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Expansion of Cancer Risk Profile for BRCA1 and BRCA2 Pathogenic Variants.
Momozawa, Yukihide; Sasai, Rumi; Usui, Yoshiaki; Shiraishi, Kouya; Iwasaki, Yusuke; Taniyama, Yukari; Parsons, Michael T; Mizukami, Keijiro; Sekine, Yuya; Hirata, Makoto; Kamatani, Yoichiro; Endo, Mikiko; Inai, Chihiro; Takata, Sadaaki; Ito, Hidemi; Kohno, Takashi; Matsuda, Koichi; Nakamura, Seigo; Sugano, Kokichi; Yoshida, Teruhiko; Nakagawa, Hidewaki; Matsuo, Keitaro; Murakami, Yoshinori; Spurdle, Amanda B; Kubo, Michiaki.
Afiliação
  • Momozawa Y; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Sasai R; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Usui Y; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Shiraishi K; Division of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, Japan.
  • Iwasaki Y; Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceuticals Sciences, Okayama, Japan.
  • Taniyama Y; Division of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
  • Parsons MT; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Mizukami K; Division of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, Japan.
  • Sekine Y; Division of Genetics and Population Health, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Hirata M; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Kamatani Y; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Endo M; Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.
  • Inai C; Department of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
  • Takata S; Institute of Medical Science, Division of Molecular Pathology, Department of Cancer Biology, The University of Tokyo, Tokyo, Japan.
  • Ito H; Laboratory of Complex Trait Genomics, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • Kohno T; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Matsuda K; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Nakamura S; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Sugano K; Division of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, Japan.
  • Yoshida T; Division of Descriptive Cancer Epidemiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Nakagawa H; Division of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
  • Matsuo K; Laboratory of Clinical Genome Sequencing, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.
  • Murakami Y; Division of Breast Surgical Oncology, Department of Surgery, Showa University School of Medicine, Tokyo, Japan.
  • Spurdle AB; Department of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.
  • Kubo M; Department of Genetic Medicine, Kyoundo Hospital, Sasaki Foundation, Tokyo, Japan.
JAMA Oncol ; 8(6): 871-878, 2022 06 01.
Article em En | MEDLINE | ID: mdl-35420638
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Neoplasias Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Neoplasias Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article