---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '21378'
abstract:
- lang: eng
  text: From insects to mammals, essential brain functions, such as forming long-term
    memories (LTMs), increase metabolic activity in stimulated neurons to meet the
    energetic demand associated with brain activation. However, while impairing neuronal
    metabolism limits brain performance, whether expanding the metabolic capacity
    of neurons boosts brain function remains poorly understood. Here, we show that
    LTM formation of flies and mice can be enhanced by increasing mitochondrial metabolism
    in central memory circuits. By knocking down the mitochondrial Ca2+ exporter Letm1,
    we favour Ca2+ retention in the mitochondrial matrix of neurons due to reduction
    of mitochondrial H+/Ca2+ exchange. The resulting increase in mitochondrial Ca2+
    over-activates mitochondrial metabolism in neurons of central memory circuits,
    leading to improved LTM storage in training paradigms in which wild-type counterparts
    of both species fail to remember. Our findings unveil an evolutionarily conserved
    mechanism that controls mitochondrial metabolism in neurons and indicate its involvement
    in shaping higher brain functions, such as LTM.
acknowledgement: We thank all members of the laboratory of J.d.J.-S. for insightful
  discussions and comments. We thank S. Perez for technical assistance. This work
  was made possible by the Paris Brain Institute Diane Barriere Chair in Synaptic
  Bioenergetics awarded to J.d.J.-S., who is also supported by an ERC Starting Grant
  (SynaptoEnergy, European Research Council; ERC-StG-852873), 2019 ATIP-Avenir Grant
  (CNRS, Inserm), a Big Brain Theory Grant (ICM Foundation) and a Kavli Exploratory
  Award (Kavli Foundation). This work was also supported by an ERC Advanced Grant
  (EnergyMeMo; ERC-AdG-741550) to T.P. and grants from the Agence Nationale de la
  Recherche to P.Y.P. (ANR-20-CE92-0047-01), T.P. (ANR-23-CE16-0029-01), A.P. and
  J.d.J.-S. (ANR-22-CE16-0020) and J.d.J.-S. (ANR-24-CE16-0221). T.P., P.Y.P. and
  J.d.J.-S. are permanent CNRS researchers. A.P. is a permanent ESPCI associate professor.
  T.C. was funded by the French Ministry of Research and the Fondation pour la Recherche
  Médicale. V.R. was funded by the Max Planck Society, the Chan Zuckerberg Initiative
  DAF, an advised fund of the Silicon Valley Community Foundation grant number 2024-349543
  and the NIH Director’s New Innovator Award (DP2 MH140148). A.B.-G. and C.R.-D. received
  funding from an ERC Starting Grant (HighMemory; ERC-StG-948217), the Ministry of
  Economy and Competitiveness (PID2021-122795OB-I00) and the Departament d’Economia
  i Coneixement de la Generalitat de Catalunya (SGR 00022). T.P.V. was funded by the
  Wellcome Trust and a Royal Society Sir Henry Dale Research Fellowship (WT100000)
  and a Wellcome Trust Senior Research Fellowship (214316/Z/18/Z). K.G. was supported
  by the DIM C-BRAINS, funded by the Conseil Régional d’Ile-de-France. The contributions
  of H.F. and E.R.S. were supported by the Howard Hughes Medical Institute. The PHENO-ICMice
  animal Core at ICM is supported by two ‘Investissements d’avenir’ (ANR-10- IAIHU-06
  and ANR-11-INBS-0011-NeurATRIS) and the Fondation pour la Recherche Médicale.
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Anjali
  full_name: Amrapali Vishwanath, Anjali
  last_name: Amrapali Vishwanath
- first_name: Typhaine
  full_name: Comyn, Typhaine
  last_name: Comyn
- first_name: Rodrigo G.
  full_name: Mira, Rodrigo G.
  last_name: Mira
- first_name: Claire
  full_name: Brossier, Claire
  last_name: Brossier
- first_name: Carlos
  full_name: Pascual-Caro, Carlos
  last_name: Pascual-Caro
- first_name: Maya
  full_name: Faour, Maya
  last_name: Faour
- first_name: Kahina
  full_name: Boumendil, Kahina
  last_name: Boumendil
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: Carla
  full_name: Ramon-Duaso, Carla
  last_name: Ramon-Duaso
- first_name: Ruolin
  full_name: Fan, Ruolin
  last_name: Fan
- first_name: Kishalay
  full_name: Ghosh, Kishalay
  last_name: Ghosh
- first_name: Helen
  full_name: Farrants, Helen
  last_name: Farrants
- first_name: Jean-Paul
  full_name: Berwick, Jean-Paul
  last_name: Berwick
- first_name: Riya
  full_name: Sivakumar, Riya
  last_name: Sivakumar
- first_name: Mario
  full_name: Lopez-Manzaneda, Mario
  last_name: Lopez-Manzaneda
- first_name: Eric R.
  full_name: Schreiter, Eric R.
  last_name: Schreiter
- first_name: Thomas
  full_name: Preat, Thomas
  last_name: Preat
- 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: Vidhya
  full_name: Rangaraju, Vidhya
  last_name: Rangaraju
- first_name: Arnau
  full_name: Busquets-Garcia, Arnau
  last_name: Busquets-Garcia
- first_name: Pierre-Yves
  full_name: Plaçais, Pierre-Yves
  last_name: Plaçais
- first_name: Alice
  full_name: Pavlowsky, Alice
  last_name: Pavlowsky
- first_name: Jaime
  full_name: de Juan-Sanz, Jaime
  last_name: de Juan-Sanz
citation:
  ama: Amrapali Vishwanath A, Comyn T, Mira RG, et al. Mitochondrial Ca2+ efflux controls
    neuronal metabolism and long-term memory across species. <i>Nature Metabolism</i>.
