Ott J - Search Results

1

Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia.

Shmulewitz D, Auerbach SB, Lehner T, Blundell ML, Winick JD, Youngman LD, Skilling V, Heath SC, Ott J, Stoffel M, Breslow JL, Friedman JM. Shmulewitz D, et al. Among authors: ott j. Hum Hered. 2001;51(1-2):8-19. doi: 10.1159/000022953. Hum Hered. 2001. PMID: 11096265

2

Heterogeneity for multiple disease loci in linkage analysis.

Bhat A, Heath SC, Ott J. Bhat A, et al. Among authors: ott j. Hum Hered. 1999 Jul;49(4):229-31. doi: 10.1159/000022879. Hum Hered. 1999. PMID: 10436385

3

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.

Gordon D, Heath SC, Liu X, Ott J. Gordon D, et al. Among authors: ott j. Am J Hum Genet. 2001 Aug;69(2):371-80. doi: 10.1086/321981. Epub 2001 Jul 5. Am J Hum Genet. 2001. PMID: 11443542 Free PMC article.

4

True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms.

Gordon D, Heath SC, Ott J. Gordon D, et al. Among authors: ott j. Hum Hered. 1999 Mar;49(2):65-70. doi: 10.1159/000022846. Hum Hered. 1999. PMID: 10077724

5

Power loss for multiallelic transmission/disequilibrium test when errors introduced: GAW11 simulated data.

Gordon D, Matise TC, Heath SC, Ott J. Gordon D, et al. Among authors: ott j. Genet Epidemiol. 1999;17 Suppl 1:S587-92. doi: 10.1002/gepi.1370170795. Genet Epidemiol. 1999. PMID: 10597497

6

An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design.

Gordon D, Leal SM, Heath SC, Ott J. Gordon D, et al. Among authors: ott j. Pac Symp Biocomput. 2000:663-74. doi: 10.1142/9789814447331_0064. Pac Symp Biocomput. 2000. PMID: 10902214 Free PMC article.

7

Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator.

Mérette C, Lehner T, Ott J. Mérette C, et al. Among authors: ott j. Genet Epidemiol. 1993;10(6):455-9. doi: 10.1002/gepi.1370100621. Genet Epidemiol. 1993. PMID: 8314043

8

Linkage analysis for a disease with a complex mode of inheritance in a simulated data set.

Lehner T, Sandkuyl LA, Ott J. Lehner T, et al. Among authors: ott j. Prog Clin Biol Res. 1989;329:141-6. Prog Clin Biol Res. 1989. PMID: 2622943 No abstract available.

9

Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.

Brzustowicz LM, Mérette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TC. Brzustowicz LM, et al. Among authors: ott j. Hum Hered. 1993 Nov-Dec;43(6):380-7. doi: 10.1159/000154164. Hum Hered. 1993. PMID: 7904586

10

Preliminary ranking procedures for multilocus ordering based on radiation hybrid data.

Weeks DE, Lehner T, Ott J. Weeks DE, et al. Among authors: ott j. Cytogenet Cell Genet. 1992;59(2-3):125-7. doi: 10.1159/000133222. Cytogenet Cell Genet. 1992. PMID: 1737477 No abstract available.

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