(Q22122153)

6 February 2023

6

Richard M. Durbin (Co-Chair)

Richard M.

Durbin (Co-Chair)

1 reference

6 February 2023

3

0 references

Robert E Handsaker

object named as

Robert E Handsaker

7

0 references

Vineet Bafna

1 reference

Klaudia Walter

1 reference

Andrew G. Clark

Andrew G.

Clark

7

2 references

6 February 2023

1 reference

Matthew E.

Hurles

14

Matthew E. Hurles

1 reference

6 February 2023

9

Gabor T.

Marth

Gabor T Marth

1 reference

6 February 2023

Bartha M.

Knoppers

15

Bartha M. Knoppers

1 reference

6 February 2023

Richard A.

Gibbs

12

Richard A. Gibbs

1 reference

6 February 2023

Lisa D Brooks

4

0 references

Mark A DePristo

5

0 references

Hyun Min Kang

8

0 references

Gil A. McVean

Gil A.

McVean

1

1 reference

6 February 2023

David M. Altshuler (Co-Chair)

David M.

Altshuler (Co-Chair)

2

1 reference

6 February 2023

David R. Bentley

David R.

Bentley

5

1 reference

6 February 2023

Aravinda Chakravarti

Aravinda

Chakravarti

6

1 reference

6 February 2023

Peter Donnelly

Peter

Donnelly

8

1 reference

6 February 2023

Evan E. Eichler

Evan E.

Eichler

9

1 reference

6 February 2023

Paul Flicek

Paul

Flicek

10

1 reference

6 February 2023

Stacey B. Gabriel

Stacey B.

Gabriel

11

1 reference

6 February 2023

Eric D. Green

Eric D.

Green

13

1 reference

6 February 2023

Jan O. Korbel

Jan O.

Korbel

16

1 reference

6 February 2023

Eric S. Lander

Eric S.

Lander

17

1 reference

6 February 2023

Charles Lee

Charles

Lee

18

1 reference

6 February 2023

Hans Lehrach

Hans

Lehrach

19

1 reference

6 February 2023

Elaine R. Mardis

Elaine R.

Mardis

20

1 reference

6 February 2023

Gil A. McVean

Gil A.

McVean

22

1 reference

6 February 2023

Deborah A. Nickerson

Deborah A.

Nickerson

23

1 reference

6 February 2023

Jeanette P. Schmidt

Jeanette P.

Schmidt

24

1 reference

6 February 2023

Stephen T. Sherry

Stephen T.

Sherry

25

1 reference

6 February 2023

Jun Wang

Jun

Wang

26

1 reference

6 February 2023

Richard K. Wilson

Richard K.

Wilson

27

1 reference

Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

6 February 2023

language of work or name

English

0 references

publication date

1 November 2012

0 references

published in

Nature

0 references

volume

491

0 references

issue

7422

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page(s)

56-65

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copyright license

start time

31 October 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability

19 March 2017

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19 March 2017

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19 March 2017

1 reference

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19 March 2017

1 reference

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19 March 2017

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19 March 2017

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Genome-wide patterns of population structure and admixture in West Africans and African Americans

19 March 2017

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19 March 2017

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

19 March 2017

1 reference

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Analysis of the vertebrate insulator protein CTCF-binding sites in the human genome

19 March 2017

1 reference

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Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

19 March 2017

1 reference

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Integrated genomic analyses of ovarian carcinoma

19 March 2017

1 reference

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Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

19 March 2017

1 reference

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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

19 March 2017

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The mystery of missing heritability: Genetic interactions create phantom heritability

19 March 2017

1 reference

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

19 March 2017

1 reference

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A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

19 March 2017

1 reference

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KEGG for integration and interpretation of large-scale molecular data sets

7 April 2017

1 reference

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

7 April 2017

1 reference

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Exome sequencing as a tool for Mendelian disease gene discovery

7 April 2017

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Inference of population structure using dense haplotype data

7 April 2017

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Efficiency and power as a function of sequence coverage, SNP array density, and imputation

10 May 2017

1 reference

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DNase I sensitivity QTLs are a major determinant of human expression variation

12 September 2017

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A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.

12 September 2017

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Clan genomics and the complex architecture of human disease

12 September 2017

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The functional spectrum of low-frequency coding variation

12 September 2017

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Demographic history and rare allele sharing among human populations

12 September 2017

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Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

12 September 2017

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12 September 2017

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Efficient construction of an assembly string graph using the FM-index

12 September 2017

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Fine mapping of the association with obesity at the FTO locus in African-derived populations

12 September 2017

1 reference

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Genetic loci influencing kidney function and chronic kidney disease

12 September 2017

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Gene--environment-wide association studies: emerging approaches

12 September 2017

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Sequence variations in the public human genome data reflect a bottlenecked population history

12 September 2017

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Expression cloning of a novel Gal beta (1-3/1-4) GlcNAc alpha 2,3-sialyltransferase using lectin resistance selection.

12 September 2017

1 reference

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De novo assembly and genotyping of variants using colored de Bruijn graphs

12 September 2017

1 reference

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Recent explosive human population growth has resulted in an excess of rare genetic variants

27 September 2017

1 reference

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Differential confounding of rare and common variants in spatially structured populations

30 May 2018

1 reference

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Low-coverage sequencing: implications for design of complex trait association studies

30 May 2018

1 reference

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The Human Gene Mutation Database: 2008 update

30 May 2018

1 reference

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The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.

30 May 2018

1 reference

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

29 November 2018

1 reference

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29 November 2018

Identifiers

DOI

10.1038/NATURE11632

1 reference

ADS bibcode

2012Natur.491...56T

0 references

7227b20c-d34a-3632-93cc-97863eb04b46

0 references

Mendeley publication ID

1 reference

https://www.mendeley.com/catalogue/7227b20c-d34a-3632-93cc-97863eb04b46/

title

An integrated map of genetic vari... preview & related info | Mendeley (British English)

8 October 2022

1 reference

1 reference

PubMed publication ID

23128226

1 reference