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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

1992

1. JF Arena, C Schwartz, R Stevenson, L Lawrence, A Carpenter, R Duara, D Ledbetter, T Huang, T Lehner, J Ott, HA Lubs (1992)
   "Spastic paraplegia with iron deposits in the basal ganglia A new X-linked mental retardation syndrome",
   American Journal of Medical Genetics, 43, 479-490
   [ abstract]

2. LM Brzustowicz, PW Kleyn, FM Boyce, LL Lien, AP Monaco, GK Penchaszadeh, K Das, CH Wang, TL Munsat, J Ott, LM Kunkel, TC Gilliam (1992)
   "Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6",
   Genomics, 13, 991-998.
   [ abstract ]

3. RJ Daniels, NH Thomas, RN MacKinnon, T Lehner, J Ott, TJ Flint, V Dubowitz, J Ignatius, M Donner, K Zerres, M Rietschel, WOC Cookson, LM Brzustowicz, TC Gilliam, KE Davies (1992)
   "Linkage analysis of spinal muscular atrophy",
   Genomics, 12, 335-339
   [ abstract]

4. KA Ellison, CP Fill, J Terwilliger, LJ DeGennaro, A Martin-Gallardo, M Anvret, AK Percy, J Ott, H Zoghbi (1992)
   "Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis",
   American Journal of Human Genetics, 50:278-287.
   [ abstract]

5. M Maziade, MA Roy, JP Fournier, D Cliche, C Merette, C Caron, Y Garneau, M Montgrain, C Shriqui, C Dion, et al (1992)
   "Reliability of best-estimate diagnosis in genetic linkage studies of major psychoses: results from the Quebec pedigree studies",
   American Journal of Psychiatry , 149(12), 1674-1686 (1992)
   [ abstract]

6. R Medori, H-J Tritschler, A LeBlanc, F Villare, V Manetto, HY Chen, R Xue, S Leal, P Montagna, P Cortelli, P Tinuper, P Avoni, M Mochi, A Baruzzi, JJ Hauw, J Ott, E Lugaresi, L Autilio-Gambetti, P Gambetti (1992)
   "Fatal familial insomnia: a prion disease with a mutation at codon 178 of the prion protein gene",
   New England Journal of Medicine, 326: 444-449.
   [ abstract]

7. C Merette, M-C King, J Ott (1992)
   "Heterogeneity analysis of breast cancer families by using age at onset as a covariate",
   American Journal of Human Genetics, 50:515-519.
   [ abstract]

8. HW Moser, AB Moser, KD Smith, A Bergin, J Boral, J Shankroff, OC Stine, C Merette, J Ott, W Krivit, E Shapiro (1992)
   "Adreno-leukodystrophy: Phenotypic variability; implications for therapy",
   Journal of Inher Metab Dis, 15: 645-664.
   [ abstract]

9. J Ott (1992)
   "Strategies for characterizing highly polymorphic markers in human gene mapping",
   American Journal of Human Genetics, 51:283-290.
   [ abstract]

10. J Ott (1992)
    "Introductory remarks: genetic models and statistical approaches",
    Ann Med, 24, 375-377

11. J Ott (1992)
    "The future of multilocus linkage analysis",
    Ann Med, 24:401-403.
    [ abstract]

12. RB Petersen, M Tabaton, L Berg, B Schrank, RM Torack, S Leal , J Julien, C Vital, B Deleplanque, WW Pendlebury, D Drachman, TW Smith, JJ Martin, M Oda, P Montagna, J Ott , L Autilio-Gambetti, E Lugaresi, P Gambetti (1992)
    Analysis of the prion protein gene in thalamic dementia ,
    Neurology 42, 1859-1863

13. JD Terwilliger, Y Ding, J Ott (1992)
    On the relative importance of marker heterozygosity and intermarker distance in gene mapping ,
    Genomics, 13: 951-956.
    [ Medline entry]

14. JD Terwilliger, J Ott (1992)
    "A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions",
    Cytogenetics and Cell Genetics, 59, 142-144

15. J Terwilliger, J Ott (1992)
    A haplotype-based 'haplotype relative risk' approach to detecting allelic associations ,
    Human Heredity 42:337-346
    [Medline entry]

16. V Vieland, DA Greenberg, SE Hodge, J Ott (1992)
    "Linkage analysis of two-locus diseases under single-locus and two-locus analysis models",
    Cytogenetics and Cell Genetics, 59, 145-146

17. J Wagstaff, JH Knoll, KA Glatt, YYShugart , A Sommer, M Lalande (1992)
    "Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression ",
    Nature Genetics, 1:291-294
    [ abstract ]

18. DE Weeks, T Lehner, J Ott (1992)
    "Preliminary ranking procedures for multilocus ordering based on radiation hybrid data",
    Cytogenetics and Cell Genetics, 59:125-127.