المؤلفون: Xiao, Sheng

المساهمون: Brigham and Women's Hospital, Boston, MA 02215

مصطلحات موضوعية: eosinophilia, PDGFRA, PDGFRB, FGFR1, PCM1/JAK2, Leukaemia Section, Biomarkers, Tumor/*genetics, Bone Marrow Cells/metabolism/pathology, Chromosomes, Human, Pair 2/genetics, Pair 5/genetics, Golgi Matrix Proteins/*genetics, Humans, Hypereosinophilic Syndrome/*genetics/pathology, Leukemia/*genetics/pathology, Male, Middle Aged, Oncogene Fusion, Oncogene Proteins, Fusion/*genetics, Receptor, Platelet-Derived Growth Factor beta/*genetics, Translocation, Genetic, Blood Cell Count, Pair 9/genetics, Hypereosinophilic Syndrome/blood/drug therapy/*genetics, Imatinib Mesylate/therapeutic use

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/PDGFRAPDGFRBFGFR1PCM1-JAK2ID1855.htmlTest; Sheng, Xiao. Myeloid/lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2: Overview 2019. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2020, 4, p. 174-179; http://hdl.handle.net/2042/70698Test; https://doi.org/10.4267/2042/70698Test

الإتاحة: https://doi.org/10.4267/2042/70698Test
http://hdl.handle.net/2042/70698Test

المؤلفون: Zamecnikova, Adriana

المساهمون: Kuwait Cancer Control Center, Kuwait

مصطلحات موضوعية: Reports Section, Acute Disease, Adult, Aged, 80 and over, Chromosomes, Human, Pair 6/*genetics, Cytogenetic Analysis, Female, Humans, In Situ Hybridization, Fluorescence, Leukemia, Myeloid/diagnosis/*genetics, Male, Middle Aged, Myelodysplastic Syndromes/diagnosis/*genetics, Neoplasms, Second Primary/diagnosis/*genetics, Sensitivity and Specificity, Translocation, Genetic/*genetics, Anemia, Refractory/*genetics/pathology, Pair 22/genetics, Pair 9/genetics

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Reports/t0617p21p13AdrianaMECOMID100092.htmlTest; Adriana, Zamecnikova. t(6;17)(p21;p13) associated with t(3;3)(q21;q26.2) in AML. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 07, p. 213-215; http://hdl.handle.net/2042/70476Test; https://doi.org/10.4267/2042/70476Test

الإتاحة: https://doi.org/10.4267/2042/70476Test
http://hdl.handle.net/2042/70476Test

المساهمون: Jihye Ha, Borahm Kim, Seungmin Hahn, Seung-Tae Lee, Chuhl Joo Lyu, Jong rak Choi, Kim, Borahm, Lyu, Chuhl Joo, Lee, Seung-Tae, Choi, Jong Rak, Hahn, Seung Min

مصطلحات موضوعية: Adolescent, Chromosomes, Human, Pair 12/genetics, Pair 9/genetics, Humans, Male, Oligonucleotide Array Sequence Analysis, Oncogene Proteins, Fusion/genetics, PAX5 Transcription Factor/genetics, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma*/diagnosis, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma*/genetics, Proto-Oncogene Proteins c-ets/genetics, Repressor Proteins/genetics, Translocation, Genetic

العلاقة: ANNALS OF HEMATOLOGY; J00161; OAK-2018-05737; https://ir.ymlib.yonsei.ac.kr/handle/22282913/165506Test; https://link.springer.com/article/10.1007%2Fs00277-018-3291-zTest; T201804100; ANNALS OF HEMATOLOGY, Vol.97(8) : 1505-1507, 2018; 59117

الإتاحة: https://doi.org/10.1007/s00277-018-3291-zTest
https://ir.ymlib.yonsei.ac.kr/handle/22282913/165506Test

المؤلفون: Sanford Biggerstaff, Julie

المساهمون: Idaho Cytogenetics Diagnostic Laboratory, Boise, ID 83706

مصطلحات موضوعية: chromosome 3, chromosome 9, FOXP1, ABL1, B Cell Acute Lymphoblastic Leukemia, Follicular Lymphoma, Leukaemia Section, Adolescent, Adult, Chromosomes, Human, Pair 3/genetics, Pair 5/genetics, Pair 9/genetics, Fatal Outcome, Female, Forkhead Transcription Factors/*genetics, Humans, Male, Oncogene Proteins, Fusion/*genetics, Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics, Proto-Oncogene Proteins c-abl/*genetics, Repressor Proteins/*genetics

