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1
المؤلفون: Semanti Mukherjee, Chaitanya Bandlamudi, Matthew D. Hellmann, Yelena Kemel, Esther Drill, Hira Rizvi, Kaitlyn Tkachuk, Aliya Khurram, Michael F. Walsh, Marjorie G. Zauderer, Diana Mandelker, Sabine Topka, Ahmet Zehir, Preethi Srinivasan, Myvizhi Esai Selvan, Maria I. Carlo, Karen A. Cadoo, Alicia Latham, Jada G. Hamilton, Ying L. Liu, Steven M. Lipkin, Sami Belhadj, Gareth L. Bond, Zeynep H. Gümüş, Robert J. Klein, Marc Ladanyi, David B. Solit, Mark E. Robson, David R. Jones, Mark G. Kris, Joseph Vijai, Zsofia K. Stadler, Christopher I. Amos, Barry S. Taylor, Michael F. Berger, Charles M. Rudin, Kenneth Offit
المصدر: Cancer Epidemiol Biomarkers Prev
مصطلحات موضوعية: Germ Cells, Lung Neoplasms, Oncology, Epidemiology, Humans, Genetic Predisposition to Disease, Prospective Studies, Germ-Line Mutation, Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f14b3108bc280a9e40a27f4e7b70806Test
https://doi.org/10.1158/1055-9965.epi-21-1287Test -
2
المؤلفون: Anna Arutyunova, Maria I. Carlo, Jada G. Hamilton, Rebecca Gebert, Mark E. Robson, Erin E. Salo-Mullen, Vivek Narayan, Melissa Batson, Heather Symecko, Kelsey Spielman, Amanda Catchings, Zsofia K. Stadler, Ibrahim H Shah, Stacy Pundock, Elizabeth Schofield, Susan M. Domchek, Kenneth Offit, Karen Cadoo, Rebecca Mueller, Kelsey Breen, Magan Trottier, Kim A. Reiss
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics
مصطلحات موضوعية: Male, medicine.medical_specialty, Genetic counseling, MEDLINE, Genetic Counseling, Mainstreaming, Article, treatment-focused genetic testing, Prostate cancer, multigene panel testing, psychosocial outcomes, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Genetic Testing, Prospective Studies, Genetics (clinical), Depression (differential diagnoses), Genetic testing, medicine.diagnostic_test, business.industry, Prostatic Neoplasms, medicine.disease, Distress, hereditary cancer, business, Patient education
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d65921dfb8882a8a828209c579ff688Test
https://doi.org/10.1038/s41436-021-01262-2Test -
3
المؤلفون: Marc Ladanyi, Gowtham Jayakumaran, Karen Cadoo, Ahmet Zehir, Philip Jonsson, Xiang Li, Jason Hwee, Meera Prasad, Michael Walsh, Jinru Shia, Allison Richards, Alexander V Penson, Aijazuddin Syed, Joseph Vijai, Roy Cambria, Michael F. Berger, Barry S. Taylor, Mark E. Robson, Semanti Mukherjee, Chaitanya Bandlamudi, Jianjiong Gao, Christopher J. Fong, Ozge Ceyhan-Birsoy, Maria I. Carlo, Liying Zhang, David M. Hyman, Preethi Srinivasan, Ino de Bruijn, Diana Mandelker, Jesse Galle, Selcuk Onur Sumer, Craig M. Bielski, Kenneth Offit, Shweta S. Chavan, Nikolaus Schultz, Yelena Kemel, David B. Solit, Zsofia K. Stadler
المصدر: Nature genetics, vol 53, iss 11
مصطلحات موضوعية: Heterozygote, DNA Copy Number Variations, Carcinogenesis, Somatic cell, Biology, medicine.disease_cause, DNA Mismatch Repair, Medical and Health Sciences, Germline, Rare Diseases, Clinical Research, Neoplasms, Genetics, medicine, Humans, 2.1 Biological and endogenous factors, Genetic Predisposition to Disease, Aetiology, Allele, Gene, Germ-Line Mutation, Cancer, Human Genome, Biological Sciences, medicine.disease, Phenotype, Penetrance, Developmental Biology
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1307a6c613516d022f0084adcb249133Test
https://doi.org/10.1038/s41588-021-00949-1Test -
4
المؤلفون: Ozge Ceyhan-Birsoy, Gowtham Jayakumaran, Yelena Kemel, Maksym Misyura, Umut Aypar, Sowmya Jairam, Ciyu Yang, Yirong Li, Nikita Mehta, Anna Maio, Angela Arnold, Erin Salo-Mullen, Margaret Sheehan, Aijazuddin Syed, Michael Walsh, Maria Carlo, Mark Robson, Kenneth Offit, Marc Ladanyi, Jorge S. Reis-Filho, Zsofia K. Stadler, Liying Zhang, Alicia Latham, Ahmet Zehir, Diana Mandelker
