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11 results for author:"Mcclay J."Drop in Literature Citations

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AKT1 is associated with schizophrenia across multiple symptom dimensions in the Irish study of high density schizophrenia families.

Thiselton D.L., Vladimirov V.I., Kuo P.H., McClay J., Wormley B., Fanous A., O'Neill F.A., Walsh D., Van den Oord E.J., Kendler K.S. et al.

Biol. Psychiatry 63:449-457(2008) · Mapped (7)

A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families.

Vladimirov V., Thiselton D.L., Kuo P.H., McClay J., Fanous A., Wormley B., Vittum J., Ribble R., Moher B., van den Oord E. et al.

Mol. Psychiatry 12:842-853(2007) · Mapped (1)

Catechol-O-methyltransferase and the clinical features of psychosis.

McClay J.L., Fanous A., van den Oord E.J., Webb B.T., Walsh D., O'Neill F.A., Kendler K.S., Chen X.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 141B:935-938(2006) · Mapped (7)

Four mutations in Epidermodysplasia verruciformis 1 (EVER1) gene are not contributors to susceptibility in RRP.

Donfack J., Buchinsky F.J., Derkay C.S., Steinberg B.M., Choi S.S., Conley S.F., Meyer C.M., McClay J.E., Campisi P., Hu F.Z. et al.

Int. J. Pediatr. Otorhinolaryngol. 70:1235-1240(2006) · Mapped (6)

Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction.

Caspi A., Moffitt T.E., Cannon M., McClay J., Murray R., Harrington H., Taylor A., Arseneault L., Williams B., Braithwaite A. et al.

Biol. Psychiatry 57:1117-1127(2005) · Mapped (7)

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene.

Caspi A., Sugden K., Moffitt T.E., Taylor A., Craig I.W., Harrington H., McClay J., Mill J., Martin J., Braithwaite A. et al.

Science 301:386-389(2003) · UniProtKB (1) · Mapped (3)

Association analysis of MAOA and COMT with neuroticism assessed by peers.

Eley T.C., Tahir E., Angleitner A., Harriss K., McClay J., Plomin R., Riemann R., Spinath F., Craig I.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 120B:90-96(2003) · Mapped (16)

Role of genotype in the cycle of violence in maltreated children.

Caspi A., McClay J., Moffitt T.E., Mill J., Martin J., Craig I.W., Taylor A., Poulton R.

Science 297:851-854(2002) · Mapped (9)

The dopamine D4 receptor and the hyperactivity phenotype: a developmental-epidemiological study.

Mill J.S., Caspi A., McClay J., Sugden K., Purcell S., Asherson P., Craig I., McGuffin P., Braithwaite A., Poulton R. et al.

Mol. Psychiatry 7:383-391(2002) · Mapped (59)

Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb.

Koch H.G., McClay J., Loh E.W., Higuchi S., Zhao J.H., Sham P., Ball D., Craig I.W.

Hum. Mol. Genet. 9:2993-2999(2000) · Mapped (4)

The DNA sequence of human chromosome 22.

Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K. et al.

Nature 402:489-495(1999) · UniProtKB (1,027) · Mapped (3)

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