(Q39787996)

14 September 2017

title

Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci (English)

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14 September 2017

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1

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Stefan Schreiber

series ordinal

3

object named as

Stefan Schreiber

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14 September 2017

4

Andre Franke

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14 September 2017

David Ellinghaus

2

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14 September 2017

Tim Becker

series ordinal

5

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14 September 2017

language of work or name

English

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publication date

21 March 2016

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14 September 2017

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14 September 2017

volume

32

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14 September 2017

issue

14

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14 September 2017

page(s)

2136-2142

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An integrated map of genetic variation from 1,092 human genomes

14 September 2017

cites work

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https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW125

Synthetic associations are unlikely to account for many common disease genome-wide association signals

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21 January 2018

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Rare variants create synthetic genome-wide associations

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Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

21 January 2018

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Common genetic variation and human traits

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The importance of synthetic associations will only be resolved empirically

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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

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Genome-wide association study signal at the 12q12 locus for Crohn's disease may represent associations with the MUC19 gene.

21 January 2018

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

21 January 2018

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21 January 2018

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21 January 2018

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Conditions under which genome-wide association studies will be positively misleading.

21 January 2018

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Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locus

21 January 2018

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A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose

21 January 2018

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Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants

21 January 2018

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Association of warfarin dose with genes involved in its action and metabolism

21 January 2018

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Interpretation of association signals and identification of causal variants from genome-wide association studies

21 January 2018

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Synthetic associations created by rare variants do not explain most GWAS results

21 January 2018

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10.1093/BIOINFORMATICS/BTW125

21 January 2018

Identifiers

DOI

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journals/bioinformatics/LacourESFB16

14 September 2017

DBLP publication ID

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DBLP Dataset 2021-01-02

28 January 2021

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