المؤلفون: Assad H; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA. assadh@karmanos.org., Levitin M; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA., Petrucelli N; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA., Manning M; Department of Psychology, Oakland University, Rochester, MI, USA., Thompson HS; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA., Chen W; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA., Jang H; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA., Simon MS; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, MI, USA.

المصدر: Breast cancer research and treatment [Breast Cancer Res Treat] 2024 Jul; Vol. 206 (2), pp. 261-272. Date of Electronic Publication: 2024 Apr 12.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Kluwer Academic Country of Publication: Netherlands NLM ID: 8111104 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7217 (Electronic) Linking ISSN: 01676806 NLM ISO Abbreviation: Breast Cancer Res Treat Subsets: MEDLINE

مواضيع طبية MeSH: Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , BRCA1 Protein*/genetics , Genetic Testing* , BRCA2 Protein*/genetics, Humans ; Female ; Middle Aged ; Adult ; Early Detection of Cancer ; Genetic Predisposition to Disease ; Aged ; Risk Reduction Behavior ; Ovarian Neoplasms/genetics ; Ovarian Neoplasms/prevention & control ; Ovarian Neoplasms/diagnosis ; Breast Neoplasms/genetics ; Breast Neoplasms/diagnosis ; Breast Neoplasms/epidemiology ; Mutation ; Salpingo-oophorectomy

المؤلفون: Trevisan L; Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy., Godino L; Unit of Medical Genetics, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy., Battistuzzi L; Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy., Innella G; Unit of Medical Genetics, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy., Luppi E; Unit of Medical Genetics, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy., Buzzatti G; Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy., Gismondi V; Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy., Blondeaux E; U.O. Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Largo Rosanna Benzi 10, Genova, 16132, Italy. evablondeaux@gmail.com., Bonelli LA; U.O. Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Largo Rosanna Benzi 10, Genova, 16132, Italy., Turchetti D; Unit of Medical Genetics, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy., Varesco L; Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

المصدر: Familial cancer [Fam Cancer] 2024 Jun; Vol. 23 (2), pp. 197-207. Date of Electronic Publication: 2023 Nov 16.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , Hereditary Breast and Ovarian Cancer Syndrome*/prevention & control , Genetic Testing*/methods , Genetic Predisposition to Disease*, Humans ; Female ; Italy ; Middle Aged ; Adult ; BRCA2 Protein/genetics ; Aged ; BRCA1 Protein/genetics ; Ovarian Neoplasms/genetics ; Ovarian Neoplasms/prevention & control ; Ovarian Neoplasms/diagnosis ; Male ; Breast Neoplasms/genetics ; Breast Neoplasms/prevention & control ; Breast Neoplasms/diagnosis

SCR Disease Name: Breast Cancer, Familial

المؤلفون: Evans DG; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK. gareth.evans@mft.nhs.uk.; Division of Evolution Infection and Genomic Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, School of Biological Sciences, University of Manchester, Manchester, M13 9PL, UK. gareth.evans@mft.nhs.uk., Green K; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK., Burghel GJ; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK., Forde C; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK., Lalloo F; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK., Schlecht H; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK., Woodward ER; Manchester Centre for Genomic Medicine and North-West Genomics Hub, Manchester University Hospitals NHS Foundation Trust, Manchester, M13 9WL, UK.; Division of Evolution Infection and Genomic Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, School of Biological Sciences, University of Manchester, Manchester, M13 9PL, UK.

المصدر: Familial cancer [Fam Cancer] 2024 Jun; Vol. 23 (2), pp. 187-195. Date of Electronic Publication: 2024 Mar 13.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Genetic Testing*/methods , Genetic Testing*/standards , Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , Practice Guidelines as Topic* , Genetic Predisposition to Disease*, Humans ; Female ; United Kingdom ; BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; MutS Homolog 2 Protein/genetics ; Early Detection of Cancer/methods ; MutL Protein Homolog 1/genetics ; Germ-Line Mutation ; DNA-Binding Proteins/genetics ; Mismatch Repair Endonuclease PMS2/genetics ; Male ; Ovarian Neoplasms/genetics ; Ovarian Neoplasms/diagnosis

المؤلفون: de Freitas Ribeiro AA; Universidade Federal de São João del Rei (UFSJ), 400 Sebastião Gonçalves Coelho St, Divinópolis, MG, 35501-296, Brazil., Junior NMC; Universidade Federal de São João del Rei (UFSJ), 400 Sebastião Gonçalves Coelho St, Divinópolis, MG, 35501-296, Brazil., Dos Santos LL; Universidade Federal de São João del Rei (UFSJ), 400 Sebastião Gonçalves Coelho St, Divinópolis, MG, 35501-296, Brazil. llaramg@hotmail.com.

المصدر: European journal of medical research [Eur J Med Res] 2024 Mar 20; Vol. 29 (1), pp. 187. Date of Electronic Publication: 2024 Mar 20.

