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1. Full Text A Bayesian Method for Detecting and Characterizing Allelic Heterogeneity and Boosting Signals in Genome-Wide Association Studies
by Zhan Su and Niall Cardin and Wellcome Trust Case Control Consortium and Peter Donnelly and Jonathan Marchini and Wellcome Trust Case Control and The Wellcome Trust Case Control Consortium
Statistical science, ISSN 0883-4237, 11/2009, Volume 24, Issue 4, pp. 430 - 450
Haplotypes | Plant diseases | Crohn disease | Genealogy | Disease models | Genetic loci | Genomes | Genetic mutation | Modeling | Genotypes | Complex disease | Bayesian methods | Genome-wide association | Allelic heterogeneity | Statistics & Probability | Physical Sciences | Mathematics | Science & Technology | Models | Statistical analysis | Bayesian analysis | Genomics | Innovations | genome-wide association | allelic heterogeneity
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2. Full Text Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
by Barrett, Jeffrey C and Hansoul, Sarah and Nicolae, Dan L and Cho, Judy H and Duerr, Richard H and Rioux, John D and Brant, Steven R and Silverberg, Mark S and Taylor, Kent D and Barmada, M Michael and Bitton, Alain and Dassopoulos, Themistocles and Datta, Lisa Wu and Green, Todd and Griffiths, Anne M and Kistner, Emily O and Murtha, Michael T and Regueiro, Miguel D and Rotter, Jerome I and Schumm, L Philip and Steinhart, A Hillary and Targan, Stephan R and Xavier, Ramnik J and Libioulle, Cécile and Sandor, Cynthia and Lathrop, Mark and Belaiche, Jacques and Dewit, Olivier and Gut, Ivo and Heath, Simon and Laukens, Debby and Mni, Myriam and Rutgeerts, Paul and Van Gossum, André and Zelenika, Diana and Franchimont, Denis and Hugot, Jean-Pierre and De Vos, Martine and Vermeire, Severine and Louis, Edouard and Cardon, Lon R and Anderson, Carl A and Drummond, Hazel and Nimmo, Elaine and Ahmad, Tariq and Prescott, Natalie J and Onnie, Clive M and Fisher, Sheila A and Marchini, Jonathan and Ghori, Jilur and Bumpstead, Suzannah and Gwilliam, Rhian and Tremelling, Mark and Deloukas, Panos and Mansfield, John and Jewell, Derek and Satsangi, Jack and Mathew, Christopher G and Parkes, Miles and Georges, Michel and Daly, Mark J and Wellcome Trust Case Control and NIDDK IBD Genetics Consortium and Belgian-French IBD Consortium and Wellcome Trust Case Control Consortium and the NIDDK IBD Genetics Consortium and the Belgian-French IBD Consortium and the Wellcome Trust Case Control Consortium
Nature genetics, ISSN 1061-4036, 2008, Volume 40, Issue 8, pp. 955 - 962
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Crohn Disease - genetics | Genetic Predisposition to Disease | Genome, Human | Quantitative Trait Loci | Humans | Physiological aspects | Crohn's disease | Genetic aspects | Research | Genetic susceptibility | Risk factors | Inflammatory bowel disease | Studies | Medical research | Genetics | Genomics | Crohns disease | Index Medicus
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3. Full Text Genome-wide association analysis identifies 20 loci that influence adult height
by Weedon, Michael N and Lango, Hana and Lindgren, Cecilia M and Wallace, Chris and Evans, David M and Mangino, Massimo and Freathy, Rachel M and Perry, John R. B and Stevens, Suzanne and Hall, Alistair S and Samani, Nilesh J and Shields, Beverly and Prokopenko, Inga and Farrall, Martin and Dominiczak, Anna and Johnson, Toby and Bergmann, Sven and Beckmann, Jacques S and Vollenweider, Peter and Waterworth, Dawn M and Mooser, Vincent and Palmer, Colin N. A and Morris, Andrew D and Ouwehand, Willem H and Zhao, Jing Hua and Li, Shengxu and Loos, Ruth J. F and Barroso, Inês and Deloukas, Panagiotis and Sandhu, Manjinder S and Wheeler, Eleanor and Soranzo, Nicole and Inouye, Michael and Wareham, Nicholas J and Caulfield, Mark and Munroe, Patricia B and Hattersley, Andrew T and McCarthy, Mark I and Frayling, Timothy M and Diabet Genetics Initiat and Cambridge GEM Consortium and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Diabetes Genetics Initiative and The Wellcome Trust Case Control Consortium
Nature genetics, ISSN 1061-4036, 05/2008, Volume 40, Issue 5, pp. 575 - 583
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Extracellular Matrix Proteins - genetics | Humans | Middle Aged | Genotype | Male | Body Height - genetics | Hedgehog Proteins - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome, Human | Neoplasm Proteins - genetics | Stature | Quantitative trait loci | Genetic variation | Physiological aspects | Genetic aspects | Research | Identification and classification | Studies | Genetic research | Genetics | Gene loci | Height | Genes | Index Medicus
