يعرض 1 - 10 نتائج من 56 نتيجة بحث عن '"Xiaoqing, Chen"', وقت الاستعلام: 1.21s تنقيح النتائج
  1. 1
    Impact of TP53 mutations in breast cancer: Clinicopathological features and prognosisImpact of TP53 mutations in breast CA

    المؤلفون: Liping Guo, Ning Liao, Xiaoqing Chen, Yunlian Xue, Bo Chen, Xuerui Li, Lingzhu Wen, Yulei Wang

    المصدر: Thoracic Cancer, Vol 11, Iss 7, Pp 1861-1868 (2020)
    Thoracic Cancer

    مصطلحات موضوعية: 0301 basic medicine, Oncology, endocrine system diseases, Receptor, ErbB-2, DNA Mutational Analysis, next‐generation sequencing, Tp53 mutation, medicine.disease_cause, Cohort Studies, Breast cancer, 0302 clinical medicine, TP53, Mutation, General Medicine, Middle Aged, Prognosis, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Gene Expression Regulation, Neoplastic, Receptors, Estrogen, Lymphatic Metastasis, 030220 oncology & carcinogenesis, Correlation analysis, Cohort, Clinicopathological features, Original Article, Female, Receptors, Progesterone, Pulmonary and Respiratory Medicine, medicine.medical_specialty, Tumor suppressor gene, Breast Neoplasms, lcsh:RC254-282, 03 medical and health sciences, Internal medicine, Biomarkers, Tumor, medicine, Humans, Neoplasm Invasiveness, neoplasms, Receiver operating characteristic, business.industry, Original Articles, medicine.disease, 030104 developmental biology, Tumor Suppressor Protein p53, genomic mutation, business

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf33f3c684e559f0dc8391c4851195dd
    https://doi.org/10.1111/1759-7714.13467

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  2. 2
    Genetic and immune characteristics of sentinel lymph node metastases and multiple lymph node metastases compared to their matched primary breast tumours

    المؤلفون: Bo Chen, Yuchen Zhang, Kai Li, Yulei Wang, Li Cao, Yingzi Li, Min Li, Jianguo Lai, Ning Liao, Chongyang Ren, Xiaoqing Chen, Xueying Wu, Jiali Lin, Henghui Zhang, Xuerui Li, Charles M. Balch, Weikai Xiao, Cheukfai Li, Jing Liu, Minghan Jia, Hsiaopei Mok, Guangnan Wei, Guochun Zhang, Lingzhu Wen

    المصدر: EBioMedicine, Vol 71, Iss, Pp 103542-(2021)
    EBioMedicine

    مصطلحات موضوعية: Oncology, medicine.medical_specialty, Medicine (General), Angiogenesis, Sentinel lymph node, Breast Neoplasms, General Biochemistry, Genetics and Molecular Biology, Metastasis, Lymphocytes, Tumor-Infiltrating, Breast cancer, Immune system, R5-920, Internal medicine, Biomarkers, Tumor, Tumor Microenvironment, medicine, Humans, Neoplasm Invasiveness, Lymph node, Genome, business.industry, Gene Expression Profiling, Computational Biology, High-Throughput Nucleotide Sequencing, Multiple lymph node metastases, Oncogenes, General Medicine, Sentinel node, medicine.disease, Immune characteristics, medicine.anatomical_structure, Lymphatic Metastasis, Sentinel lymph node metastases, Mutation, Medicine, Female, Disease Susceptibility, Lymph, Sentinel Lymph Node, business, Research Paper

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c9ea60ad9803c24283f5cadf546919
    http://www.sciencedirect.com/science/article/pii/S2352396421003352

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  3. 3
    Distinct clinical and somatic mutational features of breast tumors with high-, low-, or non-expressing human epidermal growth factor receptor 2 status

    المؤلفون: Guochun Zhang, Chongyang Ren, Cheukfai Li, Yulei Wang, Bo Chen, Lingzhu Wen, Minghan Jia, Kai Li, Hsiaopei Mok, Li Cao, Xiaoqing Chen, Jiali Lin, Guangnan Wei, Yingzhi Li, Yuchen Zhang, Charles M. Balch, Ning Liao

    المصدر: BMC medicine. 20(1)

    مصطلحات موضوعية: Phosphatidylinositol 3-Kinases, Receptor, ErbB-2, Humans, Breast Neoplasms, Female, General Medicine, In Situ Hybridization, Fluorescence

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d1cf13a202c8a721bb62186ed2e086
    https://pubmed.ncbi.nlm.nih.gov/35484593

