McIntosh I - Search Results

1

Testing candidate genes for non-syndromic oral clefts using a case-parent trio design.

Beaty TH, Hetmanski JB, Zeiger JS, Fan YT, Liang KY, VanderKolk CA, McIntosh I. Beaty TH, et al. Among authors: mcintosh i. Genet Epidemiol. 2002 Jan;22(1):1-11. doi: 10.1002/gepi.1039. Genet Epidemiol. 2002. PMID: 11754469

2

Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996.

Beaty TH, Maestri NE, Hetmanski JB, Wyszynski DF, Vanderkolk CA, Simpson JC, McIntosh I, Smith EA, Zeiger JS, Raymond GV, Panny SR, Tifft CJ, Lewanda AF, Cristion CA, Wulfsberg EA. Beaty TH, et al. Among authors: mcintosh i. Cleft Palate Craniofac J. 1997 Sep;34(5):447-54. doi: 10.1597/1545-1569_1997_034_0447_tfibms_2.3.co_2. Cleft Palate Craniofac J. 1997. PMID: 9345615

3

Application of transmission disequilibrium tests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the models.

Maestri NE, Beaty TH, Hetmanski J, Smith EA, McIntosh I, Wyszynski DF, Liang KY, Duffy DL, VanderKolk C. Maestri NE, et al. Among authors: mcintosh i. Am J Med Genet. 1997 Dec 19;73(3):337-44. doi: 10.1002/(sici)1096-8628(19971219)73:3<337::aid-ajmg21>3.0.co;2-j. Am J Med Genet. 1997. PMID: 9415696

4

A case-control study of nonsyndromic oral clefts in Maryland.

Beaty TH, Wang H, Hetmanski JB, Fan YT, Zeiger JS, Liang KY, Chiu YF, Vanderkolk CA, Seifert KC, Wulfsberg EA, Raymond G, Panny SR, McIntosh I. Beaty TH, et al. Among authors: mcintosh i. Ann Epidemiol. 2001 Aug;11(6):434-42. doi: 10.1016/s1047-2797(01)00222-8. Ann Epidemiol. 2001. PMID: 11454503

5

Haplotype diversity in 11 candidate genes across four populations.

Beaty TH, Fallin MD, Hetmanski JB, McIntosh I, Chong SS, Ingersoll R, Sheng X, Chakraborty R, Scott AF. Beaty TH, et al. Among authors: mcintosh i. Genetics. 2005 Sep;171(1):259-67. doi: 10.1534/genetics.105.043075. Epub 2005 Jun 18. Genetics. 2005. PMID: 15965248 Free PMC article.

6

High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts.

Park JW, Cai J, McIntosh I, Jabs EW, Fallin MD, Ingersoll R, Hetmanski JB, Vekemans M, Attie-Bitach T, Lovett M, Scott AF, Beaty TH. Park JW, et al. Among authors: mcintosh i. J Med Genet. 2006 Jul;43(7):598-608. doi: 10.1136/jmg.2005.040162. Epub 2006 Jan 13. J Med Genet. 2006. PMID: 16415175 Free PMC article.

7

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.

Beaty TH, Hetmanski JB, Fallin MD, Park JW, Sull JW, McIntosh I, Liang KY, Vanderkolk CA, Redett RJ, Boyadjiev SA, Jabs EW, Chong SS, Cheah FS, Wu-Chou YH, Chen PK, Chiu YF, Yeow V, Ng IS, Cheng J, Huang S, Ye X, Wang H, Ingersoll R, Scott AF. Beaty TH, et al. Among authors: mcintosh i. Hum Genet. 2006 Nov;120(4):501-18. doi: 10.1007/s00439-006-0235-9. Epub 2006 Sep 5. Hum Genet. 2006. PMID: 16953426

8

Association study of transforming growth factor alpha (TGF alpha) TaqI polymorphism and oral clefts: indication of gene-environment interaction in a population-based sample of infants with birth defects.

Hwang SJ, Beaty TH, Panny SR, Street NA, Joseph JM, Gordon S, McIntosh I, Francomano CA. Hwang SJ, et al. Among authors: mcintosh i. Am J Epidemiol. 1995 Apr 1;141(7):629-36. doi: 10.1093/oxfordjournals.aje.a117478. Am J Epidemiol. 1995. PMID: 7702037

9

Family-based analysis of MSX1 haplotypes for association with oral clefts.

Fallin MD, Hetmanski JB, Park J, Scott AF, Ingersoll R, Fuernkranz HA, McIntosh I, Beaty TH. Fallin MD, et al. Among authors: mcintosh i. Genet Epidemiol. 2003 Sep;25(2):168-75. doi: 10.1002/gepi.10255. Genet Epidemiol. 2003. PMID: 12916025

10

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.

Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I. Zeiger JS, et al. Among authors: mcintosh i. Eur J Hum Genet. 2003 Nov;11(11):835-9. doi: 10.1038/sj.ejhg.5201052. Eur J Hum Genet. 2003. PMID: 14571267

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