Huiping Zhu, Publications
Zhu H, Kartiko S, Finnell RH. Importance of Gene-Environment Interactions in the Etiology of Selected Birth Defects. Clinic Genet. 2009: 75: 409-423. Review
Naufal Z, Zhiwen L, Zhu L, Zhou GD, McDonald T, He LY, Mitchell L, Ren A, Zhu H, Finnell R, Donnelly KC. Biomarkers of exposure to combustion by-products in a human population in Shanxi, China. : J Expo Sci Environ Epidemiol. 2009 Mar 11. [Epub ahead of print]
Shu W, Lu W, Zhu H, Yang W, Shaw GM, Lammer EJ, Islam A, Finnell RH. Genetic Polymorphisms in the Thrioredoxin 2 (TXN2) Gene and Risk for Spina Bifida. Am J Med Genet. 2009 Jan 15;149A(2):155-60.
Pei L, Liu J, Zhang Y, Zhu H, Ren A. Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects.Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 22. [Epub ahead of print] PMID: 19105199.
Lu W, Zhu H, Wen S, Yang W, Shaw GM, Lammer EJ, Finnell RH.Nicotinamide N-methyl transferase (NNMT) gene polymorphisms and risk for spina bifida.Birth Defects Res A Clin Mol Teratol. 2008 Oct; 82(10):670-5.
Zhu H, Cabrera RM, Wlodarczyk BJ, Bozinov D, Wang D, Schwartz RJ, Finnell RH. Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity. BMC Dev Biol. 2007 Nov 20;7:128. PMCID: PMC2206038
Zhu H, Enaw JO, Ma C, Shaw GM, Lammer EJ, Finnell RH.Association between CFL1 gene polymorphisms and spina bifida risk in a California population. BMC Med Genet. 2007 Mar 12;8:12. PMCID: PMC1831766
Zhu H, Wlodarczyk BJ, Scott M, Yu W, Merriweather M, Gelineau-van Waes J, Schwartz RJ, Finnell RH. Cardiovascular abnormalities in Folr1 knockout mice and folate rescue.Birth Defects Res A Clin Mol Teratol. 2007 Apr;79(4):257-68.
Chevrier C, Perret C, Bahuau M, Zhu H, Nelva A, Herman C, Francannet C,Robert-Gnansia E, Finnell RH, Cordier S.Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts. Am J Med Genet A. 2007 Feb 1;143(3):248-57.
Enaw JO, Zhu H, Yang W, Lu W, Shaw GM, Lammer EJ, Finnell RH.CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population. BMC Med. 2006 Dec 21;4:36. PMCID: PMC1770928
Shaw GM, Jelliffe-Pawlowski L, Nelson V, Zhu H, Harris JA, Finnell RH. Infant C677T MTHFR polymorphism and severe mental retardation. Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):24-6.
Lu W, Zhu H, Wen S, Laurent C, Shaw GM, Lammer EJ, Finnell RH. Screening for novel PAX3 polymorphisms and risks of spina bifida.Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):45-9.
Wlodarczyk BJ, Cabrera RM, Hill DS, Bozinov D, Zhu H, Finnell RH. Arsenic-induced gene expression changes in the neural tube of folate transport defective mouse embryos. Neurotoxicology. 2006 Jul;27(4):547-57.
Zhang J, Zhu H, Yang W, Shaw GM, Lammer EJ, Finnell RH. Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida. Am J Med Genet A. 2006 Apr 1;140(7):785-9.
Zhu J, Ren A, Hao L, Pei L, Liu J, Zhu H, Li S, Finnell RH, Li Z. Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China. Am J Med Genet A. 2006 Mar 15;140(6):551-7. PMID: 16470725
Zhu H, Yang W, Lu W, Zhang J, Shaw GM, Lammer EJ, Finnell RH. A known functional polymorphism (Ile120Val) of the human PCMT1 gene and risk of spina bifida. Mol Genet Metab. 2006 Jan;87(1):66-70. PMID: 16256389
Zhu H, Lu W, Laurent C, Shaw GM, Lammer EJ, Finnell RH. Genes encoding catalytic subunits of protein kinase A and risk of spina bifida. Birth Defects Res A Clin Mol Teratol. 2005 Sep;73(9):591-6. PMID: 16080189
Lu W, Volcik K, Zhu H, Wen S, Shaw GM, Lammer EJ, Finnell RH. Genetic variation in the proto-oncogene SKI and risk for orofacial clefting. Mol Genet Metab. 2005 Nov;86(3):412-6. PMID: 16054854
Pei L, Zhu H, Zhu J, Ren A, Finnell RH, Li Z. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China. Ann Epidemiol. 2006 May;16(5):352-6. PMID: 16019224
Pei LJ, Li ZW, Zhang W, Ren AG, Zhu HP, Hao L, Zhu JH, Li Z. [Epidemiological study on reduced folate carrier gene(RFC1 A80G) polymorphism and other risk factors of neural tube defects]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 2005 Aug 18;37(4):341-5.