    2026;8(2):467-488. doi:<a href="https://doi.org/10.1038/s42255-026-01451-w">10.1038/s42255-026-01451-w</a>
  apa: Amrapali Vishwanath, A., Comyn, T., Mira, R. G., Brossier, C., Pascual-Caro,
    C., Faour, M., … de Juan-Sanz, J. (2026). Mitochondrial Ca2+ efflux controls neuronal
    metabolism and long-term memory across species. <i>Nature Metabolism</i>. Springer
    Nature. <a href="https://doi.org/10.1038/s42255-026-01451-w">https://doi.org/10.1038/s42255-026-01451-w</a>
  chicago: Amrapali Vishwanath, Anjali, Typhaine Comyn, Rodrigo G. Mira, Claire Brossier,
    Carlos Pascual-Caro, Maya Faour, Kahina Boumendil, et al. “Mitochondrial Ca2+
    Efflux Controls Neuronal Metabolism and Long-Term Memory across Species.” <i>Nature
    Metabolism</i>. Springer Nature, 2026. <a href="https://doi.org/10.1038/s42255-026-01451-w">https://doi.org/10.1038/s42255-026-01451-w</a>.
  ieee: A. Amrapali Vishwanath <i>et al.</i>, “Mitochondrial Ca2+ efflux controls
    neuronal metabolism and long-term memory across species,” <i>Nature Metabolism</i>,
    vol. 8, no. 2. Springer Nature, pp. 467–488, 2026.
  ista: Amrapali Vishwanath A, Comyn T, Mira RG, Brossier C, Pascual-Caro C, Faour
    M, Boumendil K, Chintaluri C, Ramon-Duaso C, Fan R, Ghosh K, Farrants H, Berwick
    J-P, Sivakumar R, Lopez-Manzaneda M, Schreiter ER, Preat T, Vogels TP, Rangaraju
    V, Busquets-Garcia A, Plaçais P-Y, Pavlowsky A, de Juan-Sanz J. 2026. Mitochondrial
    Ca2+ efflux controls neuronal metabolism and long-term memory across species.
    Nature Metabolism. 8(2), 467–488.
  mla: Amrapali Vishwanath, Anjali, et al. “Mitochondrial Ca2+ Efflux Controls Neuronal
    Metabolism and Long-Term Memory across Species.” <i>Nature Metabolism</i>, vol.
    8, no. 2, Springer Nature, 2026, pp. 467–88, doi:<a href="https://doi.org/10.1038/s42255-026-01451-w">10.1038/s42255-026-01451-w</a>.
  short: A. Amrapali Vishwanath, T. Comyn, R.G. Mira, C. Brossier, C. Pascual-Caro,
    M. Faour, K. Boumendil, C. Chintaluri, C. Ramon-Duaso, R. Fan, K. Ghosh, H. Farrants,
    J.-P. Berwick, R. Sivakumar, M. Lopez-Manzaneda, E.R. Schreiter, T. Preat, T.P.
    Vogels, V. Rangaraju, A. Busquets-Garcia, P.-Y. Plaçais, A. Pavlowsky, J. de Juan-Sanz,
    Nature Metabolism 8 (2026) 467–488.
das_tickbox: '1'
date_created: 2026-03-02T10:04:49Z
date_published: 2026-02-11T00:00:00Z
date_updated: 2026-07-13T12:30:14Z
day: '11'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.1038/s42255-026-01451-w
external_id:
  pmid:
  - '41673453'
file:
- access_level: open_access
  checksum: 365932a599d05bc9ce8a57204e7a1465
  content_type: application/pdf
  creator: dernst
  date_created: 2026-03-02T15:21:27Z
  date_updated: 2026-03-02T15:21:27Z
  file_id: '21392'
  file_name: 2026_NatureMetab_AmrapaliVishwanath.pdf
  file_size: 5326608
  relation: main_file
  success: 1
file_date_updated: 2026-03-02T15:21:27Z
has_accepted_license: '1'
intvolume: '         8'
issue: '2'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 467-488
pmid: 1
project:
- _id: c084a126-5a5b-11eb-8a69-d75314a70a87
  grant_number: 214316/Z/18/Z
  name: What’s in a memory? Spatiotemporal dynamics in strongly coupled recurrent
    neuronal networks.
publication: Nature Metabolism
publication_identifier:
  eissn:
  - 2522-5812
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mitochondrial Ca2+ efflux controls neuronal metabolism and long-term memory
  across species
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2026'
...
---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '22295'
abstract:
- lang: eng
  text: 'Despite the functional diversity of over 100 causal genes1,2,3, phenotypic
    convergence across models may reveal common neurobiological processes in autism
    spectrum disorder (ASD). Here we profiled 251 samples from 11 monogenic mouse
    models of ASD using single-nucleus multi-omic sequencing across three developmental
    stages, both sexes and two brain regions. Despite genetic heterogeneity, ASD-linked
    mutations converged on perturbations of the radial glial cell lineage. These alterations
    reflect a transient developmental delay rather than lasting lineage misspecification
    and resolve by postnatal stages. Molecularly, the largest transcriptional differences
    emerged in neurons at early postnatal stages. These changes included downregulation
    of synaptic and ion channel-related genes, consistent with homeostatic adaptation
    or delayed maturation. Network analysis showed molecular convergence across models
    within each developmental stage, suggesting that diverse mutations linked to ASD
    impinge on common, stage-specific processes. Convergence becomes less pronounced
    by postnatal day 14, highlighting the dynamic nature of ASD-associated changes.