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  4. 4
    Genetic mutation profile of Chinese HER2-positive breast cancers and genetic predictors of responses to Neoadjuvant anti-HER2 therapy

    المؤلفون: Li Cao, Zhou Zhang, Bo Chen, Liping Guo, Ning Liao, Xiaoqing Chen, Min Li, Kai Li, Charles M. Balch, Jiali Lin, Guochun Zhang, Yulei Wang, Chongyang Ren, Minghan Jia, Cheukfai Li, Jing Liu, Ting Hou, Lingzhu Wen, Guangnan Wei, Hsiaopei Mok

    المصدر: Breast Cancer Research and Treatment

    مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, Cancer Research, medicine.medical_specialty, Receptor, ErbB-2, medicine.medical_treatment, Breast Neoplasms, medicine.disease_cause, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Preclinical Study, Asian People, Internal medicine, Antineoplastic Combined Chemotherapy Protocols, ROS1, Biomarkers, Tumor, Medicine, Missense mutation, Humans, skin and connective tissue diseases, Pathological, neoplasms, Aged, Chemotherapy, Mutation, business.industry, High-Throughput Nucleotide Sequencing, Middle Aged, medicine.disease, Neoadjuvant Therapy, 030104 developmental biology, Ki-67 Antigen, Treatment Outcome, 030220 oncology & carcinogenesis, Cohort, Female, Anti her2, Tumor Suppressor Protein p53, business

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4464d36dd150b15dab7ef06a4b8398ab
    https://pubmed.ncbi.nlm.nih.gov/32638235

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  5. 5
    Association between histone lysine methyltransferase KMT2C mutation and clinicopathological factors in breast cancer

    المؤلفون: Li Cao, Guochun Zhang, Liping Guo, Xiaoqing Chen, Ning Liao, Bo Chen, Lingzhu Wen, Chongyang Ren, Yulei Wang

    المصدر: Biomedicine & Pharmacotherapy, Vol 116, Iss, Pp 108997-(2019)

    مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Mutation rate, Breast Neoplasms, Kaplan-Meier Estimate, RM1-950, Molecular taxonomy, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Histone-lysine methyltransferase, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, In patient, Epigenetics, Genetic Association Studies, Proportional Hazards Models, Pharmacology, business.industry, Hazard ratio, KMT2C mutation, General Medicine, Middle Aged, medicine.disease, DNA-Binding Proteins, Treatment Outcome, 030104 developmental biology, 030220 oncology & carcinogenesis, Multivariate Analysis, Mutation, Cohort, Female, Therapeutics. Pharmacology, Next-generation sequencing technique, business

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::047805e2a79e92b966db9ee40ca34bf2
    http://www.sciencedirect.com/science/article/pii/S0753332219316828

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  6. 6
    A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

