المؤلفون: Martine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, Corinna Ernst, Arnaud Droit, Bing-Jian Feng, Stéphane Dubois, Annie-Claude Collin-Deschesnes, Penny Soucy, Maxime Vallée, Frédéric Fournier, Audrey Lemaçon, Muriel A. Adank, Jamie Allen, Janine Altmüller, Norbert Arnold, Margreet G. E. M. Ausems, Riccardo Berutti, Manjeet K. Bolla, Shelley Bull, Sara Carvalho, Sten Cornelissen, Michael R. Dufault, Alison M. Dunning, Christoph Engel, Andrea Gehrig, Willemina R. R. Geurts-Giele, Christian Gieger, Jessica Green, Karl Hackmann, Mohamed Helmy, Julia Hentschel, Frans B. L. Hogervorst, Antoinette Hollestelle, Maartje J. Hooning, Judit Horváth, M. Arfan Ikram, Silke Kaulfuß, Renske Keeman, Da Kuang, Craig Luccarini, Wolfgang Maier, John W. M. Martens, Dieter Niederacher, Peter Nürnberg, Claus-Eric Ott, Annette Peters, Paul D. P. Pharoah, Alfredo Ramirez, Juliane Ramser, Steffi Riedel-Heller, Gunnar Schmidt, Mitul Shah, Martin Scherer, Antje Stäbler, Tim M. Strom, Christian Sutter, Holger Thiele, Christi J. van Asperen, Lizet van der Kolk, Rob B. van der Luijt, Alexander E. Volk, Michael Wagner, Quinten Waisfisz, Qin Wang, Shan Wang-Gohrke, Bernhard H. F. Weber, Genome of the Netherlands Project Genome of the Netherlands Project, GHS Study Group GHS Study Group, Peter Devilee, Sean Tavtigian, Gary D. Bader, Alfons Meindl, David E. Goldgar, Irene L. Andrulis, Rita K. Schmutzler, Douglas F. Easton, Marjanka K. Schmidt, Eric Hahnen, Jacques Simard

المصدر: Cancers; Volume 14; Issue 14; Pages: 3363

مصطلحات موضوعية: breast cancer, genetic susceptibility, whole-exome sequencing, moderate-penetrance genes

وصف الملف: application/pdf

العلاقة: Cancer Epidemiology and Prevention; https://dx.doi.org/10.3390/cancers14143363Test

الإتاحة: https://doi.org/10.3390/cancers14143363Test

المؤلفون: Colin Mackenzie, Colin C. Young, Sean V. Tavtigian, Yukihide Momozawa, Elodie Girard, Elad Ziv, Fabienne Lesueur, Donglei Hu, Bing Jian Feng, Susan L. Neuhausen, Yusuke Iwasaki

مصطلحات موضوعية: medicine.medical_specialty, Breast cancer, In silico, Multiple comparisons problem, medicine, Missense mutation, Medical genetics, Genomics, Computational biology, Biology, medicine.disease, CHEK2, Sequence (medicine)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6de57b1d363618497743a147afbce7eTest

المؤلفون: Margaret Akinhanmi, Brigette Tippin Davis, Priyanka Sharma, Drakoulis Yannoukakos, Eric C. Polley, Raymond Moore, David E. Goldgar, Peter A. Fasching, Jill S. Dolinsky, Abigail Thomas, Heli Nevanlinna, Judy Garber, Diana Eccles, Hiltrud Brauch, Andrew K. Godwin, Bing Jian Feng, Holly LaDuca, Angela Cox, Song Yao, Hermela Shimelis, Jie Na, Florentia Fostira, Steven N. Hart, Fergus J. Couch, Tina Pesaran, Amanda Ewart-Toland, Chunling Hu, Jenna Lilyquist, Irene Konstantopoulou

المساهمون: Doctoral Programme in Biomedicine, Department of Obstetrics and Gynecology, Clinicum

