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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

1997

1. LM Brzustowicz, JP Gardner, L Hopp, E Jeanclos, J Ott, XY Yang, Z Fekete, A Aviv (1997)
   "Linkage analysis using platelet-activating factor Ca2+ response in transformed lymphoblasts",
   Hypertension, 29:158-164.
   [abstract] [ Medline entry]

2. D Cusi, C Barlassina, T Azzani, G Casari, L Citterio, M Devoto , N Glorioso, C Lanzani, P Manunta, M Righetti, R Rivera, P Stella, C Troffa, L Zagato, G Bianchi (1997),
   "Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertension",
   LANCET, 349(9062):1353-1357
   [Medline entry]

3. Dann J, DeLisi LE, M Devoto, Laval S, Nancarrow DJ, Shields G, Smith A, Loftus J, Peterson P, Vita A, Comazzi M, Invernizzi G, Levinson DF, Wildenauer D, Mowry BJ, Collier D, Powell J, Crowe RR, Andreasen NC, Silverman JM, Mohs RC, Murray RM, Walters MK, Lennon DP, Hayward NK, Albus M, Lerer B, Maier W, Crow TJ (1997),
   "Linkage study of schizophrenia to markers within Xp11 near the MAOB gene",
   Psychiatry Research, 70(3):131-143
   [Medline entry]

4. Esterling LE, Matise TC, Sanders AR, Yoshikawa T, Overhauser J, Gershon ES, Moskowitz MT, Detera-Wadleigh SD (1997),
   "An integrated physical map of 18p112: a susceptibility region for bipolar disorder",
   Molecular Psychiatry, 2(6):501-504

5. D Gordon , Stephen J Finch, Adam L Jacobs, Nancy R Mendell, Richard M Single, Thomas G Marr (1997),
   "Association of posterior p-values of SAGE SIBPAL proportion-IBD and Haseman-Elson Statistics for ACTHR112",
   Genetic Epidemiology, 14(6), 629-634.
   [abstract]

6. HH Göring, J Ott (1997)
   "Relationship estimation in affected sib pair analysis of late onset diseases",
   European Journal of Human Genetics, 5(2):69-77.
   [abstract] [ Medline entry]

7. F Haghighi, W Li, CSJ Fann (1997)
   "Affected sibpair analysis of bipolar disorder using data on chromosome 18",
   Genetic Epidemiology, 14, 641-646.
   [ abstract] [ Medline entry]

8. F Haghighi, J Ott (1997)
   "Estimating recessive disease allele frequency based on genetic maps",
   European Journal of Human Genetics , 5(4), 203-205.
   [abstract] [ Medline entry]

9. SJ Jensen, EP Sulman, JM Marks, TC Matise, PJ Vojta, JC Barrett, GM Brodeur, PS White (1997)
   "An integrated transcript map of human chromosome 1p35-36",
   Genomics, 42(1):126-136.
   [abstract] [ Medline entry]

10. SH Juo, TH Beaty, PO Kwiterovich Jr (1997)
    "Etiologic heterogeneity of hyperapobetalipoproteinemia (HyperapoB): the results from segregation analysis in families enriched for coronary artery disease",
    Arterioscler Thromb Vasc Biol 17: 2729-2736.
    [ Medline entry]

11. SH Juo , TH Beaty, LD Duffy, NE Maestri, VL Prenger, J Zeiger, HH Lei, J Coresh, (1997)
    "A comprehensive analysis of a common disease and its underlying traits",
    Genetic Epidemiology, 14(6):815-820.
    [ Medline entry]

12. M Karayiorgou, M Altemus, BL Galke, D Goldman, DL Murphy, J Ott , JA Gogos (1997)
    "Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder",
    Proceedings of National Academy of Sciences (USA), 94(9), 4572-4575.
    [abstract] [ Medline entry] [ Full Text (PDF)] [ Full Text (postscript)]