    المؤلفون: Harald Surowy, Rulla M. Tamimi, Javier Benitez, Wing-Yee Lo, Celine M. Vachon, Nadege Presneau, John J. Spinelli, Ann Smeets, Hoda Anton-Culver, Veli-Matti Kosma, Christopher A. Haiman, Martha J. Shrubsole, Ross L. Prentice, Diana Eccles, Ursula Eilber, Loic Le Marchand, Katri Pylkäs, Jirong Long, Michael P. Lux, Sara Margolin, Hedy S. Rennert, Tom Maishman, Mary B. Daly, Rita K. Schmutzler, Julian Peto, Sune F. Nielsen, Eric Hahnen, Niclas Håkansson, Børge G. Nordestgaard, Mitul Shah, Matthias W. Beckmann, Anthony J. Swerdlow, Barbara Burwinkel, Rudolf Kaaks, Usha Menon, William J. Tapper, Argyrios Ziogas, Peter Hillemanns, Fares Al-Ejeh, Roger L. Milne, Wolfgang Janni, Pascal Guénel, Mikael Eriksson, Clarice R. Weinberg, Kyriaki Michailidou, Jonathan Beesley, Marike Gabrielson, J. Esteban Castelao, Margriet Collée, Janet E. Olson, Gad Rennert, Per Broberg, Rob A. E. M. Tollenaar, David Cox, Paolo Peterlongo, Helian Feng, Brian D. Carter, Nichola Johnson, Emmanouil Saloustros, Dijana Plaseska-Karanfilska, Kimberly F. Doheny, Paul L. Auer, Hans Wildiers, Jacques Simard, Michael Untch, Per Hall, Martine Dumont, Julie M. Cunningham, Thilo Dörk, Mary Beth Terry, Jenny Chang-Claude, Lang Wu, Irene L. Andrulis, Xiaohong R. Yang, Caroline Baynes, Isabel dos-Santos-Silva, Douglas F. Easton, Wei Shi, Emily Hallberg, Camilla Wendt, Hiltrud Brauch, Diana Torres, Olufunmilayo I. Olopade, David Van Den Berg, Georgia Chenevix-Trench, Alfons Meindl, Stig E. Bojesen, Jonine D. Figueroa, Dale P. Sandler, Vessela N. Kristensen, Christine L. Clarke, Wei Zheng, Manuela Gago-Dominguez, E Rozali, Henrik Flyger, Sheila Seal, Guanmengqian Huang, Marjanka K. Schmidt, Håkan Olsson, Christopher G. Scott, Kamila Czene, Laura Fachal, Rodney J. Scott, Jennifer Stone, Sara Y. Brucker, Qin Wang, David J. Hunter, Maya Ghoussaini, Christoph Engel, Keith Humphreys, Susan M. Gapstur, Daniel C. Tessier, Paolo Radice, John L. Hopper, Audrey Y. Jung, Lucy Xia, Atocha Romero, Chenjie Zeng, Peter A. Fasching, Jan Lubinski, Anna González-Neira, Nazneen Rahman, Robert N. Hoover, Thérèse Truong, Fergus J. Couch, Anna Marie Mulligan, Robert J. MacInnis, Ute Hamann, Hanne Meijers-Heijboer, Brigitte Rack, Simon S. Cross, Federico Canzian, J.-P. Meyer, Sara Lindström, Natalia Bogdanova, Trinidad Caldés, Olivia Fletcher, Peter Kraft, Elinor J. Sawyer, Alexander Gusev, Louise A. Brinton, Diether Lambrechts, Bingshan Li, Kristan J. Aronson, Jane Romm, Anja Rudolph, Peter Devilee, Qiuyin Cai, Arto Mannermaa, Elad Ziv, Alice S. Whittemore, Abigail Thomas, Hermann Brenner, Montserrat Garcia-Closas, Patrick Neven, Kristine Jones, Miriam Dwek, Sibylle Loibl, Heli Nevanlinna, Jolanta Lissowska, Susan L. Neuhausen, Elza Khusnutdinova, Marina Bermisheva, Alicja Wolk, Lin Fritschi, Xingyi Guo, Angela Cox, Michael Jones, Xiaoqing Chen, Esther M. John, Richard Barfield, Volker Arndt, Patricia Harrington, Quinten Waisfisz, Daniel Vincent, Antoinette Hollestelle, Dimitrios Mavroudis, JoAnn E. Manson, Joe Dennis, Walter C. Willett, Stacey L. Edwards, Melissa C. Southey, Andreas Schneeweiss, Jack A. Taylor, Robert Winqvist, Mia M. Gaudet, David E. Goldgar, Anna Jakubowska, Paul D.P. Pharoah, Kathrin Thöne, Dieter Flesch-Janys, Mark S. Goldberg, Craig Luccarini, Sten Cornelissen, Jingmei Li, Michael J. Kerin, Myrto Barrdahl, Xiao-Ou Shu, Alison M. Dunning, Manjeet K. Bolla, Carl Blomqvist, Graham G. Giles, Hans Christiansen, A. Heather Eliassen, Valerie Rhenius, Alexander Hein, Belynda Hicks, Ivana Maleva Kostovska, Tongguang Cheng, Yingchang Lu

