المؤلفون: Paschalis Nicolaou, Kyproula Christodoulou, Paraskevi Chairta, Sofia Symeonidou, Christiana A. Demetriou, Kyriaki Michailidou, Savvas Psarelis

المصدر: Genetic Testing and Molecular Biomarkers

مصطلحات موضوعية: Male, Oncology, systemic sclerosis, Pilot Projects, 0302 clinical medicine, Gene Frequency, skin and connective tissue diseases, Predictive testing, HLA-DP beta-Chains, Genetics (clinical), Sanger sequencing, 0303 health sciences, education.field_of_study, population study, Greece, integumentary system, autoimmunity, General Medicine, Middle Aged, 3. Good health, Phenotype, symbols, Population study, Female, Restriction fragment length polymorphism, Adult, medicine.medical_specialty, Genotype, Population, Short Report, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, 03 medical and health sciences, symbols.namesake, Internal medicine, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, education, Allele frequency, Alleles, 030304 developmental biology, 030203 arthritis & rheumatology, Scleroderma, Systemic, business.industry, Histocompatibility Antigens Class I, Histocompatibility Antigens Class II, susceptibility loci, Case-Control Studies, Cyprus, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a32f2f19b52f01bc214f334768a13e0c
https://doi.org/10.1089/gtmb.2019.0255

