المؤلفون: Kyproula Christodoulou, Andreas Hadjisavvas, Maria A. Loizidou, Maria Zanti, Kyriacos Kyriacou, Kyriaki Michailidou, Christina Machattou, Panagiota Pirpa, George M. Spyrou

المصدر: BMC Bioinformatics, Vol 22, Iss 1, Pp 1-21 (2021)
BMC Bioinformatics

مصطلحات موضوعية: Pipeline comparison, Computer science, QH301-705.5, Computer applications to medicine. Medical informatics, R858-859.7, Interval (mathematics), Computational biology, Biochemistry, Padding, Polymorphism, Single Nucleotide, Germline, 03 medical and health sciences, Germline NGS data analysis, Structural Biology, Variant calling, Humans, Biology (General), Molecular Biology, 030304 developmental biology, Alignment, 0303 health sciences, Next-generation sequencing (NGS), Research, Applied Mathematics, 030305 genetics & heredity, Computational Biology, High-Throughput Nucleotide Sequencing, Interval padding, Pipeline (software), Computer Science Applications, Pipeline transport, Identification (information), Germ Cells, Null (SQL), DNA microarray, Software

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c1b23847c361a0ae8917356847828d
https://doaj.org/article/2504d4d34e724e00946dd853e8e06165

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: Panayiotis Kouis, Andreas Hadjisavvas, Louiza Potamiti, Kyriaki Michailidou, Aigli Evriviadou, Panayiotis K. Yiallouros, Pinelopi Anagnostopoulou, Kyriacos Kyriacou, Panayiota Pirpa, Ioannis Tsiolakis, Maria A. Loizidou, Andreas M. Matthaiou

المصدر: Human mutationREFERENCES. 42(6)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, DNA Mutational Analysis, Prevalence, Disease, Biology, Cohort Studies, 03 medical and health sciences, FEV1/FVC ratio, Young Adult, Internal medicine, Genetics, medicine, Humans, Family, Genetic Testing, Child, Genetics (clinical), 030304 developmental biology, Primary ciliary dyskinesia, Aged, 0303 health sciences, Greece, 030305 genetics & heredity, Respiratory disease, High-Throughput Nucleotide Sequencing, Infant, Middle Aged, medicine.disease, Genetic epidemiology, Molecular Diagnostic Techniques, Child, Preschool, Cohort, Cyprus, Mutation, Female, Genetic diagnosis, Ciliary Motility Disorders

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8641233b77b7f05a78fd444fffed1ce8
https://pubmed.ncbi.nlm.nih.gov/33715250

المؤلفون: Christopher A. Haiman, Pascal Guénel, Hidemi Ito, Susan L. Neuhausen, Christy G. Woolcott, Graham G. Giles, Anthony J. Swerdlow, Per Hall, Kamila Czene, Artitaya Lophatananon, Åslaug Helland, Yu-Tang Gao, Vessela N. Kristensen, Manjeet K. Bolla, Anna H. Wu, Jacques Simard, John L. Hopper, Robert Luben, Julia A. Knight, Mark S. Goldberg, Thilo Dörk, Kay-Tee Khaw, Christopher G. Scott, Giuseppe Floris, Jennifer Stone, Madeleine M.A. Tilanus-Linthorst, Stig E. Bojesen, Daehee Kang, Qin Wang, Angela Cox, Fergus J. Couch, Jonathan Beesley, Maartje J. Hooning, Natalia Bogdanova, Brian E. Henderson, Paolo Peterlongo, Rulla M. Tamimi, Soo Hwang Teo, Diether Lambrechts, Ute Hamann, Wei Zheng, Volker Arndt, Juliet D. French, Stacey L. Edwards, Julian Peto, Ian Tomlinson, Ji Yeob Choi, Elinor J. Sawyer, Melissa C. Southey, Annegien Broeks, Arif B. Ekici, Heli Nevanlinna, Celine M. Vachon, Thérèse Truong, Amanda E. Toland, Javier Benitez, Barbara Burwinkel, Xiao-Ou Shu, Robert Winqvist, Pierre Antoine Dugué, Karen McCue, Mikael Hartman, Minouk J. Schoemaker, Keitaro Matsuo, Norbert Arnold, Deborah J. Thompson, Paolo Radice, Anna Jakubowska, Marjanka K. Schmidt, Hermann Brenner, Hoda Anton-Culver, Argyrios Ziogas, Jenny Chang-Claude, Alicia Beeghly-Fadiel, Veli-Matti Kosma, Hatef Darabi, Drakoulis Yannoukakos, Maya Ghoussaini, Rodney J. Scott, Maria Kabisch, Chen-Yang Shen, Suleeporn Sangrajrang, Montserrat Garcia-Closas, James McKay, Alfons Meindl, Christoph Engel, Joe Dennis, Chiu-Chen Tseng, Catriona McLean, Arja Jukkola-Vuorinen, Peter A. Fasching, Katharina Heusinger, Georgia Chenevix-Trench, Robert A.E.M. Tollenaar, Kyriaki Michailidou, Rita K. Schmutzler, Shivaani Mariapun, Silje Nord, Hiltrud Brauch, Peter Devilee, Isabel dos-Santos-Silva, Douglas F. Easton, Frederik Marmé, Vilde D. Haakensen, Wei-Yen Lim, Keith Humphreys, Siddhartha Kar, Anja Rudolph, Arto Mannermaa, Jan Lubinski, Anna González-Neira, Sara Margolin, Matthias W. Beckmann, Simon S. Cross, Anne Lise Børresen-Dale, Jonine D. Figueroa, Alison M. Dunning, Kenneth Muir, Sander Canisius, Jingmei Li, Carmel Apicella, Jyh-Cherng Yu, Gertraud Maskarinec, Roger L. Milne, Henrik Flyger, Irene L. Andrulis, Annika Lindblom, Sofia Khan, Diana Torres