    المساهمون: CCA - Cancer biology and immunology, Amsterdam Neuroscience - Complex Trait Genetics, Human genetics, Amsterdam Reproduction & Development (AR&D), Clinical Genetics, Medical Oncology, Guo, Xingyi [0000-0001-5269-1294], Al-Ejeh, Fares [0000-0002-1553-0077], Li, Bingshan [0000-0003-2129-168X], Gusev, Alexander [0000-0002-7980-4620], Andrulis, Irene L [0000-0002-4226-6435], Arndt, Volker [0000-0001-9320-8684], Brauch, Hiltrud [0000-0001-7531-2736], Collée, Margriet [0000-0002-9272-9346], Cox, Angela [0000-0002-5138-1099], Cunningham, Julie M [0000-0002-8159-3025], Fachal, Laura [0000-0002-7256-9752], Fletcher, Olivia [0000-0001-9387-7116], Hein, Alexander [0000-0003-2601-3398], Hicks, Belynda [0000-0001-8014-4888], Hollestelle, Antoinette [0000-0003-1166-1966], Jakubowska, Anna [0000-0002-5650-0501], Khusnutdinova, Elza [0000-0003-2987-3334], Li, Jingmei [0000-0001-8587-7511], Menon, Usha [0000-0003-3708-1732], Nevanlinna, Heli [0000-0002-0916-2976], Nordestgaard, Børge G [0000-0002-1954-7220], Pylkäs, Katri [0000-0002-2449-0521], Rennert, Gad [0000-0002-8512-068X], Romero, Atocha [0000-0002-1634-7397], Saloustros, Emmanouil [0000-0002-0485-0120], Scott, Christopher G [0000-0003-1340-0647], Shrubsole, Martha J [0000-0002-5591-7575], Wolk, Alicja [0000-0001-7387-6845], Ziogas, Argyrios [0000-0003-4529-3727], Pharoah, Paul DP [0000-0001-8494-732X], Milne, Roger L [0000-0001-5764-7268], Easton, Douglas F [0000-0003-2444-3247], Zheng, Wei [0000-0003-1226-070X], Apollo - University of Cambridge Repository, Human Genetics, ARD - Amsterdam Reproduction and Development

    المصدر: Wu, L, Shi, W, Long, J, Guo, X, Michailidou, K, Beesley, J, Bolla, M K, Shu, X-O, Lu, Y, Cai, Q, Al-Ejeh, F, Rozali, E, Wang, Q, Dennis, J, Li, B, Zeng, C, Feng, H, Gusev, A, Barfield, R T, Andrulis, I L, Anton-Culver, H, Arndt, V, Aronson, K J, Auer, P L, Barrdahl, M, Baynes, C, Beckmann, M W, Benitez, J, Bermisheva, M, Blomqvist, C, Bogdanova, N V, Bojesen, S E, Brauch, H, Brenner, H, Brinton, L, Broberg, P, Brucker, S Y, Burwinkel, B, Caldés, T, Canzian, F, Carter, B D, Castelao, J E, Chang-Claude, J, Chen, X, Cheng, T-Y D, Christiansen, H, Clarke, C L & Collée, M & Cornelissen, S & Figueroa, J 2018, ' A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer ', Nature Genetics, vol. 50, pp. 968–978 . https://doi.org/10.1038/s41588-018-0132-x
    Nature Genetics, 50(7), 968-+. Nature Publishing Group
    Nature genetics, 50(7), 968-978. Nature Publishing Group
    Nature Genetics
    BCAC 2018, ' A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer ', Nature Genetics, vol. 50, no. 7, pp. 968-+ . https://doi.org/10.1038/s41588-018-0132-x
    Nature Genetics, 50(7), 968
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid

    مصطلحات موضوعية: 0301 basic medicine, Risk, medicine.medical_specialty, Gene Expression, Genome-wide association study, Breast Neoplasms, Biology, Genome-wide association studies, Polymorphism, Single Nucleotide, Article, Transcriptome, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Genetic model, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetic association, medicine.disease, 3. Good health, 030104 developmental biology, 030220 oncology & carcinogenesis, Case-Control Studies, Expression quantitative trait loci, Medical genetics, Female, Gene expression, Breast Cancer Genetics, Genome-Wide Association Study

    وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/pdf; text

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51f35a0c172b8575e59db833fee5c8e9
    https://doi.org/10.1038/s41588-018-0132-x

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  7. 7
    Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab

    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

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::352a33e412bebbe61f92bb8a0e3c5f3c
    http://europepmc.org/articles/PMC5107177

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  8. 8
    Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers

    المؤلفون: Debra Frost, Frans B. L. Hogervorst, Lesley McGuffog, Amanda B. Spurdle, Tracy A. O'Mara, Xiaoqing Chen, Logan C. Walker, Conxi Lázaro, Paolo Radice, Javier Benitez, Kenneth Offit, Trinidad Caldés, Anna Jakubowska, Irene L. Andrulis, Marco Montagna, George A. R. Wiggins, Georgia Chenevix-Trench, John F. Pearson, Antonis C. Antoniou, Daniel Barrowdale, Annika Lindblom, Peter J. Hulick, Robert L. Nussbaum, Andrew K. Godwin, Alfons Meindl, Claudine Isaacs, Beth N. Peshkin, Michael T. Parsons, Louise Marquart, Rita K. Schmutzler, Thomas P. Slavin, Joe Dennis, Katherine L. Nathanson, Fergus J. Couch

