(Q28306661)

28

0 references

Thomas Werge

18

0 references

Patrick Sulem

3

0 references

Gudmar Thorleifsson

25

0 references

Kári Stefánsson

30

0 references

Augustine Kong

27

0 references

Solveig Gretarsdottir

12

0 references

Thorunn Rafnar

19

0 references

Hreinn Stefansson

17

0 references

Jona Saemundsdottir

9

0 references

Aslaug Jonasdottir

15

0 references

Dawood Darbar

Dawood Darbar

24

0 references

Daníel F. Guðbjartsson

Daniel F Gudbjartsson

2

0 references

Lambertus Kiemeney

Lambertus A Kiemeney

20

0 references

Dan Roden

23

Dan M Roden

0 references

Hilma Holm

1

Hilma Holm

0 references

Babar Parvez

21

Babar Parvez

0 references

Raafia Muhammad

22

Raafia Muhammad

0 references

G. Bragi Walters

26

G Bragi Walters

0 references

Stefan E. Matthiasson

13

Stefan E Matthiasson

0 references

Gísli Másson

4

Gisli Masson

0 references

Asgeir Sigurdsson

16

Asgeir Sigurdsson

0 references

Arnaldur Gylfason

10

Arnaldur Gylfason

0 references

Hafdis Helgadottir

5

Hafdis Th Helgadottir

0 references

Carlo Zanon

6

Carlo Zanon

0 references

Agnar Helgason

8

Agnar Helgason

0 references

author name string

Olafur Th Magnusson

7

0 references

Hrafnhildur Stefansdottir

11

0 references

Gu Mundur Thorgeirsson

14

0 references

David O Arnar

A map of human genome variation from population-scale sequencing

29

0 references

language of work or name

English

0 references

publication date

6 March 2011

0 references

published in

Nature Genetics

0 references

volume

43

0 references

issue

4

0 references

page(s)

316-20

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Genome-wide association analysis identifies multiple loci related to resting heart rate

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

A haplotype map of the human genome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Myosin heavy chain isoform expression in the failing and nonfailing human heart

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Structural organization of the human cardiac alpha-myosin heavy chain gene (MYH6)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Fast and accurate short read alignment with Burrows-Wheeler transform

20 March 2017

1 reference

https://api.crossref.org/works/10.1038/NG.781

The Sequence Alignment/Map format and SAMtools

22 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG.781

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

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Prediction of deleterious human alleles

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Myosin VI rewrites the rules for myosin motors

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

New insights into pacemaker activity: promoting understanding of sick sinus syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Association between two mu-opioid receptor gene (OPRM1) haplotype blocks and drug or alcohol dependence

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

29 September 2017

Estimating allele age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Cardiac alpha- and beta-myosin heavy chain genes are organized in tandem

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3066272

Several common variants modulate heart rate, PR interval and QRS duration

29 September 2017

1 reference

Patterns of expression in the developing myocardium: towards a morphologically integrated transcriptional model

21 January 2018

1 reference

C825T polymorphism in the human G protein beta3 subunit gene is associated with long-term clozapine treatment-induced body weight change in the Chinese population

21 January 2018

1 reference

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls

21 January 2018

1 reference

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

21 January 2018

1 reference

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

21 January 2018

1 reference

A novel endonuclease IV post-PCR genotyping system

21 January 2018

1 reference

Fine-scale recombination rate differences between sexes, populations and individuals

21 January 2018

1 reference

A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries

21 January 2018

1 reference

ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

21 January 2018

1 reference

The Sick Sinus Syndrome in Atrial Disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21378987

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/21378987

12 December 2020

inferred from PubMed ID database lookup

Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21378987

12 December 2020

inferred from PubMed ID database lookup

Common variants conferring risk of schizophrenia

1 reference

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.781

1 reference

1 reference

1 reference

PubMed publication ID

21378987

1 reference