المصدر: Genome Medicine. 14
مصطلحات موضوعية: Cohort Studies, Male, Genetics, Humans, Prostatic Neoplasms, Molecular Medicine, Genetic Predisposition to Disease, Genetic Testing, Colorectal Neoplasms, Molecular Biology, Germ-Line Mutation, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52d7e5f7a95eb106dd5da514b8c86580Test
https://doi.org/10.1186/s13073-022-01101-2Test -
5
المؤلفون: Hong Truong, Kelsey Breen, Subhiksha Nandakumar, Daniel D. Sjoberg, Yelena Kemel, Nikita Mehta, Andrew T. Lenis, Peter A. Reisz, Jessica Carruthers, Nicole Benfante, Vijai Joseph, Aliya Khurram, Anuradha Gopalan, Samson W. Fine, Victor E. Reuter, Andrew J. Vickers, Ozge Birsoy, Ying Liu, Michael Walsh, Alicia Latham, Diana Mandelker, Zsofia K. Stadler, Eugene Pietzak, Behfar Ehdaie, Karim A. Touijer, Vincent P. Laudone, Susan F. Slovin, Karen A. Autio, Daniel C. Danila, Dana E. Rathkopf, James A. Eastham, Yu Chen, Michael J. Morris, Kenneth Offit, David B. Solit, Howard I. Scher, Wassim Abida, Mark E. Robson, Maria I. Carlo
المصدر: European urology. 83(1)
مصطلحات موضوعية: Male, Urology, Humans, Prostatic Neoplasms, Genetic Predisposition to Disease, Genetic Testing, Genomics, Sequence Analysis, Germ-Line Mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de4a9f1fee4749a318caec27e76df05Test
https://pubmed.ncbi.nlm.nih.gov/36115772Test -
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المؤلفون: Kelsey E. Breen, Bryson W. Katona, Amanda Catchings, Megha Ranganathan, Vanessa Marcell, Alicia Latham, Matthew B. Yurgelun, Zsofia K. Stadler
المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 24(12)
مصطلحات موضوعية: Adult, Checkpoint Kinase 2, Heterozygote, Humans, Genetic Predisposition to Disease, Penetrance, Genetic Counseling, Middle Aged, Colorectal Neoplasms, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fb48956878ed2766da254f638c4b26fTest
https://pubmed.ncbi.nlm.nih.gov/36222830Test -
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المؤلفون: Amanda Catchings, Liying Zhang, Vikas Rai, Ciyu Yang, Angela G. Arnold, Zsofia K. Stadler
المصدر: Breast Cancer Res Treat
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, RNA Splicing, Biology, Article, 03 medical and health sciences, Exon, 0302 clinical medicine, Breast cancer, medicine, Humans, Missense mutation, Genetic Predisposition to Disease, Ovarian Neoplasms, medicine.disease, Pedigree, DNA-Binding Proteins, Serous fluid, 030104 developmental biology, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, Fallopian tube cancer, RNA splicing, Cancer research, Female, Ovarian cancer, Fallopian tube
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f37cae73291099d2ddc7e3725f5d0e8Test
https://doi.org/10.1007/s10549-020-06066-7Test -
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المؤلفون: Marco Montagna, Mark E. Robson, Daniel Barrowdale, Mark H. Greene, Adrià López-Fernández, Miquel Angel Pujana, Paul Brennan, Lucy Side, Jackie Cook, Munaza Ahmed, Christi J. van Asperen, Katherine L. Nathanson, Ian G. Campbell, Shan Wang-Gohrke, Gero Kramer, Debra Frost, Noura Mebirouk, Angel Izquierdo, Conxi Lázaro, Douglas F. Easton, Joe Dennis, Kenneth Offit, Esther Darder, Stefania Tommasi, Angela Toss, Brca, Virginia Valentini, Tu Nguyen-Dumont, Charlotte Kvist Lautrup, Manuel R. Teixeira, Mads Thomassen, Xin Yang, Susan M. Domchek, Valentina Silvestri, Paolo Radice, Marta Venturelli, Joseph Vijai, Pedro Pinto, Caroline Pottinger, Karina Rønlund, Lone Kroeldrup, Paul A. James, Alan Donaldson, Rita K. Schmutzler, Muriel Belotti, Kim De Leeneer, Lesley McGuffog, Susan L. Neuhausen, Amanda E. Toland, Siranoush Manoukian, Vishakha