المساهمون: Clinical Genetics, Obstetrics & Gynecology, Medical Oncology, Surgery, Cardiothoracic Surgery, Pulmonary Medicine, Thompson, Deborah [0000-0003-1465-5799], Ghoussaini, Maya [0000-0002-2415-2143], Dennis, Joe [0000-0003-4591-1214], Wang, Jean [0000-0002-9139-0627], Luben, Robert [0000-0002-5088-6343], Khaw, Kay-Tee [0000-0002-8802-2903], Dunning, Alison [0000-0001-6651-7166], Easton, Douglas [0000-0003-2444-3247], Apollo - University of Cambridge Repository

المصدر: American Journal of Human Genetics
American Journal of Human Genetics, 97(1), 22-34
American Journal of Human Genetics, 97(1), 22-34. Cell Press

مصطلحات موضوعية: Genotype, Quantitative Trait Loci, Autophagy-Related Proteins, Estrogen receptor, Breast Neoplasms, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Article, Body Mass Index, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Asian People, SDG 3 - Good Health and Well-being, Odds Ratio, medicine, Genetics, Humans, SNP, Genetics(clinical), Luciferases, Genetics (clinical), 030304 developmental biology, Genetic association, 0303 health sciences, Chromosomes, Human, Pair 10, Haplotype, Age Factors, Chromosome Mapping, medicine.disease, 3. Good health, DNA-Binding Proteins, Enhancer Elements, Genetic, Gene Expression Regulation, 030220 oncology & carcinogenesis, Trans-Activators, Regression Analysis, Female, Genome-Wide Association Study, Transcription Factors

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f9067006b984f33ebb541f432ace5b

المؤلفون: Amy V. Spencer, Kyriaki Michailidou, Angela Cox, Douglas F. Easton, Wei-Yu Lin, Kevin Walters

المصدر: Genetic Epidemiology

مصطلحات موضوعية: Genotype, Epidemiology, hyperparameter, single‐nucleotide polymorphism, Breast Neoplasms, Polymorphism, Single Nucleotide, 03 medical and health sciences, Bayes' theorem, expert knowledge, Prior probability, Statistics, Humans, Computer Simulation, Genetic Association Studies, Research Articles, Genetics (clinical), Probability, 030304 developmental biology, Mathematics, elicitation, Hyperparameter, 0303 health sciences, Models, Genetic, 030305 genetics & heredity, Uncertainty, Univariate, International Agencies, Bayes Theorem, Bayes factor, filtering, sensitivity, flexibility, Sample size determination, Case-Control Studies, Sample Size, fine mapping, Probability distribution, Female, empirical, Research Article, Quantile

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75497dbcb92bcabcfb123a6d06202803
https://doi.org/10.1002/gepi.21891