المؤلفون: Ana Peixoto, Ian Tomlinson, Thérèse Truong, Amanda E. Toland, Anna Marie Mulligan, Michael Untch, Susan J. Ramus, Kenneth Offit, John J. Spinelli, Clarice R. Weinberg, Kyriaki Michailidou, Javier Benitez, Rita K. Schmutzler, Lizet E. van der Kolk, Heli Nevanlinna, Annika Lindblom, Sara Margolin, Stella Koutros, Elza Khusnutdinova, Diana Eccles, Lenka Foretova, Wolfgang Janni, Jennifer T. Loud, Roger L. Milne, Patrick Neven, Thomas U. Ahearn, Hedy S. Rennert, Karolina Prajzendanc, Melissa C. Southey, Ramunas Janavicius, Finn Cilius Nielsen, Pascal Guénel, Antoinette Hollestelle, Jolanta Lissowska, Ni Zhao, Melissa Christiaens, Hoda Anton-Culver, Ans M.W. van den Ouweland, Christopher A. Haiman, Debra Frost, Vessela N. Kristensen, Bernard Peissel, Muhammad Usman Rashid, Noura Mebirouk, Claudine Isaacs, Matthias W. Beckmann, Sofia Khan, Xia Jiang, Jack A. Taylor, Peter Hillemanns, Robert Winqvist, Susan L. Neuhausen, Marina Bermisheva, Alicja Wolk, Katherine L. Nathanson, Judy Garber, Siranoush Manoukian, Simon S. Cross, Flavio Lejbkowicz, Manjeet K. Bolla, Goska Leslie, Saundra S. Buys, Banu Arun, Xiaohong R. Yang, Peter Schürmann, Irene Konstantopoulou, Mia M. Gaudet, Rob A. E. M. Tollenaar, Joe Dennis, Louise Izatt, David E. Goldgar, Anna Jakubowska, Alicja Lukomska, Fabienne Lesueur, Susanna C. Larsson, Peter Devilee, Helen Byers, Bernd Holleczek, Marc Tischkowitz, Arif B. Ekici, Austin Miller, Carl Blomqvist, Christopher R. Hake, Paul D.P. Pharoah, Harvey A. Risch, Kristin K. Zorn, Mehdi Manoochehri, Kamila Czene, Peter A. Fasching, Trinidad Caldés, Hanna Huebner, Agnes Jager, William G. Newman, Lesley McGuffog, Maren T. Scheuner, Nick Orr, Susan M. Domchek, Antonis C. Antoniou, Peter Kraft, Pooja Middha Kapoor, Daniel R. Barnes, Christine L. Clarke, Douglas F. Easton, Bernadette A M Heemskerk-Gerritsen, Ross L. Prentice, Mark E. Sherman, Elizabeth J. van Rensburg, Michael Jones, Åke Borg, Diether Lambrechts, Mark H. Greene, Mark S. Goldberg, Peter J. Hulick, Maria Elena Martinez, Arto Mannermaa, Frans B. L. Hogervorst, Christian F. Singer, Johanna Rantala, Esther M. John, Jesse Nodora, Wendy K. Chung, Csilla Szabo, Mads Thomassen, Tracy A. O'Mara, Kelly-Anne Phillips, Manuela Gago-Dominguez, Jacques Simard, John L. Hopper, Jacopo Azzollini, Rudolf Kaaks, Haoyu Zhang, Eitan Friedman, Heiko Becher, János Papp, Thomas Rüdiger, Alison M. Dunning, Daniele Campa, Alfons Meindl, Lothar Häberle, Ana Blanco, Eric Hahnen, Barbara Wappenschmidt, Elaine F. Harkness, Audrey Y. Jung, Guanghao Qi, Zumuruda Abu Ful, Maria A. Caligo, Priyanka Sharma, Håkan Olsson, Elke M van Veen, Marion Piedmonte, Linetta B. Koppert, Usha Menon, Laura Matricardi, Jonine D. Figueroa, Wei Zheng, Milena Jakimovska, Katarzyna Białkowska, Renske Keeman, Matti A. Rookus, William J. Tapper, J. Peto, Paul L. Auer, Andreas Schneeweiss, Xiao-Ou Shu, Miriam Dwek, Elvira Mingazheva, Hermann Brenner, Emilija Lazarova, Atocha Romero, Rulla M. Tamimi, Laura Papi, Hans Wildiers, Catriona McLean, Montserrat Garcia-Closas, Matthias Rübner, Thomas Brüning, Graham G. Giles, Robert J. MacInnis, Hans Christiansen, Sten Cornelissen, Paul A. James, Georgia Chenevix-Trench, Tjoung-Won Park-Simon, Nilanjan Chatterjee, D. Gareth Evans, Ignacio Briceño, Mary B. Daly, Annegien Broeks, Evgeny N. Imyanitov, Jonathan Beesley, Snezhana Smichkoska, Thilo Dörk, Yon-Dschun Ko, Paolo Peterlongo, Celine M. Vachon, Claire Mulot, Kristiina Aittomäki, Liene Nikitina-Zake, Manuel R. Teixeira, Edith Olah, Florentia Fostira, Beth N. Peshkin, Pierre Laurent-Puig, M. B. Terry, Michael T. Parsons, Anna González-Neira, Julie Lecarpentier, Jacek Gronwald, Fergus J. Couch, Mariarosaria Calvello, Leigha Senter, Ute Hamann, Brigitte Rack, Marco Montagna, Simon A. Gayther, Barbara Burwinkel, Anne-Vibeke Lænkholm, Irene L. Andrulis, Sabine Behrens, Beth Y. Karlan, Anthony J. Swerdlow, Marjanka K. Schmidt, Cari M. Kitahara, Emmanouil Saloustros, Dijana Plaseska-Karanfilska, Melissa A. Troester, Diana Torres, Daniel Barrowdale, Elinor J. Sawyer, Hiltrud Brauch, Minouk J. Schoemaker, Dale P. Sandler, José A. García-Sáenz, Jennifer Stone, Qin Wang, Conxi Lázaro, Paolo Radice, Jan Lubinski, Jose E. Castelao, Natalia Bogdanova, Drakoulis Yannoukakos, Davide Bondavalli, Kristan J. Aronson, Gad Rennert, Wing-Yee Lo, Robert N. Hoover, Dominique Stoppa-Lyonnet, Nadine Tung, Stephen J. Chanock, Andrew K. Godwin, Angela Cox, Maartje J. Hooning, Anthony Howell, Volker Arndt, Penny Soucy, Jenny Chang-Claude, Kathleen Claes, Olufunmilayo I. Olopade, Jeffrey N. Weitzel, Stig E. Bojesen, Sara Y Brucker, Darcy L. Thull, Darya Prokofyeva, Taru A. Muranen, Ben Schöttker, Orland Diez, Susan M. Gapstur, Sarah Sampson, Bernardo Bonanni, Per Hall, Ana Vega

