---
_id: '17693'
abstract:
- lang: eng
  text: We perform one-dimensional radiation hydrodynamical simulations to solve accretion
    flows onto massive black holes (BHs) with a very high rate. Assuming that photon
    trapping limits the luminosity emerging from the central region to L≲LEdd, Inayoshi,
    Haiman & Ostriker (2016) have shown that an accretion flow settles to a "hyper-Eddington"
    solution, with a steady and isothermal (T≃8000 K) Bondi profile reaching ≳5000
    times the Eddington accretion rate M˙Edd≡LEdd/c2. Here we address the possibility
    that gas accreting with finite angular momentum forms a bright nuclear accretion
    disc, with a luminosity exceeding the Eddington limit (1≲L/LEdd≲100). Combining
    our simulations with an analytic model, we find that a transition to steady hyper-Eddington
    accretion still occurs, as long as the luminosity remains below L/LEdd≲35 (MBH/10^4
    M⊙)^3/2(n∞/10^5 cm^−3)(T∞/10^4 K)^−3/2(r⋆/10^14 cm)^−1/2, where n∞ and T∞ are
    the density and temperature of the ambient gas, and r⋆ is the radius of the photosphere,
    at which radiation emerges. If the luminosity exceeds this value, accretion becomes
    episodic. Our results can be accurately recovered in a toy model of an optically
    thick spherical shell, driven by radiation force into a collapsing medium. When
    the central source is dimmer than the above critical value, the expansion of the
    shell is halted and reversed by ram pressure of the collapsing medium, and by
    shell's weight. Our results imply that rapid, unimpeded hyper-Eddington accretion
    is possible even if the luminosity of the central source far exceeds the Eddington
    limit, and can be either steady or strongly episodic.
article_processing_charge: No
article_type: original
author:
- first_name: Yuya
  full_name: Sakurai, Yuya
  last_name: Sakurai
- first_name: Kohei
  full_name: Inayoshi, Kohei
  last_name: Inayoshi
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
citation:
  ama: Sakurai Y, Inayoshi K, Haiman Z. Hyper-Eddington mass accretion on to a black
    hole with super-Eddington luminosity. <i>Monthly Notices of the Royal Astronomical
    Society</i>. 2016;461(4):4496-4504. doi:<a href="https://doi.org/10.1093/mnras/stw1652">10.1093/mnras/stw1652</a>
  apa: Sakurai, Y., Inayoshi, K., &#38; Haiman, Z. (2016). Hyper-Eddington mass accretion
    on to a black hole with super-Eddington luminosity. <i>Monthly Notices of the
    Royal Astronomical Society</i>. Oxford University Press. <a href="https://doi.org/10.1093/mnras/stw1652">https://doi.org/10.1093/mnras/stw1652</a>
  chicago: Sakurai, Yuya, Kohei Inayoshi, and Zoltán Haiman. “Hyper-Eddington Mass
    Accretion on to a Black Hole with Super-Eddington Luminosity.” <i>Monthly Notices
    of the Royal Astronomical Society</i>. Oxford University Press, 2016. <a href="https://doi.org/10.1093/mnras/stw1652">https://doi.org/10.1093/mnras/stw1652</a>.
  ieee: Y. Sakurai, K. Inayoshi, and Z. Haiman, “Hyper-Eddington mass accretion on
    to a black hole with super-Eddington luminosity,” <i>Monthly Notices of the Royal
    Astronomical Society</i>, vol. 461, no. 4. Oxford University Press, pp. 4496–4504,
    2016.
  ista: Sakurai Y, Inayoshi K, Haiman Z. 2016. Hyper-Eddington mass accretion on to
    a black hole with super-Eddington luminosity. Monthly Notices of the Royal Astronomical
    Society. 461(4), 4496–4504.
  mla: Sakurai, Yuya, et al. “Hyper-Eddington Mass Accretion on to a Black Hole with
    Super-Eddington Luminosity.” <i>Monthly Notices of the Royal Astronomical Society</i>,
    vol. 461, no. 4, Oxford University Press, 2016, pp. 4496–504, doi:<a href="https://doi.org/10.1093/mnras/stw1652">10.1093/mnras/stw1652</a>.
  short: Y. Sakurai, K. Inayoshi, Z. Haiman, Monthly Notices of the Royal Astronomical
    Society 461 (2016) 4496–4504.
date_created: 2024-09-06T08:39:53Z
date_published: 2016-07-08T00:00:00Z
date_updated: 2024-09-25T10:02:57Z
day: '08'
doi: 10.1093/mnras/stw1652
extern: '1'
intvolume: '       461'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/mnras/stw1652
month: '07'
oa: 1
oa_version: Published Version
page: 4496-4504
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
  issn:
  - 0035-8711
  - 1365-2966
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Hyper-Eddington mass accretion on to a black hole with super-Eddington luminosity
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 461
year: '2016'
...
---
_id: '17699'
abstract:
- lang: eng
  text: 'We quantify the presence of Ly\alpha\ damping wing absorption from a partially-neutral
    intergalactic medium (IGM) in the spectrum of the z=7.08 QSO, ULASJ1120+0641.
    Using a Bayesian framework, we simultaneously account for uncertainties in: (i)
    the intrinsic QSO emission spectrum; and (ii) the distribution of cosmic HI patches
    during the epoch of reionisation (EoR). For (i) we use a new intrinsic Ly\alpha\
    emission line reconstruction method (Greig et al.), sampling a covariance matrix
    of emission line properties built from a large database of moderate-z QSOs. For
    (ii), we use the Evolution of 21-cm Structure (EOS; Mesinger et al.) simulations,
    which span a range of physically-motivated EoR models. We find strong evidence
    for the presence of damping wing absorption redward of Ly\alpha\ (where there
    is no contamination from the Ly\alpha\ forest). Our analysis implies that the
    EoR is not yet complete by z=7.1, with the volume-weighted IGM neutral fraction
    constrained to x¯HI=0.40+0.21−0.19 at 1σ (x¯HI=0.40+0.41−0.32 at 2σ). This result
    is insensitive to the EoR morphology. Our detection of significant neutral HI
    in the IGM at z=7.1 is consistent with the latest Planck 2016 measurements of
    the CMB Thompson scattering optical depth (Planck Collaboration XLVII).'
article_number: stw3351
article_processing_charge: No
article_type: original
author:
- first_name: Bradley
  full_name: Greig, Bradley
  last_name: Greig
- first_name: Andrei
  full_name: Mesinger, Andrei
  last_name: Mesinger
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
- first_name: Robert A.
  full_name: Simcoe, Robert A.
  last_name: Simcoe
citation:
  ama: Greig B, Mesinger A, Haiman Z, Simcoe RA. Are we witnessing the epoch of reionization
    at z=7.1 from the spectrum of J1120+0641? <i>Monthly Notices of the Royal Astronomical
    Society</i>. 2016. doi:<a href="https://doi.org/10.1093/mnras/stw3351">10.1093/mnras/stw3351</a>
  apa: Greig, B., Mesinger, A., Haiman, Z., &#38; Simcoe, R. A. (2016). Are we witnessing
    the epoch of reionization at z=7.1 from the spectrum of J1120+0641? <i>Monthly
    Notices of the Royal Astronomical Society</i>. Oxford University Press. <a href="https://doi.org/10.1093/mnras/stw3351">https://doi.org/10.1093/mnras/stw3351</a>
  chicago: Greig, Bradley, Andrei Mesinger, Zoltán Haiman, and Robert A. Simcoe. “Are
    We Witnessing the Epoch of Reionization at Z=7.1 from the Spectrum of J1120+0641?”
    <i>Monthly Notices of the Royal Astronomical Society</i>. Oxford University Press,
    2016. <a href="https://doi.org/10.1093/mnras/stw3351">https://doi.org/10.1093/mnras/stw3351</a>.
  ieee: B. Greig, A. Mesinger, Z. Haiman, and R. A. Simcoe, “Are we witnessing the
    epoch of reionization at z=7.1 from the spectrum of J1120+0641?,” <i>Monthly Notices
    of the Royal Astronomical Society</i>. Oxford University Press, 2016.
  ista: Greig B, Mesinger A, Haiman Z, Simcoe RA. 2016. Are we witnessing the epoch
    of reionization at z=7.1 from the spectrum of J1120+0641? Monthly Notices of the
    Royal Astronomical Society., stw3351.
  mla: Greig, Bradley, et al. “Are We Witnessing the Epoch of Reionization at Z=7.1
    from the Spectrum of J1120+0641?” <i>Monthly Notices of the Royal Astronomical
    Society</i>, stw3351, Oxford University Press, 2016, doi:<a href="https://doi.org/10.1093/mnras/stw3351">10.1093/mnras/stw3351</a>.
  short: B. Greig, A. Mesinger, Z. Haiman, R.A. Simcoe, Monthly Notices of the Royal
    Astronomical Society (2016).
date_created: 2024-09-06T08:45:10Z
date_published: 2016-12-24T00:00:00Z
date_updated: 2024-09-25T11:19:08Z
day: '24'
doi: 10.1093/mnras/stw3351
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/mnras/stw3351
month: '12'
oa: 1
oa_version: Published Version
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
  issn:
  - 0035-8711
  - 1365-2966
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Are we witnessing the epoch of reionization at z=7.1 from the spectrum of J1120+0641?
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
year: '2016'
...
---
_id: '17700'
abstract:
- lang: eng
  text: We report the formation of intermediate-mass black holes (IMBHs) in suites
    of numerical N-body simulations of Population III remnant black holes (BHs) embedded
    in gas-rich protogalaxies at redshifts z≳10. We model the effects of gas drag
    on the BHs' orbits, and allow BHs to grow via gas accretion, including a mode
    of hyper-Eddington accretion in which photon trapping and rapid gas inflow suppress
    any negative radiative feedback. Most initial BH configurations lead to the formation
    of one (but never more than one) IMBH in the center of the protogalaxy, reaching
    a mass of 10^3−5M⊙ through hyper-Eddington growth. Our results suggest a viable
    pathway to forming the earliest massive BHs in the centers of early galaxies.
    We also find that the nuclear IMBH typically captures a stellar-mass BH companion,
    making these systems observable in gravitational waves as extreme mass-ratio inspirals
    (EMRIs) with eLISA.
article_processing_charge: No
article_type: original
author:
- first_name: Taeho
  full_name: Ryu, Taeho
  last_name: Ryu
- first_name: Takamitsu L.
  full_name: Tanaka, Takamitsu L.
  last_name: Tanaka
- first_name: Rosalba
  full_name: Perna, Rosalba
  last_name: Perna
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
citation:
  ama: Ryu T, Tanaka TL, Perna R, Haiman Z. Intermediate-mass black holes from Population
    III remnants in the first galactic nuclei. <i>Monthly Notices of the Royal Astronomical
    Society</i>. 2016;460(4):4122-4134. doi:<a href="https://doi.org/10.1093/mnras/stw1241">10.1093/mnras/stw1241</a>
  apa: Ryu, T., Tanaka, T. L., Perna, R., &#38; Haiman, Z. (2016). Intermediate-mass
    black holes from Population III remnants in the first galactic nuclei. <i>Monthly
    Notices of the Royal Astronomical Society</i>. Oxford University Press. <a href="https://doi.org/10.1093/mnras/stw1241">https://doi.org/10.1093/mnras/stw1241</a>
  chicago: Ryu, Taeho, Takamitsu L. Tanaka, Rosalba Perna, and Zoltán Haiman. “Intermediate-Mass
    Black Holes from Population III Remnants in the First Galactic Nuclei.” <i>Monthly
    Notices of the Royal Astronomical Society</i>. Oxford University Press, 2016.