المؤلفون: Per Hall, Hui Cai, Roger L. Milne, Douglas F. Easton, Anja Rudolph, José Ignacio Arias, Vessela N. Kristensen, Julia A. Knight, Lisa B. Signorello, Petra Seibold, Jonathan Tyrer, Arto Mannermaa, Alan Ashworth, Andreas Schneeweiss, Sandra Deming-Halverson, Katarzyna Durda, Kimael Eriksson, Thilo Dörk, Isabel dos Santos Silva, Alfons Meindl, Laura Baglietto, Fredrick R. Schumacher, Peter Devilee, Qiuyin Cai, Janet E. Olson, Keith Humphreys, Annegien Broeks, Soo Hwang Teo, Michael P. Lux, Sze Yee Phuah, Federick Marme, Pascal Guénel, Hidemi Ito, Irene L. Andrulis, Natalia Bogdanova, Christoph Engel, Juliet D. French, Nina Ditsch, Xianshu Wang, Susan L. Slager, Bernardo Bonanni, Hermann Brenner, Nick Orr, Marie Rose Christiaens, Martine Dumont, Martin O'Reilly, Annika Lindblom, Catriona McLean, Ans M.W. van den Ouweland, Marjanka K. Schmidt, Sara Margolin, Kerstin B. Meyer, Martha J. Shrubsole, Malcolm W.R. Reed, Hans Ulrich Ulmer, Georgia Chenevix-Trench, Kyriaki Michailidou, Brian E. Henderson, Nicola Miller, Sandrine Tchatchou, Stig E. Bojesen, Pornthep Siriwanarangsan, Joe Dennis, Jaana M. Hartikainen, Matthias W. Beckmann, Fergus J. Couch, David Van Den Berg, Celine M. Vachon, Pierre Laurent-Puig, Montserrat Garcia-Closas, Ian Tomlinson, Thomas Brüning, Maya Ghoussaini, Mikael Hartman, Kristiina Aittomäki, Thérèse Truong, Katarzyna Jaworska, Yon Ko, Yu Tang Gao, Paolo Peterlongo, Stacey L. Edwards, Saskia Carlebur, Hartef Darabi, Pei Ei Wu, Ute Hamann, M. Pilar Zamora, Taru A. Muranen, Jirong Long, Stephen J. Chanock, William Blot, Sonja Helbig, Heiko Müller, Christina Clarke Dur, Ji Yeob Choi, Melissa C. Southey, Olivia Fletcher, Ming-Feng Hou, Hiroji Iwata, Nichola Johnson, Wei Zheng, Robert Winqvist, Diether Lambrechts, Javier Benitez, Chen-Yang Shen, Suleeporn Sangrajrang, Chia-Ni Hsiung, James McKay, Kristen S. Purrington, Cheng Har Yip, Ann Smeets, Valerie Gaborieau, Keitaro Matsuo, Anthony J. Swerdlow, Anne Lise Børresen-Dale, Anna Jakubowska, Dong Young Noh, Paul D.P. Pharoah, Ines de Santiago, Hiltrud Brauch, Vesa Kataja, Yasushi Yatabe, Anna H. Wu, Grethe I. Grenaker Alnæs, Jonine D. Figueroa, Christopher A. Haiman, Florence Menegaux, Hoda Anton-Culver, Paul Brennan, Veli-Matti Kosma, Bruce A.J. Ponder, Dieter Flesch-Janys, Thomas Rüdiger, Shaik Ahmad Buhari, Katri Pylkäs, Gord Glendon, Rita K. Schmutzler, Julian Peto, Chiu-Chen Tseng, Sune F. Nielsen, Mark S. Goldberg, Angela Cox, Carolien H.M. van Deurzen, Artitaya Lophatananon, Radhika Prathalingham, Børge G. Nordestgaard, Arja Jukkola-Vuorinen, Wei Lu, Peter A. Fasching, Florentia Fostira, Wei-Yen Lim, Barbara Burwinkel, Jenny Chang-Claude, Michael J. Kerin, Maartje J. Hooning, Kamila Czene, Asta Försti, Loic Le Marchand, Gianluca Severi, Volker Arndt, John L. Hopper, Jan Lubinski, Jacques Simard, Frans B. L. Hogervorst, Alison M. Dunning, Kenneth Muir, Saila Kauppila, Laura J. van't Veer, John W.M. Martens, Helen Tsimiklis, Loris Bernard, Heli Nevanlinna, Jolanta Lissowska, Robert Pilarski, Qin Wang, Paolo Radice, Robert A.E.M. Tollenaar, Jianjun Liu, Graham G. Giles, Henrik Flyger, Arif B. Ekici, Xiao-Ou Shu, Manjeet K. Bolla, Carl Blomqvist, Daehee Kang, Argyrios Ziogas, Bernard Thienpont, Patricia Harrington, Sue K. Park, Christa Stegmaier, Sarah Stewart-Brown, Elinor J. Sawyer, Miao Hui, Susan L. Neuhausen, Daniel O. Stram, Christof Sohn, Minouk J. Schoemaker, Jingmei Li, Carmel Apicella, Caroline M. Seynaeve

