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Tonia C. Carter, Ph.D. - Publications

Affiliations: 
2007 State University of New York, Albany, Albany, NY, United States 
Area:
Epidemiology, Obstetrics and Gynecology
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23 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
2020 Carter TC, Ye Z, Ivacic LC, Budi N, Rose WE, Shukla SK. Association of variants in selected genes mediating host immune response with duration of Staphylococcus aureus bacteremia. Genes and Immunity. PMID 32507857 DOI: 10.1038/S41435-020-0101-0  0.341
2019 Jenkins MM, Almli LM, Pangilinan F, Chong JX, Blue EE, Shapira SK, White J, McGoldrick D, Smith JD, Mullikin JC, Bean CJ, Nembhard WN, Lou XY, Shaw GM, Romitti PA, ... ... Carter TC, et al. Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth Defects Research. PMID 31328417 DOI: 10.1002/Bdr2.1554  0.368
2017 Carter TC, Hebbring SJ, Liu J, Mosley JD, Shaffer CM, Ivacic LC, Kopitzke S, Stefanski EL, Strenn R, Sundaram ME, Meece J, Brilliant MH, Ferdinands JM, Belongia EA. Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission. Journal of Medical Virology. PMID 29053189 DOI: 10.1002/Jmv.24975  0.35
2017 Carter TC, Sicko RJ, Kay DM, Browne ML, Romitti PA, Edmunds ZL, Liu A, Fan R, Druschel CM, Caggana M, Brody LC, Mills JL. Copy-number variants and candidate gene mutations in isolated split hand/foot malformation. Journal of Human Genetics. PMID 28539665 DOI: 10.1038/Jhg.2017.56  0.555
2016 Ailes EC, Gilboa SM, Gill SK, Broussard CS, Crider KS, Berry RJ, Carter TC, Hobbs CA, Interrante JD, Reefhuis J. Association between antibiotic use among pregnant women with urinary tract infections in the first trimester and birth defects, National Birth Defects Prevention Study 1997 to 2011. Birth Defects Research. Part a, Clinical and Molecular Teratology. 106: 940-949. PMID 27891788 DOI: 10.1002/Bdra.23570  0.344
2016 VanderMeer JE, Carter TC, Pangilinan F, Mitchell A, Kurnat-Thoma E, Kirke PN, Troendle JF, Molloy AM, Munger RG, Feldkamp ML, Mansilla MA, Mills JL, Murray JC, Brody LC. Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. American Journal of Medical Genetics. Part A. PMID 26789141 DOI: 10.1002/Ajmg.A.37539  0.432
2015 Howley MM, Carter TC, Browne ML, Romitti PA, Cunniff CM, Druschel CM. Fluconazole use and birth defects in the National Birth Defects Prevention Study. American Journal of Obstetrics and Gynecology. PMID 26640069 DOI: 10.1016/J.Ajog.2015.11.022  0.552
2014 Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M. Generalized functional linear models for gene-based case-control association studies. Genetic Epidemiology. 38: 622-37. PMID 25203683 DOI: 10.1002/Gepi.21840  0.33
2014 Ye Z, Vasco DA, Carter TC, Brilliant MH, Schrodi SJ, Shukla SK. Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Frontiers in Genetics. 5: 125. PMID 24847357 DOI: 10.3389/Fgene.2014.00125  0.356
2013 Carter TC, Kay DM, Browne ML, Liu A, Romitti PA, Kuehn D, Conley MR, Caggana M, Druschel CM, Brody LC, Mills JL. Anorectal atresia and variants at predicted regulatory sites in candidate genes. Annals of Human Genetics. 77: 31-46. PMID 23127126 DOI: 10.1111/J.1469-1809.2012.00734.X  0.583