    Cross-genotype heterogeneity is superimposed on stage-specific effects. Electrophysiology
    corroborated this pattern: mutants generally showed altered neuronal excitability
    and synaptic properties with model-specific nuances. Our study also highlighted
    sex-specific gene expression alterations, with female mice often displaying larger
    effect sizes than male mice. Together, our findings provide a comprehensive view
    of developmental cellular and molecular dynamics across models of ASD.'
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
acknowledgement: We thank F. Freeman, V. Voronin and M. Ladron de Guevara for technical
  assistance; A. Stichelberger and S. Liegenfeld for the management of our animal
  colony; M. Schunn, C. Gold and the Preclinical Facility team for technical assistance;
  C. Jansen and the Scientific Computing Facility for bioinformatics support and technical
  assistance; the Biomedical Sequencing Facility at CeMM for assistance with next-generation
  sequencing; and J. Lin and T. Krausgruber in the laboratory of C. Bock for support
  with flow cytometry; J. Kirchner for illustrating the multi-omics approach depicted
  in Fig. 1; and all members of the laboratory of G.N. for their support and discussions.
  This study was supported by the Scientific Service Units of ISTA through resources
  provided by the Imaging & Optics Facility and the Laboratory Support Facility. Bulk
  RNA-seq was performed by the Next Generation Sequencing Facility at Vienna BioCenter
  Core Facilities, member of the Vienna BioCenter. This work was supported by a European
  Research Council Consolidator Grant (PR1028ERC02), by SFARI (PR1028SIM02) and by
  the Austrian Science Fund (PE1028W1232 and PR1028FG1803) to G.N. Open access funding
  provided by Institute of Science and Technology (IST Austria).
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Lena A
  full_name: Schwarz, Lena A
  id: 29A8453C-F248-11E8-B48F-1D18A9856A87
  last_name: Schwarz
- first_name: Christoph
  full_name: Dotter, Christoph
  id: 4C66542E-F248-11E8-B48F-1D18A9856A87
  last_name: Dotter
  orcid: 0000-0002-9033-9096
- first_name: Sergey
  full_name: Isaev, Sergey
  last_name: Isaev
- first_name: Michela
  full_name: Lisi, Michela
  id: 39383c1b-d3eb-11ef-8d6c-c8cdf4e10c8c
  last_name: Lisi
- first_name: Daniel
  full_name: Malzl, Daniel
  last_name: Malzl
- first_name: Christoph
  full_name: Büschl, Christoph
  id: 2a8c054c-0913-11ee-9159-f8ef515809ed
  last_name: Büschl
- first_name: Sabrina
  full_name: Ladstätter, Sabrina
  last_name: Ladstätter
- first_name: Bárbara
  full_name: Oliveira, Bárbara
  id: 3B03AA1A-F248-11E8-B48F-1D18A9856A87
  last_name: Oliveira
- first_name: Matteo
  full_name: Barel, Matteo
  id: 8959927b-2236-11ed-bd6e-ea83d94ade0e
  last_name: Barel
- first_name: Bernadette
  full_name: Basilico, Bernadette
  id: 36035796-5ACA-11E9-A75E-7AF2E5697425
  last_name: Basilico
  orcid: 0000-0003-1843-3173
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: Sarah
  full_name: Gorkiewicz, Sarah
  id: f141a35d-15a9-11ec-9fb2-fef6becc7b6f
  last_name: Gorkiewicz
- first_name: Mohammad
  full_name: Goudarzi, Mohammad
  id: 3384113A-F248-11E8-B48F-1D18A9856A87
  last_name: Goudarzi
- first_name: Tereza
  full_name: Belinova, Tereza
  id: 0bf89b6a-d28b-11eb-8bd6-f43768e4d368
  last_name: Belinova
- first_name: Stephan
  full_name: Reichl, Stephan
  last_name: Reichl
- first_name: Gintarė
  full_name: Sendžikaitė, Gintarė
  id: dd6d52f2-c50d-11eb-9548-bcf0ff82b344
  last_name: Sendžikaitė
- first_name: Satish
  full_name: Arcot Jayaram, Satish
  id: b0bbee33-09f7-11eb-909c-8b358058d28a
  last_name: Arcot Jayaram
  orcid: 0000-0002-2479-2669
- first_name: Peter
  full_name: Koppensteiner, Peter
  id: 3B8B25A8-F248-11E8-B48F-1D18A9856A87
  last_name: Koppensteiner
  orcid: 0000-0002-3509-1948
- first_name: Christoph M
  full_name: Sommer, Christoph M
  id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
  last_name: Sommer
  orcid: 0000-0003-1216-9105
- 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: Jörg
  full_name: Menche, Jörg
  last_name: Menche
- first_name: Igor
  full_name: Adameyko, Igor
  last_name: Adameyko
- first_name: Peter Vasili
  full_name: Kharchenko, Peter Vasili
  id: 0095641e-7eb7-11f1-8665-aec51a2ab5e0
  last_name: Kharchenko
- first_name: Christoph
  full_name: Bock, Christoph
  last_name: Bock
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
citation:
  ama: Schwarz LA, Dotter C, Isaev S, et al. Cortical development dynamics across
    autism spectrum disorder mouse models. <i>Nature</i>. 2026. doi:<a href="https://doi.org/10.1038/s41586-026-10679-1">10.1038/s41586-026-10679-1</a>
  apa: Schwarz, L. A., Dotter, C., Isaev, S., Lisi, M., Malzl, D., Büschl, C., … Novarino,
    G. (2026). Cortical development dynamics across autism spectrum disorder mouse
    models. <i>Nature</i>. Springer Nature. <a href="https://doi.org/10.1038/s41586-026-10679-1">https://doi.org/10.1038/s41586-026-10679-1</a>
  chicago: Schwarz, Lena A, Christoph Dotter, Sergey Isaev, Michela Lisi, Daniel Malzl,
    Christoph Büschl, Sabrina Ladstätter, et al. “Cortical Development Dynamics across
    Autism Spectrum Disorder Mouse Models.” <i>Nature</i>. Springer Nature, 2026.
