(Q28752178)

9

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

4

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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

33

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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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Strong association of de novo copy number mutations with sporadic schizophrenia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Neuregulin 1 and susceptibility to schizophrenia

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Inference of population structure using multilocus genotype data

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

7 April 2017

1 reference

https://api.crossref.org/works/10.1038/MP.2009.11

A high-resolution recombination map of the human genome

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

A HapMap harvest of insights into the genetics of common disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Allegro, a new computer program for multipoint linkage analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Genetic abnormalities of chromosome 22 and the development of psychosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Enhanced pedigree error detection

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Identification and analysis of error types in high-throughput genotyping

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Allele-sharing models: LOD scores and accurate linkage tests

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Irish study on high-density schizophrenia families: field methods and power to detect linkage

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

Incorrect specification of marker allele frequencies: effects on linkage analysis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2714870

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

20 June 2018

1 reference

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

Multicenter linkage study of schizophrenia loci on chromosome 22q.

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome-wide search for schizophrenia susceptibility loci: The NIMH genetics initiative and millennium consortium

1 reference

12 December 2020

Genome scan of schizophrenia

1 reference

12 December 2020

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

1 reference

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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

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

1040481434

0 references

Fatcat ID

release_wwzsnbamz5h6hgsxvxq62sujlm

1 reference

Fatcat

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

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

19223858

1 reference