Publications:

Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)

Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A

Publication Date: 2017-04-24

Variant appearance in text: rs4788597

PubMed Link: 28438747

Variant Present in the following documents:

• benm033277.ww1.pdf

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Recurring exon deletions in the HP (haptoglobin) gene contribute to lower blood cholesterol levels.

Nature Genetics

Boettger, Linda M LM; Salem, Rany M RM; Handsaker, Robert E RE; Peloso, Gina M GM; Kathiresan, Sekar S; Hirschhorn, Joel N JN; McCarroll, Steven A SA

Publication Date: 2016-04

Variant appearance in text: rs4788597

PubMed Link: 26901066

Variant Present in the following documents:

• NIHMS753659-supplement-1.pdf

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A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.

Plos One

Froguel, Philippe P; Ndiaye, Ndeye Coumba NC; Bonnefond, Amélie A; Bouatia-Naji, Nabila N; Dechaume, Aurélie A; Siest, Gérard G; Herbeth, Bernard B; Falchi, Mario M; Bottolo, Leonardo L; Guéant-Rodriguez, Rosa-Maria RM; Lecoeur, Cécile C; Langlois, Michel R MR; Labrune, Yann Y; Ruokonen, Aimo A; El Shamieh, Said S; Stathopoulou, Maria G MG; Morandi, Anita A; Maffeis, Claudio C; Meyre, David D; Delanghe, Joris R JR; Jacobson, Peter P; Sjöström, Lars L; Carlsson, Lena M S LM; Walley, Andrew A; Elliott, Paul P; Jarvelin, Marjo-Riita MR; Dedoussis, George V GV; Visvikis-Siest, Sophie S

Publication Date: 2012

Variant appearance in text: rs4788597

PubMed Link: 22403646

Variant Present in the following documents:

• Main text
• pone.0032327.pdf

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