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4. Full Text A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity
by Timothy M. Frayling and Nicholas J. Timpson and Michael N. Weedon and Eleftheria Zeggini and Rachel M. Freathy and Cecilia M. Lindgren and John R. B. Perry and Katherine S. Elliott and Hana Lango and Nigel W. Rayner and Beverley Shields and Lorna W. Harries and Jeffrey C. Barrett and Sian Ellard and Christopher J. Groves and Bridget Knight and Ann-Marie Patch and Andrew R. Ness and Shah Ebrahim and Debbie A. Lawlor and Susan M. Ring and Yoav Ben-Shlomo and Marjo-Riitta Jarvelin and Ulla Sovio and Amanda J. Bennett and David Melzer and Luigi Ferrucci and Ruth J. F. Loos and Inês Barroso and Nicholas J. Wareham and Fredrik Karpe and Katharine R. Owen and Lon R. Cardon and Mark Walker and Graham A. Hitman and Colin N. A. Palmer and Alex S. F. Doney and Andrew D. Morris and George Davey Smith and Andrew T. Hattersley and Mark I. McCarthy and Wellcome Trust Case Control and The Wellcome Trust Case Control Consortium
Science (American Association for the Advancement of Science), ISSN 0036-8075, 5/2007, Volume 316, Issue 5826, pp. 889 - 894
Mass | Body mass index | Obesity | Average linear density | Reports | Adults | Type 2 diabetes mellitus | Children | Population genetics | Genotypes | Overweight | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Body Mass Index | Genetic Predisposition to Disease | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Overweight - genetics | Male | United Kingdom | Obesity - genetics | Case-Control Studies | Birth Weight | Homozygote | Adolescent | Alleles | Adult | Female | Aged | Polymorphism, Single Nucleotide | Adipose Tissue | Child | Infant, Newborn | Cohort Studies | Obesity gene | Research | Diabetes | Body fat | Genomics | Risk factors | Index Medicus
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5. Full Text Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease
by Ouwehand, Willem and Keniry, Andrew and Fisher, Sheila A and Jewell, Derek P and Anderson, Carl A and Prescott, Natalie J and Deloukas, Panos and Blaszczyk, Katarzyna and Mansfield, John C and Mathew, Christopher G and Watkins, Nick and Drummond, Hazel and Cummings, Fraser R and Forbes, Alastair and Barrett, Jeffrey C and Ravindrarajah, Radhi and Sanderson, Jeremy and Inouye, Mike and Hunt, Sarah and Nimmo, Elaine R and Johnson, Christopher and Bumpstead, Suzannah and Hanson, Catherine E and Lobo, Alan and Massey, Dunecan and Cardon, Lon and Ewels, Philip and Satsangi, Jack and Tremelling, Mark and Gwilliam, Rhian and Carter, Martyn and Berzuini, Carlo and Lees, Charlie W and Onnie, Clive M and Parkes, Miles and Lewis, Cathryn M and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and the Wellcome Trust Case Control Consortium
Nature genetics, ISSN 1061-4036, 06/2008, Volume 40, Issue 6, pp. 710 - 712
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Biomarkers - metabolism | Crohn Disease - epidemiology | Crohn Disease - genetics | Interleukin-12 Subunit p40 - genetics | Autophagy-Related Proteins | Genetic Predisposition to Disease | Extracellular Matrix Proteins - genetics | Humans | Risk Factors | Colitis, Ulcerative - genetics | Protein-Serine-Threonine Kinases - genetics | Nod2 Signaling Adaptor Protein - genetics | Colitis, Ulcerative - epidemiology | GTP-Binding Proteins - genetics | Receptors, Interleukin - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Carrier Proteins - genetics | HLA-A Antigens - genetics | Polymorphism, Single Nucleotide - genetics | Cohort Studies | Physiological aspects | Crohn's disease | Genetic aspects | Diagnosis | Research | Single nucleotide polymorphisms | Risk factors | Ulcerative colitis | Inflammatory bowel disease | Medical research | Biomedical research | Bowel disease | Colorectal cancer | Genetics | Gene loci | Regression analysis | Crohns disease | Index Medicus
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6. Full Text Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
by Eleftheria Zeggini and Michael N. Weedon and Cecilia M. Lindgren and Timothy M. Frayling and Katherine S. Elliott and Hana Lango and Nicholas J. Timpson and John R. B. Perry and Nigel W. Rayner and Rachel M. Freathy and Jeffrey C. Barrett and Beverley Shields and Andrew P. Morris and Sian Ellard and Christopher J. Groves and Lorna W. Harries and Jonathan L. Marchini and Katharine R. Owen and Beatrice Knight and Lon R. Cardon and Mark Walker and Graham A. Hitman and Andrew D. Morris and Alex S. F. Doney and Mark I. McCarthy and Andrew T. Hattersley and WTCCC and Wellcome Trust Case Control Consortium (WTCCC) and The Wellcome Trust Case Control Consortium (WTCCC)
Science (American Association for the Advancement of Science), ISSN 0036-8075, 6/2007, Volume 316, Issue 5829, pp. 1336 - 1341
