Multiple phenotypes in genome-wide genetic mapping studies

Protein and Cell

Volumn 2, Issue 7, 2011, Pages 519-522

  Ott, Jurg ^a   Wang, Jing ^a  

^a INSTITUTE OF PSYCHOLOGY   (China)

Author keywords

case control; genetic mapping; multiple phenotypes; statistical method

Indexed keywords

CASE CONTROL STUDY; GENE MAPPING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC TRAIT; GENOTYPE PHENOTYPE CORRELATION; HERITABILITY; HUMAN; LINKAGE ANALYSIS; MONTE CARLO METHOD; MULTIVARIATE ANALYSIS OF VARIANCE; PHENOTYPIC VARIATION; PRINCIPAL COMPONENT ANALYSIS; PRIORITY JOURNAL; RACE DIFFERENCE; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 80052465702     PISSN: 1674800X     EISSN: 16748018     Source Type: Journal    
DOI: 10.1007/s13238-011-1059-5     Document Type: Review

References (21)

1. Allison, D. B., Thiel, B., St Jean, P., Elston, R. C., Infante, M. C., and Schork, N. J. (1998). Multiple phenotype modeling in genemapping studies of quantitative traits: power advantages. Am J Hum Genet 63, 1190-1201.
2. Benjamini, Y. (2010). Discovering the false discovery rate. J R Stat Soc, B 72, 405-416.
3. Benjamini, Y., Drai, D., Elmer, G., Kafkafi, N., and Golani, I. (2001). Controlling the false discovery rate in behavior genetics research. Behav Brain Res 125, 279-284.
4. Bookman, E. B., Taylor, R. E., Adams-Campbell, L., and Kittles, R. A. (2002). DRD4 promoter SNPs and gender effects on Extraversion in African Americans. Mol Psychiatry 7, 786-789.
5. Braff, D. L., Freedman, R., Schork, N. J., and Gottesman, I. I. (2007). Deconstructing schizophrenia: an overview of the use of endophenotypes in order to understand a complex disorder. Schizophr Bull 33, 21-32.
6. Cheverud, J. M. (2001). A simple correction for multiple comparisons in interval mapping genome scans. Heredity 87, 52-58.
7. DeVellis, R. F. (2003). Scale development: theory and applications, 2nd ed. Thousand Oaks, Calif.: Sage Publications, Inc. viii, 171.
8. Dubay, C., Vincent, M., Samani, N. J., Hilbert, P., Kaiser, M. A., Beressi, J. P., Kotelevtsev, Y., Beckmann, J. S., Soubrier, F., Sassard, J., et al. (1993). Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats. Nat Genet 3, 354-357.
9. Hoh, J., and Ott, J. (2000). Scan statistics to scan markers for susceptibility genes. Proc Natl Acad Sci U S A 97, 9615-9617.
10. Hoh, J., Wille, A., and Ott, J. (2001). Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res 11, 2115-2119.
11. Holmkvist, J., Banasik, K., Andersen, G., Unoki, H., Jensen, T. S., Pisinger, C., Borch-Johnsen, K., Sandbaek, A., Lauritzen, T., Brunak, S., et al. (2009). The type 2 diabetes associated minor allele of rs2237895 KCNQ1 associates with reduced insulin release following an oral glucose load. PLoS One 4, e5872.
12. Klei, L., Luca, D., Devlin, B., and Roeder, K. (2008). Pleiotropy and principal components of heritability combine to increase power for association analysis. Genet Epidemiol 32, 9-19.
13. Lander, E., and Kruglyak, L. (1995). Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11, 241-247.
14. Manly, B. F. J. (2007). Randomization, bootstrap, and Monte Carlo methods in biology, 3rd ed. Boca Raton, FL: Chapman & Hall/CRC, 455.
15. Nyholt, D. R. (2004). A simple correction for multiple testing for singlenucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet 74, 765-769.
16. Ott, J. (2004). Association of genetic loci: Replication or not, that is the question. Neurology 63, 955-958.
17. Ott, J., and Rabinowitz, D. (1999). A principal-components approach based on heritability for combining phenotype information. Hum Hered 49, 106-111.
18. Patterson, N., Price, A. L., and Reich, D. (2006). Population structure and eigenanalysis. PLoS Genet 2, e190.
19. Pe'er, I., Yelensky, R., Altshuler, D., and Daly, M. J. (2008). Estimation of the multiple testing burden for genomewide association studies of nearly all common variants. Genet Epidemiol 32, 381-385.
20. Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., and Reich, D. (2006). Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38, 904-909.
21. Zhang, Q., and Ott, J. (2009). Multiple Comparisons/Testing Issues. In: Handbook on Analyzing Human Genetic Data: Computational Approaches and Software. S. Lin, and H. Zhao, eds. Berlin: Springer. 277-287.