المساهمون: Medical Oncology, Surgery, Clinical Genetics

المصدر: Dipòsit Digital de la UB
Universidad de Barcelona
Nature Genetics, 52(6), 572-581. Nature Publishing Group
Nature Genetics, 52(6), 572-581. NATURE RESEARCH
Zhang, H, Ahearn, T U, Lecarpentier, J, Barnes, D, Beesley, J, Qi, G, Jiang, X, O’Mara, T A, Zhao, N, Bolla, M K, Dunning, A M, Dennis, J, Wang, Q, Ful, Z A, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Arndt, V, Aronson, K J, Arun, B K, Auer, P L, Azzollini, J, Barrowdale, D, Becher, H, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bialkowska, K, Blanco, A, Blomqvist, C, Bogdanova, N V, Bojesen, S E, Bonanni, B, Bondavalli, D, Borg, A, Brauch, H, Brenner, H, Briceno, I, Broeks, A, Brucker, S Y, Brüning, T, Burwinkel, B, Buys, S S, Byers, H, Caldés, T, Caligo, M A, Christiansen, H, Laenkholm, A V, Nielsen, F C, Thomassen, M, kConFab Investigators, ABCTB Investigators, EMBRACE Study & GEMO Study Collaborators 2020, ' Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses ', Nature Genetics, vol. 52, no. 6, pp. 572-581 . https://doi.org/10.1038/s41588-020-0609-2
2020, ' Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses ', Nature Genetics . https://doi.org/10.1038/s41588-020-0609-2
Nature Genetics

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Linkage disequilibrium, Carcinogenesis, Estrogen receptor, Genome-wide association study, Breast Neoplasms, Triple Negative Breast Neoplasms, Biology, Gene mutation, Linkage Disequilibrium, Càncer de mama, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Internal medicine, Genetics, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, Carcinogènesi, Triple-negative breast cancer, 030304 developmental biology, Medicinsk genetik, 0303 health sciences, Genetic heterogeneity, BRCA1 Protein, medicine.disease, 3. Good health, Case-Control Studies, Female, Mutation, Genome-Wide Association Study, Medical Genetics, 030217 neurology & neurosurgery

وصف الملف: application/pdf; text

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::585de0d60ba1a545a6088ff67231f7c4
https://doi.org/10.1038/s41588-020-0609-2

المؤلفون: Jean Leyland, Nazneen Rahman, Louise Eriksson, Rulla M. Tamimi, Nicholas J. Wareham, Celine M. Vachon, Lisa J. Martin, Melissa C. Southey, Jennifer Stone, Sara Lindström, Fergus J. Couch, Deborah J. Thompson, Johanna M. Rommens, Andrew D. Paterson, Ruth J. F. Loos, Per Hall, Douglas F. Easton, Norman F. Boyd, Jajini Varghese, Kamila Czene, Clare Turnbull, Jingmei Li, Carmel Apicella, Ruth Warren, Kyriaki Michailidou, Christopher G. Scott, John L. Hopper, Robert Luben, Elizabeth J. Atkinson, Judith E. Brown

