Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms (Q28752178)

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object named as

K S Kendler

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author name string

P A Holmans

1

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B Riley

2

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A E Pulver

3

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M J Owen

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D B Wildenauer

5

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P V Gejman

6

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B J Mowry

7

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C Laurent

8

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G Nestadt

10

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N M Williams

11

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S G Schwab

12

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A R Sanders

13

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D Nertney

14

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J Mallet

15

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B Wormley

16

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V K Lasseter

17

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M C O'Donovan

18

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J Duan

19

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M Albus

20

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M Alexander

21

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S Godard

22

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R Ribble

23

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K Y Liang

24

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N Norton

25

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G Papadimitriou

27

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D Walsh

28

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M Jay

29

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A O'Neill

30

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F B Lerer

31

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D Dikeos

32

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R R Crowe

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J M Silverman

34

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D F Levinson

Large recurrent microdeletions associated with schizophrenia

35

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language of work or name

English

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publication date

August 2009

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published in

Molecular Psychiatry

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volume

14

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issue

8

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page(s)

786-95

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cites work

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Association of the NRG1 gene and schizophrenia: a meta-analysis

16 March 2017

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Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

16 March 2017

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Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

16 March 2017

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

16 March 2017

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Neuregulin 1 and susceptibility to schizophrenia

16 March 2017

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

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16 March 2017

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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

16 March 2017

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Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium

16 March 2017

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NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

16 March 2017

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Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

16 March 2017

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

16 March 2017

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The allelic architecture of human disease genes: common disease-common variant... or not?

7 April 2017

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A high-resolution recombination map of the human genome

22 April 2017

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7 April 2017

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

7 April 2017

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Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

20 June 2018

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Genetics of recurrent early-onset major depression (GenRED): final genome scan report

20 June 2018

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The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees

20 June 2018

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Using linkage genome scans to improve power of association in genome scans

20 June 2018

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Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

20 June 2018

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Genetic abnormalities of chromosome 22 and the development of psychosis

20 June 2018

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A systematic genomewide linkage study in 353 sib pairs with schizophrenia

20 June 2018

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Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2

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Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

20 June 2018

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20 June 2018

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21 January 2018

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Genetics of Recurrent Early-Onset Major Depression (GenRED): Final Genome Scan Report

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Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes

21 January 2018

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Whole genome linkage scan of recurrent depressive disorder from the depression network study.

21 January 2018

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Genome Scan of Han Chinese Schizophrenia Families From Taiwan: Confirmation of Linkage to 10q22.3

21 January 2018

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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

21 January 2018

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Detecting Gene-Gene Interactions Using Affected Sib Pair Analysis with Covariates

21 January 2018

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Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder

21 January 2018

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12 December 2020

Genetic study of dopamine D1, D2, and D4 receptors in schizophrenia

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Genome scan of schizophrenia

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12 December 2020

Diagnostic accuracy and confusability analyses: an application to the Diagnostic Interview for Genetic Studies

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12 December 2020

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8

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Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study

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A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

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No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia

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BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

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12 December 2020

Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium

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7 January 2021

inferred from DOI database lookup

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.11

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/MP.2009.11

1 reference

Dimensions Publication ID

1132140

1040481434

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Fatcat ID

release_wwzsnbamz5h6hgsxvxq62sujlm

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Fatcat

https://api.fatcat.wiki/v0/release/wwzsnbamz5h6hgsxvxq62sujlm

24 November 2022

mapped directly with Wikidata item

1132140

1 reference

1 reference

1 reference