المصدر: JNCI Journal of the National Cancer Institute

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Cancer Research, Triple Negative Breast Neoplasms, PHENOTYPE, 0302 clinical medicine, Gene Frequency, Risk Factors, Odds Ratio, CONFER SUSCEPTIBILITY, Age of Onset, Triple-negative breast cancer, medicine.diagnostic_test, WOMEN, Articles, Middle Aged, 3. Good health, 030220 oncology & carcinogenesis, SURVIVAL, Female, Adult, medicine.medical_specialty, PALB2, 3122 Cancers, OVARIAN-CANCER, 03 medical and health sciences, Young Adult, Breast cancer, Internal medicine, medicine, Biomarkers, Tumor, Humans, Genetic Predisposition to Disease, Genetic Testing, INHERITED MUTATIONS, Alleles, Genetic Association Studies, Genetic testing, REPAIR, Cancer prevention, business.industry, Case-control study, Cancer, Odds ratio, medicine.disease, 030104 developmental biology, Case-Control Studies, Mutation, business, Genome-Wide Association Study

وصف الملف: text; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb12160fb9f3ea88ca976366ab9061ccTest
https://eprints.soton.ac.uk/426063Test/

المؤلفون: Peter Kraft, Emmanuella Bimeh, Bing Jian Feng, Mary Beth Terry, Georgia Chenevix-Trench, John L. Hopper, Saundra S. Buys, Hongyan Li, Melissa C. Southey, David E. Goldgar, Xiaoqing Chen, Esther M. John, Alexander Miron, Kelly-Anne Phillips, Antonis C. Antoniou, Gillian Mitchell, Daniel Barrowdale, Paul A. James, Heather Thorne, Irene L. Andrulis, Jonathan Beesley, Mary B. Daly

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics

مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, medicine.medical_specialty, Multifactorial Inheritance, Single-nucleotide polymorphism, Breast Neoplasms, non-BRCA associated, Polymorphism, Single Nucleotide, Risk Assessment, Article, 03 medical and health sciences, risk prediction, 0302 clinical medicine, Breast cancer, breast cancer, Risk Factors, Internal medicine, Cancer screening, medicine, Humans, Genetic Predisposition to Disease, Registries, Family history, Prospective cohort study, Genetics (clinical), Early Detection of Cancer, Aged, Gynecology, business.industry, Hazard ratio, Middle Aged, medicine.disease, Confidence interval, 3. Good health, 030104 developmental biology, cancer screening, 030220 oncology & carcinogenesis, polygenic risk score, Female, business, Risk assessment

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::352a33e412bebbe61f92bb8a0e3c5f3cTest
http://europepmc.org/articles/PMC5107177Test

المؤلفون: Nathalie Forey, Sandrine McKay-Chopin, F. Le Calvez-Kelm, Irene L. Andrulis, Melissa C. Southey, Amanda Gammon, Fabienne Lesueur, David E. Goldgar, Sean V. Tavtigian, Nivonirina Robinot, Wendy Kohlmann, Andrew M. Paquette, Geoffroy Durand, Jason Gertz, Mia Hashibe, T. C. Francy, J. S. Rosenthal, Erin L. Young, Tu Nguyen-Dumont, A. W. Stark, Esther M. John, Javier Oliver, Maroulio Pertesi, Kimberly A. Kaphingst, John L. Hopper, Maxime Vallée, Catherine Voegele, Bing Jian Feng, Francesca Damiola

المصدر: Journal of Medical Genetics

مصطلحات موضوعية: 0301 basic medicine, Adult, Risk, Mutation, Missense, Single-nucleotide polymorphism, Breast Neoplasms, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Polymorphism (computer science), Genotype, medicine, Cancer Genetics, Genetics, Missense mutation, Humans, Genetic Predisposition to Disease, Clinical genetics, Genetic Testing, CHEK2, Genetics (clinical), Genetic testing, medicine.diagnostic_test, business.industry, Cancer: breast, Case-control study, Middle Aged, medicine.disease, 3. Good health, 030104 developmental biology, 030220 oncology & carcinogenesis, Case-Control Studies, Screening, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b6ff5488840b1de5ee47b3c1ddede98Test
http://europepmc.org/articles/PMC4893078Test

المؤلفون: Heather Thorne, Bing Jian Feng, Igor V. Makunin, Jonathan Ellis, Melissa C. Southey, kConFab Investigators, Ian G. Campbell, Jun Li, David E. Goldgar, Huong Meeks, Sue Healey, Judy Kirk, David Clouston, Georgia Chenevix-Trench, Gillian Mitchell

