المؤلفون: Viswanathan, Srinivas R, Nogueira, Marina F, Buss, Colin G, Krill-Burger, John M, Wawer, Mathias J, Malolepsza, Edyta, Berger, Ashton C, Choi, Peter S, Shih, Juliann, Taylor, Alison M, Tanenbaum, Benjamin, Pedamallu, Chandra Sekhar, Cherniack, Andrew D, Tamayo, Pablo, Strathdee, Craig A, Lage, Kasper, Carr, Steven A, Schenone, Monica, Bhatia, Sangeeta N, Vazquez, Francisca, Tsherniak, Aviad, Hahn, William C, Meyerson, Matthew

المصدر: Nature genetics. 50(7)

مصطلحات موضوعية: Cell Line, Tumor, Chromosomes, Human, Pair 1, Cell Nucleus, Animals, Humans, Mice, Mice, Nude, Neoplasms, Karyopherins, Nuclear Proteins, RNA, Small Interfering, RNA Splicing, Gene Deletion, Exons, Female, HEK293 Cells, Cell Line, Tumor, Chromosomes, Human, Pair 1, Nude, RNA, Small Interfering, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4wx8p79gTest

المؤلفون: Houlston, Richard S, Cheadle, Jeremy, Dobbins, Sara E, Tenesa, Albert, Jones, Angela M, Howarth, Kimberley, Spain, Sarah L, Broderick, Peter, Domingo, Enric, Farrington, Susan, Prendergast, James GD, Pittman, Alan M, Theodoratou, Evi, Smith, Christopher G, Olver, Bianca, Walther, Axel, Barnetson, Rebecca A, Churchman, Michael, Jaeger, Emma EM, Penegar, Steven, Barclay, Ella, Martin, Lynn, Gorman, Maggie, Mager, Rachel, Johnstone, Elaine, Midgley, Rachel, Niittymäki, Iina, Tuupanen, Sari, Colley, James, Idziaszczyk, Shelley, COGENT Consortium, Thomas, Huw JW, Lucassen, Anneke M, Evans, D Gareth R, Maher, Eamonn R, CORGI Consortium, COIN Collaborative Group, COINB Collaborative Group, Maughan, Timothy, Dimas, Antigone, Dermitzakis, Emmanouil, Cazier, Jean-Baptiste, Aaltonen, Lauri A, Pharoah, Paul, Kerr, David J, Carvajal-Carmona, Luis G, Campbell, Harry, Dunlop, Malcolm G, Tomlinson, Ian PM

المصدر: Nature genetics. 42(11)

مصطلحات موضوعية: COGENT Consortium, CORGI Consortium, COIN Collaborative Group, COINB Collaborative Group, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 3, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 13, Humans, Colorectal Neoplasms, Genetic Predisposition to Disease, Oligonucleotide Array Sequence Analysis, Odds Ratio, Risk Assessment, Chromosome Mapping, Genotype, Polymorphism, Single Nucleotide, Female, Male, Meta-Analysis as Topic, Genome-Wide Association Study, Chromosomes, Human, Pair 1, Pair 3, Pair 12, Pair 13, Polymorphism, Single Nucleotide, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7r09g9scTest

المؤلفون: Silverberg, Mark S, Cho, Judy H, Rioux, John D, McGovern, Dermot PB, Wu, Jing, Annese, Vito, Achkar, Jean-Paul, Goyette, Philippe, Scott, Regan, Xu, Wei, Barmada, M Michael, Klei, Lambertus, Daly, Mark J, Abraham, Clara, Bayless, Theodore M, Bossa, Fabrizio, Griffiths, Anne M, Ippoliti, Andrew F, Lahaie, Raymond G, Latiano, Anna, Paré, Pierre, Proctor, Deborah D, Regueiro, Miguel D, Steinhart, A Hillary, Targan, Stephan R, Schumm, L Philip, Kistner, Emily O, Lee, Annette T, Gregersen, Peter K, Rotter, Jerome I, Brant, Steven R, Taylor, Kent D, Roeder, Kathryn, Duerr, Richard H

المصدر: Nature genetics. 41(2)

مصطلحات موضوعية: Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 6, Chromosomes, Human, Pair 12, Humans, Colitis, Ulcerative, Genetic Predisposition to Disease, Membrane Glycoproteins, Receptors, Interleukin, HLA-DQ Antigens, Risk Factors, Case-Control Studies, Recombination, Genetic, Genotype, Polymorphism, Single Nucleotide, Female, Male, Genome-Wide Association Study, HLA-DQ beta-Chains, Butyrophilins, Chromosomes, Human, Pair 1, Pair 6, Pair 12, Colitis, Ulcerative, Receptors, Interleukin, Recombination, Genetic, Polymorphism, Single Nucleotide, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2bc3d9f0Test

