Rare coding variants in ten genes confer substantial risk for schizophrenia
Published 2022 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Rare coding variants in ten genes confer substantial risk for schizophrenia
Authors
Keywords
-
Journal
NATURE
Volume 604, Issue 7906, Pages 509-516
Publisher
Springer Science and Business Media LLC
Online
2022-04-09
DOI
10.1038/s41586-022-04556-w
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mapping genomic loci implicates genes and synaptic biology in schizophrenia
- (2022) Vassily Trubetskoy et al. NATURE
- Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders
- (2020) Sónia Barbosa et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
- (2020) F. Kyle Satterstrom et al. CELL
- Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations
- (2020) Daniel P. Howrigan et al. NATURE NEUROSCIENCE
- Genetics of schizophrenia in the South African Xhosa
- (2020) S. Gulsuner et al. SCIENCE
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- Evidence for 28 genetic disorders discovered by combining healthcare and research data
- (2020) Joanna Kaplanis et al. NATURE
- SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse
- (2019) Frank Koopmans et al. NEURON
- Genetic identification of brain cell types underlying schizophrenia
- (2018) Nathan G. Skene et al. NATURE GENETICS
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
- (2018) Hilary K. Finucane et al. NATURE GENETICS
- Molecular Architecture of the Mouse Nervous System
- (2018) Amit Zeisel et al. CELL
- The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
- (2017) Tarjinder Singh et al. NATURE GENETICS
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
- (2016) Christian R Marshall et al. NATURE GENETICS
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
- (2016) Tarjinder Singh et al. NATURE NEUROSCIENCE
- Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
- (2016) Giulio Genovese et al. NATURE NEUROSCIENCE
- Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
- (2015) Po-Ru Loh et al. NATURE GENETICS
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
- (2015) NATURE NEUROSCIENCE
- Effect of predicted protein-truncating genetic variants on the human transcriptome
- (2015) M. A. Rivas et al. SCIENCE
- Rare-Variant Association Analysis: Study Designs and Statistical Tests
- (2014) Seunggeung Lee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The glutamate hypothesis of schizophrenia: evidence from human brain tissue studies
- (2014) Wei Hu et al. Annals of the New York Academy of Sciences
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- Large-scale discovery of novel genetic causes of developmental disorders
- (2014) T. W. Fitzgerald et al. NATURE
- A framework for the interpretation of de novo mutation in human disease
- (2014) Kaitlin E Samocha et al. NATURE GENETICS
- Searching for missing heritability: Designing rare variant association studies
- (2014) O. Zuk et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Pfam: the protein families database
- (2013) Robert D. Finn et al. NUCLEIC ACIDS RESEARCH
- Revolution Stalled
- (2012) S. E. Hyman Science Translational Medicine
- Spatio-temporal transcriptome of the human brain
- (2011) Hyo Jung Kang et al. NATURE
- Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
- (2010) Sabine Endele et al. NATURE GENETICS
- Reproductive patterns in psychotic patients
- (2010) T.M. Laursen et al. SCHIZOPHRENIA RESEARCH
- Schizophrenia: A Concise Overview of Incidence, Prevalence, and Mortality
- (2008) J. McGrath et al. EPIDEMIOLOGIC REVIEWS
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now