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1. Genome-wide association studies
: from polymorphism to personalized medicine
by Appasani, Krishnarao, 1959- editor
2016, ISBN 9781107042766, xxxi, 391 pages, 24 unnumbered pages of plates
Genome-Wide Association Study | Genetic Testing | Genomics | Medical genetics
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2. Full Text Genomewide Association Study of Leprosy
by Zhang, Fu-Ren and Zhang, Chi and Zhang, Lin and Zhang, Lian-Hua and Zhang, Xue-Jun and Zhang, Zheng and Huang, Wei and Chen, Shu-Min and Sun, Yi-Ping and Sun, Liang-Dan and Liu, Rui-Yu and Liu, Yu-Qiang and Liu, Jin-Xian and Liu, Hua-Xu and Liu, Hong and Liu, Jian-Jun and Li, Yong-Ping and Li, Jin-Yong and Li, Yi and Cui, Yong and Yan, Wei-Guo and Yan, Xiao-Xiao and Yang, Ning-Han and Yang, Sen and Yang, Hai-Tao and Rong-De Yang and Chu, Tong-Sheng and Han, Jian-Wen and Yu, Gong-Qi and Yu, Jing-Ping and Yu, Yong-Xiang and Quan, Cheng and Shi, Ben-Qing and Cheng, Yi-Lin and Cheng, Hui and Wang, Kui-Jun and Wang, De-Min and Wang, Xiao-Dong and Wang, Chang-Yuan and Wang, Ying and Wang, Qiang and Lin, Yan and Zheng, Hou-Feng and Fu, Xi-An and Zuo, Xian-Bo and Long, Heng and Tian, Hong-Qing and Zhou, Fu-Sheng and Lu, Wen-Sheng and He, Su-Min and Du, Wen-Li and Shen, Min and Jin, Qi-Yi and Low, Hui-Qi and Erwin, Tantoso and Zhao, Xin and Jiao, Yue-Lin and Mao, Li-Guo and Yin, Gang and Jiang, Zhen-Xia and Hu, Zong-Hou and Gong, Cui-Hua and Wei, Shi-Yu and Wei, Dong and Cao, Hong-Zhong and Cao, Wei-Kun and Hibberd, Martin L
The New England Journal of Medicine, ISSN 0028-4793, 12/2009, Volume 361, Issue 27, pp. 2609 - 2618
Little is known about genetic susceptibility to infectious disease. This study implicates variation in genes encoding molecules in the NOD2 (nucleotide-binding... 
IMMUNITY | MEDICINE, GENERAL & INTERNAL | MYCOBACTERIA | INFLAMMATORY-BOWEL-DISEASE | CROHNS-DISEASE | GENETICS | SUSCEPTIBILITY | GENES | HLA | Genetic Predisposition to Disease | Genome-Wide Association Study | Mycobacterium leprae | Oligonucleotide Array Sequence Analysis | Signal Transduction | Humans | Middle Aged | Genotype | Male | Nod2 Signaling Adaptor Protein - genetics | Gene Regulatory Networks | Leprosy, Paucibacillary - genetics | Case-Control Studies | Leprosy, Multibacillary - genetics | Female | Aged | Polymorphism, Single Nucleotide | Leprosy | Minority & ethnic groups | Developing countries--LDCs | Parkinsons disease | Index Medicus | Abridged Index Medicus
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3. Full Text Genome-Wide Association Study
by Gutierrez, AP and Yanez, JM and Fukui, S and Swift, B and Davidson, WS
PLOS ONE, ISSN 1932-6203, 03/2015, Volume 10, Issue 3
Early sexual maturation is considered a serious drawback for Atlantic salmon aquaculture as it retards growth, increases production times and affects flesh... 