المؤلفون: Petersen, Gloria M, Amundadottir, Laufey, Fuchs, Charles S, Kraft, Peter, Stolzenberg-Solomon, Rachael Z, Jacobs, Kevin B, Arslan, Alan A, Bueno-de-Mesquita, H Bas, Gallinger, Steven, Gross, Myron, Helzlsouer, Kathy, Holly, Elizabeth A, Jacobs, Eric J, Klein, Alison P, LaCroix, Andrea, Li, Donghui, Mandelson, Margaret T, Olson, Sara H, Risch, Harvey A, Zheng, Wei, Albanes, Demetrius, Bamlet, William R, Berg, Christine D, Boutron-Ruault, Marie-Christine, Buring, Julie E, Bracci, Paige M, Canzian, Federico, Clipp, Sandra, Cotterchio, Michelle, de Andrade, Mariza, Duell, Eric J, Gaziano, J Michael, Giovannucci, Edward L, Goggins, Michael, Hallmans, Göran, Hankinson, Susan E, Hassan, Manal, Howard, Barbara, Hunter, David J, Hutchinson, Amy, Jenab, Mazda, Kaaks, Rudolf, Kooperberg, Charles, Krogh, Vittorio, Kurtz, Robert C, Lynch, Shannon M, McWilliams, Robert R, Mendelsohn, Julie B, Michaud, Dominique S, Parikh, Hemang, Patel, Alpa V, Peeters, Petra HM, Rajkovic, Aleksandar, Riboli, Elio, Rodriguez, Laudina, Seminara, Daniela, Shu, Xiao-Ou, Thomas, Gilles, Tjønneland, Anne, Tobias, Geoffrey S, Trichopoulos, Dimitrios, Van Den Eeden, Stephen K, Virtamo, Jarmo, Wactawski-Wende, Jean, Wang, Zhaoming, Wolpin, Brian M, Yu, Herbert, Yu, Kai, Zeleniuch-Jacquotte, Anne, Fraumeni, Joseph F, Hoover, Robert N, Hartge, Patricia, Chanock, Stephen J

المصدر: Nature genetics. 42(3)

مصطلحات موضوعية: Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 5, Chromosomes, Human, Pair 13, Humans, Carcinoma, Pancreatic Neoplasms, Genetic Predisposition to Disease, Case-Control Studies, Cohort Studies, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Genome-Wide Association Study, Genetic Loci, Rare Diseases, Cancer, Genetics, Clinical Research, Pancreatic Cancer, Digestive Diseases, Human Genome, Biological Sciences, Medical and Health Sciences, Developmental Biology

الوصول الحر: https://escholarship.org/uc/item/3w13h0v1Test

المؤلفون: Matthew Meyerson, Sangeeta N. Bhatia, Craig A. Strathdee, Andrew D. Cherniack, John M. Krill-Burger, Ashton C. Berger, Juliann Shih, Mathias Wawer, Alison M. Taylor, Monica Schenone, Francisca Vazquez, Colin G. Buss, Steven A. Carr, Srinivas R. Viswanathan, Edyta Malolepsza, Marina F. Nogueira, Peter S. Choi, Benjamin Tanenbaum, William C. Hahn, Pablo Tamayo, Aviad Tsherniak, Chandra Sekhar Pedamallu, Kasper Lage

المساهمون: Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science, Koch Institute for Integrative Cancer Research at MIT

المصدر: Nature genetics
Nature genetics, vol 50, iss 7
PMC

مصطلحات موضوعية: 0301 basic medicine, Nude, Medical and Health Sciences, Small hairpin RNA, Mice, RNA interference, Neoplasms, 2.1 Biological and endogenous factors, CRISPR, Aetiology, RNA, Small Interfering, Lung, Cancer, Genetics, Tumor, Lung Cancer, Nuclear Proteins, Exons, Biological Sciences, Chromosomes, Human, Pair 1, Pair 1, Female, Biotechnology, Human, Pediatric Research Initiative, RNA Splicing, Mice, Nude, Context (language use), Biology, Karyopherins, Small Interfering, Chromosomes, Article, Cell Line, 03 medical and health sciences, Cell Line, Tumor, Animals, Humans, Gene, Cell Nucleus, Human Genome, Alternative splicing, RNA, 030104 developmental biology, HEK293 Cells, Exon junction complex, Gene Deletion, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555d43b594ed062f8833e6321b658443Test
http://europepmc.org/articles/PMC6143899Test