    <a href="https://doi.org/10.1093/mnras/stw1241">https://doi.org/10.1093/mnras/stw1241</a>.
  ieee: T. Ryu, T. L. Tanaka, R. Perna, and Z. Haiman, “Intermediate-mass black holes
    from Population III remnants in the first galactic nuclei,” <i>Monthly Notices
    of the Royal Astronomical Society</i>, vol. 460, no. 4. Oxford University Press,
    pp. 4122–4134, 2016.
  ista: Ryu T, Tanaka TL, Perna R, Haiman Z. 2016. Intermediate-mass black holes from
    Population III remnants in the first galactic nuclei. Monthly Notices of the Royal
    Astronomical Society. 460(4), 4122–4134.
  mla: Ryu, Taeho, et al. “Intermediate-Mass Black Holes from Population III Remnants
    in the First Galactic Nuclei.” <i>Monthly Notices of the Royal Astronomical Society</i>,
    vol. 460, no. 4, Oxford University Press, 2016, pp. 4122–34, doi:<a href="https://doi.org/10.1093/mnras/stw1241">10.1093/mnras/stw1241</a>.
  short: T. Ryu, T.L. Tanaka, R. Perna, Z. Haiman, Monthly Notices of the Royal Astronomical
    Society 460 (2016) 4122–4134.
date_created: 2024-09-06T08:46:28Z
date_published: 2016-05-24T00:00:00Z
date_updated: 2024-09-25T11:22:16Z
day: '24'
doi: 10.1093/mnras/stw1241
extern: '1'
intvolume: '       460'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/mnras/stw1241
month: '05'
oa: 1
oa_version: Published Version
page: 4122-4134
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
  issn:
  - 0035-8711
  - 1365-2966
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Intermediate-mass black holes from Population III remnants in the first galactic
  nuclei
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 460
year: '2016'
...
---
_id: '17709'
abstract:
- lang: eng
  text: 'We study very-high rate spherically symmetric accretion flows onto a massive
    black hole (BH; 10^2 < M_BH < 10^6 Msun) embedded in a dense gas cloud with a
    low abundance of metals, performing one-dimensional hydrodynamical simulations
    which include multi-frequency radiation transfer and non-equilibrium primordial
    chemistry. We find that rapid gas supply from the Bondi radius at a hyper-Eddington
    rate can occur without being impeded by radiation feedback when (n/10^5 cm^-3)
    > (M_BH/10^4Msun)^{-1}(T/10^4 K)^{3/2}, where n and T are the density and temperature
    of ambient gas outside of the Bondi radius. The resulting accretion rate in this
    regime is steady, and larger than 3000 times the Eddington rate. At lower Bondi
    rates, the accretion is episodic due to radiative feedback and the average rate
    is limited below the Eddington rate. For the hyper-Eddington case, the steady
    solution consists of two parts: a radiation-dominated central core, where photon
    trapping due to electron scattering is important, and an accreting envelope which
    follows a Bondi profile with T~8000 K. When the emergent luminosity is limited
    below the Eddington luminosity because of photon trapping, radiation from the
    central region does not affect the gas dynamics at larger scales. We apply our
    result to the rapid formation of massive BHs in protogalaxies with a virial temperature
    of T_vir> 10^4 K. Once a seed BH forms at the center of the galaxy, it can grow
    up to a maximum ~10^5 (T_vir/10^4 K) Msun via gas accretion independent of the
    initial BH mass. Finally, we discuss possible observational signatures of rapidly
    accreting BHs with/without allowance for dust. We suggest that these systems could
    explain Lya emitters without X-rays and luminous infrared sources with hot dust
    emission, respectively.'
article_processing_charge: No
article_type: original
author:
- first_name: Kohei
  full_name: Inayoshi, Kohei
  last_name: Inayoshi
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
- first_name: Jeremiah P.
  full_name: Ostriker, Jeremiah P.
  last_name: Ostriker
citation:
  ama: Inayoshi K, Haiman Z, Ostriker JP. Hyper-Eddington accretion flows on to massive
    black holes. <i>Monthly Notices of the Royal Astronomical Society</i>. 2016;459(4):3738-3755.
    doi:<a href="https://doi.org/10.1093/mnras/stw836">10.1093/mnras/stw836</a>
  apa: Inayoshi, K., Haiman, Z., &#38; Ostriker, J. P. (2016). Hyper-Eddington accretion
    flows on to massive black holes. <i>Monthly Notices of the Royal Astronomical
    Society</i>. Oxford University Press. <a href="https://doi.org/10.1093/mnras/stw836">https://doi.org/10.1093/mnras/stw836</a>
  chicago: Inayoshi, Kohei, Zoltán Haiman, and Jeremiah P. Ostriker. “Hyper-Eddington
    Accretion Flows on to Massive Black Holes.” <i>Monthly Notices of the Royal Astronomical
    Society</i>. Oxford University Press, 2016. <a href="https://doi.org/10.1093/mnras/stw836">https://doi.org/10.1093/mnras/stw836</a>.
  ieee: K. Inayoshi, Z. Haiman, and J. P. Ostriker, “Hyper-Eddington accretion flows
    on to massive black holes,” <i>Monthly Notices of the Royal Astronomical Society</i>,
    vol. 459, no. 4. Oxford University Press, pp. 3738–3755, 2016.
  ista: Inayoshi K, Haiman Z, Ostriker JP. 2016. Hyper-Eddington accretion flows on
    to massive black holes. Monthly Notices of the Royal Astronomical Society. 459(4),
    3738–3755.
  mla: Inayoshi, Kohei, et al. “Hyper-Eddington Accretion Flows on to Massive Black
    Holes.” <i>Monthly Notices of the Royal Astronomical Society</i>, vol. 459, no.
    4, Oxford University Press, 2016, pp. 3738–55, doi:<a href="https://doi.org/10.1093/mnras/stw836">10.1093/mnras/stw836</a>.
  short: K. Inayoshi, Z. Haiman, J.P. Ostriker, Monthly Notices of the Royal Astronomical
    Society 459 (2016) 3738–3755.
date_created: 2024-09-06T08:54:12Z
date_published: 2016-04-12T00:00:00Z
date_updated: 2024-09-25T12:00:22Z
day: '12'
doi: 10.1093/mnras/stw836
extern: '1'
intvolume: '       459'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/mnras/stw836
month: '04'
oa: 1
oa_version: Published Version
page: 3738-3755
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
  issn:
  - 0035-8711
  - 1365-2966
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Hyper-Eddington accretion flows on to massive black holes
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 459
year: '2016'
...
---
_id: '7737'
abstract:
- lang: eng
  text: Genome-wide association studies (GWAS) have identified thousands of genetic
    variants associated with human complex traits. However, the genes or functional
    DNA elements through which these variants exert their effects on the traits are
    often unknown. We propose a method (called SMR) that integrates summary-level
    data from GWAS with data from expression quantitative trait locus (eQTL) studies
    to identify genes whose expression levels are associated with a complex trait
    because of pleiotropy. We apply the method to five human complex traits using
    GWAS data on up to 339,224 individuals and eQTL data on 5,311 individuals, and
    we prioritize 126 genes (for example, TRAF1 and ANKRD55 for rheumatoid arthritis
    and SNX19 and NMRAL1 for schizophrenia), of which 25 genes are new candidates;
    77 genes are not the nearest annotated gene to the top associated GWAS SNP. These
    genes provide important leads to design future functional studies to understand
    the mechanism whereby DNA variation leads to complex trait variation.
article_processing_charge: No
article_type: original
author:
- first_name: Zhihong
  full_name: Zhu, Zhihong
  last_name: Zhu
- first_name: Futao
  full_name: Zhang, Futao
  last_name: Zhang
- first_name: Han
  full_name: Hu, Han
  last_name: Hu
- first_name: Andrew
  full_name: Bakshi, Andrew
  last_name: Bakshi
- first_name: Matthew Richard
  full_name: Robinson, Matthew Richard
  id: E5D42276-F5DA-11E9-8E24-6303E6697425
  last_name: Robinson
  orcid: 0000-0001-8982-8813
- first_name: Joseph E
  full_name: Powell, Joseph E
  last_name: Powell
- first_name: Grant W
  full_name: Montgomery, Grant W
  last_name: Montgomery
- first_name: Michael E
  full_name: Goddard, Michael E
  last_name: Goddard
- first_name: Naomi R
  full_name: Wray, Naomi R
  last_name: Wray
- first_name: Peter M
  full_name: Visscher, Peter M
  last_name: Visscher
- first_name: Jian
  full_name: Yang, Jian
  last_name: Yang
citation:
  ama: Zhu Z, Zhang F, Hu H, et al. Integration of summary data from GWAS and eQTL
    studies predicts complex trait gene targets. <i>Nature Genetics</i>. 2016;48(5):481-487.
    doi:<a href="https://doi.org/10.1038/ng.3538">10.1038/ng.3538</a>
  apa: Zhu, Z., Zhang, F., Hu, H., Bakshi, A., Robinson, M. R., Powell, J. E., … Yang,
    J. (2016). Integration of summary data from GWAS and eQTL studies predicts complex
    trait gene targets. <i>Nature Genetics</i>. Springer Nature. <a href="https://doi.org/10.1038/ng.3538">https://doi.org/10.1038/ng.3538</a>
  chicago: Zhu, Zhihong, Futao Zhang, Han Hu, Andrew Bakshi, Matthew Richard Robinson,
    Joseph E Powell, Grant W Montgomery, et al. “Integration of Summary Data from
    GWAS and EQTL Studies Predicts Complex Trait Gene Targets.” <i>Nature Genetics</i>.
    Springer Nature, 2016. <a href="https://doi.org/10.1038/ng.3538">https://doi.org/10.1038/ng.3538</a>.
  ieee: Z. Zhu <i>et al.</i>, “Integration of summary data from GWAS and eQTL studies
    predicts complex trait gene targets,” <i>Nature Genetics</i>, vol. 48, no. 5.
    Springer Nature, pp. 481–487, 2016.
  ista: Zhu Z, Zhang F, Hu H, Bakshi A, Robinson MR, Powell JE, Montgomery GW, Goddard
    ME, Wray NR, Visscher PM, Yang J. 2016. Integration of summary data from GWAS
    and eQTL studies predicts complex trait gene targets. Nature Genetics. 48(5),
    481–487.
  mla: Zhu, Zhihong, et al. “Integration of Summary Data from GWAS and EQTL Studies
    Predicts Complex Trait Gene Targets.” <i>Nature Genetics</i>, vol. 48, no. 5,
    Springer Nature, 2016, pp. 481–87, doi:<a href="https://doi.org/10.1038/ng.3538">10.1038/ng.3538</a>.
  short: Z. Zhu, F. Zhang, H. Hu, A. Bakshi, M.R. Robinson, J.E. Powell, G.W. Montgomery,
    M.E. Goddard, N.R. Wray, P.M. Visscher, J. Yang, Nature Genetics 48 (2016) 481–487.
date_created: 2020-04-30T10:50:26Z
date_published: 2016-03-28T00:00:00Z
date_updated: 2021-01-12T08:15:11Z
day: '28'
doi: 10.1038/ng.3538
extern: '1'
intvolume: '        48'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1038/ng.3538
month: '03'
oa: 1
oa_version: Published Version
page: 481-487
publication: Nature Genetics
publication_identifier:
  issn:
  - 1061-4036
  - 1546-1718
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Integration of summary data from GWAS and eQTL studies predicts complex trait
  gene targets
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 48
year: '2016'
...