Zhu H, Curry S, Wen S, Wicker NJ, Shaw GM, Lammer EJ, Yang W, Jafarov T, Finnell RH. Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts? Am J Med Genet A. 2005 Jun 15;135(3):274-7. PMID: 15887275
Pei L, Zhu H, Ren A, Li Z, Hao L, Finnell RH, Li Z. Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population. Birth Defects Res A Clin Mol Teratol. 2005 Jun;73(6):430-3. PMID: 15799025
Jafarov T, Zhu H, Finnell R, Kulieva S. Epidemiologic study on HFE C282Y mutation in Azerbaijan. Eur J Haematol. 2005 Feb;74(2):180-1. No abstract available. PMID: 15654913 [PubMed - indexed for MEDLINE]
Pei LJ, Ren AG, Hao L, Zhu HP, Zhu JH, Zhao WR, Zhou MX, Sun XM, Jiang MF, Chen HL, Zhang BL, Li Z. [Study on the association between reduced folate carrier gene polymorphism and congenital heart defects and cleft lip with or without cleft palate]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi. 2004 Dec;25(12):1063-7.
Pei LJ, Ren AG, Zhu HP, Hao L, Zhao WR, Li Z, Hou GW, Zhang BL, Jiang YY, Wu LM, Pan YJ, Zhang ML.[Study on reduced folate carrier gene (RFC1) polymorphism in the southern and northern Chinese population]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi. 2004 Jun;25(6):499-502.
Volcik KA, Zhu H, Finnell RH, Shaw GM, Canfield M, Lammer EJ. Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects. Am J Med Genet A. 2004 Apr 15;126A(2):215-7. No abstract available. PMID: 15057990
Volcik KA, Zhu H, Finnell RH, Shaw GM, Canfield M, Lammer EJ. Evaluation of the Cited2 gene and risk for spina bifida and congenital heart defects. Am J Med Genet A. 2004 Apr 30;126A(3):324-5. No abstract available. PMID: 15054851
Carmichael SL, Shaw GM, Yang W, Lammer EJ, Zhu H, Finnell RH. Limb deficiency defects, MSX1, and exposure to tobacco smoke. Am J Med Genet A. 2004 Mar 15;125A(3):285-9. PMID: 14994238
Volcik KA, Shaw GM, Zhu H, Lammer EJ, Laurent C, Finnell RH. Associations between polymorphisms within the thymidylate synthase gene and spina bifida. Birth Defects Res A Clin Mol Teratol. 2003 Nov;67(11):924-8.PMID: 14745930
Zhu H, Wicker NJ, Volcik K, Zhang J, Shaw GM, Lammer EJ, Suarez L, Canfield M, Finnell RH. Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects. Mol Genet Metab. 2004 Feb;81(2):127-32. PMID: 14741194
Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Renlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick OM, López MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martínez-Frías ML, Gallagher M, Erickson JD, Vollset SE, Mastroiacovo P, Andria G, Botto LD, Redlund M. Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide. Journal of medical genetics. 2003 Aug;40(8):619-25.
Shaw GM, Zhu H, Lammer EJ, Yang W, Finnell RH. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects. Am J Epidemiol. 2003 Oct 15;158(8):747-52.PMID: 14561664
Volcik KA, Shaw GM, Zhu H, Lammer EJ, Finnell RH. Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.Birth Defects Res A Clin Mol Teratol. 2003 Mar;67(3):158-61. PMID: 12797456
Volcik KA, Shaw GM, Lammer EJ, Zhu H, Finnell RH. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects. Birth Defects Res A Clin Mol Teratol. 2003 Mar;67(3):154-7. PMID: 12797455
De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. Reduced folate carrier polymorphism (80A-->G) and neural tube defects. Eur J Hum Genet. 2003 Mar;11(3):245-52.PMID: 12673279
Zhu H, Wicker NJ, Shaw GM, Lammer EJ, Hendricks K, Suarez L, Canfield M, Finnell RH. Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab. 2003 Mar;78(3):216-21.PMID: 12649067
Zhu H, Barber R, Shaw GM, Lammer EJ, Finnell RH. Is Sonic hedgehog (SHH) a candidate gene for spina bifida? A pilot study. Am J Med Genet A. 2003 Feb 15;117A(1):87-8. No abstract available. PMID: 12548748
Zhu H, Junker WM, Finnell RH, Brown S, Shaw GM, Lammer EJ, Canfield M, Hendricks K. Lack of association between ZIC2 and ZIC3 genes and the risk of neural tube defects (NTDs) in Hispanic populations. Am J Med Genet A. 2003 Feb 1;116A(4):414-5. No abstract available. PMID: 12522805
Volcik KA, Zhu H, Shaw GM, Lammer EJ, Finnell RH. Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida. Teratology. 2002 Nov;66(5):257-9. PMID: 12397634
De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet. 2002;47(6):319-24.PMID: 12111380
Shaw GM, Lammer EJ, Zhu H, Baker MW, Neri E, Finnell RH. Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida. Am J Med Genet. 2002 Feb 15;108(1):1-6. Erratum in: Am J Med Genet 2002 Dec 15;113(4):392. PMID: 11857541.
For other publications, see PubMed (search: Zhu, Huiping)
