(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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5 February 2018

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2

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Jennifer L. Moran

11

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5 February 2018

Michael C O'Donovan

15

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5 February 2018

Katherine Gordon-Smith

object named as

K Gordon-Smith

4

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Nick Craddock

16

object named as

N Craddock

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5 February 2018

author name string

E K Green

1

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5 February 2018

L Forty

3

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E Russell

5

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A Farmer

6

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M Hamshere

7

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I R Jones

8

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L Jones

9

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5 February 2018

P McGuffin

10

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S Purcell

12

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P Sklar

13

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M J Owen

14

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language of work or name

English

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publication date

8 May 2012

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5 February 2018

published in

Molecular Psychiatry

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5 February 2018

volume

18

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issue

5

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5 February 2018

page(s)

614-617

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5 February 2018

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

exact match

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cites work

Genetics of bipolar disorder: successful start to a long journey

1 reference

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

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

21 January 2018

1 reference

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

Genomewide association studies: history, rationale, and prospects for psychiatric disorders

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

The Kraepelinian dichotomy - going, going... but still not gone

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Gene expression and genetic variation data implicate PCLO in bipolar disorder

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Identification of loci associated with schizophrenia by genome-wide association and follow-up

21 January 2018

1 reference

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

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

21 January 2018

1 reference

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

SCAN. Schedules for Clinical Assessment in Neuropsychiatry

21 January 2018

1 reference

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

A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system

21 January 2018

1 reference

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

Concurrent validity of the OPCRIT diagnostic system. Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnoses.

21 January 2018

1 reference

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

Research diagnostic criteria: rationale and reliability

21 January 2018

1 reference

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

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

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

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

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

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

21 January 2018

1 reference

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

The Bipolar Affective Disorder Dimension Scale (BADDS)--a dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

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

Family, twin, and adoption studies of bipolar disorder

21 January 2018

1 reference

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

Design of Case-controls Studies with Unscreened Controls

21 January 2018

1 reference

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

Genetics of bipolar disorder.

21 January 2018

1 reference

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

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

1 reference

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

1 reference

5 February 2018