نتائج البحث - "Suzannah Bumpstead"

المساهمون: Pregnancy and Genes, Department of Medical and Clinical Genetics, University of Helsinki, Helsinki University Hospital Area, Research Programs Unit, CAMM - Research Program for Clinical and Molecular Metabolism, Genomics of Neurological and Neuropsychiatric Disorders, Institute for Molecular Medicine Finland, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, HUS Children and Adolescents, Lastentautien yksikkö, Clinicum, Children's Hospital, STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Tampere University, Department of Gynaecology and Obstetrics, Clinical Medicine, University of Helsinki, Research Programs Unit, University of Helsinki, Genomics of Neurological and Neuropsychiatric Disorders, University of Helsinki, HUS Gynecology and Obstetrics, University of Helsinki, HUS Children and Adolescents, University of Helsinki, STEMM - Stem Cells and Metabolism Research Program, Steinthorsdottir, Valgerdur [0000-0003-1846-6274], McGinnis, Ralph [0000-0003-4540-9857], Williams, Nicholas O [0000-0003-3989-9167], Berezina, Galina [0000-0002-5442-4461], Bybjerg-Grauholm, Jonas [0000-0003-1705-4008], Dudbridge, Frank [0000-0002-8817-8908], Franklin, Christopher S [0000-0003-3893-0759], Geller, Frank [0000-0002-9238-3269], Gudbjartsson, Daniel F [0000-0002-5222-9857], Hougaard, David Michael [0000-0001-5928-3517], Helgadottir, Anna [0000-0002-1806-2467], Jääskeläinen, Tiina [0000-0002-1202-0936], Jonsdottir, Ingileif [0000-0001-8339-150X], Kemp, John P [0000-0002-9105-2249], Kivinen, Katja [0000-0002-1135-7625], Melbye, Mads [0000-0001-8264-6785], Moffett, Ashley [0000-0002-8388-9073], Pipkin, Fiona Broughton [0000-0002-6209-5987], Prescott, Gordon [0000-0002-9156-2361], Saevarsdottir, Saedis [0000-0001-9392-6184], Skotte, Line [0000-0002-7398-1271], Stefansson, Olafur A [0000-0002-9663-3018], Simpson, Nigel AB [0000-0002-0758-7583], Dominiczak, Anna F [0000-0003-4913-3608], Walker, James J [0000-0002-8922-083X], Iversen, Ann-Charlotte [0000-0001-7726-7684], Feenstra, Bjarke [0000-0003-1478-649X], Lawlor, Deborah A [0000-0002-6793-2262], Boyd, Heather Allison [0000-0001-6849-9985], Laivuori, Hannele [0000-0003-3212-7826], Svyatova, Gulnara [0000-0001-5092-3143], Stefansson, Kari [0000-0003-1676-864X], Morgan, Linda [0000-0002-2995-4081], Apollo - University of Cambridge Repository

المصدر: Nature Communications
Steinthorsdottir, V, McGinnis, R, Williams, N O, Stefansdottir, L, Thorleifsson, G, Shooter, S, Fadista, J, Sigurdsson, J K, Auro, K M, Berezina, G, Borges, M C, Bumpstead, S, Bybjerg-Grauholm, J, Colgiu, I, Dolby, V A, Dudbridge, F, Engel, S M, Franklin, C S, Frigge, M L, Frisbaek, Y, Geirsson, R T, Geller, F, Gretarsdottir, S, Gudbjartsson, D F, Harmon, Q, Hougaard, D M, Hegay, T, Helgadottir, A, Hjartardottir, S, Jääskeläinen, T, Johannsdottir, H, Jonsdottir, I, Juliusdottir, T, Kalsheker, N, Kasimov, A, Kemp, J P, Kivinen, K, Klungsøyr, K, Lee, W K, Melbye, M, Miedzybrodska, Z, Moffett, A, Najmutdinova, D, Nishanova, F, Olafsdottir, T, Perola, M, Pipkin, F B, Skotte, L, Sørensen, K M, Kere, J, FINNPEC Consortium & GOPEC Consortium 2020, ' Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women ', Nature Communications, vol. 11, no. 1, 5976 . https://doi.org/10.1038/s41467-020-19733-6
et al. 2020, ' Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women ', Nature Communications, vol. 11, 5976 (2020) . https://doi.org/10.1038/s41467-020-19733-6
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
2020, ' Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women ', Nature Communications, vol. 11, no. 1, 5976 . https://doi.org/10.1038/s41467-020-19733-6

