Increased exonic de novo mutation rate in individuals with schizophrenia

Girard, Simon L, Gauthier, Julie, Noreau, Anne, Xiong, Lan, Zhou, Sirui, Jouan, Loubna, Dionne-Laporte, Alexandre, Spiegelman, Dan +14 more·2011·Nature Genetics
DOI 10.1038/ng.886

Cited by (435)

Items 401–435 of 435

  1. Association analysis of potentially functional variants within 8p12 with schizophrenia in the Han Chinese population
    Ruirui Chen, Jianhua Chen, Chengwen Gao, Chuanhong Wu, Dun Pan, Jinmai Zhang, Juan Zhou, Ke Wang, Qian Zhang, Qiangzhen Yang et al. · 2020 · The World Journal of Biological Psychiatry
  2. Whole-exome capture and next-generation sequencing to discover rare variants predisposing to congenital heart disease
    Matthieu J. Miossec · 2016
  3. Genetic risk factors of childhood onset schizophrenia
    Amirthagowri Ambalavanan · 2017 · eScholarship@McGill (McGill)
  4. Investigating the molecular basis of concussion using whole exome sequencing and bioinformatics
    Omar Ezzeldin Ibrahim Abdelrahman · 2021 · Queensland University of Technology
  5. Genetics of Multiple Sclerosis
    Virpi Leppä · 2013 · Työväentutkimus Vuosikirja
  6. Sporadiese skisofrenie
    Johannes Lodewikus Roos · 2019
  7. Geïsoleerde populasies
    Johannes Lodewikus Roos · 2019
  8. Familiële skisofrenie
    Johannes Lodewikus Roos · 2019
  9. Analytical Approaches for Exome Sequence Data
    Andrew R Collins · 2018 · Translational bioinformatics
  10. Next-generation clinical sequencing in a children’s hospital
    Stephen Francis Kingsmore · 2011 · Genome biology
  11. Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen
    Wolfgang Maier, Ina Giegling, Dan Rujescu · 2016 · Springer eBooks
  12. Abstract not submitted for online publication
    2011 · Genome biology
  13. Genome-forward oncology: how do we get there?
    Matthew S. Ellis · 2011 · Genome biology
  14. Faculty Opinions recommendation of Clinical application of exome sequencing in undiagnosed genetic conditions.
    Sue Malcolm · 2012 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
  15. Reconstructing microbial communities
    Mihai Pop · 2011 · Genome biology
  16. Are clinical genomes already becoming semi-routine for patient care?
    Mark S. Boguski · 2011 · Genome biology
  17. De novo mutations in mental retardation
    Joris Andre Veltman · 2011 · Genome biology
  18. Harnessing New Genomics Technologies to Assess Environmental Risk Factors That May Cause Heritable Genetic Disease
    Marc A. Beal · 2017
  19. Faculty Opinions recommendation of Genetics of congenital anomalies of the kidney and urinary tract: the current state of play.
    Andreas Schedl · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
  20. Abstract not submitted for online publication
    2011 · Genome biology
  21. Abstract not submitted for online publication
    2011 · Genome biology
  22. Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen
    Wolfgang Maier, Ina Giegling, Dan Rujescu · 2017 · Springer eBooks
  23. Faculty Opinions recommendation of InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines.
    Stephen Turner · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
  24. The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis
    Natalie Wellard, Nicholas E. Clifton, Elliott Rees, Kerrie L. Thomas, Jérémy Hall · 2024 · International Journal of Molecular Sciences
  25. Microdeletion 3q13.33-3q21.2: A Rare Cause of Neurodevelopmental Disorder
    Yi Huang, Rongpu Jia, Yuan Qiu Chen, Liang Ji Zhou, Chen Yu Gou, Meiqiong Fan, Si Li, Maofa Chen, Hua Ming Lin, Yu Gao · 2024 · Journal of Pediatric Genetics
  26. Systematic evaluation of de novo mutation calling tools using whole genome sequencing data
    Anushi Shah, Steven Monger, Michael Troup, Eddie Ip, Eleni Giannoulatou · 2025 · Briefings in Bioinformatics
  27. Additional file 1 of The complete chloroplast genome of Ulmus mianzhuensis with insights into structural variations, adaptive evolution, and phylogenetic relationships of Ulmus (Ulmaceae)
    Lin, Nan, Liu, Rui, Wang, Yakun, Guo, Peng, Wang, Yihan, Yanpei Liu, 尚富德 SHANG Fude · 2023 · Figshare
  28. Identification de nouvelles bases moléculaires des cancers précoces par séquençage à haut débit.
    Pierre Fermey · 2017
  29. L'apport de la génétique dans la nosographie en psychiatrie : l’exemple des troubles bipolaires et de la schizophrénie
    Elisa Courtois · 2020
  30. Approche neuropsychologique des patients souffrant de Troubles Complexes du Développement (TCD) à l’âge adulte
    Charlotte Danset-Alexandre · 2019
  31. Comprehensive Assessment of the KDM2B ‐Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome
    Amber S E van Oirsouw, Tzung‐Chien Hsieh, Martijn J. Koetsier, Alali Abdulrazak, Fatimah Albuainain, Elena Bacchelli, Tahsin Stefan Barakat, Yline Capri, Sandra Chantot‐Bastaraud, Valeria Capra et al. · 2026 · Clinical Genetics
  32. Involvement of strawberry notch homologue 1 in neurite outgrowth of cortical neurons.
    金田勇人, 大 井原, 裕 勝山, Munkhsoyol Erkhembaatar, Iroha Yamamoto, Fuduki Inoguchi, Kosuke Taki, Satoru Yamagishi, Leanne M. Delaney, Mariko Nishibe et al. · Institutional Repositories DataBase (IRDB)
  33. The Molecular Machinery of Synaptic Plasticity and Its Potential Role in the Aetiology of Schizophrenia
    BRIAN J. MORRIS · 2026 · Molecular Neurobiology
  34. KPNA1/importin α5 localizes to the nucleolus and associates with box C/D snoRNP complexes
    Osamu Kutomi, Katsutoshi Mizuno, Takafumi Itoh, Masami Yamada · 2026 · Biochemical and Biophysical Research Communications
  35. Clinical, genetic and functional characterization of intellectual disability disorders
    Christiane Zweier · 2014 · Radboud Repository (Radboud University)