Detection of sharing by descent, long-range phasing and haplotype imputation (Q34928818)

5 August 2017

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

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5 August 2017

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Daníel F. Guðbjartsson

15

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5 August 2017

Unnur Þorsteinsdóttir

14

Unnur Thorsteinsdottir

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Gudmar Thorleifsson

6

Gudmar Thorleifsson

1 reference

5 August 2017

10

Thorunn Rafnar

1 reference

5 August 2017

Hreinn Stefansson

16

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Augustine Kong

Augustine Kong

1

0 references

Patrick Sulem

Patrick Sulem

11

1 reference

5 August 2017

17

Kari Stefansson

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5 August 2017

9

Stacy Steinberg

1 reference

5 August 2017

8

Andres Ingason

1 reference

5 August 2017

2

Gisli Masson

1 reference

5 August 2017

3

Michael L Frigge

1 reference

5 August 2017

4

Arnaldur Gylfason

1 reference

5 August 2017

12

Magali Mouy

1 reference

5 August 2017

Pasha Zusmanovich

5

1 reference

5 August 2017

Pall I Olason

7

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5 August 2017

Frosti Jonsson

13

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5 August 2017

language of work or name

English

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publication date

1 September 2008

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5 August 2017

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5 August 2017

40

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5 August 2017

9

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5 August 2017

1068-1075

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https://scigraph.springernature.com/pub.10.1038/ng.216

5 August 2017

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cites work

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Association between microdeletion and microduplication at 16p11.2 and autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

In silico method for inferring genotypes in pedigrees

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A comparison of phasing algorithms for trios and unrelated individuals

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A fine-scale map of recombination rates and hotspots across the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Haplotype reconstruction from genotype data using Imperfect Phylogeny

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A high-resolution recombination map of the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Factors influencing recombination frequency and distribution in a human meiotic crossover hotspot.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Comparison of fine-scale recombination rates in humans and chimpanzees.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4540081

Large recurrent microdeletions associated with schizophrenia

26 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.216

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.216

1 reference

5 August 2017

1 reference

5 August 2017

1 reference