Publications:

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Olaparib-Resistant BRCA2MUT Ovarian Cancer Cells with Restored BRCA2 Abrogate Olaparib-Induced DNA Damage and G2/M Arrest Controlled by the ATR/CHK1 Pathway for Survival.

Cells

Biegała, Łukasz Ł; Gajek, Arkadiusz A; Marczak, Agnieszka A; Rogalska, Aneta A

Publication Date: 2023-03-29

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 37048111

Variant Present in the following documents:

• cells-12-01038.pdf

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Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?

International Journal Of Oncology

Lavoro, Alessandro A; Scalisi, Aurora A; Candido, Saverio S; Zanghì, Guido Nicola GN; Rizzo, Roberta R; Gattuso, Giuseppe G; Caruso, Giuseppe G; Libra, Massimo M; Falzone, Luca L

Publication Date: 2022-05

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 35383859

Variant Present in the following documents:

• ijo-60-05-05349.pdf

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Sequencing of BRCA1/2-alterations using NGS-based technology: annotation as a challenge.

Oncotarget

Ebner, Silvana S; Winkelmann, Ria R; Martin, Saskia S; Köllermann, Jens J; Wild, Peter J PJ; Demes, Melanie M

Publication Date: 2022

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 35251494

Variant Present in the following documents:

• Main text
• oncotarget-13-28213.pdf

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Impressive effect of cisplatin monotherapy on a patient with heavily pretreated triple-negative breast cancer with poor performance.

Yeungnam University Journal Of Medicine

Baek, Dong Won DW; Park, Ji-Young JY; Lee, Soo Jung SJ; Chae, Yee Soo YS

Publication Date: 2020-07

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 31962039

Variant Present in the following documents:

• yujm-2019-00423.pdf

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Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia.

Hereditary Cancer In Clinical Practice

Cortés, Carolina C; Rivera, Ana Lucía AL; Trochez, David D; Solarte, Melissa M; Gómez, Daniela D; Cifuentes, Laura L; Barreto, Guillermo G

Publication Date: 2019

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 31341521

Variant Present in the following documents:

• Main text
• 13053_2019_Article_120.pdf

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Genetics of breast cancer in African populations: a literature review.

Global Health, Epidemiology And Genomics

Abbad, A A; Baba, H H; Dehbi, H H; Elmessaoudi-Idrissi, M M; Elyazghi, Z Z; Abidi, O O; Radouani, F F

Publication Date: 2018

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 30263132

Variant Present in the following documents:

• S2054420018000088a.pdf

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A Chinese family affected by lynch syndrome caused by MLH1 mutation.

Bmc Medical Genetics

Jia, Shuqin S; Zhang, Meng M; Sun, Yu Y; Yan, Hai H; Zhao, Fangping F; Li, Ziyu Z; Ji, Jiafu J

Publication Date: 2018-06-22

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 29929473

Variant Present in the following documents:

• 12881_2018_605_MOESM2_ESM.xlsx, sheet 1

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Germline mutation in the TP53 gene in uveal melanoma.

Scientific Reports

Hajkova, Nikola N; Hojny, Jan J; Nemejcova, Kristyna K; Dundr, Pavel P; Ulrych, Jan J; Jirsova, Katerina K; Glezgova, Johana J; Ticha, Ivana I

Publication Date: 2018-05-16

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 29769598

Variant Present in the following documents:

• 41598_2018_26040_MOESM2_ESM.xlsx, sheet 1

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Mutational analysis of BRCA1 and BRCA2 genes in Peruvian families with hereditary breast and ovarian cancer.

Molecular Genetics & Genomic Medicine

Buleje, Jose J; Guevara-Fujita, Maria M; Acosta, Oscar O; Huaman, Francia D P FDP; Danos, Pierina P; Murillo, Alexis A; Pinto, Joseph A JA; Araujo, Jhajaira M JM; Aguilar, Alfredo A; Ponce, Jaime J; Vigil, Carlos C; Castaneda, Carlos C; Calderon, Gabriela G; Gomez, Henry L HL; Fujita, Ricardo R

Publication Date: 2017-09

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 28944232

Variant Present in the following documents:

• MGG3-5-481.pdf

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A comparative study of germline BRCA1 and BRCA2 mutation screening methods in use in 20 European clinical diagnostic laboratories.

British Journal Of Cancer

Ellison, Gillian G; Wallace, Andrew A; Kohlmann, Alexander A; Patton, Simon S

Publication Date: 2017-08-22

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 28751759

Variant Present in the following documents:

• Main text

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Amplification of overlapping DNA amplicons in a single-tube multiplex PCR for targeted next-generation sequencing of BRCA1 and BRCA2.

Plos One

Schenk, Desiree D; Song, Gang G; Ke, Yue Y; Wang, Zhaohui Z

Publication Date: 2017

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 28704513

Variant Present in the following documents:

• pone.0181062.pdf

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Comparison of Ion Personal Genome Machine Platforms for the Detection of Variants in BRCA1 and BRCA2.

Cancer Research And Treatment

Hwang, Sang Mee SM; Lee, Ki Chan KC; Lee, Min Seob MS; Park, Kyoung Un KU

Publication Date: 2018-01

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 28392550

Variant Present in the following documents:

• crt-2017-062-suppl1.pdf

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Improved Efficiency and Reliability of NGS Amplicon Sequencing Data Analysis for Genetic Diagnostic Procedures Using AGSA Software.

Biomed Research International

Poulet, Axel A; Privat, Maud M; Ponelle, Flora F; Viala, Sandrine S; Decousus, Stephanie S; Perin, Axel A; Lafarge, Laurence L; Ollier, Marie M; El Saghir, Nagi S NS; Uhrhammer, Nancy N; Bignon, Yves-Jean YJ; Bidet, Yannick Y

Publication Date: 2016

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 27656653

Variant Present in the following documents:

• BMRI2016-5623089.pdf

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A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.

Biomed Research International

Karami, Fatemeh F; Mehdipour, Parvin P

Publication Date: 2013

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 24312913

Variant Present in the following documents:

• Main text

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BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families.

Bmc Medical Genetics

Berzina, Dace D; Nakazawa-Miklasevica, Miki M; Zestkova, Jekaterina J; Aksenoka, Karina K; Irmejs, Arvids A; Gardovskis, Andris A; Kalniete, Dagnija D; Gardovskis, Janis J; Miklasevics, Edvins E

Publication Date: 2013-06-14

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 23767878

Variant Present in the following documents:

• 1471-2350-14-61.pdf

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Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.

European Journal Of Human Genetics : Ejhg

Caux-Moncoutier, Virginie V; Pagès-Berhouet, Sabine S; Michaux, Dorothée D; Asselain, Bernard B; Castéra, Laurent L; De Pauw, Antoine A; Buecher, Bruno B; Gauthier-Villars, Marion M; Stoppa-Lyonnet, Dominique D; Houdayer, Claude C

Publication Date: 2009-11

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 19471317

Variant Present in the following documents:

• Main text

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BRCA1 and BRCA2 germline mutations in Malaysian women with early-onset breast cancer without a family history.

Plos One

Toh, Gaik Theng GT; Kang, Peter P; Lee, Sharlene S W SS; Lee, Daphne Shin-Chi DS; Lee, Sheau Yee SY; Selamat, Suhaida S; Mohd Taib, Nur Aishah NA; Yoon, Sook-Yee SY; Yip, Cheng Har CH; Teo, Soo-Hwang SH

Publication Date: 2008-04-23

Variant appearance in text: BRCA2: 4308T>C

PubMed Link: 18431501

Variant Present in the following documents:

• Main text

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