المساهمون: Clinical Genetics, Medical Oncology, Pathology, Cardiothoracic Surgery

المصدر: The American Journal of Human Genetics; Vol 93
American Journal of Human Genetics, 93(6), 1046-1060. Cell Press
American Journal of Human Genetics, 93(6), 1046-1060
The American Journal of Human Genetics
American journal of human genetics, vol 93, iss 6

مصطلحات موضوعية: Fibroblast Growth Factor, african-american, Genome-wide association study, Medical and Health Sciences, Chromosome conformation capture, 0302 clinical medicine, 2.1 Biological and endogenous factors, Genetics(clinical), Aetiology, Promoter Regions, Genetic, Genetics (clinical), Cancer, African Continental Ancestry Group, Genetics & Heredity, Genetics, 0303 health sciences, Tumor, Chromosome Mapping, Biological Sciences, 3. Good health, Chromatin, Gene Expression Regulation, Neoplastic, 030220 oncology & carcinogenesis, kConFab Investigators, Female, RNA Interference, women, GENICA Network, transcription, reveals, Type 2, Alleles, Asian Continental Ancestry Group, Binding Sites, Breast Neoplasms, Case-Control Studies, Cell Line, Tumor, Chromatin Immunoprecipitation, E2F1 Transcription Factor, European Continental Ancestry Group, Genetic Association Studies, Haplotypes, Hepatocyte Nuclear Factor 3-alpha, Humans, Position-Specific Scoring Matrices, Protein Binding, Receptor, Fibroblast Growth Factor, Type 2, Genetic Loci, Receptor, Australian Ovarian Cancer Study Group, Black People, Single-nucleotide polymorphism, Locus (genetics), Biology, determinant, White People, Article, Cell Line, estrogen-receptor binding, Promoter Regions, 03 medical and health sciences, Genetic, SDG 3 - Good Health and Well-being, Asian People, Breast Cancer, expression, ddc:610, Allele, 030304 developmental biology, Neoplastic, Prevention, Human Genome, Molecular biology, susceptibility loci, Gene Expression Regulation, genome-wide association, chromatin, Hypersensitive site, Chromatin immunoprecipitation

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55648b7cdc44d12a453f032be172b093

المؤلفون: Joe Dennis, Sarah Stewart-Brown, Per Hall, Hui Cai, Pei Ei Wu, Soo Chin Lee, Alison M. Dunning, Kenneth Muir, Wenjin Wang, Min Hyuk Lee, Francois Bacot, Hyuna Sung, Chiu-Chen Tseng, Zefang Ren, Hidemi Ito, Artitaya Lophatananon, Ben Zhang, Wei Lu, Kexin Chen, Jong Won Lee, Daniel O. Stram, Mi Kyung Kim, Wonshik Han, Chiun-Sheng Huang, Soo Hwang Teo, Ji Yeob Choi, David Van Den Berg, Hui Miao, Xiao-Ou Shu, Jiajun Shi, Wei Zheng, Mikael Hartman, Hongbing Shen, Jirong Long, Douglas F. Easton, Qin Wang, Javier Benitez, Chun Li, Hideo Tanaka, Jyh Cherng Yu, Bu Tian Ji, Motoki Iwasaki, Daniel C. Tessier, Thomas C. Putti, Daniel Vincent, Tien Yin Wong, Ming-Feng Hou, Ui-Soon Khoo, Keitaro Matsuo, Cheng Har Yip, Hiroji Iwata, Keun-Young Yoo, Dong Young Noh, Paul D.P. Pharoah, Anna H. Wu, Sung-Won Kim, In Nee Kang, Yong-Bing Xiang, Ying Zheng, Wanqing Wen, Jong-Young Lee, Pornthep Siriwanarangsan, Chen-Yang Shen, Suleeporn Sangrajrang, Daehee Kang, Aiko Sueta, Yu Tang Gao, Qiuyin Cai, Kyriaki Michailidou, Manjeet K. Humphreys, Sue K. Park, Christopher A. Haiman

