Moore JH - Search Results

1

Genetics, statistics and human disease: analytical retooling for complexity.

Thornton-Wells TA, Moore JH, Haines JL. Thornton-Wells TA, et al. Among authors: moore jh. Trends Genet. 2004 Dec;20(12):640-7. doi: 10.1016/j.tig.2004.09.007. Trends Genet. 2004. PMID: 15522460 Review.

2

Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data.

Thornton-Wells TA, Moore JH, Haines JL. Thornton-Wells TA, et al. Among authors: moore jh. BMC Bioinformatics. 2006 Apr 12;7:204. doi: 10.1186/1471-2105-7-204. BMC Bioinformatics. 2006. PMID: 16611359 Free PMC article.

3

The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings?

Williams SM, Haines JL, Moore JH. Williams SM, et al. Among authors: moore jh. Bioessays. 2004 Feb;26(2):170-9. doi: 10.1002/bies.10401. Bioessays. 2004. PMID: 14745835

4

Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.

Thornton-Wells TA, Moore JH, Martin ER, Pericak-Vance MA, Haines JL. Thornton-Wells TA, et al. Among authors: moore jh. Genet Epidemiol. 2008 Apr;32(3):187-203. doi: 10.1002/gepi.20294. Genet Epidemiol. 2008. PMID: 18076107 Free PMC article.

5

Recurrent tissue-specific mtDNA mutations are common in humans.

Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, Hoffman RD, Haines JL, Murdock DG, Mortlock DP, Williams SM. Samuels DC, et al. Among authors: moore jh. PLoS Genet. 2013 Nov;9(11):e1003929. doi: 10.1371/journal.pgen.1003929. Epub 2013 Nov 7. PLoS Genet. 2013. PMID: 24244193 Free PMC article.

6

Problems with genome-wide association studies.

Williams SM, Canter JA, Crawford DC, Moore JH, Ritchie MD, Haines JL. Williams SM, et al. Among authors: moore jh. Science. 2007 Jun 29;316(5833):1840-2. Science. 2007. PMID: 17605173 No abstract available.

7

Analysis of the RELN gene as a genetic risk factor for autism.

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Skaar DA, et al. Among authors: moore jh. Mol Psychiatry. 2005 Jun;10(6):563-71. doi: 10.1038/sj.mp.4001614. Mol Psychiatry. 2005. PMID: 15558079 Clinical Trial.

8

Basic statistics.

Moore JH, Thornton TA, Ritchie MD. Moore JH, et al. Curr Protoc Hum Genet. 2003 Aug;Appendix 3:Appendix 3M. doi: 10.1002/0471142905.hga03ms37. Curr Protoc Hum Genet. 2003. PMID: 18428338 Review.

9

A cellular automata approach to detecting interactions among single-nucleotide polymorphisms in complex multifactorial diseases.

Moore JH, Hahn LW. Moore JH, et al. Pac Symp Biocomput. 2002:53-64. Pac Symp Biocomput. 2002. PMID: 11928505 Free article.

10

Power of multifactor dimensionality reduction for detecting gene-gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity.

Ritchie MD, Hahn LW, Moore JH. Ritchie MD, et al. Among authors: moore jh. Genet Epidemiol. 2003 Feb;24(2):150-7. doi: 10.1002/gepi.10218. Genet Epidemiol. 2003. PMID: 12548676

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