(Q24532517)

28

0 references

Jouko Lönnqvist

27

0 references

Stilianos Antonarakis

35

0 references

Michael C O'Donovan

29

0 references

Stephen Faraone

10

0 references

Hans W. Moises

Hans W Moises

17

0 references

Jill M Harkavy-Friedman

Jill M Harkavy-Friedman

42

0 references

Andrew McQuillin

Andrew McQuillin

47

0 references

Iiris Hovatta

Iiris Hovatta

6

0 references

Thordur Sigmundsson

49

Thordur Sigmundsson

0 references

Tiina Paunio

26

Tiina Paunio

0 references

Cathryn Lewis

Cathryn M Lewis

1

0 references

Kenneth Kendler

24

Kenneth S Kendler

0 references

Dolores Malaspina

41

Dolores Malaspina

0 references

C. Robert Cloninger

39

C Robert Cloninger

0 references

Dermot Walsh

23

Dermot Walsh

0 references

Gerald Nestadt

33

Gerald Nestadt

0 references

author name string

Douglas F Levinson

2

0 references

Lesley H Wise

3

0 references

Lynn E DeLisi

4

0 references

Richard E Straub

5

0 references

Nigel M Williams

7

0 references

Sibylle G Schwab

8

0 references

Ann E Pulver

9

0 references

Linda M Brzustowicz

11

0 references

Charles A Kaufmann

12

0 references

David L Garver

13

0 references

Hugh M D Gurling

14

0 references

Eva Lindholm

15

0 references

Hilary Coon

16

0 references

William Byerley

18

0 references

Sarah H Shaw

19

0 references

Andrea Mesen

20

0 references

Robin Sherrington

21

0 references

F Anthony O'Neill

22

0 references

Jesper Ekelund

25

0 references

Michael J Owen

30

0 references

Dieter B Wildenauer

31

0 references

Wolfgang Maier

32

0 references

Jean-Louis Blouin

34

0 references

Bryan J Mowry

36

0 references

Jeremy M Silverman

37

0 references

Raymond R Crowe

38

0 references

Ming T Tsuang

40

0 references

Dragan M Svrakic

43

0 references

Anne S Bassett

44

0 references

Jennifer Holcomb

45

0 references

Gursharan Kalsi

46

0 references

Jon Brynjolfson

48

0 references

Hannes Petursson

50

0 references

Elena Jazin

51

0 references

Tomas Zoëga

52

0 references

Tomas Helgason

American Journal of Human Genetics

53

0 references

language of work or name

English

0 references

publication date

July 2003

0 references

number of pages

15

0 references

published in

0 references

volume

73

0 references

page(s)

34-48

0 references

issue

1

0 references

cites work

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Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

24 March 2017

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Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

24 March 2017

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Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

24 March 2017

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Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

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24 March 2017

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7 April 2017

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Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

27 September 2017

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Large upward bias in estimation of locus-specific effects from genomewide scans

27 September 2017

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Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

27 September 2017

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Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

27 September 2017

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The relationship between the sibling recurrence-risk ratio and genotype relative risk

27 September 2017

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27 September 2017

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Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

27 September 2017

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A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

30 May 2018

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Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families

30 May 2018

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Meta-analysis of genome searches

29 November 2018

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Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.

29 November 2018

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Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families

29 November 2018

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Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

29 November 2018

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

29 November 2018

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Autosome search for schizophrenia susceptibility genes in multiply affected families

29 November 2018

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12 December 2020

Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder

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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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A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes

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Schizophrenia spectrum disorders: an autosomal-wide scan in multiplex pedigrees

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Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q

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Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q

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Genomic scan for genes predisposing to schizophrenia

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Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

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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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Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis

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Genome scan of schizophrenia

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Evidence for a chromosome 2p13-14 schizophrenia susceptibility locus in families from Palau, Micronesia

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

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Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

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Crossref

https://api.crossref.org/works/10.1086%2F376549

7 January 2021

inferred from DOI database lookup

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

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F376549

7 January 2021

inferred from DOI database lookup

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F376549

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/376549

1 reference

release_3znvewv6ibdd3pzyhq2gzaxzbu

624474

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3znvewv6ibdd3pzyhq2gzaxzbu

24 November 2022

mapped directly with Wikidata item

624474

1 reference

1 reference

1 reference