Related references
Note: Only part of the references are listed.Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
Joost Kummeling et al.
MOLECULAR PSYCHIATRY (2021)
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun et al.
NATURE (2021)
Genetic architecture of schizophrenia: a review of major advancements
Sophie E. Legge et al.
PSYCHOLOGICAL MEDICINE (2021)
CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scores
Philipp Rentzsch et al.
GENOME MEDICINE (2021)
SETD1A Mediated H3K4 Methylation and Its Role in Neurodevelopmental and Neuropsychiatric Disorders
Shan Wang et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2021)
Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia
Todd Lencz et al.
NEURON (2021)
jMorp updates in 2020: large enhancement of multi-omics data resources on the general Japanese population
Shu Tadaka et al.
NUCLEIC ACIDS RESEARCH (2021)
Aberrant Cortical Ensembles and Schizophrenia-like Sensory Phenotypes in Setd1a+/- Mice
Jordan P. Hamm et al.
BIOLOGICAL PSYCHIATRY (2020)
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations
Daniel P. Howrigan et al.
NATURE NEUROSCIENCE (2020)
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski et al.
NATURE (2020)
The polygenic architecture of schizophrenia - rethinking pathogenesis and nosology
Olav B. Smeland et al.
NATURE REVIEWS NEUROLOGY (2020)
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis et al.
NATURE (2020)
Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities
Kenichiro Nagahama et al.
CELL REPORTS (2020)
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Else Eising et al.
MOLECULAR PSYCHIATRY (2019)
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan et al.
CELL (2019)
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy
Xiuya Yu et al.
NEUROSCIENCE BULLETIN (2019)
Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice
Jun Mukai et al.
NEURON (2019)
Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study
Hirofumi Igeta et al.
NEUROPSYCHIATRIC DISEASE AND TREATMENT (2019)
High-resolution copy number variation analysis of schizophrenia in Japan
I. Kushima et al.
MOLECULAR PSYCHIATRY (2017)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R. Marshall et al.
NATURE GENETICS (2017)
Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese
Zhiqiang Li et al.
BIOLOGICAL PSYCHIATRY (2016)
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Tarjinder Singh et al.
NATURE NEUROSCIENCE (2016)
De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia
Atsushi Takata et al.
NEURON (2016)
Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility
Hiroki Kimura et al.
SCHIZOPHRENIA RESEARCH (2016)
SIFT web server: predicting effects of amino acid substitutions on proteins
Ngak-Leng Sim et al.
NUCLEIC ACIDS RESEARCH (2012)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
The dopamine D3 receptor (DRD3) gene and risk of schizophrenia: Case-control studies and an updated meta-analysis
Ayako Nunokawa et al.
SCHIZOPHRENIA RESEARCH (2010)
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: A cohort allelic sums test (CAST)
Stephan Morgenthaler et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2007)
No association between the brain-derived neurotrophic factor gene and schizophrenia in a Japanese population
Yuichiro Watanabe et al.
SCHIZOPHRENIA RESEARCH (2006)
Share Paper