QUANTITATIVE TRAIT LOCI | BODY-WEIGHT | RAINBOW-TROUT | GENETIC-IMPROVEMENT | MULTIDISCIPLINARY SCIENCES | QTL | COHO SALMON | MATURITY | CHARR SALVELINUS-ALPINUS | TROUT ONCORHYNCHUS-MYKISS | SNP ARRAY
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4. Full Text Genome-wide association study identifies five new schizophrenia loci
by Ripke, Stephan and Sanders, Alan R and Kendler, Kenneth S and Levinson, Douglas F and Sklar, Pamela and Holmans, Peter A and Lin, Dan-Yu and Duan, Jubao and Ophoff, Roel A and Aneassen, Ole A and Scolnick, Edward and Cichon, Sven and St Clair, David and Corvin, Aiden and Gurling, Hugh and Werge, Thomas and Rujescu, Dan and Blackwood, Douglas H. R and Pato, Carlos N and Malhotra, Anil K and Purcell, Shaun and Dudbridge, Frank and Neale, Benjamin M and Rossin, Lizzy and Visscher, Peter M and Posthuma, Danielle and Ruderfer, Douglas M and Fanous, Ayman and Stefansson, Hreinn and Steinberg, Stacy and Mowry, Bryan J and Golimbet, Vera and de Hert, Marc and Jönsson, Erik G and Bitter, István and Pietiläinen, Olli P. H and Collier, David A and Tosato, Sarah and Agartz, Ingrid and Albus, Margot and Alexander, Madeline and Amdur, Richard L and Amin, Farooq and Bass, Nicholas and Bergen, Sarah E and Black, Donald W and Børglum, Anders D and Brown, Matthew A and Bruggeman, Richard and Buccola, Nancy G and Byerley, William F and Cahn, Wiepke and Cantor, Rita M and Carr, Vaughan J and Catts, Stanley V and Choudhury, Khalid and Cloninger, C. Robert and Cormican, Paul and Craddock, Nicholas and Danoy, Patrick A and Datta, Susmita and de Haan, Lieuwe and Demontis, Ditte and Dikeos, Dimitris and Djurovic, Srdjan and Donnelly, Peter and Donohoe, Gary and Duong, Linh and Dwyer, Sarah and Fink-Jensen, Anders and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Georgieva, Lyudmila and Giegling, Ina and Gill, Michael and Glenthøj, Birte and Godard, Stephanie and Hamshere, Marian and Hansen, Mark and Hansen, Thomas and Hartmann, Annette M and Henskens, Frans A and Hougaard, David M and Hultman, Christina M and Ingason, Anés and Jablensky, Assen V and Jakobsen, Klaus D and Jay, Maurice and Jürgens, Gesche and Kahn, René S and Keller, Matthew C and Kenis, Gunter and Kenny, Elaine and Kim, Yunjung and Kirov, George K and Konnerth, Heike and Konte, Bettina and Krabbendam, Lydia and Krasucki, Robert and ... and Schizophrenia Psychiat Genome-Wide and Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium and The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 10, pp. 969 - 976
We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856... 
INDIVIDUALS | HUMAN HEIGHT | VARIANTS | SUSCEPTIBILITY | GENETICS & HEREDITY | LARGE PROPORTION | COMMON SNPS EXPLAIN | BIPOLAR DISORDER | ANCESTRY | HERITABILITY | MICRORNA | Haplotypes | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Gene Expression Regulation | European Continental Ancestry Group | Logistic Models | Male | MicroRNAs - metabolism | Gene Dosage | Genetic Loci | Case-Control Studies | Linkage Disequilibrium | Bipolar Disorder | Schizophrenia - genetics | Alleles | Female | MicroRNAs - genetics | Polymorphism, Single Nucleotide | Mutation | Genome, Human | MicroRNA | Genetic variation | Physiological aspects | Schizophrenia | Genetic aspects | Research | Risk factors | Studies | Genomes | Genealogy | Index Medicus
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5. Full Text Genome-wide association study of PR interval
by Pfeufer, Arne and Noord, Charlotte and Marciante, Kristin and Arking, Dan and Larson, Martin and Smith, Albert Vernon and Tarasov, Kirill and Müller, Martina and Sotoodehnia, Nona and Sinner, Moritz and Verwoert, Germaine and Li, Man and Kao, Wen and Köttgen, Anna and Coresh, Josef and Bis, Joshua and Psaty, Bruce and Rice, Kenneth and Rotter, Jerome and Rivadeneira Ramirez, Fernando and Hofman, Albert and Kors, Jan and Stricker, Bruno and Uitterlinden, Ané and Tikka-Kleemola, Päivi and Beckmann, Britt and Sauter, Wiebke and Gieger, Christian and Lubitz, Steven and Newton-Cheh, Christopher and Wang, Thomas and Magnani, Jared and Schnabel, Renate and Chung, Mina and Barnard, John and Wagoner, David and Vasan, Ramachanan Srini and Aspelund, Thor and Eiriksdottir, Gudny and Harris, Tamara and Launer, Lenore and Najjar, Samer and Lakatta, Edward and Schlessinger, David and Uda, Manuela and Abecasis, Gonçalo and Artto, Ville and Ehret, Georg and Boerwinkle, Eric and Chakravarti, Aravinda and Soliman, Elsayed and Lunetta, Kathryn and Perz, Siegfried and Wichmann, Erich and Meitinger, Thomas and Levy, Daniel and Gudnason, Vilmundur and Ellinor, Patrick and Sanna, Serena and Kääb, Stefan and Witteman, Jacqueline and Alonso, Alvaro and Benjamin, Emelia and Heckbert, Susan
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 153 - 159
textabstractThe electrocardiographic PR interval (or PQ interval) reflects atrial and atrioventricular nodal conduction, disturbances of which increase risk of... 