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0309p13q34ID1619.htmlTest; Julie, Sanford Biggerstaff. t(3;9)(p13;q34.1) FOXP1/ABL1. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 7, p. 263-264; http://hdl.handle.net/2042/68265Test; https://doi.org/10.4267/2042/68265Test

الإتاحة: https://doi.org/10.4267/2042/68265Test
http://hdl.handle.net/2042/68265Test

المؤلفون: Vigorito, Elena, Kuchenbaecker, Karoline B, Beesley, Jonathan, Adlard, Julian, Agnarsson, Bjarni A, Andrulis, Irene L, Arun, Banu K, Barjhoux, Laure, Belotti, Muriel, Benitez, Javier, Berger, Andreas, Caldes, Trinidad, Greene, Mark H, Couch, Fergus J, Offit, Kenneth, Pharoah, Paul D P, Chenevix-Trench, Georgia, Antoniou, Antonis C, Caligo, Maria A, Campbell, Ian, Chan, Salina B, Hansen, Thomas V O, Claes, Kathleen B M, Cohn, David E, Cook, Jackie, Daly, Mary B, Damiola, Francesca, Davidson, Rosemarie, Pauw, Antoine de, Delnatte, Capucine, Diez, Orland, Domchek, Susan M, Healey, Sue, Dumont, Martine, Durda, Katarzyna, Dworniczak, Bernd, Easton, Douglas F, Eccles, Diana, Edwinsdotter Ardnor, Christina, Eeles, Ros, Ejlertsen, Bent, Ellis, Steve, Evans, D Gareth, Hodgson, Shirley, Feliubadalo, Lidia, Fostira, Florentia, Foulkes, William D, Friedman, Eitan, Frost, Debra, Gaddam, Pragna, Ganz, Patricia A, Garber, Judy, Garcia-Barberan, Vanesa, Gauthier-Villars, Marion, Hogervorst, Frans B L, Gehrig, Andrea, Gerdes, Anne-Marie, Giraud, Sophie, Godwin, Andrew K, Goldgar, David E, Hake, Christopher R, Houdayer, Claude, Hulick, Peter J, Imyanitov, Evgeny N, Isaacs, Claudine, Izatt, Louise, Izquierdo, Angel, Pfeiler, Georg, Jacobs, Lauren, Jakubowska, Anna, Janavicius, Ramunas, Jaworska-Bieniek, Katarzyna, Jensen, Uffe Birk, John, Esther M, Vijai, Joseph, Karlan, Beth Y, Kast, Karin, Investigators, KConFab, Phelan, Catherine M, Khan, Sofia, Kwong, Ava, Laitman, Yael, Lester, Jenny, Lesueur, Fabienne, Liljegren, Annelie, Lubinski, Jan, Mai, Phuong L, Manoukian, Siranoush, Mazoyer, Sylvie, Piedmonte, Marion, Meindl, Alfons, Mensenkamp, Arjen R, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Ong, Kai-Ren, Poppe, Bruce, Osorio, Ana, Park, Sue Kyung, Paulsson-Karlsson, Ylva, Pedersen, Inge Sokilde, Peissel, Bernard, Peterlongo, Paolo, Pujana, Miquel Angel, Radice, Paolo, Rennert, Gad, Rodriguez, Gustavo C, Rookus, Matti A, Ross, Eric A, Bojesen, Anders, Schmutzler, Rita Katharina, Simard, Jacques, Singer, Christian F, Slavin, Thomas P, Soucy, Penny, Southey, Melissa, Steinemann, Doris, Stoppa-Lyonnet, Dominique, Sukiennicki, Grzegorz, Sutter, Christian, Bonanni, Bernardo, Szabo, Csilla I, Tea, Muy-Kheng, Teixeira, Manuel R, Teo, Soo-Hwang, Terry, Mary Beth, Thomassen, Mads, Tibiletti, Maria Grazia, Tihomirova, Laima, Tognazzo, Silvia, van Rensburg, Elizabeth J, Brewer, Carole, Varesco, Liliana, Varon-Mateeva, Raymonda, Vratimos, Athanassios, Weitzel, Jeffrey N, McGuffog, Lesley, Kirk, Judy, Toland, Amanda Ewart, Hamann, Ute, Lindor, Noralane, Ramus, Susan J