---
_id: '786'
abstract:
- lang: eng
  text: Lock-free concurrent algorithms guarantee that some concurrent operation will
    always make progress in a finite number of steps. Yet programmers prefer to treat
    concurrent code as if it were wait-free, guaranteeing that all operations always
    make progress. Unfortunately, designing wait-free algorithms is generally a very
    complex task, and the resulting algorithms are not always efficient. Although
    obtaining efficient wait-free algorithms has been a long-time goal for the theory
    community, most nonblocking commercial code is only lock-free. This article suggests
    a simple solution to this problem.We show that for a large class of lock-free
    algorithms, under scheduling conditions that approximate those found in commercial
    hardware architectures, lock-free algorithms behave as if they are wait-free.
    In other words, programmers can continue to design simple lock-free algorithms
    instead of complex wait-free ones, and in practice, they will get wait-free progress.
    Our main contribution is a new way of analyzing a general class of lock-free algorithms
    under a stochastic scheduler. Our analysis relates the individual performance
    of processes to the global performance of the system using Markov chain lifting
    between a complex per-process chain and a simpler system progress chain. We show
    that lock-free algorithms are not only wait-free with probability 1 but that in
    fact a general subset of lock-free algorithms can be closely bounded in terms
    of the average number of steps required until an operation completes. To the best
    of our knowledge, this is the first attempt to analyze progress conditions, typically
    stated in relation to a worst-case adversary, in a stochastic model capturing
    their expected asymptotic behavior.
acknowledgement: Part of this work was performed while the first author was a postdoctoral
  associate at MIT CSAIL, where he was supported by the SNF Postdoctoral Fellows Program,
  NSF grant CCF-1217921, DoE ASCR grant ER26116/DE-SC0008923, and by grants from the
  Oracle and Intel corporations. The second author was supported in part by ISF grant
  1696/14. The third author was supported in part by NSF grants CCF-1217921, CCF-1301926,
  IIS-1447786, and CCF-1561807, and the U.S. Department of Energy under grant DE-SC0008923,
  and by equipment grants from Intel Corporation.
article_processing_charge: No
arxiv: 1
author:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
- first_name: Keren
  full_name: Censor Hillel, Keren
  last_name: Censor Hillel
- first_name: Nir
  full_name: Shavit, Nir
  last_name: Shavit
citation:
  ama: Alistarh D-A, Censor Hillel K, Shavit N. Are lock free concurrent algorithms
    practically wait free . <i>Journal of the ACM</i>. 2016;63(4). doi:<a href="https://doi.org/10.1145/2903136">10.1145/2903136</a>
  apa: Alistarh, D.-A., Censor Hillel, K., &#38; Shavit, N. (2016). Are lock free
    concurrent algorithms practically wait free . <i>Journal of the ACM</i>. ACM.
    <a href="https://doi.org/10.1145/2903136">https://doi.org/10.1145/2903136</a>
  chicago: Alistarh, Dan-Adrian, Keren Censor Hillel, and Nir Shavit. “Are Lock Free
    Concurrent Algorithms Practically Wait Free .” <i>Journal of the ACM</i>. ACM,
    2016. <a href="https://doi.org/10.1145/2903136">https://doi.org/10.1145/2903136</a>.
  ieee: D.-A. Alistarh, K. Censor Hillel, and N. Shavit, “Are lock free concurrent
    algorithms practically wait free ,” <i>Journal of the ACM</i>, vol. 63, no. 4.
    ACM, 2016.
  ista: Alistarh D-A, Censor Hillel K, Shavit N. 2016. Are lock free concurrent algorithms
    practically wait free . Journal of the ACM. 63(4).
  mla: Alistarh, Dan-Adrian, et al. “Are Lock Free Concurrent Algorithms Practically
    Wait Free .” <i>Journal of the ACM</i>, vol. 63, no. 4, ACM, 2016, doi:<a href="https://doi.org/10.1145/2903136">10.1145/2903136</a>.
  short: D.-A. Alistarh, K. Censor Hillel, N. Shavit, Journal of the ACM 63 (2016).
date_created: 2018-12-11T11:48:29Z
date_published: 2016-09-01T00:00:00Z
date_updated: 2023-02-23T13:19:04Z
day: '01'
doi: 10.1145/2903136
extern: '1'
external_id:
  arxiv:
  - '1311.3200'
intvolume: '        63'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1311.3200
month: '09'
oa: 1
oa_version: Preprint
publication: Journal of the ACM
publication_status: published
publisher: ACM
publist_id: '6870'
quality_controlled: '1'
status: public
title: 'Are lock free concurrent algorithms practically wait free '
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 63
year: '2016'
...
---
_id: '8020'
abstract:
- lang: eng
  text: Balance of cortical excitation and inhibition (EI) is thought to be disrupted
    in several neuropsychiatric conditions, yet it is not clear how it is maintained
    in the healthy human brain. When EI balance is disturbed during learning and memory
    in animal models, it can be restabilized via formation of inhibitory replicas
    of newly formed excitatory connections. Here we assess evidence for such selective
    inhibitory rebalancing in humans. Using fMRI repetition suppression we measure
    newly formed cortical associations in the human brain. We show that expression
    of these associations reduces over time despite persistence in behavior, consistent
    with inhibitory rebalancing. To test this, we modulated excitation/inhibition
    balance with transcranial direct current stimulation (tDCS). Using ultra-high-field
    (7T) MRI and spectroscopy, we show that reducing GABA allows cortical associations
    to be re-expressed. This suggests that in humans associative memories are stored
    in balanced excitatory-inhibitory ensembles that lie dormant unless latent inhibitory
    connections are unmasked.
article_processing_charge: No
article_type: original
author:
- first_name: H.C.
  full_name: Barron, H.C.
  last_name: Barron
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
- first_name: U.E.
  full_name: Emir, U.E.
  last_name: Emir
- first_name: T.R.
  full_name: Makin, T.R.
  last_name: Makin
- first_name: J.
  full_name: O’Shea, J.
  last_name: O’Shea
- first_name: S.
  full_name: Clare, S.
  last_name: Clare
- first_name: S.
  full_name: Jbabdi, S.
  last_name: Jbabdi
- first_name: R.J.
  full_name: Dolan, R.J.
  last_name: Dolan
- first_name: T.E.J.
  full_name: Behrens, T.E.J.
  last_name: Behrens
citation:
  ama: Barron HC, Vogels TP, Emir UE, et al. Unmasking latent inhibitory connections
    in human cortex to reveal dormant cortical memories. <i>Neuron</i>. 2016;90(1):191-203.
    doi:<a href="https://doi.org/10.1016/j.neuron.2016.02.031">10.1016/j.neuron.2016.02.031</a>
  apa: Barron, H. C., Vogels, T. P., Emir, U. E., Makin, T. R., O’Shea, J., Clare,
    S., … Behrens, T. E. J. (2016). Unmasking latent inhibitory connections in human
    cortex to reveal dormant cortical memories. <i>Neuron</i>. Elsevier. <a href="https://doi.org/10.1016/j.neuron.2016.02.031">https://doi.org/10.1016/j.neuron.2016.02.031</a>
  chicago: Barron, H.C., Tim P Vogels, U.E. Emir, T.R. Makin, J. O’Shea, S. Clare,
    S. Jbabdi, R.J. Dolan, and T.E.J. Behrens. “Unmasking Latent Inhibitory Connections
    in Human Cortex to Reveal Dormant Cortical Memories.” <i>Neuron</i>. Elsevier,
    2016. <a href="https://doi.org/10.1016/j.neuron.2016.02.031">https://doi.org/10.1016/j.neuron.2016.02.031</a>.
  ieee: H. C. Barron <i>et al.</i>, “Unmasking latent inhibitory connections in human
    cortex to reveal dormant cortical memories,” <i>Neuron</i>, vol. 90, no. 1. Elsevier,
    pp. 191–203, 2016.
  ista: Barron HC, Vogels TP, Emir UE, Makin TR, O’Shea J, Clare S, Jbabdi S, Dolan
    RJ, Behrens TEJ. 2016. Unmasking latent inhibitory connections in human cortex
    to reveal dormant cortical memories. Neuron. 90(1), 191–203.
  mla: Barron, H. C., et al. “Unmasking Latent Inhibitory Connections in Human Cortex
    to Reveal Dormant Cortical Memories.” <i>Neuron</i>, vol. 90, no. 1, Elsevier,
    2016, pp. 191–203, doi:<a href="https://doi.org/10.1016/j.neuron.2016.02.031">10.1016/j.neuron.2016.02.031</a>.
  short: H.C. Barron, T.P. Vogels, U.E. Emir, T.R. Makin, J. O’Shea, S. Clare, S.
    Jbabdi, R.J. Dolan, T.E.J. Behrens, Neuron 90 (2016) 191–203.
date_created: 2020-06-25T13:05:33Z
date_published: 2016-04-06T00:00:00Z
date_updated: 2021-01-12T08:16:34Z
day: '06'
ddc:
- '570'
doi: 10.1016/j.neuron.2016.02.031
extern: '1'
external_id:
  pmid:
  - '26996082'
file:
- access_level: open_access
  checksum: 9ce7a1c64986dce0435c070285a7ef9b
  content_type: application/pdf
  creator: cziletti
  date_created: 2020-07-09T09:57:04Z
  date_updated: 2020-07-14T12:48:08Z
  file_id: '8104'
  file_name: 2016_Neuron_Barron.pdf
  file_size: 5334136
  relation: main_file
file_date_updated: 2020-07-14T12:48:08Z
has_accepted_license: '1'
intvolume: '        90'
issue: '1'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 191-203
pmid: 1
publication: Neuron
publication_identifier:
  issn:
  - 0896-6273
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Unmasking latent inhibitory connections in human cortex to reveal dormant cortical
  memories
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 90
year: '2016'
...
---
_id: '8094'
abstract:
- lang: eng
  text: 'With the accelerated development of robot technologies, optimal control becomes
    one of the central themes of research. In traditional approaches, the controller,
    by its internal functionality, finds appropriate actions on the basis of the history
    of sensor values, guided by the goals, intentions, objectives, learning schemes,
    and so forth. The idea is that the controller controls the world---the body plus
    its environment---as reliably as possible. This paper focuses on new lines of
    self-organization for developmental robotics. We apply the recently developed
    differential extrinsic synaptic plasticity to a muscle-tendon driven arm-shoulder
    system from the Myorobotics toolkit. In the experiments, we observe a vast variety
    of self-organized behavior patterns: when left alone, the arm realizes pseudo-random
    sequences of different poses. By applying physical forces, the system can be entrained
    into definite motion patterns like wiping a table. Most interestingly, after attaching
    an object, the controller gets in a functional resonance with the object''s internal
    dynamics, starting to shake spontaneously bottles half-filled with water or sensitively
    driving an attached pendulum into a circular mode. When attached to the crank
    of a wheel the neural system independently discovers how to rotate it. In this
    way, the robot discovers affordances of objects its body is interacting with.'
article_processing_charge: No
author:
- first_name: Georg S
  full_name: Martius, Georg S
  id: 3A276B68-F248-11E8-B48F-1D18A9856A87
  last_name: Martius
- first_name: Rafael
  full_name: Hostettler, Rafael
  last_name: Hostettler
- first_name: Alois
  full_name: Knoll, Alois
  last_name: Knoll
- first_name: Ralf
  full_name: Der, Ralf
  last_name: Der
citation:
  ama: 'Martius GS, Hostettler R, Knoll A, Der R. Self-organized control of an tendon
    driven arm by differential extrinsic plasticity. In: <i>15th International Conference
    on the Synthesis and Simulation of Living Systems</i>. Vol 28. MIT Press; 2016:142-143.
