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2023
The expression and mutation of BRCA1/2 genes in ovarian cancer: a global systematic study
Expert Review of Molecular Diagnostics
2021
Implementing NGS-basedBRCAtumour tissue testing in FFPE ovarian carcinoma specimens: hints from a real-life experience within the framework of expert recommendations
Journal of Clinical Pathology
2021
BRCA1 ve BRCA2 Mutasyonlarının Tespitine Yönelik Yeni Nesil Dizileme Temelli Kit Geliştirilmesi ve Rutinde Kullanılan Yöntemler ile Valide Edilmesi
İstanbul Gelişim Üniversitesi Sağlık Bilimleri Dergisi
2021
Correlation between the number of false positive variants and the quality of results using Ion Torrent PGM™ sequencing to screen BRCA genes
Biomédica
2018
Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection
The Journal of Molecular Diagnostics
2018
Detecting clinically actionable variants in the 3′ exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene
BMC Medical Genetics
2018
Comparison of Ion Personal Genome Machine Platforms for the Detection of Variants in BRCA1 and BRCA2
Cancer Research and Treatment
2017
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape
Scientific Reports
2017
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
PeerJ
2017
Next-generation sequencing (NGS) of cell-free circulating tumor DNA and tumor tissue in patients with advanced urothelial cancer: a pilot assessment of concordance
Annals of Oncology
2017
Impact of germline and somatic BRCA1/2 mutations: tumor spectrum and detection platforms
Gene Therapy
2017
A label-free electrochemical DNA sensor to identify breast cancer susceptibility
Microchemical Journal
2017
Rapid and cost-effective high-throughput sequencing for identification of germline mutations of BRCA1 and BRCA2
Journal of Human Genetics
2017
Recurrent large genomic rearrangements in BRCA1 and BRCA2 in an Irish case series
Cancer Genetics
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