المساهمون: 1 Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom, 2 Department of Genetics, QIMR Berghofer Medical Research Institute, Herston Road, Brisbane, Australia, 4029, 3 Yorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, United Kingdom, 4 Department of Pathology, University Hospital (Landspitali) and University of Iceland School of Medicine, Hringbraut, 101 Reykjavik, Iceland, 5 Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada, 6 Department of Breast Medical Oncology and Clinical Cancer Genetics Program, University Of Texas MD Anderson Cancer Center, 1515 Pressler Street, CBP 5, Houston, TX, United States of America, 7 Bâtiment Cheney D, Centre Léon Bérard, 28 rue Laënnec, Lyon, France, 8 Service de Génétique Oncologique, Institut Curie, 26, rue d’Ulm, Paris Cedex 05, France, 9 Human Genetics Group, Spanish National Cancer Centre (CNIO), Madrid, Spain, and Human Genotyping (CEGEN) Unit, Human Cancer Genetics Program, Spanish National Cancer Research Centre (CNIO), Madrid, Spain, 10 Dept of OB/GYN, Medical University of Vienna, Vienna, Austria, 11 Department of Clinical Genetics, Vejle Hospital, Kabbeltoft 25, Vejle, Denmark, 12 Division of Cancer Prevention and Genetics, Istituto Europeo di Oncologia (IEO), via Ripamonti 435, 20141 Milan, Italy, 13 Department of Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, United Kingdom, 14 Molecular Oncology Laboratory, Hospital Clinico San Carlos, IdISSC (El Instituto de Investigación Sanitaria del Hospital Clínico San Carlos), Martin Lagos s/n, Madrid, Spain, 15 Section of Genetic Oncology, Dept. of Laboratory Medicine, University and University Hospital of Pisa, Pisa Italy, 16 Research Division, Peter MacCallum Cancer Centre, Locked Bag 1, A'Beckett Street, Melbourne, VIC 8006, Australia, 17 1600 Divisadero Street, C415, San Francisco, CA 94143–1714, United States of America, 18 Center for Medical Genetics, Ghent University, De Pintelaan 185, 9000 Gent, Belgium, 19 Ohio State University Columbus Cancer Council GYN Oncology, 3651 Ridge Mill Drive, Columbus, OH 43026, United States of America, 20 Sheffield Clinical Genetics Service, Sheffield Children’s Hospital, Sheffield, United Kingdom, 21 Department of Clinical Oncology, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, United States of America, 22 Department of Clinical Genetics, South Glasgow University Hospitals, Glasgow, United Kingdom, 23 Unité d'oncogénétique, ICO-Centre René Gauducheau, Boulevard Jacques Monod, 44805 Nantes Saint Herblain Cedex, France, 24 Oncogenetics Group, Vall d’Hebron University Hospital, Vall d’Hebron Institute of Oncology (VHIO), and Universitat Autònoma, Passeig Vall d'Hebron 119–129, Barcelona, Spain, 25 Department of Medicine, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, 3400 Civic Center Boulevard, Philadelphia, PA 19104, United States of America, 26 Genomics Center, Centre Hospitalier Universitaire de Québec Research Center and Laval University, 2705 Laurier Boulevard, Quebec City (Quebec), Canada, 27 Department of Genetics and Pathology, Pomeranian Medical University, Polabska 4, Szczecin, Poland, 28 Institute of Human Genetics, University of Münster, Münster, Germany, 29 University of Southampton Faculty of Medicine, Southampton University Hospitals NHS Trust, Southampton, United Kingdom, 30 Department of Radiation Sciences, Oncology, Umeå University, Umea, Sweden, 31 Oncogenetics Team, The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, Sutton, United Kingdom, 32 Department of Oncology, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen, Denmark, 33 Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Worts Causeway, Cambridge, United Kingdom, 34 Genomic Medicine, Manchester Academic Health Sciences Centre, Institute of Human Development, Manchester University, Central Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom, 35 Molecular Diagnostic Unit, Hereditary Cancer Program, IDIBELL (Bellvitge Biomedical Research Institute), Catalan Institute of Oncology, Gran Via de l'Hospitalet, 199–203, 08908 L'Hospitalet, Barcelona, Spain, 36 Molecular Diagnostics Laboratory, (INRASTES) Institute of Nuclear and Radiological Sciences and Technology, National Centre for Scientific Research "Demokritos", Patriarchou Gregoriou & Neapoleos str., Aghia Paraskevi, Attiki, Athens, Greece, 37 Program in Cancer Genetics, Departments of Human Genetics and Oncology, McGill University, Montreal, Quebec, Canada, 38 The Susanne Levy Gertner Oncogenetics Unit, Institute of Human Genetics, Chaim Sheba Medical Center, Ramat Gan 52621, and Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv 69978, Israel, 39 Clinical Cancer Genetics Laboratory, Memorial Sloane Kettering Cancer Center, New York, NY, United States of America, 40 UCLA Schools of Medicine and Public Health, Division of Cancer Prevention & Control Research, Jonsson Comprehensive Cancer Center, 650 Charles Young Drive South, Room A2-125 HS, Los Angeles, CA 90095–6900, United States of America, 41 Cancer Risk and Prevention Clinic, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA, United States of America, 42 Centre of Familial Breast and Ovarian Cancer, Department of Medical Genetics, Institute of Human Genetics, University Würzburg, Würzburg, Germany, 43 Department of Clinical Genetics, Rigshospitalet 4062, Blegdamsvej 9, København Ø, Denmark, 44 Service de Génétique Moléculaire et Clinique, Hospices Civils de Lyon, Lyon cedex 04, France, 45 Department of Pathology and Laboratory Medicine, 3901 Rainbow Boulevard, 4019 Wahl Hall East, MS 3040, University of Kansas Medical Center, Kansas City, Kansas, United States of America, 46 Department of Dermatology, University of Utah School of Medicine, 30 North 1900 East, SOM 4B454, Salt Lake City, UT 84132, United States of America, 47 City of Hope Clinical Cancer Genetics Community Research Network, 1500 East Duarte Road, Duarte, CA 91010, United States of America, 48 Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen, Denmark, 49 Medical Genetics Unit, St George's, University of London, London, United Kingdom, 50 Family Cancer Clinic, Netherlands Cancer Institute, P.O. Box 90203, 1000 BE, Amsterdam, The Netherlands, 51 Center for Medical Genetics, NorthShore University Health System, University of Chicago Pritzker School of Medicine, 1000 Central Street, Suite 620, Evanston, IL 60201, United States of America, 52 N.N. Petrov Institute of Oncology, St.- Petersburg 197758, Russia, 53 Lombardi Comprehensive Cancer Center, Georgetown University, 3800 Reservoir Road NW, Washington, DC, United States of America, 54 Clinical Genetics, Guy’s and St. Thomas’ NHS Foundation Trust, London, United Kingdom, 55 Genetic Counseling Unit, Hereditary Cancer Program, IDIBGI (Institut d'Investigació Biomèdica de Girona), Catalan Institute of Oncology, Av. França s/n. 1707 Girona, Spain, 56 Clinical Genetics Research Laboratory, Dept. of Medicine, Memorial