مصطلحات موضوعية: 0301 basic medicine, Gestational hypertension, Multifactorial Inheritance, Reproductive disorders, A990, Datasets as Topic, General Physics and Astronomy, Blood Pressure, Genome-wide association study, VARIANTS, Genome-wide association studies, 0302 clinical medicine, Pre-Eclampsia, 3123 Gynaecology and paediatrics, Medicine, Prospective Studies, 030212 general & internal medicine, reproductive and urinary physiology, 2. Zero hunger, RISK, Multidisciplinary, biology, Obstetrics, Middle Aged, MEDICAL BIRTH REGISTRY, female genital diseases and pregnancy complications, 3. Good health, Europe, PREGNANCY, CARDIOVASCULAR-DISEASE, Hypertension, embryonic structures, Asia, Central, Female, Adult, medicine.medical_specialty, Fibroblast Growth Factor 5, Science, Alpha-Ketoglutarate-Dependent Dioxygenase FTO, Article, General Biochemistry, Genetics and Molecular Biology, Preeclampsia, 03 medical and health sciences, Fibroblast growth factor-5, Genetic predisposition, Humans, Genetic Predisposition to Disease, GENOME-WIDE ASSOCIATION, FETAL, METAANALYSIS, Adaptor Proteins, Signal Transducing, Aged, Pregnancy, business.industry, Case-control study, Hypertension, Pregnancy-Induced, General Chemistry, medicine.disease, MDS1 and EVI1 Complex Locus Protein, BODY-MASS INDEX, 030104 developmental biology, Genetic Loci, Case-Control Studies, COHORT PROFILE, biology.gene, business, Body mass index, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5c6a59b93fb4d8ac17970c34bafb35f
https://hdl.handle.net/11250/2754126

