Association at SYNE1 in both bipolar disorder and recurrent major depression. (Q47796306)

5 February 2018

meta-analysis

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title

Association at SYNE1 in both bipolar disorder and recurrent major depression. (English)

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2

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Jennifer L. Moran

11

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Michael C O'Donovan

15

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Katherine Gordon-Smith

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K Gordon-Smith

4

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Nick Craddock

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object named as

N Craddock

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author name string

E K Green

1

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L Forty

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E Russell

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A Farmer

6

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M Hamshere

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I R Jones

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L Jones

9

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P McGuffin

10

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S Purcell

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P Sklar

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M J Owen

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language of work or name

English

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publication date

8 May 2012

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published in

Molecular Psychiatry

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volume

18

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issue

5

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page(s)

614-617

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https://scigraph.springernature.com/pub.10.1038/mp.2012.48

exact match

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cites work

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

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Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

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Gene expression and genetic variation data implicate PCLO in bipolar disorder

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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

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Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

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Nesprins: intracellular scaffolds that maintain cell architecture and coordinate cell function?

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Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

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Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

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Genome-wide association study identifies five new schizophrenia loci

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Design of Case-controls Studies with Unscreened Controls

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Genetics of bipolar disorder.

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inferred from DOI database lookup

7 January 2021

based on heuristic

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis

1 reference

https://api.crossref.org/works/10.1038%2FMP.2012.48

inferred from DOI database lookup

7 January 2021

based on heuristic

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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https://api.crossref.org/works/10.1038%2FMP.2012.48

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/MP.2012.48

1 reference

5 February 2018

PubMed ID

22565781

1 reference

5 February 2018