(Q42747895)

6 November 2017

A Method to Assess Linkage Disequilibrium between CNVs and SNPs Inside Copy Number Variable Regions (English)

1 reference

6 November 2017

1 reference

linkage disequilibrium

1 reference

Nathan E Wineinger

1

1 reference

PMCID

3109359

6 November 2017

Nicholas M Pajewski

series ordinal

2

1 reference

PMCID

3109359

6 November 2017

Hemant K Tiwari

series ordinal

3

1 reference

6 November 2017

25 April 2011

1 reference

6 November 2017

Frontiers in Genetics

1 reference

6 November 2017

2

1 reference

6 November 2017

17

1 reference

Missing heritability and strategies for finding the underlying causes of complex disease

6 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Inferring combined CNV/SNP haplotypes from genotype data

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Population-genetic nature of copy number variations in the human genome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Finding the missing heritability of complex diseases

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Origins and functional impact of copy number variation in the human genome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

An algorithm for inferring complex haplotypes in a region of copy-number variation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Genome-wide detection and characterization of positive selection in human populations

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Copy-number variation and association studies of human disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Strong association of de novo copy number mutations with autism

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Global variation in copy number in the human genome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

Estimation of linkage disequilibrium for loci with multiple alleles: basic approach and an application using data from bighorn sheep

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

The effects of inbreeding at loci with heterozygote advantage

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3109359

THE ESTIMATION OF GENE FREQUENCIES IN A RANDOM-MATING POPULATION

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21660233

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Counting methods in genetical statistics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21660233

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3389/FGENE.2011.00017

1 reference

6 November 2017

1 reference

6 November 2017

1 reference

PMCID

3109359