مصطلحات موضوعية: Eggjastokkar, Krabbamein, Arfgengi, PTT12, Ovarian Neoplasms, Risk, Genes, BRCA1, BRCA2, Chromosomes, Human, Pair 9/genetics, Germ-Line Mutation

العلاقة: http://dx.doi.org/10.1371/journal.pone.0158801Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963094Test/; Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers., 11 (7):e0158801 PLoS ONE; http://hdl.handle.net/2336/618811Test; PloS one

الإتاحة: https://doi.org/10.1371/journal.pone.0158801Test
http://hdl.handle.net/2336/618811Test

المؤلفون: Knijnenburg, Jeroen, Beverloo, H Berna

المساهمون: Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands

مصطلحات موضوعية: chromosome 9, chromosome 11, acute myeloid leukemia, KMT2A, MLLT3, Leukaemia Section, Adolescent, Adult, Age Factors, Health Planning Guidelines, Humans, International Cooperation, Leukemia, Myeloid, Acute/*diagnosis/etiology/*therapy, Middle Aged, Prognosis, Risk Factors, Young Adult, Child, Chromosome Mapping, Chromosomes, Human, Pair 11/*genetics, Pair 9/genetics, Disease-Free Survival, Gene Rearrangement, Histone-Lysine N-Methyltransferase, In Situ Hybridization, Fluorescence

