workshop:2013:reading_list
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| + | ====== General ====== | ||
| + | |||
| + | * Heritability in the genomics era — concepts and misconceptions. Peter M. Visscher, William G. Hill & Naomi R. Wray doi: | ||
| + | * Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT. Basic statistical analysis in genetic case-control studies. Nat Protoc. 2011 Feb; | ||
| + | * Genetic Mapping in Human Disease David Altshuler, | ||
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| ====== Association: | ====== Association: | ||
| * Risch and Merikangas Science 1996 The future of genetic studies of complex disease http:// | * Risch and Merikangas Science 1996 The future of genetic studies of complex disease http:// | ||
| * Sham et al. AJHG 2000 http:// | * Sham et al. AJHG 2000 http:// | ||
| + | * Medland SE, Neale, M.C.. (2009). An Integrated Phenomic Approach to Multivariate Allelic Association. European Journal of Human Genetics.Aug. 26. [http:// | ||
| ====== GWAS ====== | ====== GWAS ====== | ||
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| * Purcell et al. 2007 AJHG http:// | * Purcell et al. 2007 AJHG http:// | ||
| * [also plink website: http:// | * [also plink website: http:// | ||
| + | * Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. https:// | ||
| + | * Genome-wide association studies for complex traits: consensus, uncertainty and challenges. https:// | ||
| + | * overview of what is GWAS Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med. 2010 Jul 8; | ||
| + | * Psychiatric GWAS Consortium Coordinating Committee, Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF. Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am J Psychiatry. 2009 May; | ||
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| ====== Sequencing: ====== | ====== Sequencing: ====== | ||
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| * DePristo et al. 2011 Nat. Genet. http:// | * DePristo et al. 2011 Nat. Genet. http:// | ||
| * 1KG 2011 Nature Genetics http:// | * 1KG 2011 Nature Genetics http:// | ||
| + | * Lander ES. Initial impact of the sequencing of the human genome. Nature. 2011 Feb 10; | ||
| + | * Patterns and rates of exonic de novo mutations in autism spectrum disorders http:// | ||
workshop/2013/reading_list.txt · Last modified: 2012/12/05 13:35 by lessem
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