    <a href="https://doi.org/10.1038/s41586-026-10679-1">https://doi.org/10.1038/s41586-026-10679-1</a>.
  ieee: L. A. Schwarz <i>et al.</i>, “Cortical development dynamics across autism
    spectrum disorder mouse models,” <i>Nature</i>. Springer Nature, 2026.
  ista: Schwarz LA, Dotter C, Isaev S, Lisi M, Malzl D, Büschl C, Ladstätter S, Oliveira
    B, Barel M, Basilico B, Chintaluri C, Gorkiewicz S, Goudarzi M, Belinova T, Reichl
    S, Sendžikaitė G, Arcot Jayaram S, Koppensteiner P, Sommer CM, Vogels TP, Menche
    J, Adameyko I, Kharchenko PV, Bock C, Novarino G. 2026. Cortical development dynamics
    across autism spectrum disorder mouse models. Nature.
  mla: Schwarz, Lena A., et al. “Cortical Development Dynamics across Autism Spectrum
    Disorder Mouse Models.” <i>Nature</i>, Springer Nature, 2026, doi:<a href="https://doi.org/10.1038/s41586-026-10679-1">10.1038/s41586-026-10679-1</a>.
  short: L.A. Schwarz, C. Dotter, S. Isaev, M. Lisi, D. Malzl, C. Büschl, S. Ladstätter,
    B. Oliveira, M. Barel, B. Basilico, C. Chintaluri, S. Gorkiewicz, M. Goudarzi,
    T. Belinova, S. Reichl, G. Sendžikaitė, S. Arcot Jayaram, P. Koppensteiner, C.M.
    Sommer, T.P. Vogels, J. Menche, I. Adameyko, P.V. Kharchenko, C. Bock, G. Novarino,
    Nature (2026).
corr_author: '1'
dataavailabilitystatement: Single-nucleus multiomics data are available from the Gene
  Expression Omnibus (GSE328363). The mm10 reference genome was used for the alignment
  (refdata-cellranger-arc-mm10-2020-A-2.0.0, obtained from https://cf.10xgenomics.com/supp/cell-arc/refdata-cellranger-arc-mm10-2020-A-2.0.0.tar.gz).
  Single-cell data can be accessed and visualized through a CELLxGENE database (https://adameykolab.hifo.meduniwien.ac.at/cellxgene_public/filecrawl/.2026_Nature_Schwarz).
  Source data are provided with this paper. Scripts and analyses that support the
  main findings of this study are accessible in a GitHub repository (https://git.ista.ac.at/research-sofware/mouseome).
date_created: 2026-07-13T09:47:21Z
date_published: 2026-06-17T00:00:00Z
date_updated: 2026-07-13T12:58:19Z
day: '17'
ddc:
- '570'
department:
- _id: AnKi
- _id: GaNo
- _id: TiVo
- _id: ScienComp
- _id: GradSch
- _id: Bio
- _id: PreCl
doi: 10.1038/s41586-026-10679-1
external_id:
  pmid:
  - '42310454'
has_accepted_license: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1038/s41586-026-10679-1
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 34ba8964-11ca-11ed-8bc3-e15864e7e9a6
  grant_number: '101044865'
  name: Toward an understanding of the brain interstitial system and the extracellular
    proteome in health and autism spectrum disorders
- _id: 9B91375C-BA93-11EA-9121-9846C619BF3A
  grant_number: '707964'
  name: Critical windows and reversibility of ASD associated with mutations in chromatin
    remodelers
- _id: 2548AE96-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232
  name: Molecular Drug Targets
- _id: ebb38b5d-77a9-11ec-83b8-a42e08120a88
  grant_number: FG1803 49015
  name: Neurobiology of anxiety in autism spectrum disorders
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: epub_ahead
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Cortical development dynamics across autism spectrum disorder mouse models
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2026'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '15169'
abstract:
- lang: eng
  text: Interpretation of extracellular recordings can be challenging due to the long
    range of electric field. This challenge can be mitigated by estimating the current
    source density (CSD). Here we introduce kCSD-python, an open Python package implementing
    Kernel Current Source Density (kCSD) method and related tools to facilitate CSD
    analysis of experimental data and the interpretation of results. We show how to
    counter the limitations imposed by noise and assumptions in the method itself.
    kCSD-python allows CSD estimation for an arbitrary distribution of electrodes
    in 1D, 2D, and 3D, assuming distributions of sources in tissue, a slice, or in
    a single cell, and includes a range of diagnostic aids. We demonstrate its features
    in a Jupyter Notebook tutorial which illustrates a typical analytical workflow
    and main functionalities useful in validating analysis results.
acknowledgement: 'The Python implementation of kCSD was started by Grzegorz Parka
  during Google Summer of Code project through the International Neuroinformatics
  Coordinating Facility. Jan Mąka implemented the first Python version of skCSD class.
