Publications:

A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk.

Hgg Advances

Yu, Yao Y; Chang, Kyle K; Chen, Jiun-Sheng JS; Bohlender, Ryan J RJ; Fowler, Jerry J; Zhang, Di D; Huang, Maosheng M; Chang, Ping P; Li, Yanan Y; Wong, Justin J; Wang, Huamin H; Gu, Jian J; Wu, Xifeng X; Schildkraut, Joellen J; Cannon-Albright, Lisa L; Ye, Yuanqing Y; Zhao, Hua H; Hildebrandt, Michelle A T MAT; Permuth, Jennifer B JB; Li, Donghui D; Scheet, Paul P; Huff, Chad D CD

Publication Date: 2022-01-13

Variant appearance in text: rs147169118

PubMed Link: 35047863

Variant Present in the following documents:

• mmc3.pdf
• mmc1.pdf

View BVdb publication page

Genetic variants affecting equivalent protein family positions reflect human diversity.

Scientific Reports

Raimondi, Francesco F; Betts, Matthew J MJ; Lu, Qianhao Q; Inoue, Asuka A; Gutkind, J Silvio JS; Russell, Robert B RB

Publication Date: 2017-10-06

Variant appearance in text: rs147169118

PubMed Link: 28986545

Variant Present in the following documents:

• 41598_2017_12971_MOESM2_ESM.xlsx, sheet 7

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XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One

Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F

Publication Date: 2015

Variant appearance in text: rs147169118

PubMed Link: 25905921

Variant Present in the following documents:

• pone.0123569.s008.xls, sheet 6
• pone.0123569.s008.xls, sheet 11
• pone.0123569.s008.xls, sheet 2

View BVdb publication page