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0911ID1001.htmlTest; Jeroen, Knijnenburg; H Berna, Beverloo. t(9;11)(p21;q23) KMT2A/MLLT3. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 12, p. 613-615; http://hdl.handle.net/2042/66949Test; https://doi.org/10.4267/2042/66949Test

الإتاحة: https://doi.org/10.4267/2042/66949Test
http://hdl.handle.net/2042/66949Test

المؤلفون: Springelkamp, Henriët, Höhn, René, Mishra, Aniket, Hysi, Pirro G, Khor, Chiea-Chuen, Loomis, Stephanie J, Bailey, Jessica N Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F, Luo, Xiaoyan, Ramdas, Wishal D, Vithana, Eranga, Nongpiur, Monisha E, Montgomery, Grant W, Xu, Liang, Mountain, Jenny E, Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C, Sim, Kar-Seng, van Leeuwen, Elisabeth M, Iglesias, Adriana I, Verhoeven, Virginie J M, Hauser, Michael A, Loon, Seng-Chee, Despriet, Dominiek D G, Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G, Schillert, Arne, Kang, Jae H, Landers, John, Jonasson, Fridbert, Cree, Angela J, van Koolwijk, Leonieke M E, Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N, de Jong, Paulus T V M, Oostra, Ben A, Uitterlinden, André G, Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P, Spector, Timothy D, Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R, Teo, Yik-Ying, Haines, Jonathan L, Wolfs, Roger C W, Lemij, Hans G, Tai, E-Shyong, Jansonius, Nomdo M, Jonas, Jost B, Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C, Klaver, Caroline C W, Craig, Jamie E, Macgregor, Stuart, Mackey, David A, Lotery, Andrew J, Stefansson, Kari, Bergen, Arthur A B, Young, Terri L, Wiggs, Janey L, Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R, Hewitt, Alex W, van Duijn, Cornelia M, Hammond, Christopher J