نوع المنشور: Journal Article; Systematic Review

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 9517857 Publication Model: Electronic Cited Medium: Internet ISSN: 2047-783X (Electronic) Linking ISSN: 09492321 NLM ISO Abbreviation: Eur J Med Res Subsets: MEDLINE

مواضيع طبية MeSH: Breast Neoplasms*/epidemiology , Breast Neoplasms*/genetics , Breast Neoplasms*/pathology , Hereditary Breast and Ovarian Cancer Syndrome*/epidemiology , Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Ovarian Neoplasms*/epidemiology , Ovarian Neoplasms*/genetics , Ovarian Neoplasms*/pathology, Female ; Humans ; Brazil/epidemiology ; Genetic Predisposition to Disease ; Germ-Line Mutation ; Mutation/genetics

SCR Disease Name: Breast Cancer, Familial

المؤلفون: Ohneda K; Division of Genomics and Disease Prevention, Tohoku Medical Megabank Organization, Tohoku University.

المصدر: Gan to kagaku ryoho. Cancer & chemotherapy [Gan To Kagaku Ryoho] 2024 Mar; Vol. 51 (3), pp. 231-236.

نوع المنشور: English Abstract; Journal Article

بيانات الدورية: Publisher: Gan To Kagaku Ryohosha Country of Publication: Japan NLM ID: 7810034 Publication Model: Print Cited Medium: Print ISSN: 0385-0684 (Print) Linking ISSN: 03850684 NLM ISO Abbreviation: Gan To Kagaku Ryoho Subsets: MEDLINE

مواضيع طبية MeSH: Hereditary Breast and Ovarian Cancer Syndrome*, Female ; Humans ; Cohort Studies ; Genetic Predisposition to Disease ; Genomics ; Germ Cells

المؤلفون: Tuncer SB; Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Türkiye. Electronic address: seref.tuncer@istanbul.edu.tr., Celik B; Erzincan Binali Yıldırım University, Department of Molecular Biology, Erzincan, Türkiye., Erciyas SK; Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Türkiye., Erdogan OS; Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Türkiye., Gültaslar BK; Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Türkiye., Odemis DA; Department of Cancer Genetics, Istanbul Faculty of Medicine, Oncology Institute, Istanbul University, Istanbul, Türkiye., Avsar M; Health Services Vocational of Higher Education, T.C. Istanbul Aydın University, Istanbul, Türkiye., Sen F; Clinic of Medical Oncology, Avrasya Hospital, Istanbul, Türkiye., Saip PM; Department of Medical Oncology, Oncology Institute, Istanbul University, Istanbul, Türkiye., Yazici H; Istanbul Arel University, Arel Medical Faculty, Department of Medical Biology and Genetics, Istanbul, Türkiye.

المصدر: Pathology, research and practice [Pathol Res Pract] 2024 Feb; Vol. 254, pp. 155075. Date of Electronic Publication: 2024 Jan 02.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Gustav Fischer Verlag Country of Publication: Germany NLM ID: 7806109 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1618-0631 (Electronic) Linking ISSN: 03440338 NLM ISO Abbreviation: Pathol Res Pract Subsets: MEDLINE

مواضيع طبية MeSH: Breast Neoplasms*/genetics , Breast Neoplasms*/diagnosis , Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Ovarian Neoplasms*/genetics, Humans ; Female ; Adult ; Genetic Predisposition to Disease ; BRCA1 Protein/genetics ; Germ-Line Mutation ; High-Throughput Nucleotide Sequencing ; Germ Cells ; Xeroderma Pigmentosum Group D Protein/genetics

SCR Disease Name: Breast Cancer, Familial

المؤلفون: Fernández Madrigal L; Hereditary and Familial Cancer Unit, Medical Oncology Service, Juan Ramón Jimenez University Hospital, Huelva, Spain. Electronic address: laurafdez1992@hotmail.com., Rodríguez Garcés MY; Hereditary and Familial Cancer Unit, Medical Oncology Service, Juan Ramón Jimenez University Hospital, Huelva, Spain., Jiménez Ruiz FJ; Hereditary and Familial Cancer Unit, Medical Oncology Service, Juan Ramón Jimenez University Hospital, Huelva, Spain.

المصدر: Current problems in cancer [Curr Probl Cancer] 2023 Dec; Vol. 47 (6), pp. 101008. Date of Electronic Publication: 2023 Sep 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Mosby Country of Publication: United States NLM ID: 7702986 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-6345 (Electronic) Linking ISSN: 01470272 NLM ISO Abbreviation: Curr Probl Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/surgery, Female ; Humans ; Male ; Genetic Predisposition to Disease ; Mastectomy ; Mutation ; Retrospective Studies

المؤلفون: Kotaka S; Department of Gynecologic Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Yasui H; Department of Gynecologic Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Tsubouchi H; Department of Gynecologic Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Mori M; Department of Gynecologic Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Kotani H; Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Yoshimura A; Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan., Ouchi A; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan., Okuno M; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan., Komori K; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan., Shimizu Y; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan., Suzuki S; Department of Gynecologic Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