المصدر: Human Molecular Genetics; Vol 22
Human Molecular Genetics

مصطلحات موضوعية: Adult, Oncology, China, medicine.medical_specialty, Population, Estrogen receptor, Breast Neoplasms, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Asian People, Internal medicine, Republic of Korea, Genetics, medicine, Humans, Genetic Predisposition to Disease, education, Molecular Biology, Genetics (clinical), Aged, 030304 developmental biology, Genetic association, 0303 health sciences, education.field_of_study, Association Studies Articles, Case-control study, Cancer, General Medicine, Middle Aged, medicine.disease, 3. Good health, Receptors, Estrogen, Case-Control Studies, 030220 oncology & carcinogenesis, Female, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::758818c189d15f1eef9278952a67a5d4
https://doi.org/10.1093/hmg/ddt089

المؤلفون: Curtis Olswold, Daniel I. Chasman, Brian E. Henderson, Peter Lichtner, Jennifer Stone, Rita K. Schmutzler, Julian Peto, Sandra L. Deming, Fredrick R. Schumacher, William J. Tapper, Gary K. Chen, Constance Chen, Kim Overvad, Diana Eccles, Nicholas G. Martin, Elio Riboli, Celine M. Vachon, Daniel J. Park, Robert C. Millikan, Timothy G. Lesnick, Matthias W. Beckmann, Gerhard A. Coetzee, Gianluca Severi, Domenico Palli, Clare Turnbull, Jenny Chang-Claude, Montserrat Garcia-Closas, Douglas F. Easton, Carla H. van Gils, Christine B. Ambrosone, Zhaoming Wang, Françoise Clavel-Chapelon, Michael F. Press, Dieter Flesch-Janys, Astrid Irwanto, Claudine Isaacs, Paul M. Ridker, Esther M. John, Wei Zheng, Nazneen Rahman, Peter Kraft, David Van Den Berg, Elisa V. Bandera, André G. Uitterlinden, Susan E. Hankinson, Loic Le Marchand, Sue A. Ingles, Arif B. Ekici, Laurence N. Kolonel, Penelope Miron, Alfons Meindl, Quinten Waisfisz, Eric A. Ross, Jianjun Liu, S Gerty, Kristen N. Stevens, Melissa C. Southey, Adam M. Lee, Daniele Campa, Kyriaki Michailidou, Regina G. Ziegler, Robert N. Hoover, Quang M. Bui, Jennifer J. Hu, Laura Baglietto, Per Hall, Mia M. Gaudet, Alison M. Dunning, Julie E. Buring, Paul D.P. Pharoah, Jorge L. Rodriguez-Gil, Jonine D. Figueroa, Afshan Siddiq, Eiliv Lund, Arndt Hartmann, Fergus J. Couch, Sarah J. Nyante, Peter A. Fasching, Louise A. Brinton, Daniel F. Schmidt, Sara Lindström, Julie R. Palmer, Graham G. Giles, Olivia Fletcher, Rebecca Hein, Lynne R. Wilkens, Carmel Apicella, Christine D. Berg, Saundra S. Buys, Angela Cox, Kevin B. Jacobs, Heather Spencer Feigelson, Fernando Rivadeneira, W. Ryan Diver, Heli Nevanlinna, Isabel dos Santos Silva, Christina Justenhoven, Hanne Meijers-Heijboer, JoEllen Weaver, Stefan Nickels, Daniel O. Stram, Pilar Amiano, Carl Blomqvist, Lorraine Durcan, Jane Carpenter, Kamila Czene, John L. Hopper, Robert B. Diasio, Rudolf Kaaks, Nikki Graham, Grant W. Montgomery, Enes Makalic, Kristine R. Monroe, Lars Beckmann, Malin Sund, Christopher A. Haiman, Scott Huntsman, Stephen J. Chanock, Xianshu Wang, Catriona McLean, Susan L. Slager, David J. Hunter, Kristiina Aittomäki, Hans-Peter Sinn, Harsh B. Pathak, Elad Ziv, Mark Lathrop, Bertram Müller-Myhsok, Leslie Bernstein, I-Min Lee, Simon S. Cross, Ruth C. Travis, Suhn K. Rhie, Hiltrud Brauch, Rüdiger Schulz-Wendtland, Michael J. Thun, Dario Greco, Judith Heinz, Andrew K. Godwin, Laura Fejerman

المساهمون: Cancer Center Amsterdam, Amsterdam Reproduction & Development (AR&D), Human Genetics, Internal Medicine, Human genetics, CCA - Oncogenesis