المساهمون: Department of Ophthalmology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands 2 Department of Epidemiology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands. 2Department of Ophthalmology, University Medical Center Mainz, Mainz 55131, Germany. 3Department of Genetics and Computational Biology, Statistical Genetics, QIMR Berghofer Medical Research Institute, Royal Brisbane Hospital, Brisbane, Queensland 4006, Australia. 4Department of Twin Research and Genetic Epidemiology, King's College London, London WC2R 2LS, UK. 51 Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119077, Singapore 2 Division of Human Genetics, Genome Institute of Singapore, Singapore 138672, Singapore. 6Department of Ophthalmology, Harvard Medical School and Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA. 71 Department of Molecular Physiology and Biophysics, Center for Human Genetics Research, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA 2 Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio 44106, USA. 8Centre for Biological Sciences, Faculty of Natural and Environmental Sciences, University of Southampton, Southampton SO17 1BJ, UK. 9deCODE/Amgen, Reykjavik 101, Iceland. 10Department of Clinical and Molecular Ophthalmogenetics, The Netherlands Institute for Neuroscience (NIN), Royal Netherlands Academy of Arts and Sciences (KNAW), Amsterdam 1105 BA, the Netherlands. 11Department of Ophthalmology, Duke University Eye Center, Durham, North Carolina 27710, USA. 12Department of Ophthalmology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands. 131 Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119077, Singapore 2 Singapore Eye Research Institute, Singapore National Eye Centre, Singapore 168751, Singapore 3 Duke-National University of Singapore, Graduate Medical School, Singapore 169857, Singapore. 141 Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119077, Singapore 2 Singapore Eye Research Institute, Singapore National Eye Centre, Singapore 168751, Singapore. 15Department of Genetics and Computational Biology, Molecular Epidemiology Laboratory, QIMR Berghofer Medical Research Institute, Royal Brisbane Hospital, Brisbane, Queensland 4006, Australia. 161 Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China 2 Beijing Ophthalmology and Visual Science Key Lab, Beijing 100730, China. 17Telethon Institute for Child Health Research, Subiaco, Western Australia 6008, Australia. 18Department of Epidemiology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands. 19Division of Human Genetics, Genome Institute of Singapore, Singapore 138672, Singapore. 20Departments of Medicine and Ophthalmology, Duke University Medical Center, Durham, North Carolina 27710, USA. 21Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119077, Singapore. 221 Department of Twin Research and Genetic Epidemiology, King's College London, London WC2R 2LS, UK 2 UCL Institute of Ophthalmology, London EC1V 9EL, UK. 23Centre for Eye Research Australia (CERA), University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Victoria 3002, Australia. 24Institute of Medical Biometry and Statistics, University of Lübeck, Lübeck 23562, Germany. 25Department of Medicine, Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA. 26Department of Ophthalmology, Flinders University, Adelaide, South Australia 5042, Australia. 271 Faculty of Medicine, University of Iceland, Reykjavik 101, Iceland 2 Department of Ophthalmology, Landspitali National University Hospital, Reykjavik 101, Iceland. 28Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK. 291 Department of Epidemiology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands 2 Department of Internal Medicine, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands 3 Netherlands Consortium for Healthy Ageing, Netherlands Genomics Initiative, The Hague 2593 CE, The Netherlands. 30Department of Ophthalmology, Landspitali National University Hospital, Reykjavik 101, Iceland. 31Department of Ophthalmology, Frimley Park Hospital NHS Foundation Trust, Frimley GU16 7UJ, UK. 32Department of Ophthalmology and Hamilton Glaucoma Center, University of California, San Diego, California 92093, USA. 331 Department of Epidemiology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands 2 Department of Retinal Signal Processing, Netherlands Institute for Neuroscience, Amsterdam 1105 BA, The Netherlands 3 Department of Ophthalmology, Academic Medical Center, Amsterdam 1105 AZ, The Netherlands 4 Department of Ophthalmology, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands. 34Department of Clinical Genetics, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands. 351 Department of Epidemiology, Erasmus Medical Center, Rotterdam 3000 CA, The Netherlands 2 Netherlands Consortium for Healthy Ageing, Netherlands Genomics Initiative, The Hague 2593 CE, The Netherlands. 36Human Development and Health, Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK. 371 deCODE/Amgen, Reykjavik 101, Iceland 2 Faculty of Medicine, University of Iceland, Reykjavik 101, Iceland. 381 Department of Ophthalmology, National University of Singapore and National University Health System, Singapore 119077, Singapore 2 Singapore Eye Research Institute, Singapore National Eye Centre, Singapore 168751, Singapore 3 Duke-National University of Singapore, Graduate Medical School, Singapore 169857, Singapore 4 Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore 117597, Singapore. 391 Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore 117597, Singapore 2 Department of Statistics and Applied Probability, National University of Singapore, Singapore 119077, Singapore. 40Glaucoma Service, The Rotterdam Eye Hospital, Rotterdam 3011 BH, The Netherlands. 411 Duke-National University of Singapore, Graduate Medical School, Singapore 169857, Singapore 2 Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore 117597, Singapore 3 Department of Medicine, National University of Singapore and National University Health System, Singapore 119077, Singapore. 42Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands. 431 Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China 2 Department of Ophthalmology, Medical Faculty Mannheim of the Ruprecht-Karls-University of Heidelberg, Seegartenklinik Heidelberg, Heidelberg 69117, Germany. 44NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London EC1V 2PD, UK. 451 Centre for Eye Research Australia (CERA), University of Melbourne, Royal Victorian Eye and Ear Hospital, Melbourne, Victoria 3002, Australia 2 Centre for Ophthalmology and Visual Science, Lions Eye Institute, University of Western Australia, Perth, Western Australia 6009, Australia. 461 Department of Clinical and Molecular Ophthalmogenetics, The Netherlands Institute for Neuroscience (NIN), Royal Netherlands Academy of Arts and Sciences (KNAW), Amsterdam 1105 BA, the Netherlands 2 Department of Ophthalmology, Academic Medical Center, Amsterdam 1105 AZ, The Netherlands 3 Department of Clinical Genetics, Academic Medical Center, Amsterdam 1105 AZ, The Netherlands. 471 Department of Ophthalmology, Harvard Medical School and Massachusetts Eye and Ear Infirmary, Boston, Massachusetts 02114, USA 2 Department of Medicine, Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

مصطلحات موضوعية: Blinda, Gláka, Erfðagreining, Arfgengi, Chromosomes, Human, Pair 14/genetics, Pair 9/genetics, Cyclin-Dependent Kinase Inhibitor p15/genetics, Glaucoma, Open-Angle/diagnosis, Open-Angle/genetics, Homeodomain Proteins, Optic Nerve Diseases/genetics

