Shi M - Search Results

1

Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth.

Ehn NL, Cooper ME, Orr K, Shi M, Johnson MK, Caprau D, Dagle J, Steffen K, Johnson K, Marazita ML, Merrill D, Murray JC. Ehn NL, et al. Among authors: shi m. Pediatr Res. 2007 Nov;62(5):630-5. doi: 10.1203/PDR.0b013e3181567bfc. Pediatr Res. 2007. PMID: 17805208 Free PMC article.

2

Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery.

Steffen KM, Cooper ME, Shi M, Caprau D, Simhan HN, Dagle JM, Marazita ML, Murray JC. Steffen KM, et al. Among authors: shi m. J Perinatol. 2007 Nov;27(11):672-80. doi: 10.1038/sj.jp.7211806. Epub 2007 Sep 13. J Perinatol. 2007. PMID: 17855807 Free PMC article.

3

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

Kim J, Stirling KJ, Cooper ME, Ascoli M, Momany AM, McDonald EL, Ryckman KK, Rhea L, Schaa KL, Cosentino V, Gadow E, Saleme C, Shi M, Hallman M, Plunkett J, Teramo KA, Muglia LJ, Feenstra B, Geller F, Boyd HA, Melbye M, Marazita ML, Dagle JM, Murray JC. Kim J, et al. Among authors: shi m. BMC Med Genet. 2013 Jul 26;14:77. doi: 10.1186/1471-2350-14-77. BMC Med Genet. 2013. PMID: 23889750 Free PMC article.

4

Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2.

Shi M, Caprau D, Romitti P, Christensen K, Murray JC. Shi M, et al. Birth Defects Res A Clin Mol Teratol. 2003 Aug;67(8):545-9. doi: 10.1002/bdra.10076. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14632302

5

Application of kinetic polymerase chain reaction and molecular beacon assays to pooled analyses and high-throughput genotyping for candidate genes.

Shi M, Caprau D, Dagle J, Christiansen L, Christensen K, Murray JC. Shi M, et al. Birth Defects Res A Clin Mol Teratol. 2004 Feb;70(2):65-74. doi: 10.1002/bdra.10153. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 14991913

6

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC. Zucchero TM, et al. Among authors: shi m. N Engl J Med. 2004 Aug 19;351(8):769-80. doi: 10.1056/NEJMoa032909. N Engl J Med. 2004. PMID: 15317890 Free article.

7

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families.

Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. Schultz RE, et al. Among authors: shi m. Am J Med Genet A. 2004 Feb 15;125A(1):17-22. doi: 10.1002/ajmg.a.20424. Am J Med Genet A. 2004. PMID: 14755461

8

Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants.

Shi M, Christensen K, Weinberg CR, Romitti P, Bathum L, Lozada A, Morris RW, Lovett M, Murray JC. Shi M, et al. Am J Hum Genet. 2007 Jan;80(1):76-90. doi: 10.1086/510518. Epub 2006 Dec 7. Am J Hum Genet. 2007. PMID: 17160896 Free PMC article.

9

X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.

Kimani JW, Shi M, Daack-Hirsch S, Christensen K, Moretti-Ferreira D, Marazita ML, Field LL, Canady JW, Murray JC. Kimani JW, et al. Among authors: shi m. Am J Med Genet A. 2007 Dec 15;143A(24):3267-72. doi: 10.1002/ajmg.a.32098. Am J Med Genet A. 2007. PMID: 18000982 Free PMC article.

10

Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects.

Shi M, Wehby GL, Murray JC. Shi M, et al. Birth Defects Res C Embryo Today. 2008 Mar;84(1):16-29. doi: 10.1002/bdrc.20117. Birth Defects Res C Embryo Today. 2008. PMID: 18383123 Free PMC article. Review.

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