Vanderbilt University School of Medicine

Dilks, Holli H , Ph.D.

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Phone Number: 615.343.2607


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1175K Light Hall

1175K Light Hall 37232-0700

Hendrickson, SL, Hutcheson, HB, Ruiz-Pesini, E, Poole, JC, Lautenberger, J, Sezgin, E, Kingsley, L, Goedert, JJ, Vlahov, D, Donfield, S, Wallace, DC, O''Brien, SJ. Mitochondrial DNA haplogroups influence AIDS progression. AIDS, 22(18), 2429-39, 2008. PMCID:2699618

Hutcheson, HB, Lautenberger, JA, Nelson, GW, Pontius, JU, Kessing, BD, Winkler, CA, Smith, MW, Johnson, R, Stephens, R, Phair, J, Goedert, JJ, Donfield, S, O''Brien, SJ. Detecting AIDS restriction genes: from candidate genes to genome-wide association discovery. Vaccine, 26(24), 2951-65, 2008.

An, P, Wang, LH, Hutcheson-Dilks, H, Nelson, G, Donfield, S, Goedert, JJ, Rinaldo, CR, Buchbinder, S, Kirk, GD, O''Brien, SJ, Winkler, CA. Regulatory polymorphisms in the cyclophilin A gene, PPIA, accelerate progression to AIDS. PLoS Pathog, 3(6), e88, 2007. PMCID:1894826

Lind, JM, Hutcheson-Dilks, HB, Williams, SM, Moore, JH, Essex, M, Ruiz-Pesini, E, Wallace, DC, Tishkoff, SA, O''Brien, SJ, Smith, MW. Elevated male European and female African contributions to the genomes of African American individuals. Hum Genet, 120(5), 713-22, 2007.

Bashirova, AA, Bleiber, G, Qi, Y, Hutcheson, H, Yamashita, T, Johnson, RC, Cheng, J, Alter, G, Goedert, JJ, Buchbinder, S, Hoots, K, Vlahov, D, May, M, Maldarelli, F, Jacobson, L, O''brien, SJ, Telenti, A, Carrington, M. Consistent effects of TSG101 genetic variability on multiple outcomes of exposure to human immunodeficiency virus type 1. J Virol, 80(14), 6757-63, 2006. PMCID:1489017

Guo, XC, O''Brien, SJ, Winkler, C, Scott, K, Hutcheson, H, David, V, Kessing, B, Zheng, YM, Liao, J, Lui, Y, Guy, de T, Zeng, Y. [Association study of chromosome 4 STRs polymorphisms with nasopharyngeal carcinoma. Yi Chuan, 28(7), 783-90, 2006.

Guo, XC, Scott, K, Liu, Y, Dean, M, David, V, Nelson, GW, Johnson, RC, Dilks, HH, Lautenberger, J, Kessing, B, Martenson, J, Guan, L, Sun, S, Deng, H, Zheng, Y, de The, G, Liao, J, Zeng, Y, O''Brien, SJ, Winkler, CA. Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: study design, methods and feasibility. Hum Genomics, 2(6), 365-75, 2006.

Walsh, EC, Sabeti, P, Hutcheson, HB, Fry, B, Schaffner, SF, de Bakker, PI, Varilly, P, Palma, AA, Roy, J, Cooper, R, Winkler, C, Zeng, Y, de The, G, Lander, ES, O''Brien, S, Altshuler, D. Searching for signals of evolutionary selection in 168 genes related to immune function. Hum Genet, 119(1-2), 92-102, 2006.

Sabeti, PC, Walsh, E, Schaffner, SF, Varilly, P, Fry, B, Hutcheson, HB, Cullen, M, Mikkelsen, TS, Roy, J, Patterson, N, Cooper, R, Reich, D, Altshuler, D, O''Brien, S, Lander, ES. The case for selection at CCR5-Delta32. PLoS Biol, 3(11), e378, 2005. PMCID:1275522

Hutcheson, HB, Olson, LM, Bradford, Y, Folstein, SE, Santangelo, SL, Sutcliffe, JS, Haines, JL. Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes. BMC Med Genet, 5, 12, 2004. PMCID:420465

Martin, MP, Lederman, MM, Hutcheson, HB, Goedert, JJ, Nelson, GW, van Kooyk, Y, Detels, R, Buchbinder, S, Hoots, K, Vlahov, D, O''Brien, SJ, Carrington, M. Association of DC-SIGN promoter polymorphism with increased risk for parenteral, but not mucosal, acquisition of human immunodeficiency virus type 1 infection. J Virol, 78(24), 14053-6, 2004. PMCID:533922

Hutcheson, HB, Bradford, Y, Folstein, SE, Gardiner, MB, Santangelo, SL, Sutcliffe, JS, Haines, JL. Defining the autism minimum candidate gene region on chromosome 7. Am J Med Genet B Neuropsychiatr Genet, 117B(1), 90-6, 2003.

Summar, ML, Hall, LD, Eeds, AM, Hutcheson, HB, Kuo, AN, Willis, AS, Rubio, V, Arvin, MK, Schofield, JP, Dawson, EP. Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I gene. Gene, 311, 51-7, 2003.

Bradford, Y, Haines, J, Hutcheson, H, Gardiner, M, Braun, T, Sheffield, V, Cassavant, T, Huang, W, Wang, K, Vieland, V, Folstein, S, Santangelo, S, Piven, J. Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet, 105(6), 539-47, 2001.

Nurmi, EL, Bradford, Y, Chen, Y, Hall, J, Arnone, B, Gardiner, MB, Hutcheson, HB, Gilbert, JR, Pericak-Vance, MA, Copeland-Yates, SA, Michaelis, RC, Wassink, TH, Santangelo, SL, Sheffield, VC, Piven, J, Folstein, SE, Haines, JL, Sutcliffe, JS. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics, 77(1-2), 105-13, 2001.

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