Publications:

Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.

Circulation. Genomic And Precision Medicine

Saad, Mohamad M; El-Menyar, Ayman A; Kunji, Khalid K; Ullah, Ehsan E; Al Suwaidi, Jassim J; Kullo, Iftikhar J IJ

Publication Date: 2022-10-12

Variant appearance in text: rs538554190

PubMed Link: 36252120

Variant Present in the following documents:

• Main text

View BVdb publication page

GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics

Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J

Publication Date: 2015-07-25

Variant appearance in text: ANGPTL4: S67R

PubMed Link: 26206375

Variant Present in the following documents:

• 12859_2015_673_MOESM1_ESM.xls, sheet 2

View BVdb publication page

Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.

Plos Genetics

Ionita-Laza, Iuliana I; Capanu, Marinela M; De Rubeis, Silvia S; McCallum, Kenneth K; Buxbaum, Joseph D JD

Publication Date: 2014-12

Variant appearance in text: ANGPTL4: Ser67Arg

PubMed Link: 25502226

Variant Present in the following documents:

• Main text
• pgen.1004729.pdf

View BVdb publication page