المصدر: Cancer Research; Vol 72
Cancer Research

مصطلحات موضوعية: Risk, Oncology, Cancer Research, medicine.medical_specialty, Breast Neoplasms, Genome-wide association study, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Gene Frequency, Internal medicine, Genetic predisposition, Humans, Medicine, Mammography, Genetic Predisposition to Disease, Risk factor, 030304 developmental biology, Genetics, 0303 health sciences, Framingham Risk Score, medicine.diagnostic_test, business.industry, Case-control study, medicine.disease, United Kingdom, 3. Good health, Postmenopause, Case-Control Studies, 030220 oncology & carcinogenesis, Female, business, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a398d9247187dd953d8bdc46ae0e924

المؤلفون: Douglas F. Easton, Rachelle Brutus, Esther M. John, Irene L. Andrulis, Quinten Waisfisz, Melissa C. Southey, Daniel F. Schmidt, Nancy J. Cox, Valerie McGuire, Fernando Rivadeneira, Paul D.P. Pharoah, Brandon L. Pierce, Mark Lathrop, Mark A. Jenkins, Carmel Apicella, Carl Blomqvist, Steve Gallinger, Daniela Seminara, Polly A. Newcomb, Graham G. Giles, Alfons Meindl, Alison M. Dunning, Kathi Malone, Heli Nevanlinna, Dieter Flesch-Janys, Habibul Ahsan, David V. Conti, Shantanu Roy, Stephanie Melkonian, Hanne Meijers-Heijboer, Rebecca Hein, Lin Tong, Maria Argos, David Duggan, Kyriaki Michailidou, Nazneen Rahman, Stephen J. Chanock, Clare Turnbull, Eric R. Gamazon, Bertram Müller-Myhsok, Jenny Chang-Claude, Isabel dos Santos Silva, Noralane M. Lindor, Anna Felberg, Olivia Fletcher, Dan L. Nicolae, Per Hall, Kamila Czene, David J. Hunter, Kristiina Aittomäki, Julia A. Knight, John L. Hopper, Astrid Irwanto, Jennifer Stone, Enes Makalic, Norbert Dahmen, Jianxin Shi, Magdalena Lochmann, Farzana Jasmine, Eunjung Lee, Robert W. Haile, Regina M. Santella, Jianjun Liu, Lars Beckmann, Daniel J. Park, Marilie D. Gammon, Jerry Halpern, André G. Uitterlinden, Graham Casey, Alice S. Whittemore, Quang M. Bui, Duncan C. Thomas, Rita K. Schmutzler, Julian Peto, Giske Ursin, Muhammad G. Kibriya

المساهمون: Other departments, CCA -Cancer Center Amsterdam, ARD - Amsterdam Reproduction and Development, Human Genetics, Human genetics, CCA - Oncogenesis, Public Health, Internal Medicine

المصدر: Cancer epidemiology, biomarkers & prevention, 23(4), 658-669. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention; Vol 23
Cancer Epidemiology Biomarkers and Prevention, 23(4), 658-669. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention, 23(4), 658-669. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention
Ahsan, H, Halpern, J, Kibriya, M G, Pierce, B L, Tong, L, Gamazon, E, McGuire, V, Felberg, A, Shi, J X, Jasmine, F, Roy, S, Brutus, R, Argos, M, Melkonian, S, Chang-Claude, J, Andrulis, I, Hopper, J L, John, E M, Malone, K, Ursin, G, Gammon, M D, Thomas, D C, Seminara, D, Casey, G, Knight, J A, Southey, M C, Giles, G G, Santella, R M, Lee, E, Conti, D, Duggan, D, Gallinger, S, Haile, R, Jenkins, M, Lindor, N M, Newcomb, P, Michailidou, K, Apicella, C, Park, D J, Peto, J, Fletcher, O, Silva, I D, Lathrop, M, Hunter, D J, Chanock, S J, Meindl, A, Schmutzler, R K, Muller-Myhsok, B, Lochmann, M, Beckmann, L, Hein, R, Makalic, E, Schmidt, D F, Bui, Q M, Stone, J, Flesch-Janys, D, Dahmen, N, Nevanlinna, H, Aittomaki, K, Blomqvist, C, Hall, P, Czene, K, Irwanto, A, Liu, J J, Rahman, N, Turnbull, C, Dunning, A M, Pharoah, P, Waisfisz, Q, Meijers-Heijboer, H, Uitterlinden, A G, Rivadeneira, F, Nicolae, D, Easton, D F, Cox, N J & Whittemore, A S 2014, ' A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age ', Cancer Epidemiology Biomarkers and Prevention, vol. 23, no. 4, pp. 658-669 . https://doi.org/10.1158/1055-9965.EPI-13-0340

