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Article detail · 2018 · article

Identification of a BRCA2 mutation in a Turkish family with early‐onset breast cancer

Journal Clinical Case Reports (discontinued)
ISSN2050-0904
YÖKSİS OpenAlex Open access · gold
Year2018
Citations2OpenAlex
Percentile%56.2
FWCI0.281.00 = world average
Scopus (SJR)Q4
OpenAlexOpenAlex record

Data source split

  • YÖKSİSYÖKSİS article record
  • YÖKSİS venueClinical Case Reports
  • Catalog match (ISSN)Clinical Case Reports (discontinued)
  • OpenAlexOpenAlex enrichment (abstract, citations, topics)

Abstract

OpenAlex English

Key Clinical Message We used a multi‐gene panel testing to identify the germline variants in a mother‐daughter pair with early‐onset breast cancer, and detected one pathogenic protein‐truncating variant in BRCA 2 . Our results highlight the importance of genetic testing in identifying the pathogenic mutation running in cancer families.

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

2citationsOpenAlex · cited_by_count (cache / database)

2 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. 2018 Identification of a BRCA 2 mutation in a Turkish family with early‐onset breast cancerCitations 2 · OpenAlex

Authors

7
  1. Elifnaz Celik 1
  2. Kubra Ermis tekkus 2
  3. Izzet Mehmet Akcay 3
  4. Gizem Alkurt 4
  5. FİKRET EZBERCİ 5
  6. GİZEM DİNLER DOĞANAY İSTANBUL TEKNİK ÜNİVERSİTESİ 6
  7. HAMDİ LEVENT DOĞANAY BAHÇEŞEHİR ÜNİVERSİTESİ 7