المصدر: Journal of Medical Genetics. 53:34-42

مصطلحات موضوعية: Male, 0301 basic medicine, Genotype, PALB2, Genes, BRCA2, Genes, BRCA1, Biology, Bioinformatics, Article, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Breast cancer, Biomarkers, Tumor, Odds Ratio, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, skin and connective tissue diseases, CHEK2, Genetic Association Studies, Germ-Line Mutation, Genetics (clinical), Genetic testing, Ovarian Neoplasms, Massive parallel sequencing, medicine.diagnostic_test, Computational Biology, High-Throughput Nucleotide Sequencing, Exons, medicine.disease, Pedigree, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, Hereditary Breast and Ovarian Cancer Syndrome, Female, Ovarian cancer

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43d19eaae6d784d350863c11b21f0658Test
https://doi.org/10.1136/jmedgenet-2015-103452Test

المؤلفون: Abigail Thomas, Bing Jian Feng, Emily Hallberg, Chunling Hu, Tina Pesaran, Robert Huether, Fergus J. Couch, Rachel McFarland, Holly LaDuca, Raymond Moore, Jill S. Dolinsky, David E. Goldgar, Hermela Shimelis, Steven N. Hart, Jie Na, Eric C. Polley, Jenna Lilyquist, Elizabeth C. Chao

المصدر: JAMA Oncology. 3:1190

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, Cell Cycle Proteins, Ataxia Telangiectasia Mutated Proteins, 0302 clinical medicine, Risk Factors, Breast, skin and connective tissue diseases, Mismatch Repair Endonuclease PMS2, Ovarian Neoplasms, MRE11 Homologue Protein, Neurofibromin 1, medicine.diagnostic_test, Nuclear Proteins, Middle Aged, Fanconi Anemia Complementation Group Proteins, Acid Anhydride Hydrolases, DNA-Binding Proteins, MutS Homolog 2 Protein, Phenotype, 030220 oncology & carcinogenesis, Population study, Female, Fanconi Anemia Complementation Group N Protein, MutL Protein Homolog 1, RNA Helicases, Adult, medicine.medical_specialty, Ubiquitin-Protein Ligases, PALB2, Breast Neoplasms, MLH1, White People, Article, 03 medical and health sciences, Breast cancer, Internal medicine, medicine, Cyclin-Dependent Kinase Inhibitor p18, Humans, Genetic Predisposition to Disease, Genetic Testing, CHEK2, Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, Genetic testing, business.industry, Tumor Suppressor Proteins, Cancer, medicine.disease, Checkpoint Kinase 2, DNA Repair Enzymes, 030104 developmental biology, Case-Control Studies, business, Ovarian cancer

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de7f0b8a965d3b2a4256befc5ad40e21Test
https://doi.org/10.1001/jamaoncol.2017.0424Test

المؤلفون: Mary B. Daly, Fabrice Odefrey, John L. Hopper, Andrew Lonie, Sean V. Tavtigian, Erin L. Young, Jun Li, Igor V. Makunin, Kayoko Tao, Hao Hu, Fleur Hammet, Graham G. Giles, Terrell C Roane, Jonathan Ellis, Russell Bell, Irene L. Andrulis, Nivonirina Robinot, Melissa C. Southey, Catherine Voegele, Carrie Snyder, Louise B. Thingholm, David E. Goldgar, Mary Beth Terry, Esther M. John, Daniel J. Park, Tu Nguyen-Dumont, Zhi Ling Teo, Shankaracharya, Henry T. Lynch, Bing Jian Feng, Saundra S. Buys, Fabienne Lesueur, Peter Devilee, Florence Le Calvez-Kelm, Helen Tsimiklis, Bernard J. Pope, Chad D. Huff

المصدر: Cancer Discovery, 4(7), 804-815

مصطلحات موضوعية: Oncology, Male, medicine.medical_specialty, Population, Breast Neoplasms, Cell Cycle Proteins, Biology, Bioinformatics, Breast cancer, Internal medicine, medicine, Humans, Exome, Genetic Predisposition to Disease, education, Exome sequencing, Genetic testing, education.field_of_study, medicine.diagnostic_test, Cancer, Family aggregation, Genetic Variation, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Pedigree, Case-Control Studies, Mutation, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234443dd802321aefd30efdffd0956d7Test
https://pubmed.ncbi.nlm.nih.gov/25002613Test

