Publications:

Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease.

Clinical Epigenetics

Nakatochi, Masahiro M; Ichihara, Sahoko S; Yamamoto, Ken K; Naruse, Keiko K; Yokota, Shigeki S; Asano, Hiroyuki H; Matsubara, Tatsuaki T; Yokota, Mitsuhiro M

Publication Date: 2017

Variant appearance in text: rs3786725

PubMed Link: 28515798

Variant Present in the following documents:

• Main text

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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: rs3786725

PubMed Link: 28438747

Variant Present in the following documents:

• benm033277.ww1.pdf

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CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.

Journal Of Neuro-Oncology

Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B

Publication Date: 2015-10

Variant appearance in text: rs3786725

PubMed Link: 26290144

Variant Present in the following documents:

• 11060_2015_1891_MOESM1_ESM.pdf

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Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.

European Journal Of Human Genetics : Ejhg

Versmissen, Jorie J; Oosterveer, Daniëlla M DM; Yazdanpanah, Mojgan M; Dehghan, Abbas A; Hólm, Hilma H; Erdman, Jeanette J; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; Schunkert, Heribert H; Huijgen, Roeland R; Vongpromek, Ranitha R; Uitterlinden, André G AG; Defesche, Joep C JC; van Duijn, Cornelia M CM; Mulder, Monique M; Dadd, Tony T; Karlsson, Hróbjartur D HD; Ordovas, Jose J; Kindt, Iris I; Jarman, Amelia A; Hofman, Albert A; van Vark-van der Zee, Leonie L; Blommesteijn-Touw, Adriana C AC; Kwekkeboom, Jaap J; Liem, Anho H AH; van der Ouderaa, Frans J FJ; Calandra, Sebastiano S; Bertolini, Stefano S; Averna, Maurizio M; Langslet, Gisle G; Ose, Leiv L; Ros, Emilio E; Almagro, Fátima F; de Leeuw, Peter W PW; Civeira, Fernando F; Masana, Luis L; Pintó, Xavier X; Simoons, Maarten L ML; Schinkel, Arend F L AF; Green, Martin R MR; Zwinderman, Aeilko H AH; Johnson, Keith J KJ; Schaefer, Arne A; Neil, Andrew A; Witteman, Jacqueline C M JC; Humphries, Steve E SE; Kastelein, John J P JJ; Sijbrands, Eric J G EJ

Publication Date: 2015-03

Variant appearance in text: rs3786725

PubMed Link: 24916650

Variant Present in the following documents:

• Main text

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Genetic variant in SWI/SNF complexes influences hepatocellular carcinoma risk: a new clue for the contribution of chromatin remodeling in carcinogenesis.

Scientific Reports

Zhong, Rong R; Liu, Li L; Tian, Yao Y; Wang, Ying Y; Tian, Jing J; Zhu, Bei-bei BB; Chen, Wei W; Qian, Jia-ming JM; Zou, Li L; Xiao, Min M; Shen, Na N; Yang, Hong H; Lou, Jiao J; Qiu, Qian Q; Ke, Jun-tao JT; Lu, Xing-hua XH; Wang, Zhen-ling ZL; Song, Wei W; Zhang, Ti T; Li, Hui H; Wang, Li L; Miao, Xiao-ping XP

Publication Date: 2014-02-21

Variant appearance in text: rs3786725

PubMed Link: 24556940

Variant Present in the following documents:

• Main text

View BVdb publication page