Tripathi, Adalgeir Arason, Pascaline Berthet, Linda Steele, Judit Horvath, Gord Glendon, Goska Leslie, Eva Gross, Anna Coppa, D. J. Gallagher, Payal D. Shah, Hebon Investigators, Alfons Meindl, Orland Diez, Irene L. Andrulis, Angela F. Brady, Giuseppe Damante, Paolo Peterlongo, Ana Sánchez de Abajo, Maria A. Caligo, Alison H. Trainer, Sophie Giraud, Saba Sharif, Christian Sutter, Johanna Rantala, Javier Benitez, Mark T. Rogers, kConFab Investigators, Lídia Feliubadaló, Inge Søkilde Pedersen, Annabeth Høgh Petersen, Jesús del Valle, Agostino Bucalo, Andrea Gehrig, Megan N. Frone, Judith Balmaña, Marc Tischkowitz, Thomas Hansen, Joan Brunet, Ines Zanna, Torben A Kruse, Carole Brewer, Bernard Peissel, Helen Gregory, Mary Porteous, Rosa B. Barkardottir, Andreas Rump, Ros Eeles, Anna Whaite, Saundra S. Buys, Fabienne Lesueur, Lisa Walker, Laura Ottini, Louise Izatt, Antonis C. Antoniou, Georgia Chenevix-Trench, Susanne E. Boonen, Hayley Cassingham, Jacques Simard, Christoph Engel, Patrick J. Morrison, Lise Lotte Christensen, Giulia Cini, Alvaro N.A. Monteiro, Kathleen Claes, Jacqueline Eason, Zoltan Matrai, Uffe Birk Jensen, Kristiina Aittomäki, Ramunas Janavicius, Olufunmilayo I. Olopade, Bjarni A. Agnarsson, Kara N. Maxwell, Julian Barwell, Bernd Auber, Julian Adlard, Esther M. John, Alex Teulé, Miguel de la Hoya, Darcy L. Thull, David E. Goldgar, Alessandra Viel, Dominique Stoppa-Lyonnet, Barbara Wappenschmidt, Phuong L. Mai, Taru A. Muranen, Eric Hahnen, Fergus J. Couch, Laura Matricardi, Domenico Palli, Yen Y. Tan, Julia Hentschel, Florentia Fostira, Ute Hamann, Trinidad Caldés, Rosemarie Davidson, Daniel R. Barnes, Åke Borg, Pedro Pérez-Segura, Aniko Bozsik, Yuan Chun Ding, Dieter Niederacher, Heli Nevanlinna, Helen Hanson, Norbert Arnold, Robin de Putter, Juliane Ramser, Alex Murray, Laura Cortesi, Christian F. Singer, Jacopo Azzollini, Zsofia K. Stadler, Oskar T. Johannsson, Andrew K. Godwin, D. Gareth Evans, Edith Olah, Michael T. Parsons
المساهمون: Medicum, Research Programs Unit, Kristiina Aittomäki / Principal Investigator, HUSLAB, Department of Medical and Clinical Genetics, University of Helsinki, Helsinki University Hospital Area, Research Program in Systems Oncology, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, Clinicum, Institut Català de la Salut, [Barnes DR, Leslie G, McGuffog L, Dennis J, Yang X] Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK. [Silvestri V] Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy. [Balmaña J] Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Diez O] Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Àrea de Genètica Clínica i Molecular, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Barnes, D R, Silvestri, V, Leslie, G, McGuffog, L, Dennis, J, Yang, X, Adlard, J, Agnarsson, B A, Ahmed, M, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Auber, B, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Barwell, J, Belotti, M, Benitez, J, Berthet, P, Boonen, S E, Borg, Å, Bozsik, A, Brady, A F, Brennan, P, Brewer, C, Brunet, J, Bucalo, A, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Cassingham, H, Christensen, L L, Cini, G, Claes, K B M, Cook, J, Coppa, A, Cortesi, L, Damante, G, Darder, E, Davidson, R, de la Hoya, M, Hansen, T V O, Horvath, J, Jensen, U B, Lautrup, C, Pedersen, I S & GEMO Study Collaborators 2022, ' Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores ', Journal of the National Cancer Institute, vol. 114, no. 1, 147, pp. 109-122 . https://doi.org/10.1093/jnci/djab147Test
JNCI Journal of the National Cancer Institute