2012 Browne ML, Carter TC, Kay DM, Kuehn D, Brody LC, Romitti PA, Liu A, Caggana M, Druschel CM, Mills JL. Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies. American Journal of Medical Genetics. Part A. 158: 2463-72. PMID 22965740 DOI: 10.1002/Ajmg.A.35565  0.575
2012 Carter TC, Kay DM, Browne ML, Liu A, Romitti PA, Kuehn D, Conley MR, Caggana M, Druschel CM, Brody LC, Mills JL. Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation. Journal of Human Genetics. 57: 485-93. PMID 22648184 DOI: 10.1038/Jhg.2012.54  0.575
2012 Mills JL, Carter TC, Kay DM, Browne ML, Brody LC, Liu A, Romitti PA, Caggana M, Druschel CM. Folate and vitamin B12-related genes and risk for omphalocele. Human Genetics. 131: 739-46. PMID 22116453 DOI: 10.1007/S00439-011-1117-3  0.566
2012 Cornman-Homonoff J, Kuehn D, Aros S, Carter TC, Conley MR, Troendle J, Cassorla F, Mills JL. Heavy prenatal alcohol exposure and risk of stillbirth and preterm delivery. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 25: 860-3. PMID 21728738 DOI: 10.3109/14767058.2011.587559  0.315
2011 Murphy LE, Mills JL, Molloy AM, Qian C, Carter TC, Strevens H, Wide-Swensson D, Giwercman A, Levine RJ. Folate and vitamin B12 in idiopathic male infertility. Asian Journal of Andrology. 13: 856-61. PMID 21857689 DOI: 10.1038/Aja.2011.96  0.327
2011 Carter TC, Olney RS, Mitchell AA, Romitti PA, Bell EM, Druschel CM. Maternal self-reported genital tract infections during pregnancy and the risk of selected birth defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 108-16. PMID 21319278 DOI: 10.1002/Bdra.20749  0.542
2011 Carter TC, Pangilinan F, Troendle JF, Molloy AM, VanderMeer J, Mitchell A, Kirke PN, Conley MR, Shane B, Scott JM, Brody LC, Mills JL. Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population. American Journal of Medical Genetics. Part A. 155: 14-21. PMID 21204206 DOI: 10.1002/Ajmg.A.33755  0.424
2010 Mills JL, Carter TC. Acyclovir exposure and birth defects: an important advance, but more are needed. Jama. 304: 905-6. PMID 20736478 DOI: 10.1001/Jama.2010.1214  0.369
2010 Mills JL, Troendle J, Conley MR, Carter T, Druschel CM. Maternal obesity and congenital heart defects: a population-based study. The American Journal of Clinical Nutrition. 91: 1543-9. PMID 20375192 DOI: 10.3945/ajcn.2009.28865  0.496
2010 Carter TC, Molloy AM, Pangilinan F, Troendle JF, Kirke PN, Conley MR, Orr DJ, Earley M, McKiernan E, Lynn EC, Doyle A, Scott JM, Brody LC, Mills JL. Testing reported associations of genetic risk factors for oral clefts in a large Irish study population. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 84-93. PMID 19937600 DOI: 10.1002/Bdra.20639  0.365
2008 Cleves MA, Malik S, Yang S, Carter TC, Hobbs CA. Maternal urinary tract infections and selected cardiovascular malformations. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 464-73. PMID 18452156 DOI: 10.1002/Bdra.20460  0.33
2008 Carter TC, Druschel CM, Romitti PA, Bell EM, Werler MM, Mitchell AA. Antifungal drugs and the risk of selected birth defects. American Journal of Obstetrics and Gynecology. 198: 191.e1-7. PMID 18226621 DOI: 10.1016/j.ajog.2007.08.044  0.542
2003 Koppel RI, Druschel CM, Carter T, Goldberg BE, Mehta PN, Talwar R, Bierman FZ. Effectiveness of pulse oximetry screening for congenital heart disease in asymptomatic newborns Pediatrics. 111: 451-455. PMID 12612220 DOI: 10.1542/Peds.111.3.451  0.509
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