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المصدر: Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-7 (2022)
Hereditary Cancer in Clinical Practice
HEREDITARY CANCER IN CLINICAL PRACTICE

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4702af71e07ca57bf19b4ffa24788c49Test
https://biblio.vub.ac.be/vubirTest/(37947d23-d669-42b0-b1d4-cf0d39f0179a).html

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The CHEK2*1100delC Mutation and Adolescent Breast Cancer: A Case Report of Breast Cancer in a 19-Year-Old and a Review of the Literature

المؤلفون: Corrie Bourdon, Mohammad Torabi, Abigail J. Engwall, Thais Fortes, Tahereh Soleimani

المصدر: Breast Care. 17:85-89

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Breast cancer, business.industry, Internal medicine, Mutation (genetic algorithm), medicine, Surgery, medicine.disease, business, Chek2 1100delc

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::4a7977865b66a13e73bfe80c1db2b5dbTest
https://doi.org/10.1159/000513679Test

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دورية أكاديمية

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

المؤلفون: Muranen, Taru A., Greco, Dario, Blomqvist, Carl, Aittomäki, Kristiina, Khan, Sofia, Hogervorst, Frans, Verhoef, Senno, Pharoah, Paul D. P., Dunning, Alison M., Shah, Mitul, Luben, Robert, Bojesen, Stig E., Nordestgaard, Borge G., Schoemaker, Minouk, Swerdlow, Anthony, Garcia-Closas, Montserrat, Figueroa, Jonine, Doerk, Thilo, Bogdanova, Natalia V., Hall, Per, Li, Jingmei, Khusnutdinova, Elza, Bermisheva, Marina, Kristensen, Vessela, Borresen-Dale, Anne-Lise, Peto, Julian, Silva, Isabel dos Santos, Couch, Fergus J., Olson, Janet E., Hillemans, Peter, Park-Simon, Tjoung-Won, Brauch, Hiltrud, Hamann, Ute, Burwinkel, Barbara, Marme, Frederik, Meindl, Alfons, Schmutzler, Rita K., Cox, Angela, Cross, Simon S., Sawyer, Elinor J., Tomlinson, Ian, Lambrechts, Diether, Moisse, Matthieu, Lindblom, Annika, Margolin, Sara, Hollestelle, Antoinette, Martens, John W. M., Fasching, Peter A., Beckmann, Matthias W., Nevanlinna, Heli, NBCS Investigators, kConFab-AOCS Investigators, Breast Canc Assoc Consortium

المساهمون: Department of Obstetrics and Gynecology, Clinicum, Department of Oncology, Medicum, Kristiina Aittomäki / Principal Investigator, Genome-Scale Biology (GSB) Research Program, Research Programs Unit, HUS Gynecology and Obstetrics, HUS Comprehensive Cancer Center

مصطلحات موضوعية: breast cancer, Breast Cancer Association Consortium, CHEK2*1100delC, common variants, polygenic risk score, FAMILY-HISTORY, MUTATION, CARRIERS, BRCA2, WOMEN, Genetics, developmental biology, physiology, Cancers

وصف الملف: application/pdf

العلاقة: Muranen , T A , Greco , D , Blomqvist , C , Aittomäki , K , Khan , S , Hogervorst , F , Verhoef , S , Pharoah , P D P , Dunning , A M , Shah , M , Luben , R , Bojesen , S E , Nordestgaard , B G , Schoemaker , M , Swerdlow , A , Garcia-Closas , M , Figueroa , J , Doerk , T , Bogdanova , N V , Hall , P , Li , J , Khusnutdinova , E , Bermisheva , M , Kristensen , V , Borresen-Dale , A-L , Peto , J , Silva , I D S , Couch , F J , Olson , J E , Hillemans , P , Park-Simon , T-W , Brauch , H , Hamann , U , Burwinkel , B , Marme , F , Meindl , A , Schmutzler , R K , Cox , A , Cross , S S , Sawyer , E J , Tomlinson , I , Lambrechts , D , Moisse , M , Lindblom , A , Margolin , S , Hollestelle , A , Martens , J W M , Fasching , P A , Beckmann , M W , Nevanlinna , H , NBCS Investigators , kConFab-AOCS Investigators & Breast Canc Assoc Consortium 2017 , ' Genetic modifiers of CHEK2*1100delC-associated breast cancer risk ' , Genetics In medicine , vol. 19 , no. 5 , pp. 599-603 . https://doi.org/10.1038/gim.2016.147Test; ORCID: /0000-0002-5895-1808/work/33744763; http://hdl.handle.net/10138/189041Test; 9ab5cfb5-9682-4841-8770-372a7dc0f97d; 85021757649; 000401247400017

