Holli B. Hutcheson, Ph.D. - Publications

Vanderbilt University, Nashville, TN 

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 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 (London, England). 22: 2429-39. PMID 19005266 DOI: 10.1097/QAD.0b013e32831940bb  0.52
2008 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: 2951-65. PMID 18325640 DOI: 10.1016/j.vaccine.2007.12.054  0.52
2006 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 = Hereditas / Zhongguo Yi Chuan Xue Hui Bian Ji. 28: 783-90. PMID 16825163  0.52
2006 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, et al. Consistent effects of TSG101 genetic variability on multiple outcomes of exposure to human immunodeficiency virus type 1 Journal of Virology. 80: 6757-6763. PMID 16809281 DOI: 10.1128/JVI.00094-06  0.52
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, et al. Searching for signals of evolutionary selection in 168 genes related to immune function. Human Genetics. 119: 92-102. PMID 16362345 DOI: 10.1007/s00439-005-0090-0  0.52
2005 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 Biology. 3: e378. PMID 16248677 DOI: 10.1371/journal.pbio.0030378  0.52
2004 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. Journal of Virology. 78: 14053-6. PMID 15564514 DOI: 10.1128/JVI.78.24.14053-14056.2004  0.52
2004 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 Medical Genetics. 5: 12. PMID 15128462 DOI: 10.1186/1471-2350-5-12  0.52
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. PMID 12853138 DOI: 10.1016/S0378-1119(03)00528-6  0.52
2003 Hutcheson HB, Bradford Y, Folstein SE, Gardiner MB, Santangelo SL, Sutcliffe JS, Haines JL. Defining the autism minimum candidate gene region on chromosome 7. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 90-6. PMID 12555242 DOI: 10.1002/ajmg.b.10033  0.52
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, et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics. 77: 105-13. PMID 11543639 DOI: 10.1006/geno.2001.6617  0.52
2001 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. American Journal of Medical Genetics. 105: 539-47. PMID 11496372 DOI: 10.1002/ajmg.1497  0.52
2001 Hutcheson HB, Haines JL. Examination of candidate genes for autism on chromosome 7 American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 594.  0.52
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