  This work was supported by the Polish National Science Centre (2013/08/W/NZ4/00691
  to DKW; 2015/17/B/ST7/04123 to DKW). '
article_number: e1011941
article_processing_charge: Yes
article_type: original
author:
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: Marta
  full_name: Bejtka, Marta
  last_name: Bejtka
- first_name: Wladyslaw
  full_name: Sredniawa, Wladyslaw
  last_name: Sredniawa
- first_name: Michal
  full_name: Czerwinski, Michal
  last_name: Czerwinski
- first_name: Jakub M.
  full_name: Dzik, Jakub M.
  last_name: Dzik
- first_name: Joanna
  full_name: Jedrzejewska-Szmek, Joanna
  last_name: Jedrzejewska-Szmek
- first_name: Daniel K.
  full_name: Wojciki, Daniel K.
  last_name: Wojciki
citation:
  ama: Chintaluri C, Bejtka M, Sredniawa W, et al. kCSD-python, reliable current source
    density estimation with quality control. <i>PLoS Computational Biology</i>. 2024;20(3).
    doi:<a href="https://doi.org/10.1371/journal.pcbi.1011941">10.1371/journal.pcbi.1011941</a>
  apa: Chintaluri, C., Bejtka, M., Sredniawa, W., Czerwinski, M., Dzik, J. M., Jedrzejewska-Szmek,
    J., &#38; Wojciki, D. K. (2024). kCSD-python, reliable current source density
    estimation with quality control. <i>PLoS Computational Biology</i>. Public Library
    of Science. <a href="https://doi.org/10.1371/journal.pcbi.1011941">https://doi.org/10.1371/journal.pcbi.1011941</a>
  chicago: Chintaluri, Chaitanya, Marta Bejtka, Wladyslaw Sredniawa, Michal Czerwinski,
    Jakub M. Dzik, Joanna Jedrzejewska-Szmek, and Daniel K. Wojciki. “KCSD-Python,
    Reliable Current Source Density Estimation with Quality Control.” <i>PLoS Computational
    Biology</i>. Public Library of Science, 2024. <a href="https://doi.org/10.1371/journal.pcbi.1011941">https://doi.org/10.1371/journal.pcbi.1011941</a>.
  ieee: C. Chintaluri <i>et al.</i>, “kCSD-python, reliable current source density
    estimation with quality control,” <i>PLoS Computational Biology</i>, vol. 20,
    no. 3. Public Library of Science, 2024.
  ista: Chintaluri C, Bejtka M, Sredniawa W, Czerwinski M, Dzik JM, Jedrzejewska-Szmek
    J, Wojciki DK. 2024. kCSD-python, reliable current source density estimation with
    quality control. PLoS Computational Biology. 20(3), e1011941.
  mla: Chintaluri, Chaitanya, et al. “KCSD-Python, Reliable Current Source Density
    Estimation with Quality Control.” <i>PLoS Computational Biology</i>, vol. 20,
    no. 3, e1011941, Public Library of Science, 2024, doi:<a href="https://doi.org/10.1371/journal.pcbi.1011941">10.1371/journal.pcbi.1011941</a>.
  short: C. Chintaluri, M. Bejtka, W. Sredniawa, M. Czerwinski, J.M. Dzik, J. Jedrzejewska-Szmek,
    D.K. Wojciki, PLoS Computational Biology 20 (2024).
corr_author: '1'
das_tickbox: '1'
date_created: 2024-03-24T23:00:59Z
date_published: 2024-03-14T00:00:00Z
date_updated: 2026-07-13T12:30:33Z
day: '14'
ddc:
- '000'
- '570'
department:
- _id: TiVo
doi: 10.1371/journal.pcbi.1011941
external_id:
  isi:
  - '001190689800001'
  pmid:
  - '38484020'
file:
- access_level: open_access
  checksum: c09718d0d09614642d877d0716ce32e8
  content_type: application/pdf
  creator: dernst
  date_created: 2025-06-25T05:47:36Z
  date_updated: 2025-06-25T05:47:36Z
  file_id: '19897'
  file_name: 2024_PLoSCompBio_Chintaluri.pdf
  file_size: 2540277
  relation: main_file
  success: 1
file_date_updated: 2025-06-25T05:47:36Z
has_accepted_license: '1'
intvolume: '        20'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLoS Computational Biology
publication_identifier:
  eissn:
  - 1553-7358
  issn:
  - 1553-734X
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/Neuroinflab/kCSD-python
scopus_import: '1'
status: public
title: kCSD-python, reliable current source density estimation with quality control
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 20
year: '2024'
...
---
OA_place: publisher
OA_type: hybrid
_id: '14666'
abstract:
- lang: eng
  text: So-called spontaneous activity is a central hallmark of most nervous systems.
    Such non-causal firing is contrary to the tenet of spikes as a means of communication,
    and its purpose remains unclear. We propose that self-initiated firing can serve
    as a release valve to protect neurons from the toxic conditions arising in mitochondria
    from lower-than-baseline energy consumption. To demonstrate the viability of our
    hypothesis, we built a set of models that incorporate recent experimental results
    indicating homeostatic control of metabolic products—Adenosine triphosphate (ATP),
    adenosine diphosphate (ADP), and reactive oxygen species (ROS)—by changes in firing.
