DE08559/DE/NIDCR NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1989	3
1990	2
1991	1
1992	4
1993	2
1995	1
1996	1
1997	2
1998	1
1999	6
2000	2
2001	1
2002	5
2003	7
2004	8
2005	5
2006	7
2007	5
2008	7
2009	7
2010	9
2011	12
2012	10
2013	5
2014	2
2015	4
2016	1
2024	0

1

Cleft lip and palate: understanding genetic and environmental influences.

Dixon MJ, Marazita ML, Beaty TH, Murray JC. Dixon MJ, et al. Nat Rev Genet. 2011 Mar;12(3):167-78. doi: 10.1038/nrg2933. Nat Rev Genet. 2011. PMID: 21331089 Free PMC article. Review.

2

Genetics of nonsyndromic orofacial clefts.

Rahimov F, Jugessur A, Murray JC. Rahimov F, et al. Cleft Palate Craniofac J. 2012 Jan;49(1):73-91. doi: 10.1597/10-178. Epub 2011 May 5. Cleft Palate Craniofac J. 2012. PMID: 21545302 Free PMC article. Review.

3

Face facts: genes, environment, and clefts.

Murray JC. Murray JC. Am J Hum Genet. 1995 Aug;57(2):227-32. Am J Hum Genet. 1995. PMID: 7668246 Free PMC article. No abstract available.

4

Orofacial clefting: recent insights into a complex trait.

Jugessur A, Murray JC. Jugessur A, et al. Curr Opin Genet Dev. 2005 Jun;15(3):270-8. doi: 10.1016/j.gde.2005.03.003. Curr Opin Genet Dev. 2005. PMID: 15917202 Free PMC article. Review.

5

Cleft palate: players, pathways, and pursuits.

Murray JC, Schutte BC. Murray JC, et al. J Clin Invest. 2004 Jun;113(12):1676-8. doi: 10.1172/JCI22154. J Clin Invest. 2004. PMID: 15199400 Free PMC article.

6

Linkage localization of Börjeson-Forssman-Lehmann syndrome.

Mathews KD, Ardinger HH, Nishimura DY, Buetow KH, Murray JC, Bartley JA. Mathews KD, et al. Am J Med Genet. 1989 Dec;34(4):470-4. doi: 10.1002/ajmg.1320340403. Am J Med Genet. 1989. PMID: 2624254

7

Digital imaging analysis to assess scar phenotype.

Smith BJ, Nidey N, Miller SF, Moreno Uribe LM, Baum CL, Hamilton GS 3rd, Wehby GL, Dunnwald M. Smith BJ, et al. Wound Repair Regen. 2014 Mar-Apr;22(2):228-38. doi: 10.1111/wrr.12141. Wound Repair Regen. 2014. PMID: 24635173 Free PMC article.

8

Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q.

Nishimura DY, Purchio AF, Murray JC. Nishimura DY, et al. Genomics. 1993 Feb;15(2):357-64. doi: 10.1006/geno.1993.1068. Genomics. 1993. PMID: 8095486

9

Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome.

Ferreira de Lima RL, Moretti-Ferreira D, Richieri-Costa A, Murray JC. Ferreira de Lima RL, et al. Am J Med Genet A. 2003 Sep 15;122A(1):56-8. doi: 10.1002/ajmg.a.20270. Am J Med Genet A. 2003. PMID: 12949973

10

X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts.

Patel PJ, Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Wu T, Murray T, Rose M, Redett RJ, Jin SC, Lie RT, Wu-Chou YH, Wang H, Ye X, Yeow V, Chong S, Jee SH, Shi B, Scott AF. Patel PJ, et al. Eur J Oral Sci. 2013 Apr;121(2):63-8. doi: 10.1111/eos.12025. Eur J Oral Sci. 2013. PMID: 23489894 Free PMC article.

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