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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

1989

1. K Hsiao, HF Baker, TJ Crow, M Poulter, F Owen, JD Terwilliger, D Westaway, J Ott, SB Prusiner (1989),
   "Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome",
   Nature, 338:342-345.
   [abstract] [Medline entry]

2. CA Kaufmann, LE DeLisi, T Lehner , TC Gilliam (1989),
   "Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q",
   Schizophrenia Bulletin, 15, 441-452

3. B Keats, J Ott, M Conneally (1989),
   "Human Gene Mapping 10 - Report of the committee on linkage and gene order" (Meeting Report),
   Cytogenetics and Cell Genetics, 51, 459-502

4. T Lehner, LA Sandkuyl, J Ott (1989),
   "Linkage analysis for a disease with a complex mode of inheritance in a simulated data set",
   Progress in Clinical & Biological Research, 329:,141-146

5. J Ott (1989) ,
   "Computer-simulation methods in human linkage analysis",
   Proceeding of National Academy of Sciences (USA), 86: 4175-4178.
   [abstract ] [ Medline entry]

6. J Ott (1989) ,
   "Statistical properties of the haplotype relative risk",
   Genetic Epidemiology, 6:127-130.
   [abstract] [ Medline entry]

7. A Palotie, P Vaisanen, J Ott, L Ryhanen, K Elima, M Vikkula, K Cheah, E Vuorio, L Peltonen (1989),
   "Predisposition to familial osteoarthrosis is linked to type II collagen gene",
   Lancet, 1:924-927 (April 29)
   [ abstract] [ Medline entry ]

8. LA Sandkuyl (1989),
   "Analysis of affected sib-pairs using information from extended families",
   in Multipoint mapping and linkage based upon affected pedigree members, Genetic Analysis Workshop 6, eds RC Elston, A Spence, SE Hodge, J MacCluer (Alan R Liss, New York), 117-122

9. LA Sandkuyl, J Ott (1989),
   "Affective disorders: Evaluation of a three-allele model accounting for clinical heterogeneity",
   Genetic Epidemiology, 6:265-269.
   [abstract] [ Medline entry]

10. LA Sandkuyl, J Ott (1989) ,
    "Determining informativity of marker typing for genetic counseling in a pedigree",
    Human Genetics, 82:159-162.
    [abstract] [ Medline entry]

11. E-M Sankila, T Lehner, AW Eriksson, H Forsius, J Karna, D Page, J Ott , A de la Chapelle (1989),
    "Haplotype and multipoint linkage analysis in Finnish choroideremia families",
    Human Genetics, 84:66-70.
    [ abstract] [ Medline entry]

12. DE Weeks, J Ott (1989),
    "Risk calculations under heterogeneity" (Letter to the Editor),
    American Journal of Human Genetics, 45, 819-821

13. HY Zoghbi, LA Sandkuyl, J Ott, SP Daiger, M Pollack, WE O'Brien, AL Beaudet (1989),
    "Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6 using multilocus linkage analysis",
    American Journal of Human Genetics, 44:255-263
    [ abstract] [ Medline entry]