    We explore the relationship of metabolic cost of spiking with its effect on the
    temporal patterning of spikes and reproduce experimentally observed changes in
    intrinsic firing in the fruitfly dorsal fan-shaped body neuron in a model with
    ROS-modulated potassium channels. We also show that metabolic spiking homeostasis
    can produce indefinitely sustained avalanche dynamics in cortical circuits. Our
    theory can account for key features of neuronal activity observed in many studies
    ranging from ion channel function all the way to resting state dynamics. We finish
    with a set of experimental predictions that would confirm an integrated, crucial
    role for metabolically regulated spiking and firmly link metabolic homeostasis
    and neuronal function.
acknowledgement: We thank Prof. C. Nazaret and Prof. J.-P. Mazat for sharing the code
  of their mitochondrial model. We also thank G. Miesenböck, E. Marder, L. Abbott,
  A. Kempf, P. Hasenhuetl, W. Podlaski, F. Zenke, E. Agnes, P. Bozelos, J. Watson,
  B. Confavreux, and G. Christodoulou, and the rest of the Vogels Lab for their feedback.
  This work was funded by Wellcome Trust and Royal Society Sir Henry Dale Research
  Fellowship (WT100000), a Wellcome Trust Senior Research Fellowship (214316/Z/18/Z),
  and a UK Research and Innovation, Biotechnology and Biological Sciences Research
  Council grant (UKRI-BBSRC BB/N019512/1).
article_number: e2306525120
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
citation:
  ama: Chintaluri C, Vogels TP. Metabolically regulated spiking could serve neuronal
    energy homeostasis and protect from reactive oxygen species. <i>Proceedings of
    the National Academy of Sciences of the United States of America</i>. 2023;120(48).
    doi:<a href="https://doi.org/10.1073/pnas.2306525120">10.1073/pnas.2306525120</a>
  apa: Chintaluri, C., &#38; Vogels, T. P. (2023). Metabolically regulated spiking
    could serve neuronal energy homeostasis and protect from reactive oxygen species.
    <i>Proceedings of the National Academy of Sciences of the United States of America</i>.
    National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.2306525120">https://doi.org/10.1073/pnas.2306525120</a>
  chicago: Chintaluri, Chaitanya, and Tim P Vogels. “Metabolically Regulated Spiking
    Could Serve Neuronal Energy Homeostasis and Protect from Reactive Oxygen Species.”
    <i>Proceedings of the National Academy of Sciences of the United States of America</i>.
    National Academy of Sciences, 2023. <a href="https://doi.org/10.1073/pnas.2306525120">https://doi.org/10.1073/pnas.2306525120</a>.
  ieee: C. Chintaluri and T. P. Vogels, “Metabolically regulated spiking could serve
    neuronal energy homeostasis and protect from reactive oxygen species,” <i>Proceedings
    of the National Academy of Sciences of the United States of America</i>, vol.
    120, no. 48. National Academy of Sciences, 2023.
  ista: Chintaluri C, Vogels TP. 2023. Metabolically regulated spiking could serve
    neuronal energy homeostasis and protect from reactive oxygen species. Proceedings
    of the National Academy of Sciences of the United States of America. 120(48),
    e2306525120.
  mla: Chintaluri, Chaitanya, and Tim P. Vogels. “Metabolically Regulated Spiking
    Could Serve Neuronal Energy Homeostasis and Protect from Reactive Oxygen Species.”
    <i>Proceedings of the National Academy of Sciences of the United States of America</i>,
    vol. 120, no. 48, e2306525120, National Academy of Sciences, 2023, doi:<a href="https://doi.org/10.1073/pnas.2306525120">10.1073/pnas.2306525120</a>.
  short: C. Chintaluri, T.P. Vogels, Proceedings of the National Academy of Sciences
    of the United States of America 120 (2023).
corr_author: '1'
das_tickbox: '1'
date_created: 2023-12-10T23:01:00Z
date_published: 2023-11-21T00:00:00Z
date_updated: 2026-07-13T12:30:49Z
day: '21'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.1073/pnas.2306525120
external_id:
  isi:
  - '001157389000005'
  pmid:
  - '37988463'
file:
- access_level: open_access
  checksum: bf4ec38602a70dae4338077a5a4d497f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-12-11T12:45:12Z
  date_updated: 2023-12-11T12:45:12Z
  file_id: '14678'
  file_name: 2023_PNAS_Chintaluri.pdf
  file_size: 16891602
  relation: main_file
  success: 1
file_date_updated: 2023-12-11T12:45:12Z
has_accepted_license: '1'
intvolume: '       120'
isi: 1
issue: '48'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: c084a126-5a5b-11eb-8a69-d75314a70a87
  grant_number: 214316/Z/18/Z
  name: What’s in a memory? Spatiotemporal dynamics in strongly coupled recurrent
    neuronal networks.
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/ccluri/metabolic_spiking
scopus_import: '1'
status: public
title: Metabolically regulated spiking could serve neuronal energy homeostasis and
  protect from reactive oxygen species
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 120
year: '2023'
...
---
_id: '17132'
abstract:
- lang: eng
  text: <jats:p>Extracellular recording is an accessible technique used in animals
    and humans to study the brain physiology and pathology. As the number of recording
    channels and their density grows it is natural to ask how much improvement the
    additional channels bring in and how we can optimally use the new capabilities
    for monitoring the brain. Here we show that for any given distribution of electrodes
    we can establish exactly what information about current sources in the brain can
    be recovered and what information is strictly unobservable. We demonstrate this
    in the general setting of previously proposed kernel Current Source Density method
    and illustrate it with simplified examples as well as using evoked potentials
    from the barrel cortex obtained with a Neuropixels probe and with compatible model
    data. We show that with conceptual separation of the estimation space from experimental
    setup one can recover sources not accessible to standard methods.</jats:p>
article_number: e1008615
article_processing_charge: No
article_type: original
author:
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: Marta
  full_name: Bejtka, Marta
  last_name: Bejtka
- first_name: Władysław
  full_name: Średniawa, Władysław
  last_name: Średniawa
- first_name: Michał
  full_name: Czerwiński, Michał
  last_name: Czerwiński
- first_name: Jakub M.
  full_name: Dzik, Jakub M.
