Publications - Sudden Infant Death Syndrome
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Association of the serotonin transporter gene with Sudden Infant Death Syndrome: a haplotype analysis. Weese-Mayer, D., Zhou, L., Berry-Kravis, E., Maher, B., Silvestri, J. and Marazita, M. Amer. J. Med. Gen. 122A: 238-245, 2003. [paper]
Cytochrome P450 2D6 and glutathione S-transferase genotype in Sudden Infant Death Syndrome. Chen, C.L., Liu, Q., Evans, W.E., Sander, C.H. and Relling, M.V. J. Paed. & Child Health.33:31-37, 1997. [paper]
Endotoxemia in Sudden Infant Death Syndrome. Platt, M.S., Elin, R.J., Hossieni, J.M. and Smialek, J.E. American J. Forensic Med. Path. 15:261-265, 1994. [paper]
Endotoxiemia - a possible mechanims of death in blunt force injury to the abdomen. Fowler, D.R., Platt, M.S., Chute, D., Elin, R.J., Niemela, J.E. and Smialek, J.E. Proc. Amer. Acad. Forensic Sci. Annual Meeting, Nashville, TN, 1996. [abstract]
Failure to detect elevated levels of carboxyhemoglobin in infants dying from SIDS. Meny, R.G., Vreman, H.J., Stevenson, D.K., Hauck, F.R., Donoghue, E.R., Smialek, J.E., Fowler, D.R., Zielke, H.R. J. Forensic Sciences 47: 660-662, 2002. [paper]
Genetic variation in 5-HT gene and Sudden Infant Death syndrome. Morley, M., Rand, C., Berry-Kravis, E., Zhou, L., Fan, W. and Weese-Mayer, D. PAS meeting, 2007. [abstract]
Genetic variation in the HTR1A gene and sudden infant death syndrome. Morley, M., Rand, C., Berry-Kravis, E., Zhou, L., Fan, W. and Weese-Mayer, D. Amer. J. Med. Gen. Part A 146A:930-933, 2008. [paper]
Involvement of mast cells in Sudden Infant Death Syndrome. Platt, M.S., Yunginger, J.W., Sekula-Perlman, A., Irani, A.M., Smialek, J.E., Mirchandani, H.G. and Schwartz, L.B. J. Allergy Clin. Immunol. 94:250-256, 1994. [paper]
Mast cells in heart tissue of fetuses, SIDS and explained-death infants, and adults. Platt, M.S., Irani, A.A., Dasu, S., Vigorito, R., Smialek, J.E. and Schwartz, L.B. American Acadamy of Allergy and Clinical Immunology Meeting, 1996. [abstract]
Molecular epidemiological studies of common bacterial and viral respiratory pathogens in sudden infant death syndrome (SIDS). Ehrlich, G.D., Hoffman, H.J., Zielke, H.R., White, G.J., Hu, F.Z., Vigorito, R., Dingman, J.R., Liebert, T., Smailek, J.E. and Post, J.C. Proc. 7th Int. Symp. On Recent Adv. in Otitis Media, 2000. [abstract]
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome. Rand, C., Weese-Mayer, D., Maher, B., Zhou, L., Marazita, M. and Berry-Kravis, E. Amer. J. Med. Gen. 140: 1447-1452, 2006. [paper]
Nicotine metabolizing genes in sudden infant death syndrome. Rand, C., Weese-Mayer, D., Maher, B., Zhou, L., Marazita, M. and Berry-Kravis, E. Society for Ped. Res., San Francisco, CA, 2006. [abstract]
Preliminary findings of hair analysis in SIDS-related deaths. Ropero, J.D., Gardise, D., Goldberger, B.A., Smialek, J.E., Zielke, R. and Vigorito, R. J. Anal. Toxicol. 21;89, 1997. [abstract]
Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life. Boles, R.G., Buck, E.A., Blitzer, M.G., Platt, M.S., Cowan, T.M., Martin, S.K., Yoon, H.-R., Madsen, J.A., Reyes-Mugica, M. and Rinaldo, P. J. Pediatr. 132:924-933, 1998. [paper]
Sudden Infant Death Syndrome (SIDS): analysis of genes pertinent to early autonomic nervous system (ANS) embryologic development. Weese-Mayer, D., Berry-Kravis, E., Zhou, L., Maher, B., Curran M., Silvestri, J. and Marazita, M. Am. J .Respir. Crit. Care Med. 169: A263, 2004. [abstract]
Sudden Infant Death Syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Weese-Mayer, D., Zhou, L., Berry-Kravis, E., Silvestri, B., Maher, B., Curran, M and Marazita, M Pediatric Research 56: 391-395, 2004. [paper]
Sudden Infant Death Syndrome: rare mutation in the serotonin system FEV gene. Rand, C., Berry-Kravis, E., Zhou, L, Fan, W. and Weese-Mayer, D. PAS meeting, 2007. [abstract]
Sudden Infant Death Syndrome: rare mutation in the serotonin system FEV sene. Rand, C., Berry-Kravis, E., Zhou, L., Fan, W and Weese-Mayer, D. Pediatric Research 62: 180-182, 2007. [paper]
Sudden Infant Death Syndrome: review of implicated genetic factors. Weese-Mayer, D., Ackerman, M., Marazita, M. and Berry-Kravis, E. Am J of Med Genetics 143A: 771-788, 2007. [paper]
Sudden infant death syndrome: Case-Control frequency differences in paired like homeobox (PHOX) 2B gene. Rand, C., Weese-Mayer, D., Zhou, L., Maher, B., Cooper, M., Marazita, M. and Berry-Kravis, E. Amer. J. Med. Gen,.140:1687-1691, 2006. [paper]
Sudden infant death syndrome: Case-control frequency differences in the PHOX2B gene. Rand, C. Weese-Mayer, D., Zhou, L., Maher, B., Cooper, M., Marazita, M. and Berry-Kravis, E. Society for Ped. Res., San Francisco, CA, 2006. [abstract]
Sudden infant death syndrome: association with a promotor polymorphism of the serotonin transporter gene. Weese-Mayer, D.E., Berry-Kravis, E.M., Maher, B.S., Silvestri, J.M., Curran, M.E., Marazita, M.L. Amer. J. Med. Gen. 117A: 268-274, 2003. [paper]
The 3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: a haplotype analysis. Maher, B., Marazita, M., Zhou, L., Berry-Kravis, E. and Weese-Mayer, D. Amer. J .Med. Gen. 140A: 1453-1457, 2006. [paper]
The effect of tobacco smoking on nicotine and cotinine levels in lung tissue of SIDS and non-SIDS cases. McMartin, L.I., Klein, J., Platt, M.S. and Koren, G. Royal College of Physicians & Surgeons of Canada, Halifax, 1996. [abstract]
Vascular endothelial growth factor (VEGF) levels as an hypoxic marker in the cerebrospinal fluid (CSF) of SIDS. Jones, K.L., Krous, H.F., Nadeau, J, Zielke, H.R. and Gozal, D. ATS meeting, Toronto, Canada, May 5-10, 2000. [abstract]
Vascular endothelial growth factor in the cerebrospinal fluid of infants who died of sudden infant death syndrome: evidence for antecedent hypoxia. Jones, K., Krous, H., Nadeau, J., Blackbourne, B., Zielke, H.R., and Gozal, D. Pediatrics 111:358-363, 2003. [paper]