الإتاحة: http://hdl.handle.net/10138/189041Test

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دورية أكاديمية

CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population

المؤلفون: Hallamies, Sanna, Pelttari, Liisa M., Poikonen-Saksela, Paula, Jekunen, Antti, Jukkola-Vuorinen, Arja, Auvinen, Paivi, Blomqvist, Carl, Aittomaki, Kristiina, Mattson, Johanna, Nevanlinna, Heli

المساهمون: Department of Obstetrics and Gynecology, University of Helsinki, Clinicum, Department of Oncology, Medicum, Kristiina Aittomäki / Principal Investigator, Department of Medical and Clinical Genetics, HUS Comprehensive Cancer Center

مصطلحات موضوعية: Male breast cancer, CHEK2 c.1100delC, OVARIAN-CANCER, BRCA2 MUTATIONS, CONFER SUSCEPTIBILITY, GENE, CHEK2-ASTERISK-1100DELC, VARIANT, FAMILIES, 1100DELC, PROSTATE, RAD51C, 3122 Cancers

وصف الملف: application/pdf

العلاقة: This study was supported by the Helsinki University Hospital Research Fund, the Academy of Finland (266528), the Sigrid Juselius Foundation, and the Finnish Cancer Society. The funders had no role in study design, collection, analysis, or interpretation of data, or in writing the manuscript.; Hallamies , S , Pelttari , L M , Poikonen-Saksela , P , Jekunen , A , Jukkola-Vuorinen , A , Auvinen , P , Blomqvist , C , Aittomaki , K , Mattson , J & Nevanlinna , H 2017 , ' CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population ' , BMC Cancer , vol. 17 , 620 . https://doi.org/10.1186/s12885-017-3631-8Test; 85028889884; 6c90fb45-6282-4e7a-8232-9893dd36e5b8; http://hdl.handle.net/10138/224440Test; 000409193300003

الإتاحة: http://hdl.handle.net/10138/224440Test

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دورية أكاديمية

Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium

المؤلفون: Muranen, Taru A., Blomqvist, Carl, Dörk, Thilo, Jakubowska, Anna, Heikkilä, Päivi, Fagerholm, Rainer, Greco, Dario, Aittomäki, Kristiina, Bojesen, Stig E., Shah, Mitul, Dunning, Alison M., Rhenius, Valerie, Hall, Per, Czene, Kamila, Brand, Judith S., Darabi, Hatef, Chang-Claude, Jenny, Rudolph, Anja, Nordestgaard, Børge G., Couch, Fergus J., Hart, Steven N., Figueroa, Jonine, García-Closas, Montserrat, Fasching, Peter A., Beckmann, Matthias W., Li, Jingmei, Liu, Jianjun, Andrulis, Irene L., Winqvist, Robert, Pylkäs, Katri, Mannermaa, Arto, Kataja, Vesa, Lindblom, Annika, Margolin, Sara, Lubinski, Jan, Dubrowinskaja, Natalia, Bolla, Manjeet K., Dennis, Joe, Michailidou, Kyriaki, Wang, Qin, Easton, Douglas F., Pharoah, Paul D. P., Schmidt, Marjanka K., Nevanlinna, Heli

المصدر: Breast Cancer Research 18(1) 98

مصطلحات موضوعية: Breast cancer, CHEK2, CHK2, I157T, 1100delC, Survival, Pathology, Gene expression

العلاقة: info:eu-repo/grantAgreement/EC/FP7/223175/; https://zenodo.org/communities/ecfundedTest; https://zenodo.org/communities/fp7-bmcTest; https://zenodo.org/record/160104Test; https://doi.org/10.1186/s13058-016-0758-5Test; oai:zenodo.org:160104

الإتاحة: https://doi.org/10.1186/s13058-016-0758-5Test
https://zenodo.org/record/160104Test

View record in BASE

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