المؤلفون: Douglas F. Easton, Olga M. Sinilnikova, Jacques Simard, Rosa B. Barkardottir, Mads Thomassen, Bing Jian Feng, Anders Kvist, Thomas Hansen, Francesca Damiola, Javier Benitez, Therese Törngren, Daniel J. Park, Inge Søkilde Pedersen, Jirong Long, Penny Soucy, Rita K. Schmutzler, Sofia Khan, Jeffrey N. Weitzel, Katherine L. Nathanson, Paolo Radice, Ian G. Campbell, Michael R. Dufault, Susan L. Neuhausen, Georgia Chenevix-Trench, T. L. Chris Chan, Paolo Peterlongo, Eric Hahnen, Heli Nevanlinna, San Ming Wang, Sylvie Mazoyer, David J. Hunter, Sean V. Tavtigian, Fabienne Lesueur, Peter Devilee, Yu-Tang Gao, Ava Kwong, Fergus J. Couch, Alfons Meindl, Wei Zheng, Lars Jønson, Martine Dumont, Carrie Snyder, Ella R. Thompson, Kasmintan A. Schrader, Melissa C. Southey, David E. Goldgar, Alison H. Trainer, S. Lindstrom, Mark E. Robson, Florentine Hilbers, Yeong C. Kim, Kenneth Offit, Susan J. Ramus, Tu Nguyen-Dumont, Peter Kraft, Henry T. Lynch, Vijai Joseph

المصدر: Europe PubMed Central
Breast Cancer Research; 15(3) (2013)
Breast Cancer Research : BCR
Southey, M C, Park, D J, Nguyen-Dumont, T, Campbell, I, Thompson, E, Trainer, A H, Chenevix-Trench, G, Simard, J, Dumont, M, Soucy, P, Thomassen, M, Jønson, L, Pedersen, I S, Hansen, T VO, Nevanlinna, H, Khan, S, Sinilnikova, O, Mazoyer, S, Lesueur, F, Damiola, F, Schmutzler, R, Meindl, A, Hahnen, E, Dufault, M R, Chris Chan, T, Kwong, A, Barkardóttir, R, Radice, P, Peterlongo, P, Devilee, P, Hilbers, F, Benitez, J, Kvist, A, Törngren, T, Easton, D, Hunter, D, Lindstrom, S, Kraft, P, Zheng, W, Gao, Y-T, Long, J, Ramus, S, Feng, B-J, Weitzel, J N, Nathanson, K, Offit, K, Joseph, V, Robson, M, Schrader, K, Wang, S M & COMPLEXO 2013, ' COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration ', Breast Cancer Research (Online Edition), vol. 15, no. 3, pp. 402 . https://doi.org/10.1186/bcr3434Test
Southey, M C, Park, D J, Nguyen-Dumont, T, Campbell, I, Thompson, E, Trainer, A H, Chenevix-Trench, G, Simard, J, Dumont, M, Soucy, P, Thomassen, M, Jønson, L, Pedersen, I S, Hansen, T V, Nevanlinna, H, Khan, S, Sinilnikova, O, Mazoyer, S, Lesueur, F, Damiola, F, Schmutzler, R, Meindl, A, Hahnen, E, Dufault, M R, Chris Chan, T, Kwong, A, Barkardóttir, R, Radice, P, Peterlongo, P, Devilee, P, Hilbers, F, Benitez, J, Kvist, A, Törngren, T, Easton, D, Hunter, D, Lindstrom, S, Kraft, P, Zheng, W, Gao, Y-T, Long, J, Ramus, S, Feng, B-J, Weitzel, J N, Nathanson, K, Offit, K, Joseph, V, Robson, M, Schrader, K, Wang, S M & COMPLEXO 2013, ' COMPLEXO : identifying the missing heritability of breast cancer via next generation collaboration ', Breast Cancer Research (Online Edition), vol. 15, no. 3, 402 . https://doi.org/10.1186/bcr3434Test
Breast Cancer Research, 15(3)

مصطلحات موضوعية: Candidate gene, Letter, Positional cloning, Genetic Linkage, Genome-wide association study, Breast Neoplasms, Biology, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Missing heritability problem, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, Exome, 030304 developmental biology, Genetics, 0303 health sciences, Massive parallel sequencing, medicine.disease, 3. Good health, 030220 oncology & carcinogenesis, Cancer and Oncology, Mutation, Female, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f5d277618241a943c17dd4b928e1dfTest
http://europepmc.org/abstract/med/23809231Test