Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder-Reference-Cited by-同舟云学术

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Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder

Published:2017-06 Issue:3 Volume:27 Page:81-88
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:

Author:

Sharp Sally I.,Lange Jenny,Kandaswamy Radhika,Daher Mazen,Anjorin Adebayo,Bass Nicholas J.,McQuillin Andrew

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics (clinical),Genetics

Reference88 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat Methods,2010

2. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis;Attali;Hum Mol Genet,2009

3. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia;Badner;Mol Psychiatry,2002

4. The genetics of bipolar disorder;Barnett;Neuroscience,2009

5. Coiled coils: a highly versatile protein folding motif;Burkhard;Trends Cell Biol,2001

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3. Rare Variant in the SLC6A2 Encoding a Norepinephrine Transporter Is Associated with Elite Athletic Performance in the Polish Population;Genes;2021-06-15

4. Targeted exon sequencing in deceased schizophrenia patients in Denmark;International Journal of Legal Medicine;2019-11-26

5. Evolutionary coupling analysis identifies the impact of disease-associated variants at less-conserved sites;Nucleic Acids Research;2019-06-14

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