    doi:<a href="https://doi.org/10.7551/978-0-262-33936-0-ch029">10.7551/978-0-262-33936-0-ch029</a>'
  apa: 'Martius, G. S., Hostettler, R., Knoll, A., &#38; Der, R. (2016). Self-organized
    control of an tendon driven arm by differential extrinsic plasticity. In <i>15th
    International Conference on the Synthesis and Simulation of Living Systems</i>
    (Vol. 28, pp. 142–143). Cancun, Mexico: MIT Press. <a href="https://doi.org/10.7551/978-0-262-33936-0-ch029">https://doi.org/10.7551/978-0-262-33936-0-ch029</a>'
  chicago: Martius, Georg S, Rafael Hostettler, Alois Knoll, and Ralf Der. “Self-Organized
    Control of an Tendon Driven Arm by Differential Extrinsic Plasticity.” In <i>15th
    International Conference on the Synthesis and Simulation of Living Systems</i>,
    28:142–43. MIT Press, 2016. <a href="https://doi.org/10.7551/978-0-262-33936-0-ch029">https://doi.org/10.7551/978-0-262-33936-0-ch029</a>.
  ieee: G. S. Martius, R. Hostettler, A. Knoll, and R. Der, “Self-organized control
    of an tendon driven arm by differential extrinsic plasticity,” in <i>15th International
    Conference on the Synthesis and Simulation of Living Systems</i>, Cancun, Mexico,
    2016, vol. 28, pp. 142–143.
  ista: 'Martius GS, Hostettler R, Knoll A, Der R. 2016. Self-organized control of
    an tendon driven arm by differential extrinsic plasticity. 15th International
    Conference on the Synthesis and Simulation of Living Systems. ALIFE 2016: Conference
    on the Synthesis and Simulation of Living Systems vol. 28, 142–143.'
  mla: Martius, Georg S., et al. “Self-Organized Control of an Tendon Driven Arm by
    Differential Extrinsic Plasticity.” <i>15th International Conference on the Synthesis
    and Simulation of Living Systems</i>, vol. 28, MIT Press, 2016, pp. 142–43, doi:<a
    href="https://doi.org/10.7551/978-0-262-33936-0-ch029">10.7551/978-0-262-33936-0-ch029</a>.
  short: G.S. Martius, R. Hostettler, A. Knoll, R. Der, in:, 15th International Conference
    on the Synthesis and Simulation of Living Systems, MIT Press, 2016, pp. 142–143.
conference:
  end_date: 2016-07-08
  location: Cancun, Mexico
  name: 'ALIFE 2016: Conference on the Synthesis and Simulation of Living Systems'
  start_date: 2016-07-04
corr_author: '1'
date_created: 2020-07-05T22:00:47Z
date_published: 2016-09-01T00:00:00Z
date_updated: 2025-07-10T11:55:05Z
day: '01'
ddc:
- '610'
department:
- _id: ChLa
- _id: GaTk
doi: 10.7551/978-0-262-33936-0-ch029
ec_funded: 1
file:
- access_level: open_access
  checksum: cff63e7a4b8ac466ba51a9c84153a940
  content_type: application/pdf
  creator: cziletti
  date_created: 2020-07-06T12:59:09Z
  date_updated: 2020-07-14T12:48:09Z
  file_id: '8096'
  file_name: 2016_ProcALIFE_Martius.pdf
  file_size: 678670
  relation: main_file
file_date_updated: 2020-07-14T12:48:09Z
has_accepted_license: '1'
intvolume: '        28'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 142-143
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: 15th International Conference on the Synthesis and Simulation of Living
  Systems
publication_identifier:
  isbn:
  - '9780262339360'
publication_status: published
publisher: MIT Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Self-organized control of an tendon driven arm by differential extrinsic plasticity
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 28
year: '2016'
...
---
_id: '8128'
abstract:
- lang: eng
  text: The stimulus selectivity of synaptic currents in cortical neurons often shows
    a co-tuning of excitation and inhibition, but the mechanisms that underlie the
    emergence and plasticity of this co-tuning are not fully understood. Using a computational
    model, we show that an interaction of excitatory and inhibitory synaptic plasticity
    reproduces both the developmental and – when combined with a disinhibitory gate
    – the adult plasticity of excitatory and inhibitory receptive fields in auditory
    cortex. The co-tuning arises from inhibitory plasticity that balances excitation
    and inhibition, while excitatory stimulus selectivity can result from two different
    mechanisms. Inhibitory inputs with a broad stimulus tuning introduce a sliding
    threshold as in Bienenstock-Cooper-Munro rules, introducing an excitatory stimulus
    selectivity at the cost of a broader inhibitory receptive field. Alternatively,
    input asymmetries can be amplified by synaptic competition. The latter leaves
    any receptive field plasticity transient, a prediction we verify in recordings
    in auditory cortex.
article_processing_charge: No
author:
- first_name: Claudia
  full_name: Clopath, Claudia
  last_name: Clopath
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
- first_name: Robert C.
  full_name: Froemke, Robert C.
  last_name: Froemke
- first_name: Henning
  full_name: Sprekeler, Henning
  last_name: Sprekeler
citation:
  ama: Clopath C, Vogels TP, Froemke RC, Sprekeler H. Receptive field formation by
    interacting excitatory and inhibitory synaptic plasticity. <i>bioRxiv</i>. 2016.
  apa: Clopath, C., Vogels, T. P., Froemke, R. C., &#38; Sprekeler, H. (2016). Receptive
    field formation by interacting excitatory and inhibitory synaptic plasticity.
    <i>bioRxiv</i>. Cold Spring Harbor Laboratory.
  chicago: Clopath, Claudia, Tim P Vogels, Robert C. Froemke, and Henning Sprekeler.
    “Receptive Field Formation by Interacting Excitatory and Inhibitory Synaptic Plasticity.”
    <i>BioRxiv</i>. Cold Spring Harbor Laboratory, 2016.
  ieee: C. Clopath, T. P. Vogels, R. C. Froemke, and H. Sprekeler, “Receptive field
    formation by interacting excitatory and inhibitory synaptic plasticity,” <i>bioRxiv</i>.
    Cold Spring Harbor Laboratory, 2016.
  ista: Clopath C, Vogels TP, Froemke RC, Sprekeler H. 2016. Receptive field formation
    by interacting excitatory and inhibitory synaptic plasticity. bioRxiv, .
  mla: Clopath, Claudia, et al. “Receptive Field Formation by Interacting Excitatory
    and Inhibitory Synaptic Plasticity.” <i>BioRxiv</i>, Cold Spring Harbor Laboratory,
    2016.
  short: C. Clopath, T.P. Vogels, R.C. Froemke, H. Sprekeler, BioRxiv (2016).
date_created: 2020-07-16T12:26:55Z
date_published: 2016-07-29T00:00:00Z
date_updated: 2021-01-12T08:17:02Z
day: '29'
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: 'https://doi.org/10.1101/066589 '
month: '07'
oa: 1
oa_version: Preprint
page: '43'
publication: bioRxiv
publication_status: published
publisher: Cold Spring Harbor Laboratory
status: public
title: Receptive field formation by interacting excitatory and inhibitory synaptic
  plasticity
type: preprint
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
year: '2016'
...
---
_id: '8241'
abstract:
- lang: eng
  text: 'Background: Anticancer vaccines could represent a valuable complementary
    strategy to established therapies, especially in settings of early stage and minimal
    residual disease. HER-2 is an important target for immunotherapy and addressed
    by the monoclonal antibody trastuzumab. We have previously generated HER-2 mimotope
    peptides from phage display libraries. The synthesized peptides were coupled to
    carriers and applied for epitope-specific induction of trastuzumab-like IgG. For
    simplification and to avoid methodological limitations of synthesis and coupling
    chemistry, we herewith present a novel and optimized approach by using adeno-associated
    viruses (AAV) as effective and high-density mimotope-display system, which can
    be directly used for vaccination. Methods: An AAV capsid display library was constructed
    by genetically incorporating random peptides in a plasmid encoding the wild-type
    AAV2 capsid protein. AAV clones, expressing peptides specifically reactive to
    trastuzumab, were employed to immunize BALB/c mice. Antibody titers against human
    HER-2 were determined, and the isotype composition and functional properties of
    these were tested. Finally, prophylactically immunized mice were challenged with
    human HER-2 transfected mouse D2F2/E2 cells. Results: HER-2 mimotope AAV-vaccines
    induced antibodies specific to human HER-2. Two clones were selected for immunization
    of mice, which were subsequently grafted D2F2/E2 cells. Both mimotope AAV clones
    delayed the growth of tumors significantly, as compared to controls. Conclusion:
    In this study, a novel mimotope AAV-based platform was created allowing the isolation
    of mimotopes, which can be directly used as anticancer vaccines. The example of
    trastuzumab AAV-mimotopes demonstrates that this vaccine strategy could help to
    establish active immunotherapy for breast-cancer patients.'
article_number: e1171446
article_processing_charge: No
article_type: original
author:
- first_name: Josef
  full_name: Singer, Josef
  last_name: Singer
- first_name: Krisztina
  full_name: Manzano-Szalai, Krisztina
  last_name: Manzano-Szalai
- first_name: Judit
  full_name: Fazekas, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Fazekas
  orcid: 0000-0002-8777-3502
- first_name: Kathrin
  full_name: Thell, Kathrin
  last_name: Thell
- first_name: Anna
  full_name: Bentley-Lukschal, Anna
  last_name: Bentley-Lukschal
- first_name: Caroline
  full_name: Stremnitzer, Caroline
  last_name: Stremnitzer
- first_name: Franziska
  full_name: Roth-Walter, Franziska
  last_name: Roth-Walter
- first_name: Margit
  full_name: Weghofer, Margit
  last_name: Weghofer
- first_name: Mirko
  full_name: Ritter, Mirko
  last_name: Ritter
- first_name: Kerstin
  full_name: Pino Tossi, Kerstin
  last_name: Pino Tossi
- first_name: Markus
  full_name: Hörer, Markus
  last_name: Hörer
- first_name: Uwe
  full_name: Michaelis, Uwe
  last_name: Michaelis
- first_name: Erika
  full_name: Jensen-Jarolim, Erika
  last_name: Jensen-Jarolim
citation:
  ama: Singer J, Manzano-Szalai K, Singer J, et al. Proof of concept study with an
    HER-2 mimotope anticancer vaccine deduced from a novel AAV-mimotope library platform.
    <i>OncoImmunology</i>. 2016;5(7). doi:<a href="https://doi.org/10.1080/2162402x.2016.1171446">10.1080/2162402x.2016.1171446</a>
  apa: Singer, J., Manzano-Szalai, K., Singer, J., Thell, K., Bentley-Lukschal, A.,
    Stremnitzer, C., … Jensen-Jarolim, E. (2016). Proof of concept study with an HER-2
    mimotope anticancer vaccine deduced from a novel AAV-mimotope library platform.
    <i>OncoImmunology</i>. Taylor &#38; Francis. <a href="https://doi.org/10.1080/2162402x.2016.1171446">https://doi.org/10.1080/2162402x.2016.1171446</a>
  chicago: Singer, Josef, Krisztina Manzano-Szalai, Judit Singer, Kathrin Thell, Anna
    Bentley-Lukschal, Caroline Stremnitzer, Franziska Roth-Walter, et al. “Proof of
    Concept Study with an HER-2 Mimotope Anticancer Vaccine Deduced from a Novel AAV-Mimotope
    Library Platform.” <i>OncoImmunology</i>. Taylor &#38; Francis, 2016. <a href="https://doi.org/10.1080/2162402x.2016.1171446">https://doi.org/10.1080/2162402x.2016.1171446</a>.
  ieee: J. Singer <i>et al.</i>, “Proof of concept study with an HER-2 mimotope anticancer
    vaccine deduced from a novel AAV-mimotope library platform,” <i>OncoImmunology</i>,
    vol. 5, no. 7. Taylor &#38; Francis, 2016.
  ista: Singer J, Manzano-Szalai K, Singer J, Thell K, Bentley-Lukschal A, Stremnitzer
    C, Roth-Walter F, Weghofer M, Ritter M, Pino Tossi K, Hörer M, Michaelis U, Jensen-Jarolim
    E. 2016. Proof of concept study with an HER-2 mimotope anticancer vaccine deduced
    from a novel AAV-mimotope library platform. OncoImmunology. 5(7), e1171446.
  mla: Singer, Josef, et al. “Proof of Concept Study with an HER-2 Mimotope Anticancer
    Vaccine Deduced from a Novel AAV-Mimotope Library Platform.” <i>OncoImmunology</i>,
    vol. 5, no. 7, e1171446, Taylor &#38; Francis, 2016, doi:<a href="https://doi.org/10.1080/2162402x.2016.1171446">10.1080/2162402x.2016.1171446</a>.
  short: J. Singer, K. Manzano-Szalai, J. Singer, K. Thell, A. Bentley-Lukschal, C.