7

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

المؤلفون: Nicholas G. Martin, René Höhn, Paul Mitchell, Gavin Band, Pamela Whittaker, Michelle Ricketts, Pirro G. Hysi, Jenefer M. Blackwell, Grant W. Montgomery, Elena Rochtchina, Manfred E. Beutel, Richard A. Mills, Anna Rautanen, Alagurevathi Jayakumar, Colin Freeman, Stephen Sawcer, Stuart MacGregor, Irene Schmidtmann, Cornelia M. van Duijn, Nicholas W. Wood, Sayoko E. Moroi, Jonathan L. Haines, Aniket Mishra, Ananth C. Viswanathan, Jie Jin Wang, Donald L. Budenz, Seyhan Yazar, Janey L. Wiggs, Garrett Hellenthal, Kathryn P. Burdon, Jerome I. Rotter, Jamie E Craig, Puya Gharahkhani, Juan P. Casas, R. Rand Allingham, Jost B. Jonas, Ozren Polasek, Julia E. Richards, Sarah Edkins, Rodney J. Scott, Abhishek Nag, Tanja Zeller, Rhian Gwilliam, Chris C. A. Spencer, David S. Friedman, Adriana I Iglesias, Radhi Ravindrarajah, Kent D. Taylor, Caroline Hayward, Eleni Giannoulatou, David A. Mackey, Michael A. Hauser, Paul J. Foster, Emma Gray, Audrey Duncanson, Yih Chung Tham, Murray H. Brilliant, Ching-Yu Cheng, William K. Scott, Robert N. Weinreb, Hugh S. Markus, Xueling Sim, David S. Siscovick, Matti Pirinen, John H. Fingert, Yelena Bykhovskaya, Louis R. Pasquale, Peter Donnelly, Donald J. Zack, Kuldev Singh, Cordelia Langford, Zhan Su, Céline Bellenguez, Joel S. Schuman, Peter Kraft, Christopher G. Mathew, Hannah Blackburn, Sara Widaa, Yuan Shi, Gabriel Cuellar-Partida, André G. Uitterlinden, Naomi Hammond, Panos Deloukas, Richard K. Lee, Robert Plomin, Jessica N. Cooke Bailey, Jae H. Kang, John Attia, Yutao Liu, Simon C. Potter, Jennifer Liddle, Matthew Gillman, Alex W. Hewitt, Margaret A. Pericak-Vance, James F. Wilson, Tien Yin Wong, Elvira Bramon, Janusz Jankowski, Henriët Springelkamp, Sarah E. Hunt, Anthony P Khawaja, Veronique Vitart, Xiaohui Li, Pieter W.M. Bonnemaijer, Damjan Vukcevic, Paul R. Lichter, Aiden Corvin, Sionne E. M. Lucas, Matthew Waller, Caroline C W Klaver, Douglas E. Gaasterland, Terry Gaasterland, Norbert Pfeiffer, Douglas Vollrath, Anthony Realini, Eranga N. Vithana, Gadi Wollstein, Thibaud Boutin, Owen T. McCann, Paul A. Weston, Lisa S. Kearns, Inês Barroso, Richard G. Pearson, Christopher J Hammond, Colin N. A. Palmer, Michael Inouye, Chiea Chuen Khor, Stephanie Loomis, Sandra E Staffieri, Yaron S. Rabinowitz, Richard C. Trembath, Tin Aung, William G. Christen, Paul N. Baird, Jing Xie, Elisabeth M. van Leeuwen, Serge Dronov, Arthur J. Sit, Colin E. Willoughby, Kang Zhang, Matthew A. Brown, Suzannah Bumpstead, Amy Strange, Elizabeth G. Holliday

المساهمون: Clinical Genetics, Epidemiology, Ophthalmology, Internal Medicine, Experimental Immunology, Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Iglesias, Adriana I [0000-0001-5532-764X], Gharahkhani, Puya [0000-0002-4203-5952], Bailey, Jessica N Cooke [0000-0002-4001-8702], Li, Xiaohui [0000-0002-5037-3572], Khawaja, Anthony P [0000-0001-6802-8585], Haines, Jonathan L [0000-0002-4351-4728], Hayward, Caroline [0000-0002-9405-9550], Bonnemaijer, Pieter [0000-0001-5154-6765], Staffieri, Sandra E [0000-0003-3131-9359], Jonas, Jost B [0000-0003-2972-5227], Kang, Jae H [0000-0003-4812-0557], Wilson, James F [0000-0001-5751-9178], Foster, Paul J [0000-0002-4755-177X], Hysi, Pirro G [0000-0001-5752-2510], Hewitt, Alex W [0000-0002-5123-5999], Khor, Chiea Chuen [0000-0002-1128-4729], Pasquale, Louis R [0000-0002-5835-3496], Montgomery, Grant W [0000-0002-4140-8139], Klaver, Caroline CW [0000-0002-2355-5258], Hammond, Christopher J [0000-0002-3227-2620], Wiggs, Janey L [0000-0003-1890-3278], Burdon, Kathryn P [0000-0001-8217-1249], MacGregor, Stuart [0000-0001-6731-8142], Apollo - University of Cambridge Repository

