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: MSH6: 3079G>C; V1027L; rs876658397

PubMed Link: 36922933

Variant Present in the following documents:

• crc-22-0136-s01.xlsx, sheet 1

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RNA Sequencing of Primary Cutaneous and Breast-Implant Associated Anaplastic Large Cell Lymphomas Reveals Infrequent Fusion Transcripts and Upregulation of PI3K/AKT Signaling via Neurotrophin Pathway Genes.

Cancers

Di Napoli, Arianna A; Vacca, Davide D; Bertolazzi, Giorgio G; Lopez, Gianluca G; Piane, Maria M; Germani, Aldo A; Rogges, Evelina E; Pepe, Giuseppina G; Santanelli Di Pompeo, Fabio F; Salgarello, Marzia M; Jobanputra, Vaidehi V; Hsiao, Susan S; Wrzeszczynski, Kazimierz O KO; Berti, Emilio E; Bhagat, Govind G

Publication Date: 2021-12-07

Variant appearance in text: MSH6: V1027L

PubMed Link: 34944796

Variant Present in the following documents:

• Main text
• cancers-13-06174.pdf

View BVdb publication page

RNA Sequencing of Primary Cutaneous and Breast-Implant Associated Anaplastic Large Cell Lymphomas Reveals Infrequent Fusion Transcripts and Upregulation of PI3K/AKT Signaling via Neurotrophin Pathway Genes.

Cancers

Di Napoli, Arianna A; Vacca, Davide D; Bertolazzi, Giorgio G; Lopez, Gianluca G; Piane, Maria M; Germani, Aldo A; Rogges, Evelina E; Pepe, Giuseppina G; Santanelli Di Pompeo, Fabio F; Salgarello, Marzia M; Jobanputra, Vaidehi V; Hsiao, Susan S; Wrzeszczynski, Kazimierz O KO; Berti, Emilio E; Bhagat, Govind G

Publication Date: 2021-12-07

Variant appearance in text: MSH6: V1027L

PubMed Link: 34944796

Variant Present in the following documents:

• Main text
• cancers-13-06174.pdf

View BVdb publication page

A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports

Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM

Publication Date: 2021-07-12

Variant appearance in text: MSH6: 3079G>C; Val1027Leu

PubMed Link: 34253785

Variant Present in the following documents:

• 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8

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Sources of discordance among germ-line variant classifications in ClinVar.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics

Yang, Shan S; Lincoln, Stephen E SE; Kobayashi, Yuya Y; Nykamp, Keith K; Nussbaum, Robert L RL; Topper, Scott S

Publication Date: 2017-10

Variant appearance in text: MSH6: 3079G>C; Val1027Leu

PubMed Link: 28569743

Variant Present in the following documents:

• gim201760x7.xlsx, sheet 2

View BVdb publication page