المؤلفون: Qingfeng Cao, Meilin Wang, Hong Li, Chaokui Wang, Liang Liang, Liping Du, Yan Zhou, Ke Hu, Lulin Huang, Meifen Zhang, Jian Qi, Bo Lei, Peizeng Yang, Chi Pui Pang, Wenjuan Zhuang, Jianfeng Xu, Dan Liao, Zhenglin Yang, Hongsong Yu, Aize Kijlstra, Minglian Zhang, Lin Bai, Zi Ye, Qi Zhang, Qingyun Zhou, Shengping Hou, Yuan Tian, Bo Gong, Yunjia Liu

المساهمون: Promovendi MHN, RS: MHeNs - R3 - Neuroscience, Oogheelkunde

المصدر: Nature Genetics, 46(9), 1007-1011. Nature Publishing Group

مصطلحات موضوعية: Adult, musculoskeletal diseases, Genotype, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Ciliary body, Asian People, Polymorphism (computer science), Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Promoter Regions, Genetic, Gene, Aged, Chromosomes, Human, Pair 10, Odds ratio, Middle Aged, eye diseases, medicine.anatomical_structure, Chromosomes, Human, Pair 1, Genetic Loci, Case-Control Studies, Female, Choroid, Uveomeningoencephalitic Syndrome, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3b9ffa611677c3d3c44a5d6688f6d38Test
https://doi.org/10.1038/ng.3061Test

المؤلفون: Siew-Kee Low, Wei Lu, Min Ho Park, Yoshio Kasuga, Jiemin Liao, Sei Hyun Ahn, Ji Yeob Choi, Hyuna Sung, Michiaki Kubo, Bingshan Li, Kyota Ashikawa, Yanfeng Zhang, Hidemi Ito, Koichi Matsuda, Chen-Yang Shen, Ryan J. Delahanty, Bu Tian Ji, Yu-Tang Gao, Han Sung Kang, Yusuke Nakamura, Motoki Iwasaki, Hiroji Iwata, Chia-Ni Hsiung, Mi Kyung Kim, Ying Zheng, Ellen P S Man, Daehee Kang, Ui-Soon Khoo, Soo Hwang Teo, Xiao-Ou Shu, Yong-Bing Xiang, Wanqing Wen, Jiajun Shi, Wei Zheng, Chun Li, Shoichiro Tsugane, Keitaro Matsuo, Hui Miao, Peter B. Kang, Pei-Ei Wu, Qiuyin Cai, Sue K. Park, Kelvin Y.K. Chan, Dong-Young Noh, Jirong Long, Shivaani Mariapun, Ben Zhang, Sun-Seog Kweon, Atsushi Takahashi, Mikael Hartman, Min-Ho Shin

المصدر: Nature genetics

مصطلحات موضوعية: Adult, Risk, Breast Neoplasms, Genome-wide association study, Biology, White People, Article, Breast cancer, Asian People, Genetics, medicine, Genome-Wide Association Analysis, Humans, Genetic Predisposition to Disease, skin and connective tissue diseases, Genetic association, Chromosomes, Human, Pair 15, Asia, Eastern, Case-control study, Middle Aged, medicine.disease, 3. Good health, Chromosomes, Human, Pair 1, Genetic Loci, Case-Control Studies, Susceptibility locus, Chromosomes, Human, Pair 5, Female, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41690ee65f134c0e9e1d14d3713395acTest
https://doi.org/10.1038/ng.3041Test

المؤلفون: Michael L. Frigge, Margret Thorsteinsdottir, André G. Uitterlinden, Helgi Jonsson, Unnur Styrkarsdottir, Gisli Masson, Olafur T. Magnusson, Nigel K Arden, P. Eline Slagboom, Hafdis T. Helgadottir, Margreet Kloppenburg, Rob G H H Nelissen, Tim D. Spector, Joyce B. J. van Meurs, Augustine Kong, Annelieke M Strijbosch, S.M.A. Bierma-Zeinstra, Ingrid Meulenbelt, Fernando Rivadeneira, Nils Bomer, Ana M. Valdes, Aslaug Jonasdottir, Deborah J. Hart, Ingileif Jonsdottir, Stefan Lohmander, Sigurjon A. Gudjonsson, Sarah Metrustry, Gudmar Thorleifsson, Finnur F. Eiriksson, Marian Beekman, Thorvaldur Ingvarsson, Unnur Thorsteinsdottir, Asgeir Sigurdsson, Evangelos Evangelou, Kari Stefansson, Albert Hofman