المصدر: Nature Communications, 9,
Nature Communications, 9:1864. Nature Publishing Group
Nature communications, 9(1):1864. Nature Publishing Group
Nature Communications
Nature Communications, Nature Publishing Group, 2018, 9 (1), pp.1864. ⟨10.1038/s41467-018-03646-6⟩
Iglesias, Adriana I; Mishra, Aniket; Vitart, Veronique; Bykhovskaya, Yelena; Höhn, René Gerhard Joachim; Springelkamp, Henriët; Cuellar-Partida, Gabriel; Gharahkhani, Puya; Bailey, Jessica N Cooke; Willoughby, Colin E; Li, Xiaohui; Yazar, Seyhan; Nag, Abhishek; Khawaja, Anthony P; Polašek, Ozren; Siscovick, David; Mitchell, Paul; Tham, Yih Chung; Haines, Jonathan L; Kearns, Lisa S; ... (2018). Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature communications, 9(1), p. 1864. Nature Publishing Group 10.1038/s41467-018-03646-6 <http://dx.doi.org/10.1038/s41467-018-03646-6>
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Nature Communications, 9, pp.
Iglesias, A I, Vitart, V, Li, X, Yazar, S, Nag, A, Khawaja, A P, Polašek, O, Siscovick, D, Mitchell, P, Chung Tham, Y, Haines, J L, Kearns, L S, Hayward, C, Shi, Y, van Leeuwen, E M, Taylor, K D, Bonnemaijer, P, Rotter, J I, Martin, N G, Zeller, T, Mills, R A, Souzeau, E, Staffieri, S E, Jonas, J B, Schmidtmann, I, Boutin, T, Kang, J H, Lucas, S E M, Wong, T Y, Beutel, M E, Uitterlinden, A G, Vithana, E N, Foster, P J, Hysi, P G, Hewitt, A W, Khor, C C, Pasquale, L R, Montgomery, G W, Klaver, C C W, Aung, T, Pfeiffer, N, Mackey, D A, Hammond, C J, Cheng, C-Y, Craig, J E, Rabinowitz, Y S & Wiggs, J L & Burdon, K P & van Duijn, C M & MacGregor, S 2018, ' Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases ', Nature Communications, vol. 9, 1864 . https://doi.org/10.1038/s41467-018-03646-6

مصطلحات موضوعية: 0301 basic medicine, Lumican, Candidate gene, genetic structures, Fibrillin-1, Gene Expression, General Physics and Astronomy, Glaucoma, Genome-wide association study, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Corneal Diseases, Marfan Syndrome, Cornea, ADAMTS Proteins, 0302 clinical medicine, Myopia, lcsh:Science, Corneal Dystrophies, Hereditary, Genetics, Multidisciplinary, Eye Diseases, Hereditary, Mendelian Randomization Analysis, 3. Good health, medicine.anatomical_structure, Proteoglycans, Decorin, Glaucoma, Open-Angle, Keratoconus, Science, Quantitative Trait Loci, 610 Medicine & health, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, White People, General Biochemistry, Genetics and Molecular Biology, Transforming Growth Factor beta2, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Quantitative Trait, Heritable, Asian People, medicine, Humans, CHROMATIN STATES, GENE-EXPRESSION, RISK-FACTOR, MUTATIONS, LUMICAN, MOUSE, KERATOCONUS, DECORIN, POLYMORPHISMS, HERITABILITY, [SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs, Loeys-Dietz Syndrome, [SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE], Genome, Human, General Chemistry, medicine.disease, eye diseases, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, 030221 ophthalmology & optometry, lcsh:Q, Ehlers-Danlos Syndrome, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, sense organs, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e97e1815813f732504c32b827988a988
http://hdl.handle.net/2066/191586