  last_name: Dzik
- first_name: Joanna
  full_name: Jędrzejewska-Szmek, Joanna
  last_name: Jędrzejewska-Szmek
- first_name: Kacper
  full_name: Kondrakiewicz, Kacper
  last_name: Kondrakiewicz
- first_name: Ewa
  full_name: Kublik, Ewa
  last_name: Kublik
- first_name: Daniel K.
  full_name: Wójcik, Daniel K.
  last_name: Wójcik
citation:
  ama: Chintaluri C, Bejtka M, Średniawa W, et al. What we can and what we cannot
    see with extracellular multielectrodes. <i>PLOS Computational Biology</i>. 2021;17(5).
    doi:<a href="https://doi.org/10.1371/journal.pcbi.1008615">10.1371/journal.pcbi.1008615</a>
  apa: Chintaluri, C., Bejtka, M., Średniawa, W., Czerwiński, M., Dzik, J. M., Jędrzejewska-Szmek,
    J., … Wójcik, D. K. (2021). What we can and what we cannot see with extracellular
    multielectrodes. <i>PLOS Computational Biology</i>. Public Library of Science.
    <a href="https://doi.org/10.1371/journal.pcbi.1008615">https://doi.org/10.1371/journal.pcbi.1008615</a>
  chicago: Chintaluri, Chaitanya, Marta Bejtka, Władysław Średniawa, Michał Czerwiński,
    Jakub M. Dzik, Joanna Jędrzejewska-Szmek, Kacper Kondrakiewicz, Ewa Kublik, and
    Daniel K. Wójcik. “What We Can and What We Cannot See with Extracellular Multielectrodes.”
    <i>PLOS Computational Biology</i>. Public Library of Science, 2021. <a href="https://doi.org/10.1371/journal.pcbi.1008615">https://doi.org/10.1371/journal.pcbi.1008615</a>.
  ieee: C. Chintaluri <i>et al.</i>, “What we can and what we cannot see with extracellular
    multielectrodes,” <i>PLOS Computational Biology</i>, vol. 17, no. 5. Public Library
    of Science, 2021.
  ista: Chintaluri C, Bejtka M, Średniawa W, Czerwiński M, Dzik JM, Jędrzejewska-Szmek
    J, Kondrakiewicz K, Kublik E, Wójcik DK. 2021. What we can and what we cannot
    see with extracellular multielectrodes. PLOS Computational Biology. 17(5), e1008615.
  mla: Chintaluri, Chaitanya, et al. “What We Can and What We Cannot See with Extracellular
    Multielectrodes.” <i>PLOS Computational Biology</i>, vol. 17, no. 5, e1008615,
    Public Library of Science, 2021, doi:<a href="https://doi.org/10.1371/journal.pcbi.1008615">10.1371/journal.pcbi.1008615</a>.
  short: C. Chintaluri, M. Bejtka, W. Średniawa, M. Czerwiński, J.M. Dzik, J. Jędrzejewska-Szmek,
    K. Kondrakiewicz, E. Kublik, D.K. Wójcik, PLOS Computational Biology 17 (2021).
das_tickbox: '1'
date_created: 2024-06-11T14:43:37Z
date_published: 2021-05-14T00:00:00Z
date_updated: 2026-07-13T12:31:04Z
day: '14'
doi: 10.1371/journal.pcbi.1008615
extern: '1'
has_accepted_license: '1'
intvolume: '        17'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1371/journal.pcbi.1008615
month: '05'
oa: 1
oa_version: Published Version
publication: PLOS Computational Biology
publication_identifier:
  issn:
  - 1553-7358
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
status: public
title: What we can and what we cannot see with extracellular multielectrodes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2021'
...
---
_id: '8127'
abstract:
- lang: eng
  text: Mechanistic modeling in neuroscience aims to explain observed phenomena in
    terms of underlying causes. However, determining which model parameters agree
    with complex and stochastic neural data presents a significant challenge. We address
    this challenge with a machine learning tool which uses deep neural density estimators—trained
    using model simulations—to carry out Bayesian inference and retrieve the full
    space of parameters compatible with raw data or selected data features. Our method
    is scalable in parameters and data features and can rapidly analyze new data after
    initial training. We demonstrate the power and flexibility of our approach on
    receptive fields, ion channels, and Hodgkin–Huxley models. We also characterize
    the space of circuit configurations giving rise to rhythmic activity in the crustacean
    stomatogastric ganglion, and use these results to derive hypotheses for underlying
    compensation mechanisms. Our approach will help close the gap between data-driven
    and theory-driven models of neural dynamics.
acknowledgement: We thank Mahmood S Hoseini and Michael Stryker for sharing their
  data for Figure 2, and Philipp Berens, Sean Bittner, Jan Boelts, John Cunningham,
  Richard Gao, Scott Linderman, Eve Marder, Iain Murray, George Papamakarios, Astrid
  Prinz, Auguste Schulz and Srinivas Turaga for discussions and/or comments on the
  manuscript. This work was supported by the German Research Foundation (DFG) through
  SFB 1233 ‘Robust Vision’, (276693517), SFB 1089 ‘Synaptic Microcircuits’, SPP 2041
  ‘Computational Connectomics’ and Germany's Excellence Strategy – EXC-Number 2064/1
  – Project number 390727645 and the German Federal Ministry of Education and Research
  (BMBF, project ‘ADIMEM’, FKZ 01IS18052 A-D) to JHM, a Sir Henry Dale Fellowship
  by the Wellcome Trust and the Royal Society (WT100000; WFP and TPV), a Wellcome
  Trust Senior Research Fellowship (214316/Z/18/Z; TPV), a ERC Consolidator Grant
  (SYNAPSEEK; WPF and CC), and a UK Research and Innovation, Biotechnology and Biological
  Sciences Research Council (CC, UKRI-BBSRC BB/N019512/1). We gratefully acknowledge
  the Leibniz Supercomputing Centre for funding this project by providing computing
  time on its Linux-Cluster.