المساهمون: General Practice, Clinical Genetics, Epidemiology, Internal Medicine, [ 1 ] deCODE Genet Amgen, Reykjavik, Iceland [ 2 ] Leiden Univ, Med Ctr, Dept Mol Epidemiol, Leiden, Netherlands [ 3 ] Kings Coll London, St Thomas Hosp, Dept Twin Res, London, England [ 4 ] Erasmus MC, Dept Internal Med, Rotterdam, Netherlands [ 5 ] Univ Ioannina, Sch Med, Dept Hyg & Epidemiol, GR-45110 Ioannina, Greece [ 6 ] Univ London Imperial Coll Sci Technol & Med, Dept Epidemiol & Biostat, London, England [ 7 ] Integrated Res Dev Determinants Ageing & Longev I, Leiden, Netherlands [ 8 ] Netherlands Consortium Hlth Ageing, Leiden, Netherlands [ 9 ] Arctic Mass, Reykjavik, Iceland [ 10 ] Univ Iceland, Fac Med, Reykjavik, Iceland [ 11 ] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands [ 12 ] Univ Oxford, Biomed Res Unit, NIHR, Oxford, England [ 13 ] Akureyri Hosp, Dept Orthoped Surg, Akureyri, Iceland [ 14 ] Univ Akureyri, Inst Hlth Sci, Akureyri, Iceland [ 15 ] Lund Univ, Dept Orthoped, Lund, Sweden [ 16 ] Leiden Univ, Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands [ 17 ] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands [ 18 ] Leiden Univ, Med Ctr, Dept Orthopaed, Leiden, Netherlands [ 19 ] Univ Nottingham, City Hosp Nottingham, Acad Rheumatol, Nottingham NG7 2RD, England [ 20 ] Natl Univ Hosp Iceland, Dept Med, Reykjavik, Iceland

المصدر: Nature Genetics; Vol 46
Nature Genetics, 46(5), 498-502. Nature Publishing Group
Nature Genetics, 46(5), 498-502
Styrkarsdottir, U, Thorleifsson, G, Helgadottir, H T, Bomer, N, Metrustry, S, Bierma-Zeinstra, S, Strijbosch, A M, Evangelou, E, Hart, D, Beekman, M, Jonasdottir, A, Sigurdsson, A, Eiriksson, F F, Thorsteinsdottir, M, Frigge, M L, Kong, A, Gudjonsson, S A, Magnusson, O T, Masson, G, Hofman, A, Arden, N K, Ingvarsson, T, Lohmander, S, Kloppenburg, M, Rivadeneira, F, Nelissen, R G H H, Spector, T, Uitterlinden, A, Slagboom, P E, Thorsteinsdottir, U, Jonsdottir, I, Valdes, A M, Meulenbelt, I, van Meurs, J, Jonsson, H, Stefansson, K & TREAT-OA Consortium 2014, ' Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 ', Nature Genetics, vol. 46, no. 5, pp. 498-502 . https://doi.org/10.1038/ng.2957Test
Nature Genetics; 46(5), pp 498-502 (2014)

مصطلحات موضوعية: Genotype, Molecular Sequence Data, Iceland, Arthritis, Genome-wide association study, Osteoarthritis, Biology, Bioinformatics, Aldehyde Dehydrogenase 1 Family, 03 medical and health sciences, 0302 clinical medicine, Genetic variation, Genetics, medicine, Humans, Genetic Predisposition to Disease, Gene, Genetic Association Studies, 030304 developmental biology, Netherlands, 030203 arthritis & rheumatology, 0303 health sciences, Base Sequence, Gene Expression Profiling, Great Britain, Computational Biology, Genetic Variation, Retinal Dehydrogenase, Odds ratio, Sequence Analysis, DNA, medicine.disease, Hand, United Kingdom, 3. Good health, Gene expression profiling, Orthopedics, Cartilage, Chromosomes, Human, Pair 1

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6445dd09e6f275465cdea5025e570145Test

