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2015, 1st ed. 2015., ISBN 1493928244
This unique volume is the first to cover a wide range of design and analysis issues in genetic studies of rare variants, with contributions from experts in the... 
Medicine | Statistics | Human genetics
Web Resource
2008, Statistical methods for the analysis of genome-wide association studies : practical advice and guidance
Web Resource
2008, Statistical methods for the analysis of genome-wide association studies : practical advice and guidance
Web Resource
Nature Genetics, ISSN 1061-4036, 02/2011, Volume 43, Issue 4, pp. 287 - 288
Journal Article
2011, 1st ed., ISBN 012375142X
According to the National Institute of Health, a genome-wide association study is defined as any study of genetic variation across the entire human genome that... 
Genetic disorders | Variation | Human genetics | Diseases
Web Resource
2011, 1st ed., ISBN 012375142X, viii, 331, [11] p. of col. plates
According to the National Institute of Health, a genome-wide association study is defined as any study of genetic variation across the entire human genome that... 
Genetic disorders | Variation | Human genetics | Diseases | Pre-clinical Medicine: Basic Sciences
Book
Nature Methods, ISSN 1548-7091, 2014, Volume 11, Issue 3, pp. 294 - 296
Identifying functionally relevant variants against the background of ubiquitous genetic variation is a major challenge in human genetics. For variants in... 
DATABASE | BIOCHEMICAL RESEARCH METHODS | Genetic Variation | Algorithms | Untranslated Regions - genetics | Computer Simulation | Humans | Molecular Sequence Annotation | Noncoding DNA | Physiological aspects | Genomes | Research | Genetics | Genomics | Index Medicus
Journal Article
Journal of Orthopaedic Research, ISSN 0736-0266, 07/2016, Volume 34, Issue 7, pp. 1105 - 1110
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 07/2019, Volume 20, Issue 9, pp. 562 - 562
An amendment to this paper has been published and can be accessed via a link at the top of the paper. 
Journal Article
Genome Medicine, ISSN 1756-994X, 10/2014, Volume 6, Issue 10, pp. 83 - 83
Rare variation has a key role in the genetic etiology of complex traits. Genetically isolated populations have been established as a powerful resource for... 
FREQUENCY | GENETICS & HEREDITY | RARE VARIANT | APOC3 | RISK | ASSOCIATION | CONFERS | Type 2 diabetes | Development and progression | Genomics
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2013, Volume 50, Issue 11, pp. 715 - 724
Journal Article
by McCarthy, Shane and Das, Sayantan and Kretzschmar, Warren and Delaneau, Olivier and Wood, Anew R and Teumer, Alexander and Kang, Hyun Min and Fuchsberger, Christian and Danecek, Petr and Sharp, Kevin and Luo, Yang and Sidorel, Carlo and Kwong, Alan and Timpson, Nicholas and Koskinen, Seppo and Vrieze, Scott and Scott, Laura J and Zhang, He and Mahajan, Anubha and Veldink, Jan and Peters, Ulrike and Pato, Carlos and van Duijn, Cornelia M and Gillies, Christopher E and Gandin, Ilaria and Mezzavilla, Massimo and Gilly, Arthur and Cocca, Massimiliano and Traglia, Michela and Angius, Anea and Barrett, Jeffrey C and Boomsma, Dorrett and Branham, Kari and Breen, Gerome and Brummett, Chad M and Busonero, Fabio and Campbell, Harry and Chan, Anew and Che, Sai and Chew, Emily and Collins, Francis S and Corbin, Laura J and Smith, George Davey and Dedoussis, George and Dorr, Marcus and Farmaki, Aliki-Eleni and Ferrucci, Luigi and Forer, Lukas and Fraser, Ross M and Gabriel, Stacey and Levy, Shawn and Groop, Leif and Harrison, Tabitha and Hattersley, Anew and Holmen, Oddgeir