Barnes, D R, Silvestri, V, Leslie, G, McGuffog, L, Dennis, J, Yang, X, Adlard, J, Agnarsson, B A, Ahmed, M, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Auber, B, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Barwell, J, Belotti, M, Benitez, J, Berthet, P, Boonen, S E, Borg, Å, Bozsik, A, Brady, A F, Brennan, P, Brewer, C, Brunet, J, Bucalo, A, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Cassingham, H, Christensen, L L, Cini, G, Claes, K B M, Cook, J, Coppa, A, Cortesi, L, Damante, G, Darder, E, Davidson, R, de la Hoya, M, De Leeneer, K, de Putter, R, Del Valle, J, Diez, O, Ding, Y C, Domchek, S M, Donaldson, A, Eason, J, Eeles, R, Engel, C, Evans, D G, Feliubadaló, L, Fostira, F, Frone, M, Frost, D, Gallagher, D, Gehrig, A, Giraud, S, Glendon, G, Godwin, A K, Goldgar, D E, Greene, M H, Gregory, H, Gross, E, Hahnen, E, Hamann, U, Hansen, T V O, Hanson, H, Hentschel, J, Horvath, J, Izatt, L, Izquierdo, A, James, P A, Janavicius, R, Jensen, U B, Johannsson, O T, John, E M, Kramer, G, Kroeldrup, L, Kruse, T A, Lautrup, C, Lazaro, C, Lesueur, F, Lopez-Fernández, A, Mai, P L, Manoukian, S, Matrai, Z, Matricardi, L, Maxwell, K N, Mebirouk, N, Meindl, A, Montagna, M, Monteiro, A N, Morrison, P J, Muranen, T A, Murray, A, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Nguyen-Dumont, T, Niederacher, D, Olah, E, Olopade, O I, Palli, D, Parsons, M T, Pedersen, I S, Peissel, B, Perez-Segura, P, Peterlongo, P, Petersen, A H, Pinto, P, Porteous, M E, Pottinger, C, Pujana, M A, Radice, P, Ramser, J, Rantala, J, Robson, M, Rogers, M T, Rønlund, K, Rump, A, Sánchez de Abajo, A M, Shah, P D, Sharif, S, Side, L E, Singer, C F, Stadler, Z, Steele, L, Stoppa-Lyonnet, D, Sutter, C, Tan, Y Y, Teixeira, M R, Teulé, A, Thull, D L, Tischkowitz, M, Toland, A E, Tommasi, S, Toss, A, Trainer, A H, Tripathi, V, Valentini, V, van Asperen, C J, Venturelli, M, Viel, A, Vijai, J, Walker, L, Wang-Gohrke, S, Wappenschmidt, B, Whaite, A, Zanna, I, Offit, K, Thomassen, M, Couch, F J, Schmutzler, R K, Simard, J, Easton, D F, Chenevix-Trench, G, Antoniou, A C, Ottini, L & GEMO Study Collaborators 2022, ' Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores ', Journal of the National Cancer Institute, vol. 114, no. 1, pp. 109-122 . https://doi.org/10.1093/jnci/djab147Test
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of the National Cancer Institute, 114(1), 109-122. OXFORD UNIV PRESS INC
JNCI-Journal of the National Cancer Institute, Oxford : Oxford University Press, 2022, vol. 114, iss. 1, p. 109-122
GEMO Study Collaborators, EMBRACE Collaborators, kConFab Investigators, HEBON Investigators, BRCA1 & BRCA2 2022, ' Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores ', National Cancer Institute. Journal (Online), vol. 114, no. 1, 147, pp. 109-122 . https://doi.org/10.1093/jnci/djab147Test
Scientia
GEMO Study Collaborators, Kristensen, L K, Jensen, U B, Lautrup, C K & Høgh Petersen, A 2022, ' Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores ', National Cancer Institute. Journal (Online), vol. 114, no. 1, djab147, pp. 109-122 . https://doi.org/10.1093/jnci/djab147Testمصطلحات موضوعية: Oncology, Male, Cancer Research, Neoplasms::Neoplasms by Site::Breast Neoplasms [DISEASES], Genetic Phenomena::Genotype::Genetic Predisposition to Disease [PHENOMENA AND PROCESSES], Diàtesi, polygenic, male breast cancer, PRS, Medical Oncology, Prostate cancer, Breast cancer, 0302 clinical medicine, Prostate, Risk Factors, Medicine and Health Sciences, 80 and over, genetics, skin and connective tissue diseases, Aged, 80 and over, neoplasias::neoplasias por localización::neoplasias de la mama [ENFERMEDADES], 0303 health sciences, education.field_of_study, BRCA1 Protein, Men, Articles, ASSOCIATION, Single Nucleotide, prostate cancer, OVARIAN, BRCA1, BRCA2, 3. Good health, Mutation