13. Lazzarini A, Schwarz KO, Jiang S, Stenroos ES, T Lehner, Johnson WG (1997),
    "Pelizaeus-Merzbacher-like disease: exclusion of the proteolipid protein locus and documentation of a new locus on Xq",
    Neurology, 49(3):824-832

14. SM Leal, J Ott (1997)
    "Analysis of two-locus traits under heterogeneity for recessive versus dominant inheritance",
    Genetic Epidemiology, 14, 1097-1100.
    [abstract] [ Medline entry]

15. A Lernmark, G Eisenbarth, L Ducat, HA Erlich, D Faustman, J Ott , MA Permutt, RS Spielman, J-X She, J Todd (1997)
    "Family cell lines available for research - an endangered resource?"
    American Journal of Human Genetics, 61(3),778-779

16. W Li (1997)
    "The study of correlation structures of DNA sequences - a critical review",
    Computer & Chemistry (special issue on open problems of computational biology), 21(4), 257-272.
    [ abstract] [ Medline entry] [ full text (PDF)]

17. W Li (1997)
    "The Complexity of DNA: the measure of compositional heterogeneity in DNA sequences and measures of complexity",
    Complexity, 3(2), 33-37.
    [ full text (PDF) ]

18. PR Lucek, J Ott (1997)
    "Neural network analysis of complex traits",
    Genetic Epidemiology, 14, 1101-1106.
    [abstract]

19. TL McGee, M Devoto, J Ott, EL Berson, TP Dryja (1997),
    "Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele",
    American Journal of Human Genetics, 61(5):1059-1066
    [abstract] [Medline entry ] [ full text (PDF) ]

20. B Mulller-Myhsok, H-J Heiland, CR Mulller, G Meng, T Grimm, J Ott (1997)
    "Mapping undetected mutations within a gene - evidence for two preferential regions in the DMD gene",
    Human Heredity, 47, 61-65

21. J Ott,
    "Vital statistics" (Book Review),
    Trends in Genetics, 13(9), 379

22. J Ott (1997),
    "Testing for interference in human genetic maps",
    Journal of Molecular Medicine, 75(6):414-419.
    [abstract] [ Medline entry] [ full text (PDF) ]

23. J Ott, D Rabinowitz (1997)
    "The effect of marker heterozygosity on the power to detect linkage disequilibrium",
    Genetics, 147, 927-930
    [abstract] [ Medline entry]

24. U Peters, G Senger, M Rahlmann, I Du Chesne, I Stec, MR Kohler, J Weissenbach, SM Leal , HG Koch, T Deufel, E Harms (1997)
    "Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13",
    European Journal of Human Genetics , 5(1):9-14.
    [ Medline entry]

25. WK Scott, MC Speer, SM Leal , L Brzustowicz, MA Pericak-Vance (1997)
    "False positive rates in a genomic screen for complex quantitative traits",
    Genetic Epidemiology , 14, 891-896
    [ Medline entry]

26. Tsou HC, Teng DH, Ping XL, Brancolini V, Davis T, Hu R, Xie XX, Gruener AC, Schrager CA, Christiano AM, Eng C, Steck P, Ott J, Tavtigian SV, Peacocke M (1997),
    "The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in RCA1-negative cases",
    American Journal of Human Genetics, 61(5):1036-1043
    [abstract] [ Medline entry] [ full text (PDF)]

27. JM Vance, TC Matise, R Wooster, BC Schutte, GA Bruns, N van Roy, GM Brodeur, YX Tao, S Gregory, A Weith, M Vaudin, P White (1997),
    "Report and abstracts of the third international workshop on human chromosome 1 mapping 1997",
    Cytogenetics and Cell Genetics, 78(3-4):154-82

28. K Wilhelmsen, D Mirel, K Marder, SM Leal , M-XTang, R Mayeux (1997)
    "Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13?",
    Annuals of Neurology, 41, 891-896
    [ Medline entry]