GWAS: heritability missing in action?
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[1] J. Stockman. Association between Microdeletion and Microduplication at 16p11.2 and Autism , 2009 .
[2] Tomas W. Fitzgerald,et al. Origins and functional impact of copy number variation in the human genome , 2010, Nature.
[3] Ku Chee Seng,et al. The success of the genome-wide association approach: a brief story of a long struggle , 2008, European Journal of Human Genetics.
[4] Shamil Sunyaev,et al. A limited role for balancing selection. , 2005, Trends in genetics : TIG.
[5] Scott M. Williams,et al. Epistasis and its implications for personal genetics. , 2009, American journal of human genetics.
[6] Joanna L. Kelley,et al. Positive selection in the human genome: from genome scans to biological significance. , 2008, Annual review of genomics and human genetics.
[7] G. V. Ommen. Popper revisited: GWAS here, last year , 2008, European Journal of Human Genetics.
[8] Joseph A. Gogos,et al. Strong association of de novo copy number mutations with sporadic schizophrenia , 2008, Nature Genetics.
[9] K. Weiss. Tilting at Quixotic Trait Loci (QTL): An Evolutionary Perspective on Genetic Causation , 2008, Genetics.
[10] P. Green,et al. Scan of Human Genome Reveals No New Loci Under Ancient Balancing Selection , 2006, Genetics.
[11] B. Maher. Personal genomes: The case of the missing heritability , 2008, Nature.
[12] E. Génin,et al. Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? , 2007, European Journal of Human Genetics.
[13] Steven A McCarroll,et al. Extending genome-wide association studies to copy-number variation. , 2008, Human molecular genetics.
[14] Trudy F C Mackay,et al. The genetic architecture of quantitative traits: lessons from Drosophila. , 2004, Current opinion in genetics & development.
[15] Thomas W. Mühleisen,et al. Large recurrent microdeletions associated with schizophrenia , 2008, Nature.
[16] J H Moore,et al. From genotypes to genometypes: putting the genome back in genome-wide association studies , 2009, European Journal of Human Genetics.
[17] B. Maher,et al. The case of the missing heritability , 2008 .
[18] M. Nöthen,et al. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness , 2009, Human Genetics.
[19] P. Visscher,et al. Rare chromosomal deletions and duplications increase risk of schizophrenia , 2008, Nature.
[20] Xavier Estivill,et al. Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies , 2022 .
[21] J. Hein,et al. Using biological networks to search for interacting loci in genome-wide association studies , 2009, European Journal of Human Genetics.
[22] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[23] W. Bodmer,et al. Common and rare variants in multifactorial susceptibility to common diseases , 2008, Nature Genetics.
[24] M. Krawczak,et al. Hypotheses in genome-wide association scans , 2008, European Journal of Human Genetics.