Cited by 148Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomics and Rare Diseases

Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism

Ben-David, E, Shifman, S·2013·Molecular Psychiatry

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Crossref · 10.1038/mp.2012.148

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  • Gene network analyses can aid in understanding genetic association studies.

    “As shown by multiple studies, gene network analyses can aid in understanding genetic association studies.”
  • Grouping genetic findings using disease- and tissue-relevant modules can increase power to detect genetic associations by combining signals reflecting similar biology while informing mechanism by functionally annotating genetic findings.

    “Grouping genetic findings using disease- and tissue-relevant modules can increase the power to detect genetic associations with disease by combining signals that reflect similar underlying biology while simultaneously informing biological mechanism by functionally annotating genetic findings30,109,122,183.”

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References 8 · Cited by 148

Authors
Ben-David, E., & Shifman, S.
Affiliations
Hebrew University of Jerusalem (IL)
Corresponding author
Shifman, S
Venue
Molecular Psychiatry
Published
2012-11-13
Volume
18
Issue
10
Pages
1054-1056
ISSN
  • 1359-4184 (ISSN-L)
  • 1476-5578
OpenAlex
W2082107430
Cited by
148
References
8
Citations by year
2026: 4 · 2025: 2 · 2024: 2 · 2023: 6 · 2022: 7 · 2021: 8 · 2020: 11 · 2019: 19 · 2018: 9 · 2017: 11 · 2016: 11 · 2015: 27 · 2014: 17 · 2013: 13
FWCI
10.99
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
Keywords
autism spectrum disorder, brain development, transcriptional regulation, de novo mutations, exome sequencing, chromatin remodeling, gene expression regulation, intellectual disability, chromatin modification
MeSH terms
Brain, Child Development Disorders, Pervasive, DNA-Binding Proteins, Humans, Mutation, Nerve Tissue Proteins, Transcription Factors, Transcription, Genetic, Homeodomain Proteins, Gene Expression Regulation, Developmental, Polymorphism, Single Nucleotide, Chromatin Assembly and Disassembly, Multiprotein Complexes, Exome

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