    Stremnitzer, F. Roth-Walter, M. Weghofer, M. Ritter, K. Pino Tossi, M. Hörer,
    U. Michaelis, E. Jensen-Jarolim, OncoImmunology 5 (2016).
date_created: 2020-08-10T11:54:03Z
date_published: 2016-06-30T00:00:00Z
date_updated: 2021-01-12T08:17:41Z
day: '30'
doi: 10.1080/2162402x.2016.1171446
extern: '1'
intvolume: '         5'
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1080/2162402X.2016.1171446
month: '06'
oa: 1
oa_version: Published Version
publication: OncoImmunology
publication_identifier:
  issn:
  - 2162-402X
publication_status: published
publisher: Taylor & Francis
quality_controlled: '1'
status: public
title: Proof of concept study with an HER-2 mimotope anticancer vaccine deduced from
  a novel AAV-mimotope library platform
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 5
year: '2016'
...
---
_id: '8302'
abstract:
- lang: eng
  text: While showing great promise, Bitcoin requires users to wait tens of minutes
    for transactions to commit, and even then, offering only probabilistic guarantees.
    This paper introduces ByzCoin, a novel Byzantine consensus protocol that leverages
    scalable collective signing to commit Bitcoin transactions irreversibly within
    seconds. ByzCoin achieves Byzantine consensus while preserving Bitcoin’s open
    membership by dynamically forming hash power-proportionate consensus groups that
    represent recently-successful block miners. ByzCoin employs communication trees
    to optimize transaction commitment and verification under normal operation while
    guaranteeing safety and liveness under Byzantine faults, up to a near-optimal
    tolerance of f faulty group members among 3f + 2 total. ByzCoin mitigates double
    spending and selfish mining attacks by producing collectively signed transaction
    blocks within one minute of transaction submission. Tree-structured communication
    further reduces this latency to less than 30 seconds. Due to these optimizations,
    ByzCoin achieves a throughput higher than Paypal currently handles, with a confirmation
    latency of 15-20 seconds.
article_processing_charge: No
arxiv: 1
author:
- first_name: Eleftherios
  full_name: Kokoris Kogias, Eleftherios
  id: f5983044-d7ef-11ea-ac6d-fd1430a26d30
  last_name: Kokoris Kogias
- first_name: Philipp
  full_name: Jovanovic, Philipp
  last_name: Jovanovic
- first_name: Nicolas
  full_name: Gailly, Nicolas
  last_name: Gailly
- first_name: Ismail
  full_name: Khoffi, Ismail
  last_name: Khoffi
- first_name: Linus
  full_name: Gasser, Linus
  last_name: Gasser
- first_name: Bryan
  full_name: Ford, Bryan
  last_name: Ford
citation:
  ama: 'Kokoris Kogias E, Jovanovic P, Gailly N, Khoffi I, Gasser L, Ford B. Enhancing
    bitcoin security and performance with strong consistency via collective signing.
    In: <i>Proceedings of the 25th USENIX Conference on Security Symposium</i>. USENIX
    Association; 2016:279–296.'
  apa: 'Kokoris Kogias, E., Jovanovic, P., Gailly, N., Khoffi, I., Gasser, L., &#38;
    Ford, B. (2016). Enhancing bitcoin security and performance with strong consistency
    via collective signing. In <i>Proceedings of the 25th USENIX Conference on Security
    Symposium</i> (pp. 279–296). Austin, TX, United States: USENIX Association.'
  chicago: Kokoris Kogias, Eleftherios, Philipp Jovanovic, Nicolas Gailly, Ismail
    Khoffi, Linus Gasser, and Bryan Ford. “Enhancing Bitcoin Security and Performance
    with Strong Consistency via Collective Signing.” In <i>Proceedings of the 25th
    USENIX Conference on Security Symposium</i>, 279–296. USENIX Association, 2016.
  ieee: E. Kokoris Kogias, P. Jovanovic, N. Gailly, I. Khoffi, L. Gasser, and B. Ford,
    “Enhancing bitcoin security and performance with strong consistency via collective
    signing,” in <i>Proceedings of the 25th USENIX Conference on Security Symposium</i>,
    Austin, TX, United States, 2016, pp. 279–296.
  ista: 'Kokoris Kogias E, Jovanovic P, Gailly N, Khoffi I, Gasser L, Ford B. 2016.
    Enhancing bitcoin security and performance with strong consistency via collective
    signing. Proceedings of the 25th USENIX Conference on Security Symposium. SEC:
    Security Symposium, 279–296.'
  mla: Kokoris Kogias, Eleftherios, et al. “Enhancing Bitcoin Security and Performance
    with Strong Consistency via Collective Signing.” <i>Proceedings of the 25th USENIX
    Conference on Security Symposium</i>, USENIX Association, 2016, pp. 279–296.
  short: E. Kokoris Kogias, P. Jovanovic, N. Gailly, I. Khoffi, L. Gasser, B. Ford,
    in:, Proceedings of the 25th USENIX Conference on Security Symposium, USENIX Association,
    2016, pp. 279–296.
conference:
  end_date: 2016-08-12
  location: Austin, TX, United States
  name: 'SEC: Security Symposium'
  start_date: 2016-08-10
date_created: 2020-08-26T12:08:35Z
date_published: 2016-09-01T00:00:00Z
date_updated: 2021-01-12T08:18:00Z
day: '01'
extern: '1'
external_id:
  arxiv:
  - '1602.06997'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1602.06997
month: '09'
oa: 1
oa_version: Published Version
page: 279–296
publication: Proceedings of the 25th USENIX Conference on Security Symposium
publication_identifier:
  isbn:
  - '9781931971324'
publication_status: published
publisher: USENIX Association
quality_controlled: '1'
status: public
title: Enhancing bitcoin security and performance with strong consistency via collective
  signing
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2016'
...
---
_id: '9019'
abstract:
- lang: eng
  text: Targeting protein–protein interactions has long been considered as a very
    difficult if impossible task, but over the past decade, front lines have moved.
    The number of successful examples is exponentially growing. This review presents
    a rapid overview of recent advances in this field considering the strengths and
    weaknesses of the small molecule approaches and alternative strategies such as
    the selection or design of artificial antibodies, peptides or peptidomimetics.
- lang: fre
  text: Cibler les interactions protéine–protéine a longtemps été considéré comme
    une tâche très difficile, voire impossible, mais, depuis les dix dernières années,
    les lignes ont bougé. Le nombre d’exemples de réussites s’accroît exponentiellement.
    Cette revue présente un rapide panorama des avancées récentes dans ce domaine,
    considérant les forces et les faiblesses de l’approche « petite molécule » ainsi
    que des stratégies alternatives comme la sélection ou le design d’anticorps artificiels,
    de peptides ou de peptidomimétiques.
article_processing_charge: No
article_type: original
author:
- first_name: May M
  full_name: Bakail, May M
  id: FB3C3F8E-522F-11EA-B186-22963DDC885E
  last_name: Bakail
  orcid: 0000-0002-9592-1587
- first_name: Francoise
  full_name: Ochsenbein, Francoise
  last_name: Ochsenbein
citation:
  ama: Bakail MM, Ochsenbein F. Targeting protein–protein interactions, a wide open
    field for drug design. <i>Comptes Rendus Chimie</i>. 2016;19(1-2):19-27. doi:<a
    href="https://doi.org/10.1016/j.crci.2015.12.004">10.1016/j.crci.2015.12.004</a>
  apa: Bakail, M. M., &#38; Ochsenbein, F. (2016). Targeting protein–protein interactions,
    a wide open field for drug design. <i>Comptes Rendus Chimie</i>. Elsevier. <a
    href="https://doi.org/10.1016/j.crci.2015.12.004">https://doi.org/10.1016/j.crci.2015.12.004</a>
  chicago: Bakail, May M, and Francoise Ochsenbein. “Targeting Protein–Protein Interactions,
    a Wide Open Field for Drug Design.” <i>Comptes Rendus Chimie</i>. Elsevier, 2016.
    <a href="https://doi.org/10.1016/j.crci.2015.12.004">https://doi.org/10.1016/j.crci.2015.12.004</a>.
  ieee: M. M. Bakail and F. Ochsenbein, “Targeting protein–protein interactions, a
    wide open field for drug design,” <i>Comptes Rendus Chimie</i>, vol. 19, no. 1–2.
    Elsevier, pp. 19–27, 2016.
  ista: Bakail MM, Ochsenbein F. 2016. Targeting protein–protein interactions, a wide
    open field for drug design. Comptes Rendus Chimie. 19(1–2), 19–27.
  mla: Bakail, May M., and Francoise Ochsenbein. “Targeting Protein–Protein Interactions,
    a Wide Open Field for Drug Design.” <i>Comptes Rendus Chimie</i>, vol. 19, no.
    1–2, Elsevier, 2016, pp. 19–27, doi:<a href="https://doi.org/10.1016/j.crci.2015.12.004">10.1016/j.crci.2015.12.004</a>.
  short: M.M. Bakail, F. Ochsenbein, Comptes Rendus Chimie 19 (2016) 19–27.
date_created: 2021-01-19T11:11:54Z
date_published: 2016-02-06T00:00:00Z
date_updated: 2023-02-23T13:46:55Z
day: '06'
ddc:
- '570'
doi: 10.1016/j.crci.2015.12.004
extern: '1'
file:
- access_level: open_access
  checksum: c262814ffdbfe95900256ab9ff42cdf5
  content_type: application/pdf
  creator: dernst
  date_created: 2021-01-22T12:36:52Z
  date_updated: 2021-01-22T12:36:52Z
  file_id: '9035'
  file_name: 2016_ComptesRendueChimie_Bakail.pdf
  file_size: 2045260
  relation: main_file
  success: 1
file_date_updated: 2021-01-22T12:36:52Z
has_accepted_license: '1'
intvolume: '        19'
issue: 1-2
keyword:
- General Chemistry
- General Chemical Engineering
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 19-27
publication: Comptes Rendus Chimie
publication_identifier:
  issn:
  - 1631-0748
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Targeting protein–protein interactions, a wide open field for drug design
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 19
year: '2016'
...
