A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus (Q34388619)

1 August 2017

title

A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus (English)

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1 August 2017

V M Aita

1

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1 August 2017

J Liu

2

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1 August 2017

J A Knowles

3

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1 August 2017

J D Terwilliger

4

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1 August 2017

R Baltazar

5

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1 August 2017

A Grunn

6

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1 August 2017

J E Loth

7

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1 August 2017

K Kanyas

8

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1 August 2017

B Lerer

9

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1 August 2017

J Endicott

10

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1 August 2017

Z Wang

11

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1 August 2017

G Penchaszadeh

12

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1 August 2017

T C Gilliam

13

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1 August 2017

M Baron

14

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1 August 2017

language of work or name

English

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publication date

1 January 1999

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

64

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1 August 2017

issue

1

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1 August 2017

page(s)

210-217

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Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3.

1 August 2017

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Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome

6 July 2018

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6 July 2018

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6 July 2018

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Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.

6 July 2018

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Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis

6 July 2018

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Genetic linkage and bipolar affective disorder: progress and pitfalls

6 July 2018

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Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome

6 July 2018

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Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21

6 July 2018

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6 July 2018

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Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q

6 July 2018

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6 July 2018

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A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

6 July 2018

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Is there an inverse relationship between Down's syndrome and bipolar affective disorder? Literature review and genetic implications.

6 July 2018

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A transcript map of the Down syndrome critical region on chromosome 21.

6 July 2018

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Strategies for multilocus linkage analysis in humans

6 July 2018

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The familial transmission of bipolar illness.

6 July 2018

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6 July 2018

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A diagnostic interview: the schedule for affective disorders and schizophrenia

6 July 2018

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6 July 2018

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6 July 2018

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Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosomes 11p15 and 21q22.

27 October 2018

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Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis.

27 October 2018

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Bipolar disorder: evidence for a major locus

27 October 2018

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A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method.

27 October 2018

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A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.

27 October 2018

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

A pedigree series for mapping disease genes in bipolar affective disorder: sampling, assessment, and analytic considerations

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloning

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https://pubmed.ncbi.nlm.nih.gov/9915960

12 December 2020

Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group

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12 December 2020

Identifiers

DOI

10.1086/302185

1 reference

1 August 2017

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1 August 2017

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