article_number: e56261
article_processing_charge: No
article_type: original
author:
- first_name: Pedro J.
  full_name: Gonçalves, Pedro J.
  last_name: Gonçalves
  orcid: 0000-0002-6987-4836
- first_name: Jan-Matthis
  full_name: Lueckmann, Jan-Matthis
  last_name: Lueckmann
  orcid: 0000-0003-4320-4663
- first_name: Michael
  full_name: Deistler, Michael
  last_name: Deistler
  orcid: 0000-0002-3573-0404
- first_name: Marcel
  full_name: Nonnenmacher, Marcel
  last_name: Nonnenmacher
  orcid: 0000-0001-6044-6627
- first_name: Kaan
  full_name: Öcal, Kaan
  last_name: Öcal
  orcid: 0000-0002-8528-6858
- first_name: Giacomo
  full_name: Bassetto, Giacomo
  last_name: Bassetto
- first_name: Chaitanya
  full_name: Chintaluri, Chaitanya
  id: BA06AFEE-A4BA-11EA-AE5C-14673DDC885E
  last_name: Chintaluri
  orcid: 0000-0003-4252-1608
- first_name: William F.
  full_name: Podlaski, William F.
  last_name: Podlaski
  orcid: 0000-0001-6619-7502
- first_name: Sara A.
  full_name: Haddad, Sara A.
  last_name: Haddad
  orcid: 0000-0003-0807-0823
- 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: David S.
  full_name: Greenberg, David S.
  last_name: Greenberg
- first_name: Jakob H.
  full_name: Macke, Jakob H.
  last_name: Macke
  orcid: 0000-0001-5154-8912
citation:
  ama: Gonçalves PJ, Lueckmann J-M, Deistler M, et al. Training deep neural density
    estimators to identify mechanistic models of neural dynamics. <i>eLife</i>. 2020;9.
    doi:<a href="https://doi.org/10.7554/eLife.56261">10.7554/eLife.56261</a>
  apa: Gonçalves, P. J., Lueckmann, J.-M., Deistler, M., Nonnenmacher, M., Öcal, K.,
    Bassetto, G., … Macke, J. H. (2020). Training deep neural density estimators to
    identify mechanistic models of neural dynamics. <i>ELife</i>. eLife Sciences Publications.
    <a href="https://doi.org/10.7554/eLife.56261">https://doi.org/10.7554/eLife.56261</a>
  chicago: Gonçalves, Pedro J., Jan-Matthis Lueckmann, Michael Deistler, Marcel Nonnenmacher,
    Kaan Öcal, Giacomo Bassetto, Chaitanya Chintaluri, et al. “Training Deep Neural
    Density Estimators to Identify Mechanistic Models of Neural Dynamics.” <i>ELife</i>.
    eLife Sciences Publications, 2020. <a href="https://doi.org/10.7554/eLife.56261">https://doi.org/10.7554/eLife.56261</a>.
  ieee: P. J. Gonçalves <i>et al.</i>, “Training deep neural density estimators to
    identify mechanistic models of neural dynamics,” <i>eLife</i>, vol. 9. eLife Sciences
    Publications, 2020.
  ista: Gonçalves PJ, Lueckmann J-M, Deistler M, Nonnenmacher M, Öcal K, Bassetto
    G, Chintaluri C, Podlaski WF, Haddad SA, Vogels TP, Greenberg DS, Macke JH. 2020.
    Training deep neural density estimators to identify mechanistic models of neural
    dynamics. eLife. 9, e56261.
  mla: Gonçalves, Pedro J., et al. “Training Deep Neural Density Estimators to Identify
    Mechanistic Models of Neural Dynamics.” <i>ELife</i>, vol. 9, e56261, eLife Sciences
    Publications, 2020, doi:<a href="https://doi.org/10.7554/eLife.56261">10.7554/eLife.56261</a>.
  short: P.J. Gonçalves, J.-M. Lueckmann, M. Deistler, M. Nonnenmacher, K. Öcal, G.
    Bassetto, C. Chintaluri, W.F. Podlaski, S.A. Haddad, T.P. Vogels, D.S. Greenberg,
    J.H. Macke, ELife 9 (2020).
das_tickbox: '1'
date_created: 2020-07-16T12:26:04Z
date_published: 2020-09-17T00:00:00Z
date_updated: 2026-07-13T12:31:21Z
day: '17'
ddc:
- '570'
department:
- _id: TiVo
doi: 10.7554/eLife.56261
ec_funded: 1
external_id:
  isi:
  - '000584989400001'
  pmid:
  - '32940606'
file:
- access_level: open_access
  checksum: c4300ddcd93ed03fc9c6cdf1f77890be
  content_type: application/pdf
  creator: cziletti
  date_created: 2020-10-27T11:37:32Z
  date_updated: 2020-10-27T11:37:32Z
  file_id: '8709'
  file_name: 2020_eLife_Gonçalves.pdf
  file_size: 17355867
  relation: main_file
  success: 1
file_date_updated: 2020-10-27T11:37:32Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 0aacfa84-070f-11eb-9043-d7eb2c709234
  call_identifier: H2020
  grant_number: '819603'
  name: Learning the shape of synaptic plasticity rules for neuronal architectures
    and function through machine learning.
publication: eLife
publication_identifier:
  eissn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Training deep neural density estimators to identify mechanistic models of neural
  dynamics
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 9
year: '2020'
...
