Moore GE - Search Results

1

Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients.

Doudney K, Ybot-Gonzalez P, Paternotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P. Doudney K, et al. Among authors: moore ge. Am J Med Genet A. 2005 Jul 1;136(1):90-2. doi: 10.1002/ajmg.a.30766. Am J Med Genet A. 2005. PMID: 15952208 No abstract available.

2

Lack of mutations in ZIC3 in three families with neural tube defects.

Carrel T, Herman GE, Moore GE, Stanier P. Carrel T, et al. Among authors: moore ge. Am J Med Genet. 2001 Jan 22;98(3):283-5. doi: 10.1002/1096-8628(20010122)98:3<283::aid-ajmg1089>3.0.co;2-g. Am J Med Genet. 2001. PMID: 11169570 No abstract available.

3

Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects.

Doudney K, Grinham J, Whittaker J, Lynch SA, Thompson D, Moore GE, Copp AJ, Greene ND, Stanier P. Doudney K, et al. Among authors: moore ge. Am J Med Genet A. 2009 Jul;149A(7):1585-9. doi: 10.1002/ajmg.a.32937. Am J Med Genet A. 2009. PMID: 19533788 No abstract available.

4

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.

Ishida M, Cullup T, Boustred C, James C, Docker J, English C; GOSgene; Lench N, Copp AJ, Moore GE, Greene NDE, Stanier P. Ishida M, et al. Among authors: moore ge. Clin Genet. 2018 Apr;93(4):870-879. doi: 10.1111/cge.13189. Epub 2018 Feb 11. Clin Genet. 2018. PMID: 29205322 Free PMC article.

5

The emerging role of epigenetic mechanisms in the etiology of neural tube defects.

Greene ND, Stanier P, Moore GE. Greene ND, et al. Among authors: moore ge. Epigenetics. 2011 Jul;6(7):875-83. doi: 10.4161/epi.6.7.16400. Epub 2011 Jul 1. Epigenetics. 2011. PMID: 21613818 Free PMC article.

6

Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of chromosome 1 syntenic with human 1q21-q23.

Stanier P, Henson JN, Eddleston J, Moore GE, Copp AJ. Stanier P, et al. Among authors: moore ge. Genomics. 1995 Apr 10;26(3):473-8. doi: 10.1016/0888-7543(95)80165-i. Genomics. 1995. PMID: 7607670

7

Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects.

Newton R, Stanier P, Loughna S, Henderson DJ, Forbes SA, Farrall M, Jensson O, Moore GE. Newton R, et al. Among authors: moore ge. Clin Genet. 1994 May;45(5):241-9. doi: 10.1111/j.1399-0004.1994.tb04149.x. Clin Genet. 1994. PMID: 8076409

8

An analysis of common isodisomic regions in five mUPD 16 probands.

Abu-Amero SN, Ali Z, Abu-Amero KK, Stanier P, Moore GE. Abu-Amero SN, et al. Among authors: moore ge. J Med Genet. 1999 Mar;36(3):204-7. J Med Genet. 1999. PMID: 10204845 Free PMC article.

9

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P. Braybrook C, et al. Among authors: moore ge. Nat Genet. 2001 Oct;29(2):179-83. doi: 10.1038/ng730. Nat Genet. 2001. PMID: 11559848

10

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Hitchins MP, Stanier P, Preece MA, Moore GE. Hitchins MP, et al. Among authors: moore ge. J Med Genet. 2001 Dec;38(12):810-9. doi: 10.1136/jmg.38.12.810. J Med Genet. 2001. PMID: 11748303 Free PMC article. Review.

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