L and Hveem, Kristian and Kretzler, Matthias and Lee, James C and McGue, Matt and Meitinger, Thomas and Melzer, David and Min, Josine L and Mohlke, Karen L and Vincent, John B and Nauck, Matthias and Nickerson, Deborah and Palotie, Aarno and Pato, Michele and Pirastu, Nicola and McInnis, Melvin and Richards, J. Brent and Sala, Cinzia and Salomaa, Veikko and Schlessinger, David and Schoenherr, Sebastian and Slagboom, P. Eline and Small, Kerrin and Spector, Timothy and Stambolian, Dwight and Tuke, Marcus and Tuomilehto, Jaakko and van den Berg, Leonard H and Van Rheenen, Wouter and Volker, Uwe and Wijmenga, Cisca and Toniolo, Daniela and Zeggini, Eleftheria and Gasparini, Paolo and Sampson, Matthew G and Wilson, James F and Frayling, Timothy and de Bakker, Paul I. W and Swertz, Morris A and McCarroll, Steven and Kooperberg, Charles and Dekker, Annelot and Altshuler, David and Willer, Cristen and Iacono, William and Ripatti, Samuli and ... and Haplotype Reference Consortium and the Haplotype Reference Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1279 - 1283
Journal Article
Nature, ISSN 0028-0836, 01/2015, Volume 517, Issue 7534, pp. 327 - 332
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9864, pp. 373 - 373
  Obesity is a well established risk factor for osteoarthritis.1 Large-scale, prospective studies consistently show a strong relation between weight gain or... 
Internal Medicine | Health risk assessment | Medical research | Genomes
Journal Article
by Fuchsberger, Christian and Flannick, Jason and Teslovich, Tanya M and Mahajan, Anubha and Agarwala, Vineeta and Gaulton, Kyle J and Ma, Clement and Fontanillas, Pierre and Moutsianas, Loukas and McCarthy, Davis J and Rivas, Manuel A and Perry, John R. B and Sim, Xueling and Blackwell, Thomas W and Robertson, Neil R and Rayner, N. William and Cingolani, Pablo and Locke, Adam E and Fernandez Tajes, Juan and Highland, Heather M and Dupuis, Josee and Chines, Peter S and Lindgren, Cecilia M and Hartl, Christopher and Jackson, Anne U and Chen, Han and Huyghe, Jeroen R and van de Bunt, Martijn and Pearson, Richard D and Kumar, Ashish and Müller-Nurasyid, Martina and Grarup, Niels and Stringham, Heather M and Gamazon, Eric R and Lee, Jaehoon and Chen, Yuhui and Scott, Robert A and Below, Jennifer E and Chen, Peng and Huang, Jinyan and Go, Min Jin and Stitzel, Michael L and Pasko, Dorota and Parker, Stephen C. J and Varga, Tibor V and Green, Todd and Beer, Nicola L and Day-Williams, Aaron G and Ferreira, Teresa and Fingerlin, Tasha and Horikoshi, Momoko and Hu, Cheng and Huh, Iksoo and Ikram, Mohammad Kamran and Kim, Bong-Jo and Kim, Yongkang and Kim, Young Jin and Kwon, Min-Seok and Lee, Juyoung and Lee, Selyeong and Lin, Keng-Han and Maxwell, Taylor J and Nagai, Yoshihiko and Wang, Xu and Welch, Ryan P and Yoon, Joon and Zhang, Weihua and Barzilai, Nir and Voight, Benjamin F and Han, Bok-Ghee and Jenkinson, Christopher P and Kuulasmaa, Teemu and Kuusisto, Johanna and Manning, Alisa and Ng, Maggie C. Y and Palmer, Nicholette D and Balkau, Beverley and Stancáková, Alena and Abboud, Hanna E and Boeing, Heiner and Gieaitis, Vilmantas and Prabhakaran, Dorairaj and Gottesman, Omri and Scott, James and Carey, Jason and Kwan, Phoenix and Grant, George and Smith, Joshua D and Neale, Benjamin M and Purcell, Shaun and Butterworth, Adam S and Howson, Joanna M. M and Lee, Heung Man and Lu, Yingchang and Kwak, Soo-Heon and Zhao, Wei and Danesh, John and Lam, Vincent K. L and Park, Kyong Soo and Saleheen, Danish and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2016, Volume 536, Issue 7614, pp. 41 - +
Journal Article