المؤلفون: Hsin Chi, Nagib Dahdah, Paul Mitchell, J Ottenkamp, Luan-Yin Chang, Min Seob Song, Adriana H. Tremoulet, Fu Yuan Huang, Kar Seng Sim, Jer-Yuarn Wu, Xiao Jing Ma, Kwi Joo Kim, Kao Pin Huang, Pamela Palasanthiran, Gi Young Jang, Stanford T. Shulman, Young Mi Hong, Rolando Cimaz, Maarten H Biezeveld, Frank T. Christiansen, Yu-Lung Lau, Jie Jin Wang, Luc Filippini, Judy Geissler, Myung Ki Han, Robert Booy, Paul A. Brogan, Chi Di Liang, Betau Hwang, Jane W. Newburger, Miranda Odam, Ho-Chang Kuo, Ming-Ren Chen, Yhu Chering Huang, Hyoung Doo Lee, Elena Rochtchina, Jae-Jung Kim, Wilbert H. Mason, Clare Nourse, Hyo Kyoung Nam, John Attia, Taco W. Kuijpers, Jung Hye Byeon, Vanita Shah, Li-Min Huang, Ananth C. Viswanathan, Willemijn B. Breunis, Jeng Sheng Chang, Junxiong Pang, Sin Weon Yun, Kee Soo Ha, Elizabeth G. Holliday, Tien Yin Wong, David Burgner, Dong Soo Kim, Colin Michie, Rodney J. Scott, Michael Levin, Ja Young Hwang, Stephen B. Harrap, Paul N. Goldwater, Delane Shingadia, Jane C. Burns, Meng Luen Lee, Michael D. Nissen, Anu Bose, Jae Moo Lee, Sejung Sohn, Martin L. Hibberd, Jung Woo Rhim, Nigel Klein, Marian E. Melish, Young-Mi Park, Kyung-Yil Lee, In Sook Park, Irene M. Kuipers, Yi-Ching Lee, Guo Ying Huang, Thomas Mukasa, Nan Chang Chiu, Jing Zhang, Fuu Jen Tsai, Chiea Chuen Khor, Jeong Jin Yoo, Yiu-fai Cheung, Pi Chang Lee, Rae S. M. Yeung, Chisato Shimizu, Sonia Davila, Annette L. Baker, Nigel Curtis, Soo-Jong Hong, M J Dillon, Lin Wu, Carline E. Tacke, Jong-Keuk Lee, John B. Ziegler, Masato Takahashi, Robert Tulloh, Fang Liu, Victoria J. Wright, Wanling Yang, Dennis E.K. Tan, Anne H. Rowley, Campbell S. Witt

المساهمون: AII - Amsterdam institute for Infection and Immunity, General Paediatrics, Paediatric Infectious Diseases / Rheumatology / Immunology, ACS - Amsterdam Cardiovascular Sciences, Paediatric Cardiology, Other departments

المصدر: Nature genetics, 43(12), 1241-1246. Nature Publishing Group

مصطلحات موضوعية: Linkage disequilibrium, Population, Locus (genetics), Genome-wide association study, Mucocutaneous Lymph Node Syndrome, FCGR2A, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Pathogenesis, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, education, Principal Component Analysis, education.field_of_study, Receptors, IgG, medicine.disease, Haplotypes, Chromosomes, Human, Pair 1, Genetic Loci, Case-Control Studies, Multigene Family, Immunology, Kawasaki disease, Chromosomes, Human, Pair 19, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88bfcca57c8e49bc234b5370873a567fTest
https://doi.org/10.1038/ng.981Test

المؤلفون: Weidong Ji, Ping Yang, Wenjin Li, Tao Li, Markus M. Nöthen, Guoquan Zhou, Sven Cichon, Peng Wang, Zhiqiang Li, Kari Stefansson, Lin He, Jue Ji, Sarah Tosato, Engilbert Sigurdsson, Ti Wang, Baojie Li, David A. Collier, David St Clair, Yongyong Shi, Yifeng Xu, Marcella Rietschel, Aarno Palotie, Shengying Qin, Hreinn Stefansson, Roel A. Ophoff, Hairong Zhang, Linqing Zheng, Guoyin Feng, Thomas Werge, Jiawei Shen, Chunling Wan, Benxiu Liu, Stacy Steinberg, Dan Rujescu, Wensheng Sun, Guang He, Fengyu Zhang, Qi Xu, Dengtang Liu, Jianhua Chen, Qingzhong Wang

المصدر: Nature Genetics
Nature genetics 43(12), 1224-1227 (2011). doi:10.1038/ng.980
Nature Genetics; Vol 43

مصطلحات موضوعية: Adult, Asian Continental Ancestry Group, Male, medicine.medical_specialty, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, Young Adult, "genome-wide association study", 03 medical and health sciences, 0302 clinical medicine, Asian People, Risk Factors, Polymorphism (computer science), ddc:570, Internal medicine, Genetics, medicine, Humans, genetics [Schizophrenia], "schizophrenia", Young adult, Aged, 030304 developmental biology, Principal Component Analysis, 0303 health sciences, "BRP44", Case-control study, Middle Aged, Heritability, medicine.disease, 3. Good health, Chromosomes, Human, Pair 1, Genetic Loci, Schizophrenia, Case-Control Studies, Cohort, Female, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 8, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757e547735ad02a7551dd07c8e7864d6Test
https://doi.org/10.1038/ng.980Test