المصدر: Nagoya journal of medical science [Nagoya J Med Sci] 2023 Nov; Vol. 85 (4), pp. 814-821.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Nagoya University School Of Medicine Country of Publication: Japan NLM ID: 0412011 Publication Model: Print Cited Medium: Internet ISSN: 2186-3326 (Electronic) Linking ISSN: 00277622 NLM ISO Abbreviation: Nagoya J Med Sci Subsets: MEDLINE

مواضيع طبية MeSH: Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , Hereditary Breast and Ovarian Cancer Syndrome*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/surgery , Breast Neoplasms*/genetics , Breast Neoplasms*/surgery , Breast Neoplasms*/pathology , Ovarian Neoplasms*/genetics , Ovarian Neoplasms*/surgery , Ovarian Neoplasms*/pathology , Carcinoma*/surgery, Humans ; Female ; Mastectomy

المؤلفون: Cheng Y; Cancer Molecular Diagnostics Core, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China.; Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Cancer Immunology and Biotherapy, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, 300060 Tianjin, China., Dong L; Cancer Molecular Diagnostics Core, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China.; Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Cancer Immunology and Biotherapy, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, 300060 Tianjin, China., Bu D; Research Center for Ubiquitous Computing Systems, Institute of Computing Technology, Chinese Academy of Sciences, 100190 Beijing, China., Han L; Cancer Molecular Diagnostics Core, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China.; Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Cancer Immunology and Biotherapy, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, 300060 Tianjin, China., Zhao Y; Research Center for Ubiquitous Computing Systems, Institute of Computing Technology, Chinese Academy of Sciences, 100190 Beijing, China., Liu J; Cancer Prevention Center, Second Department of Breast Cancer, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China., Guo X; Department of Breast Pathology and Lab, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China., Xu H; College of Life Sciences and Bioengineering, School of Physical Science and Engineering, Beijing Jiaotong University, 100044 Beijing, China., Yu J; Cancer Molecular Diagnostics Core, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, 300060 Tianjin, China.; Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Cancer Immunology and Biotherapy, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, 300060 Tianjin, China.

المصدر: Frontiers in bioscience (Landmark edition) [Front Biosci (Landmark Ed)] 2024 Jan 09; Vol. 29 (1), pp. 2.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IMR Press Country of Publication: Singapore NLM ID: 101612996 Publication Model: Print Cited Medium: Internet ISSN: 2768-6698 (Electronic) Linking ISSN: 27686698 NLM ISO Abbreviation: Front Biosci (Landmark Ed) Subsets: MEDLINE

مواضيع طبية MeSH: Breast Neoplasms*/genetics , Chromothripsis* , Hereditary Breast and Ovarian Cancer Syndrome*, Female ; Humans ; BRCA1 Protein/genetics ; Clinical Relevance ; DNA Copy Number Variations ; BRCA2 Protein/genetics ; Chromosome Mapping

SCR Disease Name: Breast Cancer, Familial

المؤلفون: Öfverholm A; Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Göteborg, Sweden., Törngren T; Division of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden., Rosén A; Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden., Arver B; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden., Einbeigi Z; Department of Oncology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Göteborg, Sweden.; Department of Medicine and Oncology, Southern Älvsborg Hospital, Borås, Sweden., Haraldsson K; Division of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden., Ståhlbom AK; Hereditary Cancer Unit, Karolinska University Hospital Solna, Stockholm, Sweden., Kuchinskaya E; Department of Clinical Pathology and Clinical Genetics, Department of Clinical Experimental Medicine, Linköping University, Linköping, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Lindblom A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden., Melin B; Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden., Paulsson-Karlsson Y; Department of Immunology, Genetics and Pathology, Uppsala University Hospital, Uppsala, Sweden., Stenmark-Askmalm M; Department of Clinical Pathology and Clinical Genetics, Department of Clinical Experimental Medicine, Linköping University, Linköping, Sweden.; Department of Genetics, Pathology and Molecular Diagnostics, Office for Medical Services, Region Skåne, Lund, Sweden., Tham E; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden., von Wachenfeldt A; Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.; Department of Oncology, Södersjukhuset, Stockholm, Sweden., Kvist A; Division of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden., Borg Å; Division of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden., Ehrencrona H; Department of Genetics, Pathology and Molecular Diagnostics, Office for Medical Services, Region Skåne, Lund, Sweden. hans.ehrencrona@med.lu.se.; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. hans.ehrencrona@med.lu.se.

المصدر: BMC cancer [BMC Cancer] 2023 Aug 10; Vol. 23 (1), pp. 738. Date of Electronic Publication: 2023 Aug 10.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2407 (Electronic) Linking ISSN: 14712407 NLM ISO Abbreviation: BMC Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Breast Neoplasms*/diagnosis , Breast Neoplasms*/genetics , Ovarian Neoplasms*/diagnosis , Ovarian Neoplasms*/genetics , Triple Negative Breast Neoplasms*/genetics , Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis , Hereditary Breast and Ovarian Cancer Syndrome*/genetics, Humans ; Female ; BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Genetic Predisposition to Disease ; Genetic Testing ; Protein Serine-Threonine Kinases/genetics ; Germ-Line Mutation

SCR Disease Name: Breast Cancer, Familial