    المساهمون: National Science Foundation (Estados Unidos), Asociación Española Contra el Cáncer, Fundación Mutua Madrileña, Wellcome Trust, University of Kansas. Cancer Center (Estados Unidos), Netherlands Comprehensive Cancer Organisation, Instituto de Salud Carlos III, Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF), Netherlands Organization of Scientific Research, Cancer Council of South (Australia)

    المصدر: Dipòsit Digital de la UB
    Universidad de Barcelona
    European Journal of Human Genetics
    Repisalud
    Instituto de Salud Carlos III (ISCIII)
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid

    مصطلحات موضوعية: Adult, Glutamate Carboxypeptidase II, 0301 basic medicine, Heterozygote, DNA Copy Number Variations, endocrine system diseases, Etiology, Càncer d'ovari, Breast Neoplasms, Locus (genetics), Single-nucleotide polymorphism, Biology, Article, Càncer de mama, Transcription Factors, TFII, 03 medical and health sciences, Breast cancer, Ovarian cancer, Genetics, medicine, Humans, Copy-number variation, Cytochrome P450 Family 2, Allele frequency, Genetics (clinical), Genetic association, Ovarian Neoplasms, Genes, Modifier, BRCA1 Protein, Pregnancy-Specific beta 1-Glycoproteins, medicine.disease, DNA-Binding Proteins, 030104 developmental biology, Càncer d'ovaris, Etiologia, Female, Aryl Hydrocarbon Hydroxylases, SNP array

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6cb77941a4238f23f9692857de669b
    http://hdl.handle.net/2445/171642

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  9. 9
    Association analysis identifies 65 new breast cancer risk loci

