Publications:

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Analysis of the APOB Gene and Apolipoprotein B Serum Levels in a Mexican Population with Acute Coronary Syndrome: Association with the Single Nucleotide Variants rs1469513, rs673548, rs676210, and rs1042034.

Genetics Research

Aceves-Ramírez, Maricela M; Valle, Yeminia Y; Casillas-Muñoz, Fidel F; Martínez-Fernández, Diana Emilia DE; Parra-Reyna, Brenda B; López-Moreno, Víctor Arturo VA; Flores-Salinas, Héctor Enrique HE; Valdés-Alvarado, Emmanuel E; Muñoz-Valle, José Francisco JF; García-Garduño, Texali T; Padilla-Gutiérrez, Jorge Ramón JR

Publication Date: 2022

Variant appearance in text: rs1469513

PubMed Link: 35440891

Variant Present in the following documents:

• GR2022-4901090.pdf

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Prevalence of ApoB100 rs693 gene polymorphism in metabolic syndrome among female students at King Abdulaziz University.

Saudi Journal Of Biological Sciences

Alghamdi, Rana A RA; Al-Zahrani, Maryam H MH; Balgoon, Maha J MJ; Alkhattabi, Nuha A NA

Publication Date: 2021-06

Variant appearance in text: rs1469513

PubMed Link: 34121862

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Common Genetic Variations Involved in the Inter-Individual Variability of Circulating Cholesterol Concentrations in Response to Diets: A Narrative Review of Recent Evidence.

Nutrients

Abdullah, Mohammad M H MMH; Vazquez-Vidal, Itzel I; Baer, David J DJ; House, James D JD; Jones, Peter J H PJH; Desmarchelier, Charles C

Publication Date: 2021-02-22

Variant appearance in text: rs1469513

PubMed Link: 33671529

Variant Present in the following documents:

• Main text
• nutrients-13-00695.pdf

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Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.

Journal Of Human Genetics

Carlson, Jenna C JC; Weeks, Daniel E DE; Hawley, Nicola L NL; Sun, Guangyun G; Cheng, Hong H; Naseri, Take T; Reupena, Muagututi'a Sefuiva MS; Tuitele, John J; Deka, Ranjan R; McGarvey, Stephen T ST; Minster, Ryan L RL

Publication Date: 2021-02

Variant appearance in text: rs1469513

PubMed Link: 32759990

Variant Present in the following documents:

• Main text

View BVdb publication page

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs1469513

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

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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: rs1469513

PubMed Link: 28438747

Variant Present in the following documents:

• benm033277.ww1.pdf

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Genomic Variants Associated with Resistance to High Fat Diet Induced Obesity in a Primate Model.

Scientific Reports

Harris, R Alan RA; Alcott, Callison E CE; Sullivan, Elinor L EL; Takahashi, Diana D; McCurdy, Carrie E CE; Comstock, Sarah S; Baquero, Karalee K; Blundell, Peter P; Frias, Antonio E AE; Kahr, Maike M; Suter, Melissa M; Wesolowski, Stephanie S; Friedman, Jacob E JE; Grove, Kevin L KL; Aagaard, Kjersti M KM

Publication Date: 2016-11-04

Variant appearance in text: rs1469513

PubMed Link: 27811965

Variant Present in the following documents:

• Main text
• srep36123.pdf

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GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm.

Plos Genetics

Bottolo, Leonardo L; Chadeau-Hyam, Marc M; Hastie, David I DI; Zeller, Tanja T; Liquet, Benoit B; Newcombe, Paul P; Yengo, Loic L; Wild, Philipp S PS; Schillert, Arne A; Ziegler, Andreas A; Nielsen, Sune F SF; Butterworth, Adam S AS; Ho, Weang Kee WK; Castagné, Raphaële R; Munzel, Thomas T; Tregouet, David D; Falchi, Mario M; Cambien, François F; Nordestgaard, Børge G BG; Fumeron, Fredéric F; Tybjærg-Hansen, Anne A; Froguel, Philippe P; Danesh, John J; Petretto, Enrico E; Blankenberg, Stefan S; Tiret, Laurence L; Richardson, Sylvia S

Publication Date: 2013

Variant appearance in text: rs1469513

PubMed Link: 23950726

Variant Present in the following documents:

• Main text
• pgen.1003657.pdf

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