Response to browning and browning

American Journal of Human Genetics

Volumn 89, Issue 1, 2011, Pages 193-195

  Goddard, Michael E ^a,b   Lee, S Hong ^c   Yang, Jian ^c   Wray, Naomi R ^c   Visscher, Peter M ^c  

^a DEPARTMENT OF PRIMARY INDUSTRIES   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ETHNICITY; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HEREDITY; HUMAN; LETTER; PHENOTYPE; POPULATION STRUCTURE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 80051497514     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.05.022     Document Type: Letter

References (8)

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2. Yang, J., Benyamin, B., McEvoy, B.P., Gordon, S., Henders, A.K., Nyholt, D.R., Madden, P.A., Heath, A.C., Martin, N.G., Montgomery, G.W., et al. (2010). Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565-569.
3. Risch, N., Burchard, E., Ziv, E., and Tang, H. (2002). Categorization of humans in biomedical research: Genes, race and disease. Genome Biol. 3, comment2007.1-comment2007.12.
4. Browning, B.L., and Browning, S.R. (2011). A fast, powerful method for detecting identity by descent. Am. J. Hum. Genet. 88, 173-182.
5. Wellcome Trust Case Control Consortium. (2007). Genomewide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661-678.
6. Yang, J., Lee, S.H., Goddard, M.E., and Visscher, P.M. (2011). GCTA: A tool for genome-wide complex trait analysis. Am. J. Hum. Genet. 88, 76-82.
7. Haldane, J.B.S. (1919). The combination of linkage values and the calculation of distances between the loci of linked factors. J. Genet. 8, 299-309.
8. Kang, H.M., Sul, J.H., Service, S.K., Zaitlen, N.A., Kong, S.Y., Freimer, N.B., Sabatti, C., and Eskin, E. (2010). Variance component model to account for sample structure in genome-wide association studies. Nat. Genet. 42, 348-354.