carriers, medicine.anatomical_structure, Ovarian, 030220 oncology & carcinogenesis, Male breast cancer, Pròstata - Càncer - Aspectes genètics, BRCA2 Protein, Genetic Predisposition to Disease, Heterozygote, Humans, Mutation, Polymorphism, Single Nucleotide, Risk Assessment, Breast Neoplasms, Prostatic Neoplasms, AcademicSubjects/MED00010, medicine.medical_specialty, Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms [DISEASES], Urology, 3122 Cancers, Population, Single-nucleotide polymorphism, MUTATION CARRIERS, Càncer de mama, Association, 03 medical and health sciences, Internal medicine, medicine, Polymorphism, education, fenómenos genéticos::genotipo::predisposición genética a la enfermedad [FENÓMENOS Y PROCESOS], 030304 developmental biology, Aged, Càncer de pròstata, business.industry, Cancer, Odds ratio, medicine.disease, neoplasias::neoplasias por localización::neoplasias urogenitales::neoplasias de los genitales masculinos::neoplasias de la próstata [ENFERMEDADES], Homes, Mama - Càncer - Aspectes genètics, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c81f6326649ecf1e3ace95b9e9e43d8Test
https://hdl.handle.net/11380/1280528Test -
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المؤلفون: Joseph Vijai, Ryan Hausler, Kenneth Offit, Wendy Kohlmann, Wassim Abida, Sophie Hyman, Piper Nicolosi, Heather H. Cheng, Jennie Vagher, Eliezer M. Van Allen, Brian H. Shirts, Maria I. Carlo, Daniel J. Lee, Marianne E Dubard-Gault, Mercy Y. Laurino, Anh D. Le, Eric Q. Konnick, Jacquelyn Powers, Luke Maese, Lauren E. Schwartz, Anne Naumer, Kara N. Maxwell, Lorraine V. Naylor, Bruce Montgomery, Colin C. Pritchard, Joshua D. Schiffman, Casey Morrison, Roman Gulati, Bastien Nguyen, Jill E. Stopfer, Oliver Sartor, Zsofia K. Stadler, Peter S. Nelson, Samantha Greenberg, Judy Garber, Saud H. AlDubayan, Robert L. Nussbaum, Michael Walsh, Diana Mandelker, Michael J. Morris, Elisa Ledet
المصدر: Eur Urol
مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, Urology, Germline, Article, Li-Fraumeni Syndrome, Prostate cancer, Interquartile range, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Germ-Line Mutation, Genetic testing, Retrospective Studies, medicine.diagnostic_test, business.industry, Prostatic Neoplasms, Retrospective cohort study, Middle Aged, medicine.disease, Confidence interval, Li–Fraumeni syndrome, Cohort, Tumor Suppressor Protein p53, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a25f5caee2992fd009f0ea66e51f00cdTest
https://europepmc.org/articles/PMC8891030Test/ -
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المؤلفون: Kenneth Offit, Hector Diaz-Zabala, Semanti Mukherjee, Mark E. Robson, Jada G. Hamilton, Vignesh Ravichandran, Steven M. Lipkin, Melissa K. Frey, Zoe Steinsnyder, Kaitlyn Tkachuk, Jeffrey Levin, Zsofia K. Stadler, Joseph Vijai, Ravi Sharaf, Michael Walsh
المصدر: Journal of Clinical Oncology
مصطلحات موضوعية: Adult, Male, Counseling, 0301 basic medicine, Cancer Research, Genetic Testing for Cancer, MEDLINE, Computational biology, Sensitivity and Specificity, DNA sequencing, 03 medical and health sciences, 0302 clinical medicine, Neoplasms, Mass Screening, Humans, Medicine, Genetic Predisposition to Disease, Genetic Testing, Prospective Studies, Gene, Early Detection of Cancer, Germ-Line Mutation, Genetic testing, medicine.diagnostic_test, business.industry, Reproducibility of Results, Cancer susceptibility, Cancer, ORIGINAL REPORTS, Middle Aged, medicine.disease, United States, Telephone, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Linear Models, Feasibility Studies, Female, Population screening, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cd719c38030fc30e228da3e2b659af9Test
https://doi.org/10.1200/jco.19.02010Test