9 Publications

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[9]
2022 | Journal Article | IST-REx-ID: 11160 | OA
C. E. Villa et al., “CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories,” Cell Reports, vol. 39, no. 1. Elsevier, 2022.
View | Files available | DOI | PubMed | Europe PMC
 
[8]
2022 | Thesis | IST-REx-ID: 12364
C. Dotter, “Transcriptional consequences of mutations in genes associated with Autism Spectrum Disorder,” Institute of Science and Technology Austria, 2022.
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[7]
2021 | Journal Article | IST-REx-ID: 9429 | OA
J. Morandell et al., “Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development,” Nature Communications, vol. 12, no. 1. Springer Nature, 2021.
View | Files available | DOI
 
[6]
2019 | Research Data | IST-REx-ID: 6074 | OA
C. Dotter and G. Novarino, “Supplementary data for the research paper ‘Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.’” IST Austria, 2019.
View | Files available | DOI
 
[5]
2018 | Journal Article | IST-REx-ID: 3 | OA
E. Deliu et al., “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition,” Nature Neuroscience, vol. 21, no. 12. Nature Publishing Group, pp. 1717–1727, 2018.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 713 | OA
D. Andergassen et al., “Mapping the mouse Allelome reveals tissue specific regulation of allelic expression,” eLife, vol. 6. eLife Sciences Publications, 2017.
View | Files available | DOI
 
[3]
2016 | Journal Article | IST-REx-ID: 1240 | OA
A. Kornienko et al., “Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans,” Genome Biology, vol. 17, no. 1. BioMed Central, 2016.
View | Files available | DOI
 
[2]
2016 | Journal Article | IST-REx-ID: 1183 | OA
Tarlungeanu D-C, Deliu E, Dotter C, Kara M, Janiesch P, Scalise M, Galluccio M, Tesulov M, Morelli E, Sönmez F, Bilgüvar K, Ohgaki R, Kanai Y, Johansen A, Esharif S, Ben Omran T, Topcu M, Schlessinger A, Indiveri C, Duncan K, Caglayan A, Günel M, Gleeson J, Novarino G. 2016. Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell. 167(6), 1481–1494.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1497 | OA
D. Andergassen et al., “Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data,” Nucleic Acids Research, vol. 43, no. 21. Oxford University Press, 2015.
View | Files available | DOI
 

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9 Publications

Mark all

[9]
2022 | Journal Article | IST-REx-ID: 11160 | OA
C. E. Villa et al., “CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories,” Cell Reports, vol. 39, no. 1. Elsevier, 2022.
View | Files available | DOI | PubMed | Europe PMC
 
[8]
2022 | Thesis | IST-REx-ID: 12364
C. Dotter, “Transcriptional consequences of mutations in genes associated with Autism Spectrum Disorder,” Institute of Science and Technology Austria, 2022.
View | Files available | DOI
 
[7]
2021 | Journal Article | IST-REx-ID: 9429 | OA
J. Morandell et al., “Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development,” Nature Communications, vol. 12, no. 1. Springer Nature, 2021.
View | Files available | DOI
 
[6]
2019 | Research Data | IST-REx-ID: 6074 | OA
C. Dotter and G. Novarino, “Supplementary data for the research paper ‘Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.’” IST Austria, 2019.
View | Files available | DOI
 
[5]
2018 | Journal Article | IST-REx-ID: 3 | OA
E. Deliu et al., “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition,” Nature Neuroscience, vol. 21, no. 12. Nature Publishing Group, pp. 1717–1727, 2018.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 713 | OA
D. Andergassen et al., “Mapping the mouse Allelome reveals tissue specific regulation of allelic expression,” eLife, vol. 6. eLife Sciences Publications, 2017.
View | Files available | DOI
 
[3]
2016 | Journal Article | IST-REx-ID: 1240 | OA
A. Kornienko et al., “Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans,” Genome Biology, vol. 17, no. 1. BioMed Central, 2016.
View | Files available | DOI
 
[2]
2016 | Journal Article | IST-REx-ID: 1183 | OA
Tarlungeanu D-C, Deliu E, Dotter C, Kara M, Janiesch P, Scalise M, Galluccio M, Tesulov M, Morelli E, Sönmez F, Bilgüvar K, Ohgaki R, Kanai Y, Johansen A, Esharif S, Ben Omran T, Topcu M, Schlessinger A, Indiveri C, Duncan K, Caglayan A, Günel M, Gleeson J, Novarino G. 2016. Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell. 167(6), 1481–1494.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1497 | OA
D. Andergassen et al., “Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data,” Nucleic Acids Research, vol. 43, no. 21. Oxford University Press, 2015.
View | Files available | DOI
 

Search

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