Publications:

Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: PARP1: V762V

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2

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PARP-1 Val762Ala polymorphism is associated with risk of cervical carcinoma.

Plos One

Ye, Feng F; Cheng, Qi Q; Hu, Yuting Y; Zhang, Jing J; Chen, Huaizeng H

Publication Date: 2012

Variant appearance in text: PARP: Val762Val

PubMed Link: 22624032

Variant Present in the following documents:

• pone.0037446.pdf

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Polymorphisms in base excision repair genes as colorectal cancer risk factors and modifiers of the effect of diets high in red meat.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology

Brevik, Asgeir A; Joshi, Amit D AD; Corral, Román R; Onland-Moret, N Charlotte NC; Siegmund, Kimberly D KD; Le Marchand, Loïc L; Baron, John A JA; Martinez, Maria Elena ME; Haile, Robert W RW; Ahnen, Dennis J DJ; Sandler, Robert S RS; Lance, Peter P; Stern, Mariana C MC

Publication Date: 2010-12

Variant appearance in text: PARP: Val762Val

PubMed Link: 21037106

Variant Present in the following documents:

• Main text

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