Shields DC - Search Results

1

Evidence for an allelic association between bipolar disorder and a Na+, K+ adenosine triphosphatase alpha subunit gene (ATP1A3).

Mynett-Johnson L, Murphy V, McCormack J, Shields DC, Claffey E, Manley P, McKeon P. Mynett-Johnson L, et al. Among authors: shields dc. Biol Psychiatry. 1998 Jul 1;44(1):47-51. doi: 10.1016/s0006-3223(97)00343-0. Biol Psychiatry. 1998. PMID: 9646882

2

Lack of evidence for a major locus for bipolar disorder in the pericentromeric region of chromosome 18 in Irish pedigrees.

Mynett-Johnson LA, Murphy VE, Manley P, Shields DC, McKeon P. Mynett-Johnson LA, et al. Among authors: shields dc. Biol Psychiatry. 1997 Sep 15;42(6):486-94. doi: 10.1016/S0006-3223(96)00427-1. Biol Psychiatry. 1997. PMID: 9285084 Clinical Trial.

3

Preliminary evidence of an association between bipolar disorder in females and the catechol-O-methyltransferase gene.

Mynett-Johnson LA, Murphy VE, Claffey E, Shields DC, McKeon P. Mynett-Johnson LA, et al. Among authors: shields dc. Psychiatr Genet. 1998 Winter;8(4):221-5. doi: 10.1097/00041444-199808040-00004. Psychiatr Genet. 1998. PMID: 9861640

4

Pseudoautosomal gene: possible association with bipolar males but not with schizophrenia.

Hawi Z, Mynett-Johnson L, Gill M, Murphy V, Straubl RE, Kendler KS, Walsh D, Machen F, Connell H, McKeon P, Shields D. Hawi Z, et al. Psychiatr Genet. 1999 Sep;9(3):129-34. Psychiatr Genet. 1999. PMID: 10551542

5

Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury).

Shields DC, Ramsbottom D, Donoghue C, Pinjon E, Kirke PN, Molloy AM, Edwards YH, Mills JL, Mynett-Johnson L, Weir DG, Scott JM, Whitehead AS. Shields DC, et al. Am J Med Genet. 2000 May 29;92(3):206-11. Am J Med Genet. 2000. PMID: 10817656

6

Thermolabile MTHFR genotype and retinal vascular occlusive disease.

Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson LA, Mooney D, Graham IM, Whitehead AS, Shields DC. Cahill M, et al. Among authors: shields dc. Br J Ophthalmol. 2001 Jan;85(1):88-90. doi: 10.1136/bjo.85.1.88. Br J Ophthalmol. 2001. PMID: 11133719 Free PMC article.

7

No association between 5HT-2A and bipolar disorder irrespective of genomic imprinting.

Murphy VE, Mynett-Johnson LA, Claffey E, Shields DC, McKeon P. Murphy VE, et al. Among authors: shields dc. Am J Med Genet. 2001 Jul 8;105(5):422-5. Am J Med Genet. 2001. PMID: 11449393

8

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, Evans A, Graham IM, Whitehead AS. Gallagher PM, et al. Among authors: shields dc. Circulation. 1996 Nov 1;94(9):2154-8. doi: 10.1161/01.cir.94.9.2154. Circulation. 1996. PMID: 8901666

9

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.

Hawi Z, Segurado R, Conroy J, Sheehan K, Lowe N, Kirley A, Shields D, Fitzgerald M, Gallagher L, Gill M. Hawi Z, et al. Am J Hum Genet. 2005 Dec;77(6):958-65. doi: 10.1086/498174. Epub 2005 Oct 26. Am J Hum Genet. 2005. PMID: 16380908 Free PMC article.

10

Genetic polymorphisms in platelet-related proteins and coronary artery disease: investigation of candidate genes, including N-acetylgalactosaminyltransferase 4 (GALNT4) and sulphotransferase 1A1/2 (SULT1A1/2).

O'Halloran AM, Patterson CC, Horan P, Maree A, Curtin R, Stanton A, McKeown PP, Shields DC. O'Halloran AM, et al. Among authors: shields dc. J Thromb Thrombolysis. 2009 Feb;27(2):175-84. doi: 10.1007/s11239-008-0196-z. Epub 2008 Feb 8. J Thromb Thrombolysis. 2009. PMID: 18259693

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