Synthetic associations are unlikely to account for many common disease genome-wide association signals (Q33803713)

29 July 2017

title

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

1 reference

genome-wide association study

29 July 2017

main subject

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author

Nicole Soranzo

series ordinal

2

1 reference

29 July 2017

3

1 reference

29 July 2017

Jeffrey C Barrett

4

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Carl A Anderson

object named as

Carl A Anderson

series ordinal

1

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language of work or name

English

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publication date

18 January 2011

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29 July 2017

1 reference

29 July 2017

volume

9

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29 July 2017

issue

1

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29 July 2017

page(s)

e1000580

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

18 January 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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4 July 2018

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4 July 2018

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Rare variants create synthetic genome-wide associations

4 July 2018

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4 July 2018

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Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

4 July 2018

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4 July 2018

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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

4 July 2018

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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

4 July 2018

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

4 July 2018

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Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium

4 July 2018

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4 July 2018

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4 July 2018

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

4 July 2018

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4 July 2018

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Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

4 July 2018

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Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients

4 July 2018

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

4 July 2018

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Complement factor H variant increases the risk of age-related macular degeneration

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Mapping of a susceptibility locus for Crohn's disease on chromosome 16

4 July 2018

1 reference

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Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PBIO.1000580

Polymorphisms identified through genome-wide association studies and their associations with type 2 diabetes in Chinese, Malays, and Asian-Indians in Singapore

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PBIO.1000580

American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PBIO.1000580

Common NOD2 mutations are absent in patients with Crohn's disease in India.

21 January 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022527

10.1371/JOURNAL.PBIO.1000580

30 October 2018

Identifiers

DOI

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release_tlj6vp6v7ventcbe32srjipb3m

29 July 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/tlj6vp6v7ventcbe32srjipb3m

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3022527

1 reference

29 July 2017

1 reference