Publications:

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Personal Genome Project UK (PGP-UK): a research and citizen science hybrid project in support of personalized medicine.

Bmc Medical Genomics

,

Publication Date: 2018-11-27

Variant appearance in text: rs4149274

PubMed Link: 30482208

Variant Present in the following documents:

• 12920_2018_423_MOESM1_ESM.pdf

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Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.

Scientific Reports

Liu, Xin X; Hu, Cheng C; Bao, Minghui M; Li, Jing J; Liu, Xiaoyan X; Tan, Xuerui X; Zhou, Yong Y; Chen, Yequn Y; Wu, Shouling S; Chen, Shuohua S; Zhang, Rong R; Jiang, Feng F; Jia, Weiping W; Wang, Xingyu X; Yang, Xinchun X; Cai, Jun J

Publication Date: 2016-08-02

Variant appearance in text: rs4149274

PubMed Link: 27480026

Variant Present in the following documents:

• srep30811-s1.pdf

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Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Bmc Medical Genetics

Huhn, Stefanie S; Bevier, Melanie M; Rudolph, Anja A; Pardini, Barbara B; Naccarati, Alessio A; Hein, Rebecca R; Hoffmeister, Michael M; Vodickova, Ludmila L; Novotny, Jan J; Brenner, Hermann H; Chang-Claude, Jenny J; Hemminki, Kari K; Vodicka, Pavel P; Försti, Asta A

Publication Date: 2012-10-05

Variant appearance in text: rs4149274

PubMed Link: 23036011

Variant Present in the following documents:

• Main text
• 1471-2350-13-94-S1.pdf
• 1471-2350-13-94.pdf

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Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology

Panagiotou, Orestis A OA; Evangelou, Evangelos E; Ioannidis, John P A JP

Publication Date: 2010-10-15

Variant appearance in text: rs4149274

PubMed Link: 20876667

Variant Present in the following documents:

• Main text

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Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study.

Journal Of Medical Genetics

Li, X X; Monda, K L KL; Göring, H H H HH; Haack, K K; Cole, S A SA; Diego, V P VP; Almasy, L L; Laston, S S; Howard, B V BV; Shara, N M NM; Lee, E T ET; Best, L G LG; Fabsitz, R R RR; MacCluer, J W JW; North, Kari E KE

Publication Date: 2009-07

Variant appearance in text: rs4149274

PubMed Link: 19429595

Variant Present in the following documents:

• Main text

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Strategies and issues in the detection of pathway enrichment in genome-wide association studies.

Human Genetics

Hong, Mun-Gwan MG; Pawitan, Yudi Y; Magnusson, Patrik K E PK; Prince, Jonathan A JA

Publication Date: 2009-08

Variant appearance in text: rs4149274

PubMed Link: 19408013

Variant Present in the following documents:

• Main text

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

Nature Genetics

Willer, Cristen J CJ; Sanna, Serena S; Jackson, Anne U AU; Scuteri, Angelo A; Bonnycastle, Lori L LL; Clarke, Robert R; Heath, Simon C SC; Timpson, Nicholas J NJ; Najjar, Samer S SS; Stringham, Heather M HM; Strait, James J; Duren, William L WL; Maschio, Andrea A; Busonero, Fabio F; Mulas, Antonella A; Albai, Giuseppe G; Swift, Amy J AJ; Morken, Mario A MA; Narisu, Narisu N; Bennett, Derrick D; Parish, Sarah S; Shen, Haiqing H; Galan, Pilar P; Meneton, Pierre P; Hercberg, Serge S; Zelenika, Diana D; Chen, Wei-Min WM; Li, Yun Y; Scott, Laura J LJ; Scheet, Paul A PA; Sundvall, Jouko J; Watanabe, Richard M RM; Nagaraja, Ramaiah R; Ebrahim, Shah S; Lawlor, Debbie A DA; Ben-Shlomo, Yoav Y; Davey-Smith, George G; Shuldiner, Alan R AR; Collins, Rory R; Bergman, Richard N RN; Uda, Manuela M; Tuomilehto, Jaakko J; Cao, Antonio A; Collins, Francis S FS; Lakatta, Edward E; Lathrop, G Mark GM; Boehnke, Michael M; Schlessinger, David D; Mohlke, Karen L KL; Abecasis, Gonçalo R GR

Publication Date: 2008-02

Variant appearance in text: rs4149274

PubMed Link: 18193043

Variant Present in the following documents:

• Main text

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