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

+ 2005

  1. G Bart, MJ Kreek, J Ott , KS LaForge, D Proudnikov, L Pollak, M Heilig (2005), "Increased attributable risk related to a functional mu-opioid receptor gene polymorphism in association with alcohol dependence in central Sweden", Neuropsychopharmacology, 30(2):417-422.

  2. Gabriela Bleiber, Margaret May, Raquel Martinez, Pascal Meylan, Jurg Ott, Jacques S. Beckmann, Amalio Telenti, the Swiss HIV Cohort Study (2005), "Use of a combined ex vivo/in vivo population approach for screening of human genes involved in the human immunodeficiency virus type 1 life cycle for variants influencing disease progression", Journal of Virology, 79(20):12674-12680.

  3. A. Keith Dunker, Marc S. Cortese,Pedro Romero, Lilia M. Iakoucheva, Vladimir N. Uversky (2005), "The roles of intrinsic disorder in protein interaction networks", FEBS Journal, 272(20):5129-5148.

  4. P J Francis, D W Schultz, A M Gregory, M B Schain, R Barra, J Majewski, J Ott, T Acott, R G Weleber and M L Klein (2005), "Genetic and phenotypic heterogeneity in pattern dystrophy", British Journal of Ophthalmology, 89:1115-1119.

  5. Cynthia Helms, Nancy L. Saccone, Li Cao, Jil A. Wright. Daw, Kai Cao, Tony M. Hsu, Patricia Taillon-Miller, Shenghui Duan, Derek Gordon, Brandon Pierce, Jurg Ott, John Rice, Marcelo A. Fernandez-Vina, Pui-Yan Kwok, Alan Menter, Anne M. Bowcock (2005), "Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR", Human Genetics, in press.

  6. F Ji , Y Yang, C Haynes , SJ Finch, D Gordon (2005), "Computing asymptotic power and sample size for case-control genetic association studies in the presence of phenotype and/or genotype misclassification errors", Stat Appl Genet Mol Biol., 4(1):37.

  7. JJ Jim, N Noponen-Hietala, KM Cheung, J Ott, J Karppinen, A Sahraravand, KD Luk, SP Yip, PC Sham, YQ Song, JC Leong, KS Cheah, L Ala-Kokko, D Chan (2005), "The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration", Spine, 30(24):2735-2742.

  8. Robert J. Klein , Caroline Zeiss, Emily Y. Chew, Jen-Yue Tsai, Richard S. Sackler , Chad Haynes , Alice K. Henning, John Paul SanGiovanni, Shrikant M. Mane, Susan T. Mayne, Michael B. Bracken, Frederick L. Ferris, Jurg Ott , Colin Barnstable, Josephine Hoh (2005), "Complement factor H polymorphism in age-related macular degeneration", Science, 308:385-389.

  9. Orna Levran, Claire Attwooll, Rashida T Henry, Kelly L Milton, Kornelia Neveling, Paula Rio, Sat Dev Batish, Reinhard Kalb, Eunike Velleuer, Sandra Barral, Jurg Ott, John Petrini, Detlev Schindler, Helmut Hanenberg, Arleen D Auerbach (2005), "The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia", Nature Genetics, 37:931-933.

  10. Daniela Markovic, Xiagna Tang, Mallikarjunrao Guruju, Mark A. Levenstien, Josephine Hoh, Ashok Kumar, Jurg Ott (2005), "Association of angiotensinogen gene polymorphisms with essential hypertension in African-Americans and Caucasians", Human Heredity, 60(2):89-96.

  11. N Noponen-Hietala, I Virtanen, R Karttunen, S Schwenke, E Jakkula, H Li, R Merikivi, S Barral, J Ott , J Karppinen, L Ala-Kokko (2005), "Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica", Pain, 114(1-2):186-194.

  12. J Xu, Y Yang, J Ott (2005), "Survival analysis of microarray expression data by transformation models", Computational Biology and Chemistry, 29(2):91-94.

  13. Slobodan Vucetic, Zoran Obradovic, Vladimir Vacic, Predrag Radivojac, Kang Peng, Lilia M. Iakoucheva, Marc S. Cortese, J. David Lawson, Celeste J. Brown, Jason G. Sikes, Crystal D. Newton, A. Keith Dunker (2005), "DisProt: a database of protein disorder", Bioinformatics, 21(1):137-140.

  14. Sepideh Zareparsi, Kari E. H. Branham, Mingyao Li, Sapna Shah, Robert J. Klein, Jurg Ott, Josephine Hoh, Goncalo R. Abecasis, Anand Swaroop (2005), "Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration", American Journal of Human Genetics, 77:149-153.