Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
出版年份 2021 全文链接
标题
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
作者
关键词
-
出版物
Nature Communications
Volume 12, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2021-09-09
DOI
10.1038/s41467-021-25532-4
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
- (2020) F. Kyle Satterstrom et al. CELL
- Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
- (2020) Isabelle Cleynen et al. MOLECULAR PSYCHIATRY
- 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
- De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
- (2020) Elliott Rees et al. NATURE NEUROSCIENCE
- Transcript expression-aware annotation improves rare variant interpretation
- (2020) Beryl B. Cummings et al. NATURE
- 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
- Nonsocial and social cognition in schizophrenia: current evidence and future directions
- (2019) Michael F. Green et al. World Psychiatry
- MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
- (2019) Christopher C Y Mak et al. BRAIN
- Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis
- (2018) Andrew E. Jaffe et al. NATURE NEUROSCIENCE
- Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia
- (2018) Sarah E. Bergen et al. AMERICAN JOURNAL OF PSYCHIATRY
- The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
- (2017) Tarjinder Singh et al. NATURE GENETICS
- ClinVar: improving access to variant interpretations and supporting evidence
- (2017) Melissa J Landrum et al. NUCLEIC ACIDS RESEARCH
- Schizophrenia and the neurodevelopmental continuum:evidence from genomics
- (2017) Michael J. Owen et al. World Psychiatry
- De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
- (2016) Vandana Shashi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
- (2016) Chelsea Lowther et al. GENETICS IN MEDICINE
- 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
- The implications of the shared genetics of psychiatric disorders
- (2016) Michael C O'Donovan et al. NATURE MEDICINE
- 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
- Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia
- (2016) Elliott Rees et al. JAMA Psychiatry
- IQ and Schizophrenia in a Swedish National Sample: Their Causal Relationship and the Interaction of IQ With Genetic Risk
- (2015) Kenneth S. Kendler et al. AMERICAN JOURNAL OF PSYCHIATRY
- De novo variants in sporadic cases of childhood onset schizophrenia
- (2015) Amirthagowri Ambalavanan et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Common alleles contribute to schizophrenia in CNV carriers
- (2015) K E Tansey et al. MOLECULAR PSYCHIATRY
- Increased co-expression of genes harboring the damaging de novo mutations in Chinese schizophrenic patients during prenatal development
- (2015) Qiang Wang et al. Scientific Reports
- De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
- (2014) S E McCarthy et al. MOLECULAR PSYCHIATRY
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- A framework for the interpretation of de novo mutation in human disease
- (2014) Kaitlin E Samocha et al. NATURE GENETICS
- Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene
- (2014) Atsushi Takata et al. NEURON
- Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes
- (2014) Michel Guipponi et al. PLoS One
- Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
- (2013) Suleyman Gulsuner et al. CELL
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia
- (2013) Stephan Ripke et al. NATURE GENETICS
- De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
- (2012) Bin Xu et al. NATURE GENETICS
- Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
- (2012) S Hong Lee et al. NATURE GENETICS
- Genetic architectures of psychiatric disorders: the emerging picture and its implications
- (2012) Patrick F. Sullivan et al. NATURE REVIEWS GENETICS
- Neurodevelopmental hypothesis of schizophrenia
- (2011) Michael J. Owen et al. BRITISH JOURNAL OF PSYCHIATRY
- Increased exonic de novo mutation rate in individuals with schizophrenia
- (2011) Simon L Girard et al. NATURE GENETICS
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
- (2009) Helen V. Firth et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Intellectual disability co-occurring with schizophrenia and other psychiatric illness: population-based study
- (2008) Vera A. Morgan et al. BRITISH JOURNAL OF PSYCHIATRY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd 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 Now