مصطلحات موضوعية: Epidemiology, Population, Genome-wide association study, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Phosphofructokinase-1, Muscle Type, Genetic predisposition, medicine, Biomarkers, Tumor, SNP, Humans, Genetic Predisposition to Disease, education, Gene, 030304 developmental biology, Genetics, 0303 health sciences, education.field_of_study, Middle Aged, medicine.disease, 3. Good health, Oncology, PFKM, 030220 oncology & carcinogenesis, Case-Control Studies, Female, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6e75265c5cc9dabb3b6b8fafb1b90b3
https://europepmc.org/articles/PMC3990360/

المؤلفون: Qin Wang, Anna González-Neira, Betül T. Yesilyurt, Paolo Radice, Jenny Chang-Claude, Malcolm W.R. Reed, Graham G. Giles, Robert A.E.M. Tollenaar, Gianluca Severi, Gillian S. Dite, Fredrick R. Schumacher, J. Margriet Collée, Pascal Guénel, Fergus J. Couch, Núria Malats, Dieter Flesch-Janys, Ute Hamann, Michael J. Kerin, Asta Försti, Guillermo Pita, Christina A. Clarke, Heli Nevanlinna, Anja Rudolph, Jolanta Lissowska, Javier Benitez, Pilar Zamora, Brian E. Henderson, Elinor J. Sawyer, Arto Mannermaa, Hiltrud Brauch, Jesús Herranz, Henrik Flyger, Aida Karina Dieffenbach, Karin Leunen, Xianshu Wang, Angela Cox, Celine M. Vachon, Arif B. Ekici, Maartje J. Hooning, Antoinette Hollestelle, Volker Arndt, Hatef Darabi, Penny Soucy, Minouk J. Schoemaker, Thilo Dörk, Hoda Anton-Culver, Melissa C. Southey, Stig E. Bojesen, Yon-Dschun Ko, Natalia Bogdanova, Veli-Matti Kosma, Robert Winqvist, Argyrios Ziogas, Jingmei Li, Carmel Apicella, M. Rosario Alonso, Douglas F. Easton, Arja Jukkola-Vuorinen, Paolo Mariani, Hermann Brenner, Peter A. Fasching, Drakoulis Yannoukakos, Paolo Peterlongo, Annegien Broeks, Federik Marme, Caroline Seynaeve, Taru A. Muranen, Anna Jakubowska, Paul D.P. Pharoah, Joe Dennis, Vesa Kataja, Kamila Czene, Alison M. Dunning, Mikael Eriksson, Vessela N. Kristensen, Ian Tomlinson, Thérèse Truong, Jonathan Tyrer, Thomas Rüdiger, Montserrat Garcia-Closas, Manjeet K. Bolla, Amanda E. Toland, Thomas Brüning, John L. Hopper, kConFab Investigators, Carl Blomqvist, Lothar Häberle, Hans Ulrich Ulmer, Anna Marie Mulligan, Jan Lubinski, Diether Lambrechts, Ian W. Brock, Emiel J. Th. Rutgers, Anthony J. Swerdlow, Grethe I. Grenaker Alnæs, Stephen J. Chanock, Katarzyna Durda, Olivia Fletcher, Mervi Grip, Per Hall, Claire Mulot, Keith Humphreys, Jonine D. Figueroa, Julia A. Knight, Petra Seibold, Alan Ashworth, Laura Baglietto, Katarzyna Jaworska-Bieniek, José Ignacio Arias-Perez, Sara Margolin, Mitul Shah, Matthias W. Beckmann, Bernard Peissel, Kyriaki Michailidou, Peter Devilee, Anne Lise Børresen-Dale, Julian Peto, Georgia Chenevix-Trench, Børge G. Nordestgaard, Barbara Burwinkel, Kristiina Aittomäki, Nicola Miller, Isabel dos Santos Silva, Agnes Jager, Janet E. Olson, Roger L. Milne, Kristen S. Purrington, Jacques Simard, Irene L. Andrulis, Nick Orr, Martine Dumont, Annika Lindblom, Nichola Johnson, Marjanka K. Schmidt, Susan L. Neuhausen, Marie Sanchez, Christopher A. Haiman, Loic Le Marchand, Katri Pylkäs, Giuseppe Floris, Christa Stegmaier, Senno Verhoef, Jaana M. Hartikainen, Gord Glendon

