(Q42130816)

17 October 2017

Sampling strategies for rare variant tests in case-control studies (English)

1 reference

17 October 2017

Sebastian Zöllner

1

1 reference

17 October 2017

18 April 2012

1 reference

European Journal of Human Genetics

17 October 2017

1 reference

17 October 2017

20

1 reference

17 October 2017

10

1 reference

17 October 2017

1085-1091

1 reference

Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Testing for an unusual distribution of rare variants

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

You've gotta be lucky: Coverage and the elusive gene-gene interaction

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Powerful SNP-set analysis for case-control genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Power analysis for case-control association studies of samples with known family histories.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Finding the missing heritability of complex diseases

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Discovery of rare variants via sequencing: implications for the design of complex trait association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Efficient study designs for test of genetic association using sibship data and unrelated cases and controls

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Linkage strategies for genetically complex traits. I. Multilocus models

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

Implications of multilocus inheritance for gene-disease association studies

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3449077

17 August 2018

Identifiers

DOI

10.1038/EJHG.2012.58

1 reference

Dimensions Publication ID

17 October 2017

1008872104

0 references

Fatcat ID

release_ecq3wpuhwvesnfdrpsotslagri

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ecq3wpuhwvesnfdrpsotslagri

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

17 October 2017

PubMed publication ID

22510851

1 reference