Haplotype tagging for the identification of common disease genes (Q59200321)

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11 November 2019

title

Haplotype tagging for the identification of common disease genes (English)

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11 November 2019

3

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11 November 2019

Frank Dudbridge

10

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11 November 2019

Felicity Payne

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11 November 2019

author name string

Johnson GC

1

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11 November 2019

Esposito L

2

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11 November 2019

Smith AN

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11 November 2019

Heward J

5

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11 November 2019

Di Genova G

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11 November 2019

Ueda H

7

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11 November 2019

Cordell HJ

8

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11 November 2019

Eaves IA

9

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11 November 2019

Twells RC

11

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11 November 2019

Hughes W

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11 November 2019

Nutland S

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11 November 2019

Stevens H

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11 November 2019

Carr P

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11 November 2019

Tuomilehto-Wolf E

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11 November 2019

Tuomilehto J

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11 November 2019

Gough SC

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11 November 2019

Clayton DG

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11 November 2019

Todd JA

21

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11 November 2019

language of work or name

English

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publication date

1 October 2001

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11 November 2019

1 reference

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11 November 2019

volume

29

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11 November 2019

issue

2

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11 November 2019

page(s)

233-237

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A comparison of linkage disequilibrium measures for fine-scale mapping

11 November 2019

cites work

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7 January 2021

The optimal measure of allelic association

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7 January 2021

Linkage disequilibrium in humans: models and data

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7 January 2021

Linkage disequilibrium in the human genome

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7 January 2021

High-resolution haplotype structure in the human genome

1 reference

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7 January 2021

Global patterns of linkage disequilibrium at the CD4 locus and modern human origins

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7 January 2021

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

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7 January 2021

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

1 reference

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7 January 2021

Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium

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7 January 2021

Lactase haplotype diversity in the Old World

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7 January 2021

Sequence variation in the human angiotensin converting enzyme

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7 January 2021

Evidence for variable selective pressures at MC1R

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7 January 2021

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism

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7 January 2021

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

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7 January 2021

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

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7 January 2021

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease

1 reference

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7 January 2021

Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR.

1 reference

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7 January 2021

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

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7 January 2021

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

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7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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7 January 2021

Single-nucleotide polymorphisms in the public domain: how useful are they?

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7 January 2021

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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7 January 2021

Complexity and power in case-control association studies

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7 January 2021

Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

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7 January 2021

Evolution of human and non-human primate CC chemokine receptor 5 gene and mRNA. Potential roles for haplotype and mRNA diversity, differential haplotype-specific transcriptional activity, and altered transcription factor binding to polymorphic nucle

1 reference

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7 January 2021

Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects

1 reference

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7 January 2021

Identification of susceptibility loci for insulin-dependent diabetes mellitus by trans-racial gene mapping.

1 reference

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7 January 2021

Ancestral haplotypes reveal the role of the central MHC in the immunogenetics of IDDM

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7 January 2021

Fine-mapping of an ancestral recombination breakpoint in DCP1

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7 January 2021

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation

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7 January 2021

Identifiers

DOI

10.1038/NG1001-233

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11586306%20AND%20SRC:MED&resulttype=core&format=json

release_kmzqtuts2zgbfbcjultmc5u4zi

11 November 2019

Fatcat ID

0 references

1 reference