---
_id: '9051'
abstract:
- lang: eng
  text: 'Biological systems often involve the self-assembly of basic components into
    complex and functioning structures. Artificial systems that mimic such processes
    can provide a well-controlled setting to explore the principles involved and also
    synthesize useful micromachines. Our experiments show that immotile, but active,
    components self-assemble into two types of structure that exhibit the fundamental
    forms of motility: translation and rotation. Specifically, micron-scale metallic
    rods are designed to induce extensile surface flows in the presence of a chemical
    fuel; these rods interact with each other and pair up to form either a swimmer
    or a rotor. Such pairs can transition reversibly between these two configurations,
    leading to kinetics reminiscent of bacterial run-and-tumble motion.'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Megan S.
  full_name: Davies Wykes, Megan S.
  last_name: Davies Wykes
- first_name: Jérémie A
  full_name: Palacci, Jérémie A
  id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
  last_name: Palacci
  orcid: 0000-0002-7253-9465
- first_name: Takuji
  full_name: Adachi, Takuji
  last_name: Adachi
- first_name: Leif
  full_name: Ristroph, Leif
  last_name: Ristroph
- first_name: Xiao
  full_name: Zhong, Xiao
  last_name: Zhong
- first_name: Michael D.
  full_name: Ward, Michael D.
  last_name: Ward
- first_name: Jun
  full_name: Zhang, Jun
  last_name: Zhang
- first_name: Michael J.
  full_name: Shelley, Michael J.
  last_name: Shelley
citation:
  ama: Davies Wykes MS, Palacci JA, Adachi T, et al. Dynamic self-assembly of microscale
    rotors and swimmers. <i>Soft Matter</i>. 2016;12(20):4584-4589. doi:<a href="https://doi.org/10.1039/c5sm03127c">10.1039/c5sm03127c</a>
  apa: Davies Wykes, M. S., Palacci, J. A., Adachi, T., Ristroph, L., Zhong, X., Ward,
    M. D., … Shelley, M. J. (2016). Dynamic self-assembly of microscale rotors and
    swimmers. <i>Soft Matter</i>. Royal Society of Chemistry. <a href="https://doi.org/10.1039/c5sm03127c">https://doi.org/10.1039/c5sm03127c</a>
  chicago: Davies Wykes, Megan S., Jérémie A Palacci, Takuji Adachi, Leif Ristroph,
    Xiao Zhong, Michael D. Ward, Jun Zhang, and Michael J. Shelley. “Dynamic Self-Assembly
    of Microscale Rotors and Swimmers.” <i>Soft Matter</i>. Royal Society of Chemistry,
    2016. <a href="https://doi.org/10.1039/c5sm03127c">https://doi.org/10.1039/c5sm03127c</a>.
  ieee: M. S. Davies Wykes <i>et al.</i>, “Dynamic self-assembly of microscale rotors
    and swimmers,” <i>Soft Matter</i>, vol. 12, no. 20. Royal Society of Chemistry,
    pp. 4584–4589, 2016.
  ista: Davies Wykes MS, Palacci JA, Adachi T, Ristroph L, Zhong X, Ward MD, Zhang
    J, Shelley MJ. 2016. Dynamic self-assembly of microscale rotors and swimmers.
    Soft Matter. 12(20), 4584–4589.
  mla: Davies Wykes, Megan S., et al. “Dynamic Self-Assembly of Microscale Rotors
    and Swimmers.” <i>Soft Matter</i>, vol. 12, no. 20, Royal Society of Chemistry,
    2016, pp. 4584–89, doi:<a href="https://doi.org/10.1039/c5sm03127c">10.1039/c5sm03127c</a>.
  short: M.S. Davies Wykes, J.A. Palacci, T. Adachi, L. Ristroph, X. Zhong, M.D. Ward,
    J. Zhang, M.J. Shelley, Soft Matter 12 (2016) 4584–4589.
date_created: 2021-02-01T13:44:00Z
date_published: 2016-05-28T00:00:00Z
date_updated: 2023-02-23T13:47:38Z
day: '28'
doi: 10.1039/c5sm03127c
extern: '1'
external_id:
  arxiv:
  - '1509.06330'
  pmid:
  - '27121100'
intvolume: '        12'
issue: '20'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1509.06330
month: '05'
oa: 1
oa_version: Preprint
page: 4584-4589
pmid: 1
publication: Soft Matter
publication_identifier:
  eissn:
  - 1744-6848
  issn:
  - 1744-683X
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic self-assembly of microscale rotors and swimmers
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 12
year: '2016'
...
---
_id: '9052'
abstract:
- lang: eng
  text: We describe colloidal Janus particles with metallic and dielectric faces that
    swim vigorously when illuminated by defocused optical tweezers without consuming
    any chemical fuel. Rather than wandering randomly, these optically-activated colloidal
    swimmers circulate back and forth through the beam of light, tracing out sinuous
    rosette patterns. We propose a model for this mode of light-activated transport
    that accounts for the observed behavior through a combination of self-thermophoresis
    and optically-induced torque. In the deterministic limit, this model yields trajectories
    that resemble rosette curves known as hypotrochoids.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Henrique
  full_name: Moyses, Henrique
  last_name: Moyses
- first_name: Jérémie A
  full_name: Palacci, Jérémie A
  id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
  last_name: Palacci
  orcid: 0000-0002-7253-9465
- first_name: Stefano
  full_name: Sacanna, Stefano
  last_name: Sacanna
- first_name: David G.
  full_name: Grier, David G.
  last_name: Grier
citation:
  ama: Moyses H, Palacci JA, Sacanna S, Grier DG. Trochoidal trajectories of self-propelled
    Janus particles in a diverging laser beam. <i>Soft Matter</i>. 2016;12(30):6357-6364.
    doi:<a href="https://doi.org/10.1039/c6sm01163b">10.1039/c6sm01163b</a>
  apa: Moyses, H., Palacci, J. A., Sacanna, S., &#38; Grier, D. G. (2016). Trochoidal
    trajectories of self-propelled Janus particles in a diverging laser beam. <i>Soft
    Matter</i>. Royal Society of Chemistry . <a href="https://doi.org/10.1039/c6sm01163b">https://doi.org/10.1039/c6sm01163b</a>
  chicago: Moyses, Henrique, Jérémie A Palacci, Stefano Sacanna, and David G. Grier.
    “Trochoidal Trajectories of Self-Propelled Janus Particles in a Diverging Laser
    Beam.” <i>Soft Matter</i>. Royal Society of Chemistry , 2016. <a href="https://doi.org/10.1039/c6sm01163b">https://doi.org/10.1039/c6sm01163b</a>.
  ieee: H. Moyses, J. A. Palacci, S. Sacanna, and D. G. Grier, “Trochoidal trajectories
    of self-propelled Janus particles in a diverging laser beam,” <i>Soft Matter</i>,
    vol. 12, no. 30. Royal Society of Chemistry , pp. 6357–6364, 2016.
  ista: Moyses H, Palacci JA, Sacanna S, Grier DG. 2016. Trochoidal trajectories of
    self-propelled Janus particles in a diverging laser beam. Soft Matter. 12(30),
    6357–6364.
  mla: Moyses, Henrique, et al. “Trochoidal Trajectories of Self-Propelled Janus Particles
    in a Diverging Laser Beam.” <i>Soft Matter</i>, vol. 12, no. 30, Royal Society
    of Chemistry , 2016, pp. 6357–64, doi:<a href="https://doi.org/10.1039/c6sm01163b">10.1039/c6sm01163b</a>.
  short: H. Moyses, J.A. Palacci, S. Sacanna, D.G. Grier, Soft Matter 12 (2016) 6357–6364.
date_created: 2021-02-01T13:44:15Z
date_published: 2016-08-14T00:00:00Z
date_updated: 2023-02-23T13:47:40Z
day: '14'
doi: 10.1039/c6sm01163b
extern: '1'
external_id:
  arxiv:
  - '1609.01497'
  pmid:
  - '27338294'
intvolume: '        12'
issue: '30'
keyword:
- General Chemistry
- Condensed Matter Physics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1609.01497
month: '08'
oa: 1
oa_version: Preprint
page: 6357-6364
pmid: 1
publication: Soft Matter
publication_identifier:
  eissn:
  - 1744-6848
  issn:
  - 1744-683X
publication_status: published
publisher: 'Royal Society of Chemistry '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Trochoidal trajectories of self-propelled Janus particles in a diverging laser
  beam
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 12
year: '2016'
...
---
_id: '9140'
abstract:
- lang: eng
  text: 'Expected changes to future extreme precipitation remain a key uncertainty
    associated with anthropogenic climate change. Extreme precipitation has been proposed
    to scale with the precipitable water content in the atmosphere. Assuming constant
    relative humidity, this implies an increase of precipitation extremes at a rate
    of about 7% °C−1 globally as indicated by the Clausius‐Clapeyron relationship.
    Increases faster and slower than Clausius‐Clapeyron have also been reported. In
    this work, we examine the scaling between precipitation extremes and temperature
    in the present climate using simulations and measurements from surface weather
    stations collected in the frame of the HyMeX and MED‐CORDEX programs in Southern
    France. Of particular interest are departures from the Clausius‐Clapeyron thermodynamic
    expectation, their spatial and temporal distribution, and their origin. Looking
    at the scaling of precipitation extreme with temperature, two regimes emerge which
    form a hook shape: one at low temperatures (cooler than around 15°C) with rates
    of increase close to the Clausius‐Clapeyron rate and one at high temperatures
    (warmer than about 15°C) with sub‐Clausius‐Clapeyron rates and most often negative
    rates. On average, the region of focus does not seem to exhibit super Clausius‐Clapeyron
    behavior except at some stations, in contrast to earlier studies. Many factors
    can contribute to departure from Clausius‐Clapeyron scaling: time and spatial
    averaging, choice of scaling temperature (surface versus condensation level),
    and precipitation efficiency and vertical velocity in updrafts that are not necessarily
    constant with temperature. But most importantly, the dynamical contribution of
    orography to precipitation in the fall over this area during the so‐called “Cevenoles”
    events, explains the hook shape of the scaling of precipitation extremes.'
article_processing_charge: No
article_type: original
author:
- first_name: P.
  full_name: Drobinski, P.
  last_name: Drobinski
- first_name: B.
  full_name: Alonzo, B.
  last_name: Alonzo
- first_name: S.
  full_name: Bastin, S.
  last_name: Bastin
- first_name: N. Da
  full_name: Silva, N. Da
  last_name: Silva
- first_name: Caroline J
  full_name: Muller, Caroline J
  id: f978ccb0-3f7f-11eb-b193-b0e2bd13182b
  last_name: Muller
  orcid: 0000-0001-5836-5350
citation:
  ama: 'Drobinski P, Alonzo B, Bastin S, Silva ND, Muller CJ. Scaling of precipitation
    extremes with temperature in the French Mediterranean region: What explains the
    hook shape? <i>Journal of Geophysical Research: Atmospheres</i>. 2016;121(7):3100-3119.
    doi:<a href="https://doi.org/10.1002/2015jd023497">10.1002/2015jd023497</a>'
  apa: 'Drobinski, P., Alonzo, B., Bastin, S., Silva, N. D., &#38; Muller, C. J. (2016).
    Scaling of precipitation extremes with temperature in the French Mediterranean
    region: What explains the hook shape? <i>Journal of Geophysical Research: Atmospheres</i>.
    American Geophysical Union. <a href="https://doi.org/10.1002/2015jd023497">https://doi.org/10.1002/2015jd023497</a>'
  chicago: 'Drobinski, P., B. Alonzo, S. Bastin, N. Da Silva, and Caroline J Muller.
    “Scaling of Precipitation Extremes with Temperature in the French Mediterranean
    Region: What Explains the Hook Shape?” <i>Journal of Geophysical Research: Atmospheres</i>.
