No large-effect low-frequency coding variation found for myocardial infarction (Q33991765)

30 July 2017

title

No large-effect low-frequency coding variation found for myocardial infarction (English)

1 reference

30 July 2017

19

Kristian Hveem

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30 July 2017

14

Frank Skorpen

1 reference

30 July 2017

Ellen Schmidt

4

0 references

He Zhang

He Zhang

2

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Daniel H Hovelson

Daniel H Hovelson

5

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Maja-Lisa Løchen

Maja-Lisa Løchen

7

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Inger Njølstad

18

Inger Njølstad

1 reference

30 July 2017

10

Lars Vatten

1 reference

30 July 2017

16

Michael Boehnke

1 reference

30 July 2017

6

Arnulf Langhammer

1 reference

30 July 2017

12

Tom Wilsgaard

1 reference

30 July 2017

9

Ellisiv B Mathiesen

1 reference

30 July 2017

20

Cristen J Willer

1 reference

30 July 2017

8

Santhi K Ganesh

1 reference

30 July 2017

15

Håvard Dalen

1 reference

30 July 2017

Oddgeir L Holmen

1

1 reference

30 July 2017

Wei Zhou

3

1 reference

30 July 2017

Carl Platou

11

1 reference

30 July 2017

Jin Chen

13

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30 July 2017

Goncalo R Abecasis

17

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30 July 2017

publication date

12 April 2014

1 reference

30 July 2017

published in

Human Molecular Genetics

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30 July 2017

volume

23

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30 July 2017

issue

17

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30 July 2017

page(s)

4721-4728

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Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

30 July 2017

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Large-scale association analysis identifies new risk loci for coronary artery disease

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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

5 July 2018

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Cohort profile: the Tromso Study

5 July 2018

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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

5 July 2018

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5 July 2018

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5 July 2018

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Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

5 July 2018

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5 July 2018

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5 July 2018

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

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Variance component model to account for sample structure in genome-wide association studies

5 July 2018

1 reference

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Genetic variants associated with Lp(a) lipoprotein level and coronary disease.

5 July 2018

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5 July 2018

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A common variant on chromosome 9p21 affects the risk of myocardial infarction

5 July 2018

1 reference

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Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

5 July 2018

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Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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A PCSK9 missense variant associated with a reduced risk of early-onset myocardial infarction

5 July 2018

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21 January 2018

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21 January 2018

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A Polymorphism in the Protease-Like Domain of Apolipoprotein(a) Is Associated With Severe Coronary Artery Disease

21 January 2018

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21 January 2018

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21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/24728188

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDU175

1 reference

30 July 2017

1 reference

30 July 2017

1 reference