العلاقة: http://dx.doi.org/10.1038/ncomms5883Test; http://www.nature.com/ncomms/2014/140922/ncomms5883/pdf/ncomms5883.pdfTest; Nat Commun. 2014, 5:4883; http://hdl.handle.net/2336/331966Test; Nature communications

الإتاحة: https://doi.org/10.1038/ncomms5883Test
http://hdl.handle.net/2336/331966Test

المؤلفون: Nyholt, Dale, Low, Siew-Kee, Anderson, Carl, Painter, Jodie, Uno, Satoko, Morris, Andrew, Macgregor, Stuart, Gordon, Scott, Henders, Anjali, Martin, Nicholas, other, and

المصدر: Nature Genetics

مصطلحات موضوعية: Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Asian Continental Ancestry Group/genetics, Carrier Proteins/genetics, Chromosomes, Cohort Studies, Endometriosis/*genetics, European Continental Ancestry Group/genetics, Female, Human, Humans, Membrane Proteins/genetics, Neoplasm Proteins/genetics, Pair 1/genetics, Pair 2/genetics, Pair 6/genetics, Pair 7/genetics, Pair 9/genetics, Polymorphism, Risk, Severity of Illness Index, Single Nucleotide, Wnt4 Protein/genetics

وصف الملف: application/pdf

العلاقة: https://eprints.qut.edu.au/91839/1/emss-50444.pdfTest; Nyholt, Dale, Low, Siew-Kee, Anderson, Carl, Painter, Jodie, Uno, Satoko, Morris, Andrew, Macgregor, Stuart, Gordon, Scott, Henders, Anjali, Martin, Nicholas, & other, and (2012) Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44(12), pp. 1355-1359.; https://eprints.qut.edu.au/91839Test/; Faculty of Health; Institute of Health and Biomedical Innovation

الإتاحة: https://doi.org/10.1038/ng.2445Test
https://eprints.qut.edu.au/91839Test/

المساهمون: Sang-Guk Lee, Tae Sung Park, Gayoung Lim, Kyung-A Lee, Jaewoo Song, Jong Rak Choi, Song, Jae Woo, Lee, Kyung A, Choi, Jong Rak

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Child, Preschool, Chromosome Inversion, Chromosomes, Human, Pair 9/genetics, Female, Hematologic Diseases/diagnosis, Hematologic Diseases/genetics, Hematologic Diseases/therapy, Hematopoietic Stem Cell Transplantation, Humans, Infant, Korea, Male, Middle Aged, Retrospective Studies, Time Factors, Young Adult

العلاقة: ANNALS OF CLINICAL AND LABORATORY SCIENCE; J00155; OAK-2010-01583; https://ir.ymlib.yonsei.ac.kr/handle/22282913/101983Test; http://www.annclinlabsci.org/content/40/3/273.longTest; T201003123; ANNALS OF CLINICAL AND LABORATORY SCIENCE, Vol.40(3) : 273-277, 2010

الإتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/101983Test
http://www.annclinlabsci.org/content/40/3/273.longTest

المساهمون: Sang-Guk Lee, Jong Rak Choi, Jin Seok Kim, Tae Sung Park, Kyung-A Lee, Jaewoo Song, Kim, Jin Seok, Park, Tae Sung, Song, Jae Woo, Lee, Kyung A, Choi, Jong Rak

مصطلحات موضوعية: Biopsy, Fine-Needle, Bone Marrow/pathology, Chromosomes, Human, Pair 22/genetics, Pair 9/genetics, Female, Humans, Karyotyping, Middle Aged, Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy, Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics, Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology, Translocation, Genetic

العلاقة: CANCER GENETICS AND CYTOGENETICS; J00443; OAK-2009-00366; https://ir.ymlib.yonsei.ac.kr/handle/22282913/103706Test; http://www.sciencedirect.com/science/article/pii/S0165460809000843Test; T200900951; CANCER GENETICS AND CYTOGENETICS , Vol.191(1) : 51-54, 2009; 36639

الإتاحة: https://doi.org/10.1016/j.cancergencyto.2009.02.002Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/103706Test
http://www.sciencedirect.com/science/article/pii/S0165460809000843Test