Publications
Dr. Sullivan has 170 total publications (153 journal articles, 17
chapters or invited articles, and 2 miscellaneous items). Recent
papers are shown below. Click here for a PubMed search.
Furberg, H., P. Lichtenstein, N. L. Pedersen, C. M. Bulik and P. F. Sullivan (In press). Cigarettes and oral snuff use in Sweden: prevalence and transitions. Addiction.
Hemminger, B. M., B. Saelim and P. F. Sullivan (2006). TAMAL: An integrated approach to choosing SNPs for genetic studies of human complex traits. Bioinformatics 22: 626-7.
Kato, K., P. Sullivan, B. Evengård and N. L. Pedersen (In press). Chronic widespread pain and its comorbidities: A population-based study. Archives of Internal Medicine.
Lichtenstein, P., C. Bjork, C. M. Hultman, E. M. Scolnick, P. Sklar and P. F. Sullivan (In press). Recurrence risks for schizophrenia in a Swedish national cohort. Psychological Medicine.
Perkins, D. O., C. Jeffries and P. Sullivan (2004). Expanding the 'central dogma': the regulatory role of nonprotein coding genes and implications for the genetic liability to schizophrenia. Mol Psychiatry 10: 69-78.
Pinheiro, A., R. Keefe, T. Skelly, M. Olarte, K. Leviel, L. Lange, E. M. Lange, T. Stroup, J. Lieberman and P. F. Sullivan (In press). AKT1 and neurocognition in schizophrenia. Australian and New Zealand Journal of Psychiatry.
Sullivan, P. F., B. Evengard, A. Jacks and N. L. Pedersen (2005). Twin analyses of chronic fatigue in a Swedish national sample. Psychol Med 35(9): 1327-36.
Sullivan, P. F., R. S. E. Keefe, L. A. Lange, E. M. Lange, T. S. Stroup, J. A. Lieberman and P. F. Maness (In press). NCAM1 and neurocognition in schizophrenia. Biological Psychiatry.
Sullivan, P. F., K. S. Kendler and M. C. Neale (2003). Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Archives of General Psychiatry 60: 1187-92.
Sullivan, P. F., P.-H. Kuo, B. T. Webb, M. C. Neale, J. Vittum, H. Furberg, D. Walsh, D. G. Patterson, B. Riley, C. A. Prescott and K. S. Kendler (Submitted). Genomewide linkage survey of nicotine dependence phenotypes.
Sullivan, P. F., G. W. Montgomery, J. J. Hottenga, N. R. Wray, D. I. Boomsma and N. G. Martin (In press). Empirical evaluation of the genetic similarity of samples from twin registries in Australia and the Netherlands using 359 STRP markers. Twin Res Hum Genet.
Sullivan, P. F., B. M. Neale, M. C. Neale, E. J. C. G. van den Oord and K. S. Kendler (2003). Multipoint and single point non-parametric linkage analysis with imperfect data. Am J Med Genet 121B: 89-94.
van den Oord, E. J. and P. F. Sullivan (2003). A framework for controlling false discovery rates and minimizing the amount of genotyping in the search for disease mutations. Hum Hered 56(4): 188-99.
van den Oord, E. J. C. G., P. F. Sullivan, X. Jiang, D. Walsh, F. A. O'Neill, K. S. Kendler and B. Riley (2003). Identification of a high risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish Study of High Density Schizophrenia families. Molecular Psychiatry 8: 499-510.
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Trainees
Furberg, Helena - 2003-present, UNC-CH K-award mentor
Leviel, Keren - 2004-2006, UNC-CH Pre-doc
Losh, Molly - 2005 present, UNC-CH K-award mentor
Neale, Ben - 2001 2003, VCU Undergrad
Pinheiro, Andrea - 2005 2006, UNC-CH Visiting scientist
Tozzi, Federica - 2001 2002, VCU Visiting scientist
Tsai, Huei-Ting - 2004 present, UNC-CH Pre-doc
Wojczynski, Mary - 2003 2006, UNC-CH Pre-doc
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