    المؤلفون: Michael Jones, Dong-Young Noh, Martha J. Shrubsole, Chen-Yang Shen, Xiaoqing Chen, Esther M. John, Patricia Harrington, Quinten Waisfisz, Sue K. Park, Miriam Dwek, Christa Stegmaier, Sibylle Loibl, Wing-Yee Lo, Suleeporn Sangrajrang, Susan L. Neuhausen, Marina Bermisheva, Alicja Wolk, Christof Sohn, Keun-Young Yoo, Arja Jukkola-Vuorinen, Kathrin Thöne, James McKay, John J. Spinelli, Brian D. Carter, Elza Khusnutdinova, Francois Bacot, Paul L. Auer, Anna H. Wu, Christopher I. Amos, Johanna I. Kiiski, Hans Wildiers, Manjeet K. Bolla, Soo Hwang Teo, Julie M. Cunningham, Zhaoming Wang, Dieter Flesch-Janys, Argyrios Ziogas, Ann Smeets, Min Hyuk Lee, Xiaohong R. Yang, Carl Blomqvist, Natalia Antonenkova, Vassilios Georgoulias, Siranoush Manoukian, Anne Lise Børresen-Dale, Montserrat Garcia-Closas, Priyanka Sharma, Michael J. Kerin, Loic Le Marchand, Yoshio Kasuga, Michael Untch, Thomas Brüning, Natalia Bogdanova, Juliet D. French, Mark E. Sherman, Diana Eccles, Don M. Conroy, Marcia Adams, Pascal Guénel, Jonine D. Figueroa, Somchai Thanasitthichai, Jonathan Beesley, Paolo Peterlongo, Angela Cox, Graham G. Giles, Hans Christiansen, Irene L. Andrulis, Caroline Baynes, V. Shane Pankratz, Kristine Jones, Wei Zheng, Motoki Iwasaki, Rita K. Schmutzler, Julian Peto, Sara Margolin, Hedy S. Rennert, Hidemi Ito, Caroline Seynaeve, Jirong Long, Rachel Lloyd, Mark S. Goldberg, Javier Benitez, Børge G. Nordestgaard, Kathleen E. Malone, A. Heather Eliassen, Valerie Rhenius, Kristan J. Aronson, Maartje J. Hooning, Ursula Eilber, Christopher A. Haiman, Ji Yeob Choi, Jaana M. Hartikainen, Ian W. Brock, Barbara Burwinkel, Brigitte Rack, Mitul Shah, Matthias W. Beckmann, Belynda Hicks, Bernardo Bonanni, Alexander Hein, Leslie Bernstein, Christine L. Clarke, Emilie Cordina-Duverger, Sabine Behrens, Hoda Anton-Culver, Angela Brooks-Wilson, Bin Zhu, Gord Glendon, Banu Arun, José A. García-Sáenz, Jose Ignacio Arias Perez, Anne Grundy, Ans M.W. van den Ouweland, Nadege Presneau, Volker Arndt, Mikael Eriksson, Simon S. Cross, Craig Luccarini, Anthony J. Swerdlow, Veli-Matti Kosma, Hui Miao, Ming-Feng Hou, Hiroji Iwata, Christi J. van Asperen, Henrik Flyger, Jennifer Stone, Qin Wang, Penny Soucy, Heli Nevanlinna, Jane Heyworth, Shoichiro Tsugane, Annika Lindblom, Curtis Olswold, Trinidad Caldés, Laura Fachal, Ed Dicks, Shirley Hui, Katja Butterbach, Alison M. Dunning, Peter Devilee, Qiuyin Cai, Antonis C. Antoniou, Diether Lambrechts, Katarzyna Kaczmarek, Katri Pylkäs, Fredrick R. Schumacher, Arif B. Ekici, Aaron D. Norman, Jolanta Lissowska, Daniel C. Tessier, N Hamel, Paolo Radice, Håkan Olsson, Vessela N. Kristensen, Ling Tong, Harald Surowy, Rulla M. Tamimi, Jonathan Tyrer, Michael P. Lux, Stacey L. Edwards, Kathryn J. Ruddy, Giske Ursin, Myrto Barrdahl, Xiao-Ou Shu, Primitiva Menéndez, Sara Y. Brucker, Elad Ziv, Kenneth Muir, Eric Hahnen, Andy C. H. Lee, Rodney J. Scott, Lothar Haeberle, Darya Prokofyeva, Isabel dos-Santos-Silva, Peter Kraft, David G. Cox, Jong Won Lee, Sunil R. Lakhani, Kelly-Anne Phillips, Douglas