(Q34514291)

2 August 2017

Association screening of common and rare genetic variants by penalized regression (English)

1 reference

2 August 2017

3

Janet S Sinsheimer

1 reference

2 August 2017

4

Kenneth Lange

1 reference

2 August 2017

Hua Zhou

1

1 reference

PubMed ID

20693321

2 August 2017

Mary E Sehl

series ordinal

2

1 reference

PubMed ID

20693321

2 August 2017

language of work or name

English

0 references

publication date

6 August 2010

1 reference

2 August 2017

1 reference

2 August 2017

26

1 reference

2 August 2017

2375-2382

1 reference

2 August 2017

19

1 reference

Analysis of North American Rheumatoid Arthritis Consortium data using a penalized logistic regression approach

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Human genetic variation and its contribution to complex traits

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Darwinian and demographic forces affecting human protein coding genes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

A groupwise association test for rare mutations using a weighted sum statistic

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Genome-wide association analysis by lasso penalized logistic regression

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Autoimmune diseases: insights from genome-wide association studies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Genome-wide in situ exon capture for selective resequencing

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Recent and ongoing selection in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

The structure of haplotype blocks in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Identification of the breast cancer susceptibility gene BRCA2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Genome-wide association studies in cancer.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Multiple rare nonsynonymous variants in the adenomatous polyposis coli gene predispose to colorectal adenomas.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025646

The genetic attributable risk of breast and ovarian cancer

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20693321

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTQ448

1 reference

journals/bioinformatics/ZhouSSL10

2 August 2017

1 reference

DBLP Dataset 2021-01-02

release_7gb6btxzobh35ozkg4w52xxsyi

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7gb6btxzobh35ozkg4w52xxsyi

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

3025646

1 reference

2 August 2017

1 reference

PubMed ID

20693321