Walsh C - Search Results

1

Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat.

Ashworth A, Abusaad I, Walsh C, Nanko S, Murray RM, Asherson P, McGuffin P, Gill M, Owen MJ, Collier DA. Ashworth A, et al. Among authors: walsh c. Psychiatr Genet. 1996 Summer;6(2):81-6. doi: 10.1097/00041444-199622000-00008. Psychiatr Genet. 1996. PMID: 8840394

2

Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?

Asherson P, Walsh C, Williams J, Sargeant M, Taylor C, Clements A, Gill M, Owen M, McGuffin P. Asherson P, et al. Among authors: walsh c. Br J Psychiatry. 1994 May;164(5):619-24. doi: 10.1192/bjp.164.5.619. Br J Psychiatry. 1994. PMID: 7921711

3

Familiality of symptom dimensions in schizophrenia.

Wickham H, Walsh C, Asherson P, Taylor C, Sigmundson T, Gill M, Owen MJ, McGuffin P, Murray R, Sham P. Wickham H, et al. Among authors: walsh c. Schizophr Res. 2001 Mar 1;47(2-3):223-32. doi: 10.1016/s0920-9964(00)00098-0. Schizophr Res. 2001. PMID: 11278139

4

Psychiatric morbidity in the relatives of schizophrenic probands.

Walsh C, Gill M. Walsh C, et al. Br J Psychiatry. 1993 Nov;163:695. doi: 10.1192/bjp.163.5.695b. Br J Psychiatry. 1993. PMID: 8298848 No abstract available.

5

An examination of linkage of schizophrenia and schizoaffective disorder to the pseudoautosomal region (Xp22.3).

Crow TJ, Delisi LE, Lofthouse R, Poulter M, Lehner T, Bass N, Shah T, Walsh C, Boccio-Smith A, Shields G, et al. Crow TJ, et al. Among authors: walsh c. Br J Psychiatry. 1994 Feb;164(2):159-64. doi: 10.1192/bjp.164.2.159. Br J Psychiatry. 1994. PMID: 7818635

6

Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample.

Corvin A, McGhee KA, Murphy K, Donohoe G, Nangle JM, Schwaiger S, Kenny N, Clarke S, Meagher D, Quinn J, Scully P, Baldwin P, Browne D, Walsh C, Waddington JL, Morris DW, Gill M. Corvin A, et al. Among authors: walsh c. Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):949-53. doi: 10.1002/ajmg.b.30452. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17492767

7

A family history study of chronic fatigue syndrome.

Walsh CM, Zainal NZ, Middleton SJ, Paykel ES. Walsh CM, et al. Psychiatr Genet. 2001 Sep;11(3):123-8. doi: 10.1097/00041444-200109000-00003. Psychiatr Genet. 2001. PMID: 11702053

8

Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder.

Jain S, Leggo J, DeLisi LE, Crow TJ, Margolis RL, Li SH, Goodburn S, Walsh C, Paykel ES, Ferguson-Smith MA, Ross CA, Rubinsztein DC. Jain S, et al. Among authors: walsh c. Am J Med Genet. 1996 Apr 9;67(2):139-46. doi: 10.1002/(SICI)1096-8628(19960409)67:2<139::AID-AJMG3>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723040

9

cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat.

Margolis RL, Stine OC, McInnis MG, Ranen NG, Rubinsztein DC, Leggo J, Brando LV, Kidwai AS, Loev SJ, Breschel TS, Callahan C, Simpson SG, DePaulo JR, McMahon FJ, Jain S, Paykel ES, Walsh C, DeLisi LE, Crow TJ, Torrey EF, Ashworth RG, Macke JP, Nathans J, Ross CA. Margolis RL, et al. Among authors: walsh c. Hum Mol Genet. 1996 May;5(5):607-16. doi: 10.1093/hmg/5.5.607. Hum Mol Genet. 1996. PMID: 8733127

10

Analysis and metaanalysis of two polymorphisms within the tyrosine hydroxylase gene in bipolar and unipolar affective disorders.

Furlong RA, Rubinsztein JS, Ho L, Walsh C, Coleman TA, Muir WJ, Paykel ES, Blackwood DH, Rubinsztein DC. Furlong RA, et al. Among authors: walsh c. Am J Med Genet. 1999 Feb 5;88(1):88-94. doi: 10.1002/(sici)1096-8628(19990205)88:1<88::aid-ajmg16>3.0.co;2-j. Am J Med Genet. 1999. PMID: 10050974

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