    American Geophysical Union, 2016. <a href="https://doi.org/10.1002/2015jd023497">https://doi.org/10.1002/2015jd023497</a>.'
  ieee: 'P. Drobinski, B. Alonzo, S. Bastin, N. D. Silva, and C. J. Muller, “Scaling
    of precipitation extremes with temperature in the French Mediterranean region:
    What explains the hook shape?,” <i>Journal of Geophysical Research: Atmospheres</i>,
    vol. 121, no. 7. American Geophysical Union, pp. 3100–3119, 2016.'
  ista: 'Drobinski P, Alonzo B, Bastin S, Silva ND, Muller CJ. 2016. Scaling of precipitation
    extremes with temperature in the French Mediterranean region: What explains the
    hook shape? Journal of Geophysical Research: Atmospheres. 121(7), 3100–3119.'
  mla: 'Drobinski, P., et al. “Scaling of Precipitation Extremes with Temperature
    in the French Mediterranean Region: What Explains the Hook Shape?” <i>Journal
    of Geophysical Research: Atmospheres</i>, vol. 121, no. 7, American Geophysical
    Union, 2016, pp. 3100–19, doi:<a href="https://doi.org/10.1002/2015jd023497">10.1002/2015jd023497</a>.'
  short: 'P. Drobinski, B. Alonzo, S. Bastin, N.D. Silva, C.J. Muller, Journal of
    Geophysical Research: Atmospheres 121 (2016) 3100–3119.'
date_created: 2021-02-15T14:21:16Z
date_published: 2016-03-16T00:00:00Z
date_updated: 2022-01-24T13:41:02Z
day: '16'
doi: 10.1002/2015jd023497
extern: '1'
intvolume: '       121'
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1002/2015JD023497
month: '03'
oa: 1
oa_version: Published Version
page: 3100-3119
publication: 'Journal of Geophysical Research: Atmospheres'
publication_identifier:
  issn:
  - 2169-897X
  - 2169-8996
publication_status: published
publisher: American Geophysical Union
quality_controlled: '1'
status: public
title: 'Scaling of precipitation extremes with temperature in the French Mediterranean
  region: What explains the hook shape?'
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 121
year: '2016'
...
---
_id: '9456'
abstract:
- lang: eng
  text: The discovery of introns four decades ago was one of the most unexpected findings
    in molecular biology. Introns are sequences interrupting genes that must be removed
    as part of messenger RNA production. Genome sequencing projects have shown that
    most eukaryotic genes contain at least one intron, and frequently many. Comparison
    of these genomes reveals a history of long evolutionary periods during which few
    introns were gained, punctuated by episodes of rapid, extensive gain. However,
    although several detailed mechanisms for such episodic intron generation have
    been proposed, none has been empirically supported on a genomic scale. Here we
    show how short, non-autonomous DNA transposons independently generated hundreds
    to thousands of introns in the prasinophyte Micromonas pusilla and the pelagophyte
    Aureococcus anophagefferens. Each transposon carries one splice site. The other
    splice site is co-opted from the gene sequence that is duplicated upon transposon
    insertion, allowing perfect splicing out of the RNA. The distributions of sequences
    that can be co-opted are biased with respect to codons, and phasing of transposon-generated
    introns is similarly biased. These transposons insert between pre-existing nucleosomes,
    so that multiple nearby insertions generate nucleosome-sized intervening segments.
    Thus, transposon insertion and sequence co-option may explain the intron phase
    biases and prevalence of nucleosome-sized exons observed in eukaryotes. Overall,
    the two independent examples of proliferating elements illustrate a general DNA
    transposon mechanism that can plausibly account for episodes of rapid, extensive
    intron gain during eukaryotic evolution.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Jason T.
  full_name: Huff, Jason T.
  last_name: Huff
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Scott W.
  full_name: Roy, Scott W.
  last_name: Roy
citation:
  ama: Huff JT, Zilberman D, Roy SW. Mechanism for DNA transposons to generate introns
    on genomic scales. <i>Nature</i>. 2016;538(7626):533-536. doi:<a href="https://doi.org/10.1038/nature20110">10.1038/nature20110</a>
  apa: Huff, J. T., Zilberman, D., &#38; Roy, S. W. (2016). Mechanism for DNA transposons
    to generate introns on genomic scales. <i>Nature</i>. Springer Nature . <a href="https://doi.org/10.1038/nature20110">https://doi.org/10.1038/nature20110</a>
  chicago: Huff, Jason T., Daniel Zilberman, and Scott W. Roy. “Mechanism for DNA
    Transposons to Generate Introns on Genomic Scales.” <i>Nature</i>. Springer Nature
    , 2016. <a href="https://doi.org/10.1038/nature20110">https://doi.org/10.1038/nature20110</a>.
  ieee: J. T. Huff, D. Zilberman, and S. W. Roy, “Mechanism for DNA transposons to
    generate introns on genomic scales,” <i>Nature</i>, vol. 538, no. 7626. Springer
    Nature , pp. 533–536, 2016.
  ista: Huff JT, Zilberman D, Roy SW. 2016. Mechanism for DNA transposons to generate
    introns on genomic scales. Nature. 538(7626), 533–536.
  mla: Huff, Jason T., et al. “Mechanism for DNA Transposons to Generate Introns on
    Genomic Scales.” <i>Nature</i>, vol. 538, no. 7626, Springer Nature , 2016, pp.
    533–36, doi:<a href="https://doi.org/10.1038/nature20110">10.1038/nature20110</a>.
  short: J.T. Huff, D. Zilberman, S.W. Roy, Nature 538 (2016) 533–536.
date_created: 2021-06-04T11:34:55Z
date_published: 2016-10-27T00:00:00Z
date_updated: 2021-12-14T07:55:30Z
day: '27'
department:
- _id: DaZi
doi: 10.1038/nature20110
extern: '1'
external_id:
  pmid:
  - '27760113'
intvolume: '       538'
issue: '7626'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684705/
month: '10'
oa: 1
oa_version: Submitted Version
page: 533-536
pmid: 1
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: 'Springer Nature '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mechanism for DNA transposons to generate introns on genomic scales
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 538
year: '2016'
...
---
_id: '9473'
abstract:
- lang: eng
  text: Cytosine DNA methylation regulates the expression of eukaryotic genes and
    transposons. Methylation is copied by methyltransferases after DNA replication,
    which results in faithful transmission of methylation patterns during cell division
    and, at least in flowering plants, across generations. Transgenerational inheritance
    is mediated by a small group of cells that includes gametes and their progenitors.
    However, methylation is usually analyzed in somatic tissues that do not contribute
    to the next generation, and the mechanisms of transgenerational inheritance are
    inferred from such studies. To gain a better understanding of how DNA methylation
    is inherited, we analyzed purified Arabidopsis thaliana sperm and vegetative cells-the
    cell types that comprise pollen-with mutations in the DRM, CMT2, and CMT3 methyltransferases.
    We find that DNA methylation dependency on these enzymes is similar in sperm,
    vegetative cells, and somatic tissues, although DRM activity extends into heterochromatin
    in vegetative cells, likely reflecting transcription of heterochromatic transposons
    in this cell type. We also show that lack of histone H1, which elevates heterochromatic
    DNA methylation in somatic tissues, does not have this effect in pollen. Instead,
    levels of CG methylation in wild-type sperm and vegetative cells, as well as in
    wild-type microspores from which both pollen cell types originate, are substantially
    higher than in wild-type somatic tissues and similar to those of H1-depleted roots.
    Our results demonstrate that the mechanisms of methylation maintenance are similar
    between pollen and somatic cells, but the efficiency of CG methylation is higher
    in pollen, allowing methylation patterns to be accurately inherited across generations.
article_processing_charge: No
article_type: original
author:
- first_name: Ping-Hung
  full_name: Hsieh, Ping-Hung
  last_name: Hsieh
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Toby
  full_name: Buttress, Toby
  last_name: Buttress
- first_name: Hongbo
  full_name: Gao, Hongbo
  last_name: Gao
- first_name: Matthew
  full_name: Couchman, Matthew
  last_name: Couchman
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Hsieh P-H, He S, Buttress T, et al. Arabidopsis male sexual lineage exhibits
    more robust maintenance of CG methylation than somatic tissues. <i>Proceedings
    of the National Academy of Sciences</i>. 2016;113(52):15132-15137. doi:<a href="https://doi.org/10.1073/pnas.1619074114">10.1073/pnas.1619074114</a>
  apa: Hsieh, P.-H., He, S., Buttress, T., Gao, H., Couchman, M., Fischer, R. L.,
    … Feng, X. (2016). Arabidopsis male sexual lineage exhibits more robust maintenance
    of CG methylation than somatic tissues. <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1619074114">https://doi.org/10.1073/pnas.1619074114</a>
  chicago: Hsieh, Ping-Hung, Shengbo He, Toby Buttress, Hongbo Gao, Matthew Couchman,
    Robert L. Fischer, Daniel Zilberman, and Xiaoqi Feng. “Arabidopsis Male Sexual
    Lineage Exhibits More Robust Maintenance of CG Methylation than Somatic Tissues.”
    <i>Proceedings of the National Academy of Sciences</i>. National Academy of Sciences,
    2016. <a href="https://doi.org/10.1073/pnas.1619074114">https://doi.org/10.1073/pnas.1619074114</a>.
  ieee: P.-H. Hsieh <i>et al.</i>, “Arabidopsis male sexual lineage exhibits more
    robust maintenance of CG methylation than somatic tissues,” <i>Proceedings of
    the National Academy of Sciences</i>, vol. 113, no. 52. National Academy of Sciences,
    pp. 15132–15137, 2016.
  ista: Hsieh P-H, He S, Buttress T, Gao H, Couchman M, Fischer RL, Zilberman D, Feng
    X. 2016. Arabidopsis male sexual lineage exhibits more robust maintenance of CG
    methylation than somatic tissues. Proceedings of the National Academy of Sciences.
    113(52), 15132–15137.
  mla: Hsieh, Ping-Hung, et al. “Arabidopsis Male Sexual Lineage Exhibits More Robust
    Maintenance of CG Methylation than Somatic Tissues.” <i>Proceedings of the National
    Academy of Sciences</i>, vol. 113, no. 52, National Academy of Sciences, 2016,
    pp. 15132–37, doi:<a href="https://doi.org/10.1073/pnas.1619074114">10.1073/pnas.1619074114</a>.
  short: P.-H. Hsieh, S. He, T. Buttress, H. Gao, M. Couchman, R.L. Fischer, D. Zilberman,
    X. Feng, Proceedings of the National Academy of Sciences 113 (2016) 15132–15137.
date_created: 2021-06-07T06:21:39Z
date_published: 2016-12-27T00:00:00Z
date_updated: 2023-05-08T11:00:40Z
day: '27'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1073/pnas.1619074114
extern: '1'
external_id:
  pmid:
  - '27956643'
intvolume: '       113'
issue: '52'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1619074114
month: '12'
oa: 1
oa_version: Published Version
page: 15132-15137
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arabidopsis male sexual lineage exhibits more robust maintenance of CG methylation
  than somatic tissues
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 113
year: '2016'
...
---
_id: '9477'
abstract:
- lang: eng
  text: Cytosine methylation is a DNA modification with important regulatory functions
    in eukaryotes. In flowering plants, sexual reproduction is accompanied by extensive
    DNA demethylation, which is required for proper gene expression in the endosperm,
    a nutritive extraembryonic seed tissue. Endosperm arises from a fusion of a sperm
    cell carried in the pollen and a female central cell. Endosperm DNA demethylation
    is observed specifically on the chromosomes inherited from the central cell in
    Arabidopsis thaliana, rice, and maize, and requires the DEMETER DNA demethylase
    in Arabidopsis. DEMETER is expressed in the central cell before fertilization,
    suggesting that endosperm demethylation patterns are inherited from the central
    cell. Down-regulation of the MET1 DNA methyltransferase has also been proposed
    to contribute to central cell demethylation. However, with the exception of three
    maize genes, central cell DNA methylation has not been directly measured, leaving
    the origin and mechanism of endosperm demethylation uncertain. Here, we report
    genome-wide analysis of DNA methylation in the central cells of Arabidopsis and
    rice—species that diverged 150 million years ago—as well as in rice egg cells.
