Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.
about
Family studies to find rare high risk variants in migraine.Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.Progress in Genetic Studies of Tourette's Syndrome.Nervous system development and disease: A focus on trithorax related proteins and chromatin remodelers.Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers.Truncating mutations in RBM12 are associated with psychosis.A Methylome-Wide Association Study of Trajectories of Oppositional Defiant Behaviors and Biological Overlap With Attention Deficit Hyperactivity Disorder.Variance explained by whole genome sequence variants in coding and regulatory genome annotations for six dairy traits.[Genetics and epigenetics of schizophrenia and other psychoses].Shank2 Deletion in Parvalbumin Neurons Leads to Moderate Hyperactivity, Enhanced Self-Grooming and Suppressed Seizure Susceptibility in Mice.Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.Distinct Phenotypes of Mouse Models Reflect Neuropsychiatric Spectrum Disorders of Human Patients With Variants
P2860
Q36296198-8F394C7F-6F30-4ADB-A7E9-1DA6D6712098Q38705083-EFC4E1A2-9DD3-4A1D-B9ED-7D07DE51A4C5Q38939089-8282B91A-9D5A-4B6B-9EE9-2E8EB65D6FEFQ47147207-10E46B35-E623-4AE7-89E7-1073AEBBEB35Q47340829-7927380A-F09A-4AC2-9DEA-AC6202930E1BQ47631610-A307CB9B-2CD1-4066-B9CC-130A0263F8E1Q48258271-7A7595EB-A944-44DA-9F02-2AE95E5B9764Q50000961-E042A2E2-0F3B-4181-BA86-A14F2F181EE4Q52331979-773F5100-49B0-4107-A797-7C21A72D528CQ52585640-50075086-6561-445A-882C-33EA7DC17406Q55438998-9A4845EB-D074-413B-B763-25ED4F5E01CCQ55453560-B517FEBF-EC49-4C85-A1C5-AC8BEA20841DQ57175338-84463A7E-F8E7-469C-9C16-15DD166A8987
P2860
Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մարտին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Whole-genome sequencing in mul ...... enes segregating with illness.
@ast
Whole-genome sequencing in mul ...... enes segregating with illness.
@en
type
label
Whole-genome sequencing in mul ...... enes segregating with illness.
@ast
Whole-genome sequencing in mul ...... enes segregating with illness.
@en
prefLabel
Whole-genome sequencing in mul ...... enes segregating with illness.
@ast
Whole-genome sequencing in mul ...... enes segregating with illness.
@en
P2093
P2860
P3181
P356
P1433
P1476
Whole-genome sequencing in mul ...... enes segregating with illness.
@en
P2093
L E DeLisi
O R Homann
R W Sandrock
S I McDonough
P2860
P2888
P304
P3181
P356
10.1038/MP.2016.24
P407
P577
2016-03-22T00:00:00Z