المساهمون: Cancer Center Amsterdam, Oncogenomics, Clinical Genetics, Medical Oncology

المصدر: Human Molecular Genetics; Vol 23
Human Molecular Genetics, 23(7), 1934-1946
Human molecular genetics, 23(7), 1934-1946. Oxford University Press
Human Molecular Genetics, 23(7), 1934-1946. Oxford University Press
Human Molecular Genetics

مصطلحات موضوعية: Oncology, epistasis, Genome-wide association study, Bioinformatics, 0302 clinical medicine, Medizinische Fakultät, common variants, Genetics (clinical), risk, 0303 health sciences, Association Studies Articles, identifies 2, Family aggregation, General Medicine, Single Nucleotide, 030220 oncology & carcinogenesis, loci, alleles, Female, medicine.medical_specialty, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Breast cancer, SDG 3 - Good Health and Well-being, Genetic, Internal medicine, Genetics, medicine, Genetic predisposition, SNP, Humans, Genetic Predisposition to Disease, ddc:610, Allele, Polymorphism, Molecular Biology, erap1, 030304 developmental biology, Case-control study, Epistasis, Genetic, Case-Control Studies, Genome-Wide Association Study, Logistic Models, medicine.disease, confer susceptibility, genome-wide association, genetic susceptibility

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38315b853e48c396ecac49b47254e07b
https://europepmc.org/articles/PMC3943524/