F. Easton, Melissa C. Southey, Jan Lubinski, Jose E. Castelao, Hanne Meijers-Heijboer, Ivana Maleva Kostovska, Siddhartha Kar, Renske Keeman, Celine M. Vachon, Diana Torres, Stephen J. Chanock, Jack A. Taylor, Emiel J. Th. Rutgers, Chuen Neng Lee, Jason Vollenweider, Gadi Rennert, Jane Romm, Amy E. McCart Reed, Kee Seng Chia, Thomas Rüdiger, Anja Rudolph, Catriona McLean, David Van Den Berg, Christopher G. Scott, Mervi Grip, Lucy Xia, Georgia Chenevix-Trench, Robert Winqvist, Mary Beth Terry, Jenny Chang-Claude, Hans-Ulrich Ulmer, Mikael Hartman, Dona N. Ho, Maria Kabisch, Christoph Engel, Claire Mulot, Grethe I. Grenaker Alnæs, Arto Mannermaa, Nazneen Rahman, Tjoung-Won Park-Simon, Atocha Romero, Lin Fritschi, Manuela Gago-Dominguez, Matthias Ruebner, Valerie Gaborieau, Keitaro Matsuo, Asha Rostamianfar, Emmanouil Saloustros, Dijana Plaseska-Karanfilska, J.-P. Meyer, Sara Lindström, Annegien Broeks, Audrey Lemaçon, Tsun Leung Chan, Tongguang Cheng, Robert J. MacInnis, Habibul Ahsan, Federico Canzian, Paul Brennan, Mia M. Gaudet, David E. Goldgar, Anna Jakubowska, Paul D.P. Pharoah, Jacek Gronwald, Sung-Won Kim, Daehee Kang, Daniel O. Stram, Nichola Johnson, Rob B. van der Luijt, Sten Cornelissen, Camilla Wendt, Dylan M. Glubb, Olufunmilayo I. Olopade, Usha Menon, David J. Hunter, Kristiina Aittomäki, Jamie Allen, Chiu-Chen Tseng, Keith Humphreys, Edmond S. K. Ma, Peter Hillemanns, Hiltrud Brauch, Chia-Ni Hsiung, Sheila Seal, Junko Ishiguro, Dale P. Sandler, Peter Schürmann, Gary D. Bader, Sarah Stewart-Brown, Flavio Lejbkowicz, Marike Gabrielson, Wolfgang Janni, Judith S. Brand, Jingmei Li, Ava Kwong, Stig E. Bojesen, Ying Zheng, Mila Pinchev, Yu Tang Gao, Susan E. Hankinson, Elinor J. Sawyer, Per Broberg, Sofia Khan, Grace Sheng, Alfons Meindl, Margriet Collée, Jyh-Cherng Yu, Ute Krüger, Louise A. Brinton, Elizabeth W. Pugh, Thilo Dörk, Hilary K. Finucane, Peter A. Fasching, Shan Wang-Gohrke, Jenna Lilyquist, Muriel A. Adank, Marjanka K. Schmidt, Susan M. Gapstur, Sune F. Nielsen, Maya Ghoussaini, Minouk J. Schoemaker, Roger L. Milne, Jacques Simard, Clarice R. Weinberg, Kyriaki Michailidou, Shivaani Mariapun, Rob A. E. M. Tollenaar, Lizet E. van der Kolk, Nicola Miller, Anna González-Neira, Ian Tomlinson, Thérèse Truong, Ross L. Prentice, Anna Marie Mulligan, Jason S. Carroll, Taiki Yamaji, Carolina Ellberg, Mingajeva Elvira, Olivia Fletcher, Arnaud Droit, Per Hall, Maria Elena Martinez, Maria Tengström, Hui Cai, Xia Jiang, Janet E. Olson, Julia A. Knight, Nick Orr, Angel Carracedo, Guanmengqian Huang, Martine Dumont, Cheng Har Yip, Tom Maishman, Mary B. Daly, Artitaya Lophatananon, Niclas Håkansson, Steven N. Hart, Nur Aishah Taib, Andreas Schneeweiss, Daniel F. Schmidt, Daniel Vincent, Antoinette Hollestelle, Dimitrios Mavroudis, JoAnn E. Manson, Joe Dennis, Walter C. Willett, Rudolf Kaaks, Karen McCue, Enes Makalic, Kimberly F. Doheny, Eunjung Lee, Robert N. Hoover, Fergus J. Couch, Ute Hamann, Alice S. Whittemore, Hermann Brenner, Lorraine Durcan, Kamila Czene, Patrick Neven, John L. Hopper

