Publications:

Whole-exome Sequencing of Nigerian Prostate Tumors from the Prostate Cancer Transatlantic Consortium (CaPTC) Reveals DNA Repair Genes Associated with African Ancestry.

Cancer Research Communications

White, Jason A JA; Kaninjing, Ernest T ET; Adeniji, Kayode A KA; Jibrin, Paul P; Obafunwa, John O JO; Ogo, Chidiebere N CN; Mohammed, Faruk F; Popoola, Ademola A; Fatiregun, Omolara A OA; Oluwole, Olabode P OP; Karanam, Balasubramanyam B; Elhussin, Isra I; Ambs, Stefan S; Tang, Wei W; Davis, Melissa M; Polak, Paz P; Campbell, Moray J MJ; Brignole, Kathryn R KR; Rotimi, Solomon O SO; Dean-Colomb, Windy W; Odedina, Folake T FT; Martin, Damali N DN; Yates, Clayton C

Publication Date: 2022-09

Variant appearance in text: MSH2: 942+2T>G; rs587779195

PubMed Link: 36922933

Variant Present in the following documents:

• crc-22-0136-s01.xlsx, sheet 1

View BVdb publication page

Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics

Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P

Publication Date: 2023-02-23

Variant appearance in text: MSH2: 942+2T>G

PubMed Link: 36823319

Variant Present in the following documents:

• 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6

View BVdb publication page

Genomic loci susceptible to systematic sequencing bias in clinical whole genomes.

Genome Research

Freeman, Timothy M TM; , ; Wang, Dennis D; Harris, Jason J

Publication Date: 2020-03

Variant appearance in text: rs587779195

PubMed Link: 32156711

Variant Present in the following documents:

• 415.pdf

View BVdb publication page

Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition.

Plos One

Martin-Morales, Lorena L; Rofes, Paula P; Diaz-Rubio, Eduardo E; Llovet, Patricia P; Lorca, Victor V; Bando, Inmaculada I; Perez-Segura, Pedro P; de la Hoya, Miguel M; Garre, Pilar P; Garcia-Barberan, Vanesa V; Caldes, Trinidad T

Publication Date: 2018

Variant appearance in text: MSH2: 942+2T>G

PubMed Link: 30256826

Variant Present in the following documents:

• Main text
• pone.0203885.pdf

View BVdb publication page

Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.

Journal Of Medical Genetics

van der Post, R S RS; Kiemeney, L A LA; Ligtenberg, M J L MJ; Witjes, J A JA; Hulsbergen-van de Kaa, C A CA; Bodmer, D D; Schaap, L L; Kets, C M CM; van Krieken, J H J M JH; Hoogerbrugge, N N

Publication Date: 2010-07

Variant appearance in text:

PubMed Link: 20591884

Variant Present in the following documents:

• Main text

View BVdb publication page