المؤلفون: William J. Tapper, Frederik Marmé, Natalia Bogdanova, Joe Dennis, Pei-Ei Wu, Vesa Kataja, Michael Jones, Dong-Young Noh, Xiaoqing Chen, Thilo Dörk, Javier Benitez, Arif B. Ekici, André G. Uitterlinden, Karin Leunen, Chen-Yang Shen, Esther M. John, Sune F. Nielsen, Adam M. Lee, Arto Mannermaa, Dieter Flesch-Janys, Diana Eccles, Don M. Conroy, Quinten Waisfisz, Sara Margolin, Hoda Anton-Culver, Peter Devilee, Ans M.W. van den Ouweland, Ruth Swann, Chia-Ni Hsiung, Peter Schürmann, Per Hall, Bertram Müller-Myhsok, Jonathan Beesley, Graham G. Giles, Qin Wang, Mitul Shah, Matthias W. Beckmann, Veli-Matti Kosma, Carmel Apicella, Henrik Flyger, Daniel F. Schmidt, Gianluca Severi, Kristen N. Stevens, Paolo Peterlongo, Helen Tsimiklis, Betül T. Yesilyurt, Irene L. Andrulis, Louiza S. Velentzis, Peter A. Fasching, Jyh-Cherng Yu, Caroline Baynes, Jenny Chang-Claude, Craig Luccarini, Leslie Bernstein, Katarzyna Durda, Antoinette Hollestelle, Catriona McLean, Georgia Chenevix-Trench, Rebecca Hein, Heli Nevanlinna, Arja Jukkola-Vuorinen, Jolanta Lissowska, Rita K. Schmutzler, Giuseppe Floris, Christa Stegmaier, David J. Hunter, Kristiina Aittomäki, Johann H. Karstens, Alan Ashworth, Alfons Meindl, Emilie Cordina-Duverger, Stefan Nickels, Julian Peto, Jan Lubinski, Børge G. Nordestgaard, Ed Dicks, Stig E. Bojesen, Christie J. van Asperen, Malcolm W.R. Reed, Michael J. Kerin, Annika Lindblom, Barbara Burwinkel, Kristy Driver, Darya Prokofieva, Montserrat Garcia-Closas, Thomas Brüning, Christina Justenhoven, Nazneen Rahman, Annegien Broeks, Hermann Brenner, Hiltrud Brauch, Laura Baglietto, Yuri I. Rogov, Clare Turnbull, A Jakubowska, Marina Bermisheva, Heiko Müller, Hanne Meijers-Heijboer, Anne-Lise Børrensen-Dale, Pascal Guénel, Stephen J. Chanock, Siranoush Manoukian, Melissa C. Southey, Daniel J. Park, M. Rosario Alonso, Christof Sohn, Shan Wang-Gohrke, Melanie Maranian, Shahana Ahmed, Jonine D. Figueroa, Robert Winqvist, Jianjun Liu, Suthee Rattanamongkongul, Diether Lambrechts, Andreas Schneeweiss, Paul D.P. Pharoah, Alexander Miron, Ursula Eilber, Angela Cox, Anna González-Neira, Minh Bui, Frans B. L. Hogervorst, Peter Hillemanns, Peter Lichtner, Maartje J. Hooning, Roger L. Milne, Alison M. Dunning, Fernando Rivadeneira, Ian Tomlinson, Thérèse Truong, Volker Arndt, Rogier A. Oldenburg, Grethe I. Grenaker Alnæs, Senno Verhoef, Rob A. E. M. Tollenaar, Anna Marie Mulligan, Kenneth Muir, Christina Clarke Dur, Katarzyna Jaworska, Saila Kauppila, Olivia Fletcher, Jaana M. Hartikainen, Michael P. Lux, Kyriaki Michailidou, Stefano Fortuzzi, Douglas F. Easton, Anthony J. Swerdlow, Elza Khusnutdinova, Annie Perkins, Carl Blomqvist, Argyrios Ziogas, Keun-Young Yoo, Caroline Seynaeve, Natalia Antonenkova, Bruce A.J. Ponder, Vessela N. Kristensen, Gord Glendon, Daehee Kang, Elinor J. Sawyer, Michael Bremer, Louise A. Brinton, Minouk J. Schoemaker, Kamila Czene, Isabel dos Santos Silva, John L. Hopper, Astrid K. Irwanto, Nick Orr, S Gerty, Fergus J. Couch, Arkom Chaiwerawattana, Manjeet K. Humphreys, Marjanka K. Schmidt, Maya Ghoussaini, Nikki Graham, Artitaya Lophatananon, Florence Menegaux, Enes Makalic, Katri Pylkäs, Nichola Johnson, Xianshu Wang, Bernardo Bonanni, Mark Lathrop

المساهمون: Human genetics, CCA - Oncogenesis, Clinical Genetics, Internal Medicine, Medical Oncology, CCA -Cancer Center Amsterdam, ARD - Amsterdam Reproduction and Development, Human Genetics