SYSTEM | INDIVIDUALS | VARIABILITY | COMMON VARIANTS | DESIGN | GENETICS & HEREDITY | HEART-RATE | SODIUM-CHANNEL | NATIONAL HEART | ATHEROSCLEROSIS RISK | ATRIAL-FIBRILLATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Genetic Loci - genetics | Male | Atrial Fibrillation - genetics | Atrial Fibrillation - physiopathology | Heart Conduction System - physiology | Electrocardiography | Female | Aged | Cohort Studies | Usage | Care and treatment | Electrocardiogram | Atrial fibrillation | Genetic aspects | Diagnosis | Research | Health aspects | Risk factors | Studies | Cardiac arrhythmia | Medical research | Index Medicus | atrial fibrillation | quantitative trait | PQ interval | genome-wide association study | PR interval | developmental genes | voltage gated sodium channel
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6. Full Text A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
by Moffatt, Miriam F and Gut, Ivo G and Demenais, Florence and Strachan, David P and Bouzigon, Emmanuelle and Heath, Simon and von Mutius, Erika and Farrall, Martin and Lathrop, Mark and Cookson, William O.C.M and GABRIEL Consortium
The New England Journal of Medicine, ISSN 0028-4793, 09/2010, Volume 363, Issue 13, pp. 1211 - 1221
This genomewide association study implicates variants of SMAD3 in susceptibility to asthma and confirms previously observed genetic associations. The study... 
MEDICINE, GENERAL & INTERNAL | POSITIONAL CLONING | VARIANTS | ALLERGY | IN-VIVO | DISEASE | SUSCEPTIBILITY GENE | RECEPTOR | CYTOKINE | TRAITS | EXPRESSION | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Logistic Models | Male | Th2 Cells - immunology | Genetic Loci | Hypersensitivity - complications | Asthma - genetics | Case-Control Studies | Immunoglobulin E - blood | HLA-DR Antigens - genetics | Occupational Diseases - genetics | Adolescent | Age of Onset | Asthma - immunology | Female | Chromosomes, Human | Polymorphism, Single Nucleotide | Odds Ratio | Child | Usage | Immunoglobulin E | Genetic aspects | Health aspects | Risk factors | Genetic screening | Asthma | Studies | Genetics | Age | Index Medicus | Abridged Index Medicus | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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7. Full Text Genome-wide association study reveals genetic risk underlying Parkinson's disease
by Simon-Sanchez, J and Schulte, C and Bras, J.M and Sharma, M and Gibbs, J.R and Berg, D and Paisan-Ruiz, C and Lichtner, P and Scholz, S.W and Hernandez, D.G and Kruger, R and Federoff, M and Klein, C and Goate, A and Perlmutter, J and Bonin, M and Nalls, M.A and Illig, T and Gieger, C and Houlden, H and Steffens, M and Okun, M.S and Racette, B.A and Cookson, M.R and Foote, K.D and Fernandez, H.H and Traynor, B.J and Schreiber, S and Arepalli, S and Zonozi, R and Gwinn, K and Brug, van der, M and Lopez, G and Chanock, S.J and Schatzkin, A and Park, Y and Hollenbeck, A and Gao, J.T and Huang, X.M and Wood, N.W and Lorenz, D and Deuschl, G and Chen, H.L and Riess, O and Hardy, J.A and Singleton, A.B and Gasser, T
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 12, pp. 1308 - 1312
We performed a genome-wide association study (GWAS) in 1,713 individuals of European ancestry with Parkinson's disease (PD) and 3,978 controls. After... 
SYSTEM | LINKAGE DISEQUILIBRIUM | GENETICS & HEREDITY | TAU GENE | HAPLOTYPE | MUTATIONS | PROGRESSIVE SUPRANUCLEAR PALSY | SNCA | Genetic Variation | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | Japan | Risk Factors | Parkinson Disease - epidemiology | Parkinson Disease - genetics | Cohort Studies | Genetic aspects | Parkinson's disease | Research | Single nucleotide polymorphisms | Genetic susceptibility | Risk factors | Education | Environmental health | Quality control | Genetics | Regression analysis | Chromosomes | Neurological disorders | Index Medicus
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