Medical research | Forestry research | Hospital buildings | Medical genetics | Genetic research | Hospital units | Genetic loci | Reports | Type 2 diabetes mellitus | Human genetics | Research universities | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Diabetes. Impaired glucose tolerance | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Insulin-Like Growth Factor Binding Proteins - genetics | Genetic Predisposition to Disease | Meta-Analysis as Topic | Oligonucleotide Array Sequence Analysis | Introns | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Male | United Kingdom | Chromosome Mapping | Transcription Factors - genetics | Genes, p16 | Case-Control Studies | Homeodomain Proteins - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome, Human | Type 2 diabetes | Genetic aspects | Research | Risk factors | Biomedical research | Cellular biology | Genomics | Diabetes | Molecular biology | Pancreas | Population genetics | Index Medicus
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7. Full Text Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
by Nejentsev, Sergey and Bailey, Rebecca and Hardy, Matthew and Cooper, Jason D and Howson, Joanna M. M and Walker, Neil M and Maier, Lisa M and Ribas, Gloria and King, Erna and Szeszko, Jeffrey and Field, Sarah F and Reynolds, Pamela and Smyth, Deborah and Todd, John A and Hulme, John and Clayton, David G and Masters, Jennifer and Stevens, Helen E and Campbell, R. Duncan and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and The Wellcome Trust Case Control Consortium
Nature (London), ISSN 0028-0836, 12/2007, Volume 450, Issue 7171, pp. 887 - 92
Diabetes Mellitus, Type 1/genetics | European Continental Ancestry Group/genetics | HLA-B Antigens/genetics | Gene Frequency | Humans | Databases, Genetic | HLA-DR Antigens/genetics | Genetic Predisposition to Disease/genetics | Genotype | Case-Control Studies | Genes, MHC Class II/genetics | Polymorphism, Single Nucleotide/genetics | Sample Size | HLA-DRB1 Chains | Alleles | Genes, MHC Class I/genetics | HLA-A Antigens/genetics | HLA-DQ Antigens/genetics | HLA-DQ beta-Chains | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Diabetes. Impaired glucose tolerance | Medical sciences | Endocrine pancreas. Apud cells (diseases) | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genes, MHC Class I - genetics | Diabetes Mellitus, Type 1 - genetics | HLA-DR Antigens - genetics | Genes, MHC Class II - genetics | HLA-DQ Antigens - genetics | HLA-A Antigens - genetics | Polymorphism, Single Nucleotide - genetics | HLA-B Antigens - genetics | Genotype & phenotype | Statistical analysis | Genomics | Diabetes | Autoimmune diseases | Gene expression | Chromosomes | Index Medicus
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8. Full Text Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies
by Nolte, Ilja and Wallace, Chris and Newhouse, Stephen and Waggott, Daryl and Fu, Jingyuan and Soranzo, Nicole and Gwilliam, Rhian and Demissie, Serkalem and Savelieva, Irina and Zheng, Dongling and Dalageorgou, Chrysoula and Farrall, Martin and Samani, Nilesh and Connell, John and Brown, Morris and Dominiczak, Anna and Lathrop, Mark and Zeggini, Eleftheria and Wain, Louise and Newton-Cheh, Christopher and Eijgelsheim, Mark and Rice, Kenneth and Bakker, Paul and Pfeufer, Arne and Sanna, Serena and Arking, Dan and Asselbergs, Folkert and Spector, Timothy and Carter, Nicholas and Jeffery, Steve and Tobin, Martin and Caulfield, Mark and Snieder, Harold and Paterson, Anew and Munroe, Patricia and Jamshidi, Yalda and QTGEN Consortium and QTSCD Consortium and Wellcome Trust Case Control Consor and DCCT EDIC Res Grp and QTGEN consortium and DCCT/EDIC Research Group and Wellcome Trust Case Control Consortium and QTSCD consortium and for the QTGEN consortium and The DCCT/EDIC Research Group and for the The Wellcome Trust Case Control Consortium and for the QTSCD consortium
PloS one, ISSN 1932-6203, 07/2009, Volume 4, Issue 7, pp. e6138 - e6138
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic Variation | Genome-Wide Association Study | Heart - physiology | Humans | Chromosomes, Human, Pair 6 | Calcium-Binding Proteins - genetics | Cohort Studies | Consortia | Heart | Arrhythmia | Analysis | Genes | Genomics | Genetic research | Disease susceptibility | Genetic aspects | Genomes | Haplotypes | Health sciences | Calcium | Cardiovascular disease | Single-nucleotide polymorphism | Epidemiology | Population genetics | Bioinformatics | Heart diseases | Calcium (intracellular) | Susceptibility | Phospholamban | Pharmacology | Genetic diversity | College campuses | Loci | Medicine | Studies | Heart rate | Hospitals | Womens health | Diabetes | Ventricle | Index Medicus
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