Rare variants create synthetic genome-wide associations (Q29614955)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

genome-wide association study

30 April 2017

main subject

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author name string

Dickson SP

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

30 April 2017

Wang K

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

30 April 2017

Krantz I

3

1 reference

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30 April 2017

Hakonarson H

4

1 reference

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30 April 2017

Goldstein DB

5

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

30 April 2017

language of work or name

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30 April 2017

publication date

26 January 2010

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30 April 2017

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volume

8

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page(s)

e1000294

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issue

1

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Creative Commons Attribution 4.0 International

30 April 2017

copyright license

start time

26 January 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Common genetic variation and human traits

30 April 2017

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

30 April 2017

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Personal genomes: The case of the missing heritability

30 April 2017

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MYH9 is associated with nondiabetic end-stage renal disease in African Americans

30 April 2017

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Large recurrent microdeletions associated with schizophrenia

30 April 2017

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Dendroscope: An interactive viewer for large phylogenetic trees

30 April 2017

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

30 April 2017

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

30 April 2017

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GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review

30 April 2017

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A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

30 April 2017

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On the allelic spectrum of human disease

30 April 2017

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The future of genetic studies of complex human diseases

30 April 2017

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Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci

30 April 2017

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Hormone-dependent effects of FGFR2 and MAP3K1 in breast cancer susceptibility in a population-based sample of post-menopausal African-American and European-American women

3 June 2018

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Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population.

3 June 2018

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CD226 Gly307Ser association with multiple autoimmune diseases

3 June 2018

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Lack of association between the CALM1 core promoter polymorphism (-16C/T) and susceptibility to knee osteoarthritis in a Chinese Han population

3 June 2018

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Genome-wide association studies: potential next steps on a genetic journey

3 June 2018

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Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

3 June 2018

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Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

3 June 2018

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Worldwide population differentiation at disease-associated SNPs

3 June 2018

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Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies

3 June 2018

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Non-syndromic, autosomal-recessive deafness

3 June 2018

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Advances in hereditary deafness

3 June 2018

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Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review

3 June 2018

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Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

3 June 2018

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Human genetics: the hidden text of genome-wide associations

21 January 2018

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Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

21 January 2018

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GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.

21 January 2018

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Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population

21 January 2018

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Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan.

21 January 2018

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Evaluation of coverage variation of SNP chips for genome-wide association studies.

21 January 2018

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GENOME: a rapid coalescent-based whole genome simulator

21 January 2018

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SNP mapping and candidate gene sequencing in the class I region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians

21 January 2018

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Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration

26 November 2018

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12 December 2020

The CALM1 core promoter polymorphism is not associated with hip osteoarthritis in a United Kingdom Caucasian population

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12 December 2020

A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese

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Pulmonary complications of sickle cell disease

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10.1371/JOURNAL.PBIO.1000294

Identifiers

DOI

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30 April 2017

75173

75173

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

2 references

30 April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20126254

2 references

30 April 2017