Find this article in full text from ProQuest

8

Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

المؤلفون: J. Graessler, Ulf Smith, Marie-France Hivert, Antigone S. Dimas, Joshua W. Knowles, Stéphane Cauchi, Karen L. Mohlke, Michael Boehnke, David Meyre, Nicholas J. Wareham, Ci Song, Denis Rybin, Erik Ingelsson, Mario A. Morken, Anne U. Jackson, Michael R. Erdos, Peter Kovacs, Fahim Abbasi, Claudia Langenberg, Ke Hao, Andreas Pfeiffer, Thomas Quertemous, Lars Lind, Stefan R. Bornstein, Suzannah Bumpstead, Alena Stančáková, Lori L. Bonnycastle, Michael Stumvoll, Oluf Pedersen, Themistocles L. Assimes, Inês Barroso, Andrea Benazzo, Richard M. Watanabe, Magic Investigators, Josée Dupuis, Inga Prokopenko, Heather M. Stringham, Felicity Payne, Markku Laakso, Antje Fischer-Rosinsky, Francis S. Collins, Mark Walker, James B. Meigs, Torben Hansen, Peter Schwarz, Xia Yang, Yvonne Böttcher, Hans-Ulrich Häring, Anke Tönjes, Narisu Narisu, Cécile Lecoeur, Jaakko Tuomilehto, Reedik Mägi, Joachim Spranger, Amy J. Swift, Johanna Kuusisto, Jose C. Florez, Niels Grarup, Philippe Froguel, Vasiliki Lagou, Peter S. Chines, Mark I. McCarthy, Adam Barker, Trine Welløv Boesgaard, Richard N. Bergman

المصدر: Diabetes 63, 2158-2171 (2013)
Diabetes
Diabetes, vol 63, iss 6
Dimas, A S, Lagou, V, Barker, A, Knowles, J W, Magi, R, Hivert, M F, Benazzo, A, Rybin, D, Jackson, A U, Stringham, H M, Song, C, Fischer-Rosinsky, A, Boesgaard, T W, Grarup, N, Abbasi, F A, Assimes, T L, Hao, K, Yang, X, Lecoeur, C, Barroso, I, Bonnycastle, L L, Bottcher, Y, Bumpstead, S, Chines, P S, Erdos, M R, Graessler, J, Kovacs, P, Morken, M A, Narisu, N, Payne, F, Stancakova, A, Swift, A J, Tonjes, A, Bornstein, S R, Cauchi, S, Froguel, P, Meyre, D, Schwarz, P E H, Haring, H U, Smith, U, Boehnke, M, Bergman, R N, Collins, F S, Mohlke, K L, Tuomilehto, J, Quertemous, T, Lind, L, Hansen, T, Pedersen, O, Walker, M, Pfeiffer, A F H, Spranger, J, Stumvoll, M, Meigs, J B, Wareham, N J, Kuusisto, J, Laakso, M, Langenberg, C, Dupuis, J, Watanabe, R M, Florez, J C, Ingelsson, E, McCarthy, M I, Prokopenko, I & Investigators, M 2014, ' Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity ', Diabetes, vol. 63, no. 6, pp. 2158-2171 . https://doi.org/10.2337/db13-0949

مصطلحات موضوعية: Male, Endocrinology, Diabetes and Metabolism, Insulin Resistance/genetics, Type 2 diabetes, Medical and Health Sciences, Endocrinology, 0302 clinical medicine, Gene Frequency, Risk Factors, Insulin-Secreting Cells, Insulin Secretion, 2.1 Biological and endogenous factors, Cluster Analysis, Insulin, Aetiology, 2. Zero hunger, Genetics, 0303 health sciences, SLC30A8, Medicine (all), Diabetes, Single Nucleotide, Diabetes and Metabolism, Diabetes Mellitus, Type 2/genetics, Female, Type 2, Insulin processing, medicine.medical_specialty, Insulin/metabolism, Quantitative Trait Loci, Socio-culturale, 030209 endocrinology & metabolism, Biology, Autoimmune Disease, Polymorphism, Single Nucleotide, MAGIC Investigators, Endocrinology & Metabolism, 03 medical and health sciences, Insulin-Secreting Cells/metabolism, Insulin resistance, Clinical Research, Alleles, Diabetes Mellitus, Type 2, Genetic Variation, Genome-Wide Association Study, Humans, Insulin Resistance, Transcription Factors, Genetic Predisposition to Disease, Internal Medicine, Diabetes mellitus, Internal medicine, Genetic model, Diabetes Mellitus, medicine, Transcription Factors/metabolism, Polymorphism, Metabolic and endocrine, 030304 developmental biology, Glycemic, Prevention, medicine.disease, biology.protein, Quantitative Trait Loci/genetics, TCF7L2