    المساهمون: Clinical Genetics, Medical Oncology, Human Genetics, CCA - Cancer biology and immunology, Dennis, Joe [0000-0003-4591-1214], Wang, Jean [0000-0002-9139-0627], Tyrer, Jonathan [0000-0003-3724-4757], Dicks, Ed [0000-0002-0617-0401], Lee, Andrew [0000-0003-0677-0252], Allen, Jamie [0000-0002-8677-2225], Fachal Vilar, Laura [0000-0002-7256-9752], Carroll, Jason [0000-0003-3643-0080], Rhenius, Valerie [0000-0003-4215-3235], Antoniou, Antonis [0000-0001-9223-3116], Pharoah, Paul [0000-0001-8494-732X], Dunning, Alison [0000-0001-6651-7166], Easton, Douglas [0000-0003-2444-3247], Apollo - University of Cambridge Repository, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D)

    المصدر: Nature, 551(7678), 92-+. Nature Publishing Group
    Nature, 551(7678), 92-94. Nature Publishing Group
    Nature, 551(7678), 92
    Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
    Consejería de Sanidad de la Comunidad de Madrid
    Michailidou, K, Lindström, S, Dennis, J, Beesley, J, Hui, S, Kar, S, Lemaçon, A, Soucy, P, Glubb, D, Rostamianfar, A, Bolla, M K, Wang, Q, Tyrer, J, Dicks, E, Lee, A, Wang, Z, Allen, J, Keeman, R, Eilber, U, French, J D, Chen, X Q, Fachal, L, McCue, K, Reed, A E M C, Ghoussaini, M, Carroll, J S, Jiang, X, Finucane, H, Adams, M, Adank, M A, Ahsan, H, Aittomäki, K, Anton-Culver, H, Antonenkova, N N, Arndt, V, Aronson, K J, Arun, B, Auer, P L, Bacot, F, Barrdahl, M, Baynes, C, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bernstein, L, Blomqvist, C, Hooning, M J, Meijers-Heijboer, H, Waisfisz, Q, NBCS Collaborators, ABCTB Investigators & kConFab/AOCS Investigators 2017, ' Association analysis identifies 65 new breast cancer risk loci ', Nature, vol. 551, no. 7678, pp. 92-94 . https://doi.org/10.1038/nature24284
    Nature
    Michailidou, K, Lindström, S, Dennis, J, Beesley, J, Hui, S, Kar, S, Lemaçon, A, Soucy, P, Glubb, D, Rostamianfar, A, Bolla, M K, Wang, Q, Tyrer, J, Dicks, E, Lee, A, Wang, Z, Allen, J, Keeman, R, Eilber, U, French, J D, Qing Chen, X, Fachal, L, McCue, K, McCart Reed, A E, Ghoussaini, M, Carroll, J S, Jiang, X, Finucane, H, Adams, M, Adank, M A, Ahsan, H, Aittomäki, K, Anton-Culver, H, Antonenkova, N N, Arndt, V, Aronson, K J, Arun, B, Auer, P L, Bacot, F, Barrdahl, M, Baynes, C, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bernstein, L, Blomqvist, C, Bogdanova, N V, Bojesen, S E & Figueroa, J & Tomlinson, I 2017, ' Association analysis identifies 65 new breast cancer risk loci ', Nature, vol. 551, no. 7678, pp. 92–94 . https://doi.org/10.1038/nature24284
    Nature, 551(7678), 92. Nature Publishing Group
    Michailidou, K, Lindström, S, Dennis, J, Beesley, J, Hui, S, Kar, S, Lemaçon, A, Soucy, P, Glubb, D, Rostamianfar, A, Bolla, M K, Wang, Q, Tyrer, J, Dicks, E, Lee, A, Wang, Z, Allen, J, Keeman, R, Eilber, U, French, J D, Qing Chen, X, Fachal, L, McCue, K, McCart Reed, A E, Ghoussaini, M, Carroll, J S, Jiang, X, Finucane, H, Adams, M, Adank, M A, Ahsan, H, Aittomäki, K, Anton-Culver, H, Antonenkova, N N, Arndt, V, Aronson, K J, Arun, B, Auer, P L, Bacot, F, Barrdahl, M, Baynes, C, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bernstein, L, Blomqvist, C, Lophatananon, A, Muir, K, Scott, C & NBCS Collaborators 2017, ' Association analysis identifies 65 new breast cancer risk loci ', Nature, vol. 551, no. 7678, pp. 92-94 . https://doi.org/10.1038/nature24284

    مصطلحات موضوعية: 0301 basic medicine, Multifactorial Inheritance, Genome-wide association study, Regulatory Sequences, Nucleic Acid, skin and connective tissue diseases, Cancer genetics, Genetics, Multidisciplinary, medicine.diagnostic_test, 3. Good health, Europe, annotation, Medical genetics, Female, Asian Continental Ancestry Group, medicine.medical_specialty, Asia, architecture, European Continental Ancestry Group, ABCTB Investigators, Locus (genetics), Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, Risk Assessment, Article, White People, NBCS Collaborators, 03 medical and health sciences, Breast cancer, Asian People, SDG 3 - Good Health and Well-being, Genetic variation, ConFab/AOCS Investigators, expression, medicine, Genetic predisposition, Journal Article, Humans, Computer Simulation, Genetic Predisposition to Disease, biological pathways, Genetic association, Genetic testing, Genetic association study, Binding Sites, interaction networks, medicine.disease, comprehensive molecular portraits, mutations, susceptibility loci, 030104 developmental biology, Genetic Loci, genome-wide association, protein, Transcription Factors, Genome-Wide Association Study

    وصف الملف: application/pdf; image/pdf; Print-Electronic

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02ae4dc4b3b083725f91978a6ca648ed
    https://pure.eur.nl/en/publications/2325b1a7-eea4-4e72-82e9-9b12f458bce8

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest
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  10. 10
    A Role for Common Genomic Variants in the Assessment of Familial Breast Cancer

    المؤلفون: S Sawyer, David D.L. Bowtell, Jonathan Beesley, Marion Harris, Alison H. Trainer, Geoffrey J. Lindeman, Joanne McKinley, Gillian Mitchell, Georgia Chenevix-Trench, Xiaoqing Chen, Paul A. James

    المصدر: Journal of Clinical Oncology. 30:4330-4336

    مصطلحات موضوعية: Cancer Research, Genotype, Genes, BRCA2, Population, Genes, BRCA1, Breast Neoplasms, Genome-wide association study, Bioinformatics, Polymorphism, Single Nucleotide, Breast cancer, Risk Factors, Humans, Medicine, Genetic Predisposition to Disease, Allele, education, Genetic testing, Family Health, education.field_of_study, medicine.diagnostic_test, business.industry, Cancer, Genomics, Middle Aged, medicine.disease, Oncology, Mutation, Female, business, Ovarian cancer, Genome-Wide Association Study

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec1abfdc87afbd82fe4c6463cba549c
    https://doi.org/10.1200/jco.2012.41.7469

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