المصدر: Human Molecular Genetics; Vol 21
Hum. Mol. Genet. 21, 5373-5384 (2012)
Human molecular genetics, 21(24), 5373-5384. Oxford University Press
Human Molecular Genetics, 21(24), 5373-5384. Oxford University Press
Siddiq, A, Couch, F J, Chen, G K, Lindström, S, Eccles, D, Millikan, R C, Michailidou, K, Stram, D O, Beckmann, L, Rhie, S K, Ambrosone, C B, Aittomäki, K, Amiano, P, Apicella, C, Baglietto, L, Bandera, E V, Beckmann, M W, Berg, C D, Bernstein, L, Blomqvist, C, Brauch, H, Brinton, L, Bui, Q M, Buring, J E, Buys, S S, Campa, D, Carpenter, J E, Chasman, D I, Chang-Claude, J, Chen, C, Clavel-Chapelon, F, Cox, A, Cross, S S, Czene, K, Deming, S L, Diasio, R B, Diver, W R, Dunning, A M, Durcan, L, Ekici, A B, Fasching, P A, Fejerman, L, Figueroa, J D, Fletcher, O, Flesch-Janys, D, Gaudet, M M, Gerty, S M, Rodriguez-Gil, J L, Giles, G G, Overvad, K & Australian Breast Cancer Tissue Bank Investigators 2012, ' A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11 ', Human Molecular Genetics, vol. 21, no. 24, pp. 5373-5384 . https://doi.org/10.1093/hmg/dds381
Human Molecular Genetics
Siddiq, A, Couch, F J, Chen, G K, Lindstrom, S, Eccles, D, Millikan, R C, Michailidou, K, Stram, D O, Beckmann, L, Rhie, S K, Ambrosone, C B, Aittomaki, K, Amiano, P, Apicella, C, Baglietto, L, Bandera, E V, Beckmann, M W, Berg, C D, Bernstein, L, Blomqvist, C, Brauch, H, Brinton, L, Bui, Q M, Buring, J E, Buys, S S, Campa, D, Carpenter, J E, Chasman, D I, Chang-Claude, J, Chen, C, Clavel-Chapelon, F, Cox, A, Cross, S S, Czene, K, Deming, S L, Diasio, R B, Diver, W R, Dunning, A M, Durcan, L, Ekici, A B, Fasching, P A, Feigelson, H S, Fejerman, L, Figueroa, J D, Fletcher, O, Flesch-Janys, D, Gaudet, M M, Gerty, S M, Rodriguez-Gil, J L, Giles, G G, van Gils, C H, Godwin, A K, Graham, N, Greco, D, Hall, P, Hankinson, S E, Hartmann, A, Hein, R, Heinz, J, Hoover, R N, Hopper, J L, Hu, J J, Huntsman, S, Ingles, S A, Irwanto, A, Isaacs, C, Jacobs, K B, John, E M, Justenhoven, C, Kaaks, R, Kolonel, L N, Coetzee, G A, Lathrop, M, Le Marchand, L, Lee, AM, Lee, I M, Lesnick, T, Lichtner, P, Liu, J J, Lund, E, Makalic, E, Martin, N G, McLean, C A, Meijers-Heijboer, E J, Meindl, A, Miron, P, Monroe, K R, Montgomery, G W, Muller-Myhsok, B, Nickels, S, Nyante, S J, Olswold, C, Overvad, K, Palli, D, Park, D J, Palmer, J R, Pathak, H, Peto, J & Pharoah, P 2012, ' A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11 ', Human Molecular Genetics, vol. 21, no. 24, pp. 5373-5384 . https://doi.org/10.1093/hmg/dds381

مصطلحات موضوعية: Oncology, genetic association, Hispanic, Estrogen receptor, Genome-wide association study, Bioinformatics, genetic risk, Prostate cancer, 0302 clinical medicine, Japan, single nucleotide polymorphism, Genotype, genetic variability, African American, Genetics (clinical), Triple-negative breast cancer, 0303 health sciences, education.field_of_study, Association Studies Articles, article, General Medicine, prostate cancer, 3. Good health, Europe, female, Receptors, Estrogen, priority journal, 030220 oncology & carcinogenesis, chromosome 20q, medicine.medical_specialty, gene locus, Population, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Breast cancer, breast cancer, SDG 3 - Good Health and Well-being, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, controlled study, human, education, Molecular Biology, chromosome 6q, computer model, gene replication, genetic susceptibility, major clinical study, triple negative breast cancer, 030304 developmental biology, medicine.disease, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f64dd59f9871cd129ec5da82b106f2
https://pure.eur.nl/en/publications/67bfde16-8d72-4ba1-a81c-81f236e8fb8e

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: 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

وصف الملف: application/pdf

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