Genetic architecture of circulating lipid levels (Q35108611)

6 August 2017

Genetic architecture of circulating lipid levels (English)

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6 August 2017

Marjo-Riitta Järvelin

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9

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6 August 2017

Cornelia M. van Duijn

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Cornelia M van Duijn

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Samuli Ripatti

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Samuli Ripatti

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André Uitterlinden

19

André G Uitterlinden

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Jouke-Jan Hottenga

12

Jouke-Jan Hottenga

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Igor Rudan

8

Igor Rudan

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Gonneke Willemsen

16

Gonneke Willemsen

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Angela Döring

26

Angela Döring

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Leena Peltonen-Palotie

41

Leena Peltonen-Palotie

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6 August 2017

Åsa Johansson

11

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Andrew A Hicks

Andrew A Hicks

10

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Najaf Amin

Najaf Amin

2

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Patrik K E Magnusson

Patrik K E Magnusson

33

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Taina Rantanen

Taina Rantanen

24

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Grant W. Montgomery

Grant W Montgomery

22

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Nick Martin

Nicholas G Martin

38

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Kirsi H Pietiläinen

Kirsi H Pietiläinen

23

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Brenda Penninx

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Brenda W Penninx

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6 August 2017

Mark McCarthy

40

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Cecile Janssens

A Cecile J W Janssens

45

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6 August 2017

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Dorret I Boomsma

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6 August 2017

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Albert Hofman

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6 August 2017

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Ulf Gyllensten

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6 August 2017

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Eco J C de Geus

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6 August 2017

Jacqueline C M Witteman

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Jacqueline Witteman

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6 August 2017

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Heinz-Erich Wichmann

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6 August 2017

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James F Wilson

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6 August 2017

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Harry Campbell

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6 August 2017

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Tim Spector

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6 August 2017

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Nancy L Pedersen

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6 August 2017

39

Ben A Oostra

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6 August 2017

5

John B Whitfield

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6 August 2017

27

Peter P Pramstaller

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6 August 2017

14

Sarah H Wild

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6 August 2017

7

Kirsten O H M Kyvik

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6 August 2017

3

Aaron Isaacs

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6 August 2017

1

Ayşe Demirkan

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6 August 2017

Johannes J Smith

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Fernando Rivadeneria

32

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6 August 2017

Birgit Hoehne

37

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6 August 2017

ENGAGE CONSORTIUM

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6 August 2017

language of work or name

English

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publication date

30 March 2011

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European Journal of Human Genetics

6 August 2017

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published in

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6 August 2017

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813-819

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7

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https://scigraph.springernature.com/pub.10.1038/ejhg.2011.21

6 August 2017

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Finding the missing heritability of complex diseases

9 July 2018

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The Rotterdam Study: 2010 objectives and design update

9 July 2018

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Genetic scoring analysis: a way forward in genome wide association studies?

9 July 2018

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

9 July 2018

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Inherited lipodystrophies and hypertriglyceridemia

9 July 2018

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Plasma lipoproteins: genetic influences and clinical implications

9 July 2018

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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

9 July 2018

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

9 July 2018

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Common variants at 30 loci contribute to polygenic dyslipidemia

9 July 2018

1 reference

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LDL-cholesterol concentrations: a genome-wide association study

9 July 2018

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

9 July 2018

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

9 July 2018

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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

9 July 2018

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

9 July 2018

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Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: the Erasmus Rucphen Family Study

9 July 2018

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Rare APOA5 mutations--clinical consequences, metabolic and functional effects: an ENID review

9 July 2018

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A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

9 July 2018

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Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

9 July 2018

1 reference

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

9 July 2018

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Factors of risk in the development of coronary heart disease--six year follow-up experience. The Framingham Study

9 July 2018

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Monogenic hypercholesterolemia: new insights in pathogenesis and treatment

9 July 2018

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PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

9 July 2018

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Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6.

9 July 2018

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Estimation of contribution of changes in classic risk factors to trends in coronary-event rates across the WHO MONICA Project populations

9 July 2018

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Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

9 July 2018

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Familial lipoprotein disorders in patients with premature coronary artery disease

9 July 2018

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Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

9 July 2018

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Sizing up human height variation.

21 January 2018

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21 January 2018

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Novel rare mutations and promoter haplotypes in ABCA1 contribute to low-HDL-C levels.

21 January 2018

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The Collaborative Lipid Research Clinics Program Family Study. IV. Familial associations of plasma lipids and lipoproteins

21 January 2018

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https://api.fatcat.wiki/v0/release/odecdvigifa7fcaoi4fu2fqmie

27 September 2018

Identifiers

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30 July 2022

release_odecdvigifa7fcaoi4fu2fqmie

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/odecdvigifa7fcaoi4fu2fqmie

30 July 2022

https://api.fatcat.wiki/v0/release/odecdvigifa7fcaoi4fu2fqmie

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/odecdvigifa7fcaoi4fu2fqmie

1 reference

30 July 2022