publications (journal article)

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

+ 2003

  1. M Garcia-Barcelo, MH Sham, VCH Lui, BLS Chen, J Ott, PKH Tam (2003), "Association study of PHOX2B as a candidate gene for Hirschsprung's disease", Gut, 52(4):563-567.

  2. D Gordon, MB Corwin, CS Mellersh, EA Ostrander, J Ott (2003), "Establishing appropriate genome-wide significance levels for canine linkage analyses", Journal of Heredity, 94(1):1-7.

  3. D Gordon, MA Levenstien, SJ Finch, J Ott (2003), "Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies", Pacific Symposium of Biocomputing, pp.490-501.

  4. Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JAW, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM (2003), "A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis", Nature Genetics, 35(4):349-356.

  5. J Hoh , F Matsuda, X Peng, D Markovic, MG Lathrop, J Ott (2003), "SNP haplotype tagging from DNA pools of two individuals", BMC Bioinformatics, 4(1):14.

  6. Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG, Levy M, Montagutelli X, Ahmad W, Aita VM, Gordon D, Uitto J, Whiting D, Ott J, Fischer S, Gilliam TC, Jahoda CA, Morris RJ, Panteleyev AA, Nguyen VT, Christiano AM (2003), "Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris", Cell, 113(2):249-260.

  7. PM Knappskog, J Majewski , A Livneh, PTE Nilsen, JS Bringsli, J Ott , H Boman (2003), "Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene", American Journal of Human Genetics, 72(2):375-383.

  8. MA Levenstien, Y Yang, J Ott (2003), "Statistical significance for hierarchical clustering in genetic association and microarray expression studies", BMC Bioinformatics, 4(1):62.

  9. J Liu, SH Juo, A Dewan, A Grunn, X Tong, M Brito, N Park, JE Loth, K Kanyas, B Lerer, J Endicott, G Penchaszadeh, JA Knowles, J Ott, TC Gilliam, M Baron (2003), "Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12", Molecular Psychiatry, 8(3):333-342.

  10. E Louie, J Ott, J Majewski (2003), "Nucleotide frequency variation across human genes", Genome Research, 13(12):2594-2601.

  11. Majewski J (2003), "Dependence of mutational asymmetry on gene-expression levels in the human genome", American Journal of Human Genetics, 73(3):688-692.

  12. Majewski J, Schultz DW, Weleber RG, Schain MB, Edwards AO, Matise TC, Acott TS, Ott J, Klein ML (2003), "Age-related macular degeneration - a genome scan in extended families", American Journal of Human Genetics, 73(3):540-550.

  13. J Majewski, J Ott (2003), "Amino acid substituations in the human genome - evolutionary implications of sibgle nucleotide polymorphisms", Gene,

  14. Martinez-Mir A, Zlotogorski A, Ott J, Gordon D, Christiano AM (2003), "Genetic linkage studies in alopecia areata", J INVESTIG DERMATOL SYMP PROC, 8(2):199-203

  15. Noponen-Hietala N, Kyllonen E, Mannikko M, Ilkko E, Karppinen J, Ott J, Ala-Kokko L (2003), "Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis", ANN RHEUM DIS, 62(12):1208-1214.

  16. DW Schultz, ML Klein, A Humpert, J Majewski , M Schain, RG Weleber, J Ott , TS Acott (2003), "Lack of an association of apolipoprotein E gene polymorphisms with familial age-related macular degeneration", Arch Ophthalmol. 121(5):679-683.

  17. Stiburkova B, Majewski J, Hodanova K, Ondrova L, Jerabkova M, Zikanova M, Vylet'al P, Sebesta I, Marinaki A, Simmonds A, Matthijs G, Fryns JP, Torres R, Puig JG, Ott J, Kmoch S (2003), "Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes", European Journal of Human Genetics, 11(2):145-154.

  18. A Wille, J Hoh, J Ott (2003), "Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers", Genetic Epidemiology, 25(4):350-359.

  19. Y Yang, J Hoh , C Broger, M Neeb, J Edington, K Lindpaintner, J Ott (2003), "Statistical methods for analyzing microarray feature data with replications", Journal of Computational Biology, 10(2):157-169.

  20. Y Yang, J Zhang, J Hoh , F Matsuda, P Xu, M Lathrop, J Ott (2003), "Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA", Proceedings of National Academy of Sciences, 100(12):7225-7230.