المصدر: Nature Genetics, 44, 312-8
Nature Genetics
Nature Genetics, 44(3), 312-318. Nature Publishing Group
Ghoussaini, M, Fletcher, O, Michailidou, K, Turnbull, C, Schmidt, M K, Dicks, E, Dennis, J, Wang, Q, Humphreys, M K, Luccarini, C, Baynes, C, Conroy, D, Maranian, M, Ahmed, S, Driver, K, Johnson, N, Orr, N, Silva, I D, Waisfisz, Q, Meijers-Heijboer, E J, Uitterlinden, A G, Rivadeneira, F, Hall, P, Czene, K, Irwanto, A, Liu, J J, Nevanlinna, H, Aittomaki, K, Blomqvist, C, Meindl, A, Schmutzler, R K, Muller-Myhsok, B, Lichtner, P, Chang-Claude, J, Hein, R, Nickels, S, Flesch-Janys, D, Tsimiklis, H, Makalic, E, Schmidt, D, Bui, M, Hopper, J L, Apicella, C, Park, D J, Southey, M, Hunter, D J, Chanock, S J, Broeks, A, Verhoef, S, Hogervorst, F B L, Fasching, P A, Lux, M P, Beckmann, M W, Ekici, A B, Sawyer, E, Tomlinson, I, Kerin, M, Marme, F, Schneeweiss, A, Sohn, C, Burwinkel, B, Guenal, P, Truong, T, Cordina-Duverger, E, Menegaux, F, Bojesen, S E, Nordestgaard, B G, Nielsen, S F, Flyger, H, Milne, R L, Alonso, M R, Gonzalez-Neira, A, Benitez, J, Anton-Culver, H, Ziogas, A, Bernstein, L, Dur, C C, Brenner, H, Muller, H, Arndt, V, Stegmaier, C, Justenhoven, C, Brauch, H, Bruning, T, Wang-Gohrke, S, Eilber, U, Dork, T, Schurmann, P, Bremer, M, Hillemanns, P, Bogdanova, N V, Antonenkova, N N, Rogov, Y I, Karstens, J H, Bermisheva, M, Prokofieva, D, Khusnutdinova, E, Lindblom, A, Margolin, S, Peto, J & Easton, D F 2012, ' Genome-wide association analysis identifies three new breast cancer susceptibility loci ', Nature Genetics, vol. 44, no. 3, pp. 312-318 . https://doi.org/10.1038/ng.1049
Nature Genetics, 44, 3, pp. 312-8
Nature Genetics; Vol 44
Nature Genetics, 44(3), 312-U120
Nature Genetics, 44(3), 312-U120. Nature Publishing Group
Nature genetics, 44(3), 312-U120. Nature Publishing Group

مصطلحات موضوعية: Candidate gene, Chromosomes,Human,Pair 21, analysis, cell carcinoma, Mammary gland, Estrogen receptor, Genome-wide association study, developmental regulatory molecule, 0302 clinical medicine, common variants, retinoic acid, Pair 12, genetics, hormone-related protein, Genetics, Chromosomes,Human,Pair 12, Treatment - Localised Therapies – Discovery and Development, Principal Component Analysis, 0303 health sciences, Bone metastasis, Single Nucleotide, 3. Good health, medicine.anatomical_structure, 030220 oncology & carcinogenesis, epidemiology, Cancer Type - Breast Cancer, Female, Human, Risk, ulnar-mammary syndrome, parathyroid-hormone, European Continental Ancestry Group, Breast Neoplasms, Biology, Chromosomes, Polymorphism,Single Nucleotide, 03 medical and health sciences, Breast cancer, SDG 3 - Good Health and Well-being, Translational research [ONCOL 3], Genetic predisposition, medicine, cancer, Humans, Women, Genetic Predisposition to Disease, Polymorphism, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], breast, 030304 developmental biology, Hereditary cancer and cancer-related syndromes [ONCOL 1], Cancer, confer susceptibility, medicine.disease, gene-expression, Logistic Models, negative-feedback, Genetic Loci, Cancer research, Other, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 21, Genome-Wide Association Study, Polymorphism, Single Nucleotide, Pair 21, Meta-Analysis

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bfdb756063659a5c3cc42d69046f57c
https://doi.org/10.1038/ng.1049