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ec76408386665bb3ac65c80f7efd345
https://doi.org/10.2337/db13-0949

9

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

المؤلفون: Shin S-Y., Steffan D. Bos, Margreet Kloppenburg, Andres Metspalu, Ashok Rai, Karen E. Chapman, Tõnu Esko, J M Willkinson, Panagiotis Deloukas, Gudmar Thorleifsson, Nigel K Arden, Ingileif Jonsdottir, Andrew Carr, Kalliope Panoutsopoulou, Fernando Rivadeneira, Michelle Ricketts, F O'Neill, Sarah Metrustry, Massimo Mangino, Ollier Wer., Sarah E. Hunt, N Koller, Sally Doherty, M C Lopes, John Loughlin, Raine Eva., Andrew McCaskie, Bridget Watkins, Lorraine Southam, Gillian A. Wallis, Battley P-K., Vijay K. Yadav, U Stykarsdottir, N Aslam, Evangelos Evangelou, van Meurs Jbj., K Walker, Donald Salter, Mike R. Reed, K. Stefansson, I Carluke, E Arden, K Sherburn, Stuart Ralston, Tim D. Spector, Suzannah Bumpstead, Madhushika Ratnayake, Hannah Blackburn, K S Elliott, H Jonnson, Guangju Zhai, Michael Doherty, M. Wheeler, Thorvaldur Ingvarsson, Ingrid Meulenbelt, J Joseph, Fraser Birrell, D Swift, A.G. Uitterlinden, K Dixon, Ioannidis Jpa., Hanneke J. M. Kerkhof, Aaron G. Day-Williams, E Paling, Simon C. Potter, Ana M. Valdes, P E Slagboom, Richard Keen, Sheryl Mitchell, C Beazley, Eleftheria Zeggini, A Hoffman, Vesna Boraska, Jeanine J. Houwing-Duistermaat, Allan Gordon, N W Rayner

المصدر: Lancet
Zeggini, E, Panoutsopoulou, K, Southam, L, Rayner, N W, Day-Williams, A G, Lopes, M C, Boraska, V, Esko, T, Evangelou, E, Hofman, A, Houwing-Duistermaat, J J, Ingvarsson, T, Jonsdottir, I, Jonsson, H, Kerkhof, H J M, Kloppenburg, M, Bos, S D, Mangino, M, Metrustry, S, Slagboom, P E, Thorleifsson, G, Raine, E V A, Ratnayake, M, Ricketts, M, Beazley, C, Blackburn, H, Bumpstead, S, Elliott, K S, Hunt, S E, Potter, S C, Shin, S-Y, Yadav, V K, Zhai, G, Sherburn, K, Dixon, K, Arden, E, Aslam, N, Battley, P-K, Carluke, I, Doherty, S, Gordon, A, Joseph, J, Keen, R, Koller, N C, Mitchell, S, O'Neill, F, Paling, E, Reed, M R & Salter, D & Ralston, S H 2012, ' Identification of new susceptibility loci for osteoarthritis (arcOGEN) : a genome-wide association study ', The Lancet, vol. 380, no. 9844, pp. 815-823 . https://doi.org/10.1016/S0140-6736(12)60681-3
The Lancet; Vol 380

مصطلحات موضوعية: Male, medicine.medical_specialty, Linkage disequilibrium, Chromosome 9, Genome-wide association study, Polymorphism, Single Nucleotide, osteoarthritis, GWAS, FTO gene, Linkage Disequilibrium, Osteoarthritis, Hip, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Osteoarthritis, medicine, Humans, Genetic Predisposition to Disease, Arthroplasty, Replacement, Chromosome 12, 030304 developmental biology, 030203 arthritis & rheumatology, Genetics, Hip surgery, 0303 health sciences, business.industry, Articles, General Medicine, Odds ratio, Osteoarthritis, Knee, 3. Good health, Chromosome 3, Case-Control Studies, Female, business, Genome-Wide Association Study