(Q41906963)

13 October 2017

Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals (English)

1 reference

13 October 2017

1 reference

2

1 reference

13 October 2017

Lawrence H Uricchio

1

0 references

Dan L. Nicolae

object named as

Dan L Nicolae

series ordinal

5

0 references

Carole Ober

series ordinal

4

object named as

Carole Ober

1 reference

13 October 2017

Kevin D Ross

3

1 reference

13 October 2017

28 March 2012

1 reference

13 October 2017

1 reference

13 October 2017

36

1 reference

13 October 2017

4

1 reference

13 October 2017

312-319

1 reference

A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A fast, powerful method for detecting identity by descent

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

GWAS: heritability missing in action?

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Finding the missing heritability of complex diseases

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A graphical algorithm for fast computation of identity coefficients and generalized kinship coefficients

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Detection of sharing by descent, long-range phasing and haplotype imputation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Imputation-based analysis of association studies: candidate regions and quantitative traits

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A new multipoint method for genome-wide association studies by imputation of genotypes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A comparison of bayesian methods for haplotype reconstruction from population genotype data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

The genetic dissection of complex traits in a founder population

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Use of population isolates for mapping complex traits

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Base-calling of automated sequencer traces using phred. II. Error probabilities

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Genetic dissection of complex traits

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

A remark on rare variants.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3794468

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.21623

The founder effect in a human isolate: Evolutionary implications

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22460724

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The genetics of asthma. Mapping genes for complex traits in founder populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22460724

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21623

1 reference

13 October 2017

1 reference

PMC publication ID

3794468

13 October 2017

PubMed publication ID

22460724

1 reference

PMC publication ID

3794468