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books | meeting abstracts | book chapters
Rockefeller: 2007 | 2006 | 2005 | 2004 | 2003 | 2002 | 2001 | 2000 | 1999 | 1998 | 1997 | 1996
Columbia: 1995 | 1994 | 1993 | 1992 | 1991 | 1990 | 1989 | 1988
1987 | 1986 | 1985 | 1984 | 1983 | 1982 | 1981 | 1980 | 1979 | 1978 | 1977 | 1976 | 1975 | 1974

2000

1. Bulayeva KB, Leal SM, Pavlova TA, Kurbanov, Coover S, Bulayev O, Byerley W (2000),
   "The genetic epidemiology of schizophrenia in highland isolates of Daghestan (Northern Caucasus, Russia)",
   American Journal Medical Genetics, 10:67-72.

2. D Gordon, SM Leal, SC Heath, J Ott (2000),
   "An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design",
   Proceedings of the Fifth Pacific Symposium on Biocomputing, 663-674.

3. D Gordon , I Simonic, J Ott (2000)
   "Significant evidence for linkage disequilibrium over 5-cM in Afrikaners",
   Genomics, 66:87-92.

4. HHH Goring , JD Terwilliger (2000),
   "Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes",
   American Journal of Human Genetics, 66(3):1095-1106.
   [ full text (PDF) ]

5. HHH Goring , JD Terwilliger (2000),
   "Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions",
   American Journal of Human Genetics, 66(3):1107-1118
   [ full text (PDF) ]

6. HHH Goring , JD Terwilliger (2000),
   "Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters",
   American Journal of Human Genetics, 66:1298-1309.
   [ full text (PDF) ]

7. HHH Goring , JD Terwilliger (2000),
   "Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the model of inheritance cannot accurately specified",
   American Journal of Human Genetics, 66:1310-1327.
   [ full text (PDF) ]

8. FM Hafner, AA Salam, TE Linder, D Balmer, A Baumer, AA Schinzel, T Spillmann, SM Leal (2000)
   "A novel locus (DFNA24) for prelingual nonprogressive autosomal domninant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred" (report),
   American Journal of Human Genetics, 66:1437-1442.
   

9. J Hoh , SE Hodge (2000),
   "A measure of phase ambiguity in pairs of SNPs in the presence of linkage disequilibrium",
   Human Heredity, 50(6): 359-364.

10. J Hoh, J Ott (2000),
    "Complex inheritance and localizing disease genes",
    Human Heredity, 50:85-89.

11. J Hoh, J Ott (2000),
    "Scan statistics to scan markers for susceptibility genes",
    Proceedings of National Academy of Sciences (USA), 97(17):9615-9617.

12. J Hoh, A Wille, R Zee, S Cheng, R Reynolds, K Lindpaintner, J Ott (2000),
    "Selecting SNPs in two-stage analyses of disease association data: a model-free approach",
    Annals of Human Genetics, 64:413-417.

13. FZ Hu, RA Preston, JC Post, GJ White, LW Kikuchi, X Wang, SM Leal, MA Levenstien, J Ott , TW Self, G Allen, RS Stiffler, C McGraw, EA Pulsifer-Anderson, GD Ehrlich (2000),
    "Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14",
    JAMA, 28:325-334

14. SH Juo, Z Han, JD Smith, L Colangelo, K Liu (2000),
    "A common polymorphism in the promoter region of the microsomal triglyceride transfer protein gene influences cholesterol, triglyceride and ApolipoproteinB levels in young African American men: results from the CARDIA study",
    Arterioscler Thromb Vasc Biology, in press.

15. Kimonis VE, Kovach MJ, Waggoner B, Leal S, Salam A, Davis K, Khardori R, Gelber D (2000),
    "Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone",
    Genetics in Medicine, 2:232-241.

16. SM Leal, J Ott (2000),
    "Effects of stratification in the analysis of affected-sib-pair data: benefits and costs",
    American Journal of Human Genetics, 66(2):567-575.

17. W Li, J Reich (2000),
    "A complete enumeration and classification of two-locus disease models",
    Human Heredity, 50(6):334-349.

18. J Majewski, J Ott (2000),
    "GT repeats are associated with recombination on human chromosome 22",
    Genome Research, 10:1108-1114.

19. C Merette, A Brassard, A Potvin, H Bouvier, F Rousseau, C Emond, L Bissonnette, MA Roy, M Maziade, J Ott , Caron C (2000),
    "Significant Linkage for Tourette Syndrome in a Large French Canadian Family",
    American Journal of Human Genetics, 67:1008-1013.

20. M Mottes, S Mirandola, F Rigatelli, F Zolezzi, V Lisi, D Gordon , PF Pignatti (2000),
    "Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan Syndrome",
    Human Heredity, 50(3):175-179.

21. DR Nyholt (2000),
    "All LODs are not created equal",
    American Journal of Human Genetics,67:282-288.

22. J Ott (2000),
    "Predicting the range of linkage disequilibrium",
    Proceedings of National Academy of Sciences (USA), 97:2-3.

23. J Ott, J Hoh (2000),
    "Statistical approaches to gene mapping",
    American Journal of Human Genetics,67:289-294.

24. Salam AA, Haefner FM, Linder T, Spillmann T, Schinzel A, Leal SM (2000),
    "A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred",
    American Journal of Human Genetics, 66:1984-1988

25. Blanka Stiburkova, Jacek Majewski, Ivan Sebesta, Wenyong Zhang, Jurg Ott, and Stanislav Kmoch (2000),
    "Familial Juvenile Hyperuricemic Nephropathy: localization of the gene on chromosome 16p11.2and evidence for genetic heterogeneity" (report),
    American Journal of Human Genetics, 66(6):1989-1994.
    [ full text (PDF) ]

26. JD Terwilliger, HHH Goring (2000),
    "Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design",
    Human Biology , 72(1):63-132.