    We find that DNA demethylation in both species is initiated in central cells,
    which requires DEMETER in Arabidopsis. However, we do not observe a global reduction
    of CG methylation that would be indicative of lowered MET1 activity; on the contrary,
    CG methylation efficiency is elevated in female gametes compared with nonsexual
    tissues. Our results demonstrate that locus-specific, active DNA demethylation
    in the central cell is the origin of maternal chromosome hypomethylation in the
    endosperm.
article_processing_charge: No
article_type: original
author:
- first_name: Kyunghyuk
  full_name: Park, Kyunghyuk
  last_name: Park
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Jin-Sup
  full_name: Park, Jin-Sup
  last_name: Park
- first_name: Youbong
  full_name: Hyun, Youbong
  last_name: Hyun
- first_name: Takashi
  full_name: Okamoto, Takashi
  last_name: Okamoto
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Yeonhee
  full_name: Choi, Yeonhee
  last_name: Choi
- first_name: Stefan
  full_name: Scholten, Stefan
  last_name: Scholten
citation:
  ama: Park K, Kim MY, Vickers M, et al. DNA demethylation is initiated in the central
    cells of Arabidopsis and rice. <i>Proceedings of the National Academy of Sciences</i>.
    2016;113(52):15138-15143. doi:<a href="https://doi.org/10.1073/pnas.1619047114">10.1073/pnas.1619047114</a>
  apa: Park, K., Kim, M. Y., Vickers, M., Park, J.-S., Hyun, Y., Okamoto, T., … Scholten,
    S. (2016). DNA demethylation is initiated in the central cells of Arabidopsis
    and rice. <i>Proceedings of the National Academy of Sciences</i>. National Academy
    of Sciences. <a href="https://doi.org/10.1073/pnas.1619047114">https://doi.org/10.1073/pnas.1619047114</a>
  chicago: Park, Kyunghyuk, M. Yvonne Kim, Martin Vickers, Jin-Sup Park, Youbong Hyun,
    Takashi Okamoto, Daniel Zilberman, et al. “DNA Demethylation Is Initiated in the
    Central Cells of Arabidopsis and Rice.” <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences, 2016. <a href="https://doi.org/10.1073/pnas.1619047114">https://doi.org/10.1073/pnas.1619047114</a>.
  ieee: K. Park <i>et al.</i>, “DNA demethylation is initiated in the central cells
    of Arabidopsis and rice,” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 113, no. 52. National Academy of Sciences, pp. 15138–15143, 2016.
  ista: Park K, Kim MY, Vickers M, Park J-S, Hyun Y, Okamoto T, Zilberman D, Fischer
    RL, Feng X, Choi Y, Scholten S. 2016. DNA demethylation is initiated in the central
    cells of Arabidopsis and rice. Proceedings of the National Academy of Sciences.
    113(52), 15138–15143.
  mla: Park, Kyunghyuk, et al. “DNA Demethylation Is Initiated in the Central Cells
    of Arabidopsis and Rice.” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 113, no. 52, National Academy of Sciences, 2016, pp. 15138–43, doi:<a href="https://doi.org/10.1073/pnas.1619047114">10.1073/pnas.1619047114</a>.
  short: K. Park, M.Y. Kim, M. Vickers, J.-S. Park, Y. Hyun, T. Okamoto, D. Zilberman,
    R.L. Fischer, X. Feng, Y. Choi, S. Scholten, Proceedings of the National Academy
    of Sciences 113 (2016) 15138–15143.
date_created: 2021-06-07T07:10:59Z
date_published: 2016-12-27T00:00:00Z
date_updated: 2023-05-08T11:00:07Z
day: '27'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1073/pnas.1619047114
extern: '1'
external_id:
  pmid:
  - '27956642'
intvolume: '       113'
issue: '52'
keyword:
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1619047114
month: '12'
oa: 1
oa_version: Published Version
page: 15138-15143
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA demethylation is initiated in the central cells of Arabidopsis and rice
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 113
year: '2016'
...
---
_id: '948'
abstract:
- lang: eng
  text: Experience constantly shapes neural circuits through a variety of plasticity
    mechanisms. While the functional roles of some plasticity mechanisms are well-understood,
    it remains unclear how changes in neural excitability contribute to learning.
    Here, we develop a normative interpretation of intrinsic plasticity (IP) as a
    key component of unsupervised learning. We introduce a novel generative mixture
    model that accounts for the class-specific statistics of stimulus intensities,
    and we derive a neural circuit that learns the input classes and their intensities.
    We will analytically show that inference and learning for our generative model
    can be achieved by a neural circuit with intensity-sensitive neurons equipped
    with a specific form of IP. Numerical experiments verify our analytical derivations
    and show robust behavior for artificial and natural stimuli. Our results link
    IP to non-trivial input statistics, in particular the statistics of stimulus intensities
    for classes to which a neuron is sensitive. More generally, our work paves the
    way toward new classification algorithms that are robust to intensity variations.
acknowledgement: DFG Cluster of Excellence EXC 1077/1 (Hearing4all) and  LU 1196/5-1
  (JL and TM), People Programme (Marie Curie Actions) FP7/2007-2013 grant agreement
  no. 291734 (CS)
alternative_title:
- Advances in Neural Information Processing Systems
article_processing_charge: No
author:
- first_name: Travis
  full_name: Monk, Travis
  last_name: Monk
- first_name: Cristina
  full_name: Savin, Cristina
  id: 3933349E-F248-11E8-B48F-1D18A9856A87
  last_name: Savin
- first_name: Jörg
  full_name: Lücke, Jörg
  last_name: Lücke
citation:
  ama: 'Monk T, Savin C, Lücke J. Neurons equipped with intrinsic plasticity learn
    stimulus intensity statistics. In: Vol 29. Neural Information Processing Systems
    Foundation; 2016:4285-4293.'
  apa: 'Monk, T., Savin, C., &#38; Lücke, J. (2016). Neurons equipped with intrinsic
    plasticity learn stimulus intensity statistics (Vol. 29, pp. 4285–4293). Presented
    at the NIPS: Neural Information Processing Systems, Barcelona, Spaine: Neural
    Information Processing Systems Foundation.'
  chicago: Monk, Travis, Cristina Savin, and Jörg Lücke. “Neurons Equipped with Intrinsic
    Plasticity Learn Stimulus Intensity Statistics,” 29:4285–93. Neural Information
    Processing Systems Foundation, 2016.
  ieee: 'T. Monk, C. Savin, and J. Lücke, “Neurons equipped with intrinsic plasticity
    learn stimulus intensity statistics,” presented at the NIPS: Neural Information
    Processing Systems, Barcelona, Spaine, 2016, vol. 29, pp. 4285–4293.'
  ista: 'Monk T, Savin C, Lücke J. 2016. Neurons equipped with intrinsic plasticity
    learn stimulus intensity statistics. NIPS: Neural Information Processing Systems,
    Advances in Neural Information Processing Systems, vol. 29, 4285–4293.'
  mla: Monk, Travis, et al. <i>Neurons Equipped with Intrinsic Plasticity Learn Stimulus
    Intensity Statistics</i>. Vol. 29, Neural Information Processing Systems Foundation,
    2016, pp. 4285–93.
  short: T. Monk, C. Savin, J. Lücke, in:, Neural Information Processing Systems Foundation,
    2016, pp. 4285–4293.
conference:
  end_date: 2016-12-10
  location: Barcelona, Spaine
  name: 'NIPS: Neural Information Processing Systems'
  start_date: 2016-12-05
date_created: 2018-12-11T11:49:21Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2025-06-03T11:18:32Z
day: '01'
department:
- _id: GaTk
ec_funded: 1
intvolume: '        29'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://papers.nips.cc/paper/6582-neurons-equipped-with-intrinsic-plasticity-learn-stimulus-intensity-statistics
month: '01'
oa: 1
oa_version: None
page: 4285 - 4293
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication_status: published
publisher: Neural Information Processing Systems Foundation
publist_id: '6469'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Neurons equipped with intrinsic plasticity learn stimulus intensity statistics
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 29
year: '2016'
...
---
_id: '9591'
abstract:
- lang: eng
  text: We give several results showing that different discrete structures typically
    gain certain spanning substructures (in particular, Hamilton cycles) after a modest
    random perturbation. First, we prove that adding linearly many random edges to
    a dense k-uniform hypergraph ensures the (asymptotically almost sure) existence
    of a perfect matching or a loose Hamilton cycle. The proof involves an interesting
    application of Szemerédi's Regularity Lemma, which might be independently useful.
    We next prove that digraphs with certain strong expansion properties are pancyclic,
    and use this to show that adding a linear number of random edges typically makes
    a dense digraph pancyclic. Finally, we prove that perturbing a certain (minimum-degree-dependent)
    number of random edges in a tournament typically ensures the existence of multiple
    edge-disjoint Hamilton cycles. All our results are tight.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Michael
  full_name: Krivelevich, Michael
  last_name: Krivelevich
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: Benny
  full_name: Sudakov, Benny
  last_name: Sudakov
citation:
  ama: Krivelevich M, Kwan MA, Sudakov B. Cycles and matchings in randomly perturbed
    digraphs and hypergraphs. <i>Combinatorics, Probability and Computing</i>. 2016;25(6):909-927.
    doi:<a href="https://doi.org/10.1017/s0963548316000079">10.1017/s0963548316000079</a>
  apa: Krivelevich, M., Kwan, M. A., &#38; Sudakov, B. (2016). Cycles and matchings
    in randomly perturbed digraphs and hypergraphs. <i>Combinatorics, Probability
    and Computing</i>. Cambridge University Press. <a href="https://doi.org/10.1017/s0963548316000079">https://doi.org/10.1017/s0963548316000079</a>
  chicago: Krivelevich, Michael, Matthew Alan Kwan, and Benny Sudakov. “Cycles and
    Matchings in Randomly Perturbed Digraphs and Hypergraphs.” <i>Combinatorics, Probability
    and Computing</i>. Cambridge University Press, 2016. <a href="https://doi.org/10.1017/s0963548316000079">https://doi.org/10.1017/s0963548316000079</a>.
  ieee: M. Krivelevich, M. A. Kwan, and B. Sudakov, “Cycles and matchings in randomly
    perturbed digraphs and hypergraphs,” <i>Combinatorics, Probability and Computing</i>,
    vol. 25, no. 6. Cambridge University Press, pp. 909–927, 2016.
  ista: Krivelevich M, Kwan MA, Sudakov B. 2016. Cycles and matchings in randomly
    perturbed digraphs and hypergraphs. Combinatorics, Probability and Computing.
    25(6), 909–927.
  mla: Krivelevich, Michael, et al. “Cycles and Matchings in Randomly Perturbed Digraphs
    and Hypergraphs.” <i>Combinatorics, Probability and Computing</i>, vol. 25, no.
    6, Cambridge University Press, 2016, pp. 909–27, doi:<a href="https://doi.org/10.1017/s0963548316000079">10.1017/s0963548316000079</a>.
  short: M. Krivelevich, M.A. Kwan, B. Sudakov, Combinatorics, Probability and Computing
    25 (2016) 909–927.
date_created: 2021-06-22T12:35:13Z
date_published: 2016-11-01T00:00:00Z
date_updated: 2023-02-23T14:02:07Z
day: '01'
doi: 10.1017/s0963548316000079
extern: '1'
external_id:
  arxiv:
  - '1501.04816'
intvolume: '        25'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1501.04816
month: '11'
oa: 1
oa_version: Preprint
page: 909-927
publication: Combinatorics, Probability and Computing
publication_identifier:
  eissn:
  - 1469-2163
  issn:
  - 0963-5483
publication_status: published
publisher: Cambridge University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cycles and matchings in randomly perturbed digraphs and hypergraphs
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 25
year: '2016'
...
