(Q40509865)

21 September 2017

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants (English)

1 reference

21 September 2017

2

1 reference

21 September 2017

5

1 reference

21 September 2017

8

1 reference

21 September 2017

3

Andrew P Morris

1 reference

21 September 2017

Robert Lawrence

1

1 reference

21 September 2017

Xiayi Ke

4

1 reference

21 September 2017

Marta Paolucci

6

1 reference

21 September 2017

Jiannis Ragoussis

7

1 reference

21 September 2017

David Bentley

9

1 reference

21 September 2017

Lon R Cardon

10

1 reference

21 September 2017

language of work or name

1 reference

1 November 2005

1 reference

21 September 2017

1 reference

21 September 2017

15

1 reference

21 September 2017

11

1 reference

21 September 2017

1503-1510

1 reference

Optimal selection of SNP markers for disease association studies.

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Whole-genome patterns of common DNA variation in three human populations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Pattern of sequence variation across 213 environmental response genes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Genetic analysis of genome-wide variation in human gene expression

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Mapping complex disease loci in whole-genome association studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Integrating ethics and science in the International HapMap Project

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

The fine-scale structure of recombination rate variation in the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

The complex interplay among factors that influence allelic association.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

The International HapMap Project

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Estimating recombination rates from population-genetic data

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Haplotype blocks and linkage disequilibrium in the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Using haplotype blocks to map human complex trait loci

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Efficient selective screening of haplotype tag SNPs

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

What makes a good case-control study? Design issues for complex traits such as endometriosis.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

A dynamic programming algorithm for haplotype block partitioning

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

The structure of haplotype blocks in the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Generating samples under a Wright-Fisher neutral model of genetic variation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Linkage disequilibrium in the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Association study designs for complex diseases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Statistical properties of the number of recombination events in the history of a sample of DNA sequences

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Ancestral inference from samples of DNA sequences with recombination.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Genotype prediction using a dense map of SNPs

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

The impact of SNP density on fine-scale patterns of linkage disequilibrium

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Linkage disequilibrium patterns of the human genome across populations

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

High-resolution haplotype structure in the human genome

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots

2 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

A first-generation linkage disequilibrium map of human chromosome 22

2 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310638

Evidence for substantial fine-scale variation in recombination rates across the human genome

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16251460

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Variation is the spice of life

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16251460

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Haplotype tagging for the identification of common disease genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16251460

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1101/GR.4217605

1 reference

21 September 2017

1 reference

21 September 2017

PubMed publication ID

16251460

1 reference