Williams J - Search Results

1

A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability.

Plomin R, Turic DM, Hill L, Turic DE, Stephens M, Williams J, Owen MJ, O'Donovan MC. Plomin R, et al. Among authors: williams j. Mol Psychiatry. 2004 Jun;9(6):582-6. doi: 10.1038/sj.mp.4001441. Mol Psychiatry. 2004. PMID: 14981524

2

A novel Alzheimer disease locus located near the gene encoding tau protein.

Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj AC, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, Destefano AL, Grenier-Boley B, Sims R, Beecham GW, Smith AV, Chouraki V, Hamilton-Nelson KL, Ikram MA, Fievet N, Denning N, Martin ER, Schmidt H, Kamatani Y, Dunstan ML, Valladares O, Laza AR, Zelenika D, Ramirez A, Foroud TM, Choi SH, Boland A, Becker T, Kukull WA, van der Lee SJ, Pasquier F, Cruchaga C, Beekly D, Fitzpatrick AL, Hanon O, Gill M, Barber R, Gudnason V, Campion D, Love S, Bennett DA, Amin N, Berr C, Tsolaki M, Buxbaum JD, Lopez OL, Deramecourt V, Fox NC, Cantwell LB, Tárraga L, Dufouil C, Hardy J, Crane PK, Eiriksdottir G, Hannequin D, Clarke R, Evans D, Mosley TH Jr, Letenneur L, Brayne C, Maier W, De Jager P, Emilsson V, Dartigues JF, Hampel H, Kamboh MI, de Bruijn RF, Tzourio C, Pastor P, Larson EB, Rotter JI, O'Donovan MC, Montine TJ, Nalls MA, Mead S, Reiman EM, Jonsson PV, Holmes C, St George-Hyslop PH, Boada M, Passmore P, Wendland JR, Schmidt R, Morgan K, Winslow AR, Powell JF, Carasquillo M, Younkin SG, Jakobsdóttir J, Kauwe JS, Wilhelmsen KC, Rujescu D, Nöthen MM, Hofman A, Jones L; IGAP Consortium; Haines JL, Psaty BM, Van … See abstract for full author list ➔ Jun G, et al. Among authors: williams j. Mol Psychiatry. 2016 Jan;21(1):108-17. doi: 10.1038/mp.2015.23. Epub 2015 Mar 17. Mol Psychiatry. 2016. PMID: 25778476 Free PMC article.

3

Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia.

Asherson P, Mant R, Holmans P, Williams J, Cardno A, Murphy K, Jones L, Collier D, McGuffin P, Owen MJ. Asherson P, et al. Among authors: williams j. Mol Psychiatry. 1996 May;1(2):125-32. Mol Psychiatry. 1996. PMID: 9118322

4

A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter.

Spurlock G, Heils A, Holmans P, Williams J, D'Souza UM, Cardno A, Murphy KC, Jones L, Buckland PR, McGuffin P, Lesch KP, Owen MJ. Spurlock G, et al. Among authors: williams j. Mol Psychiatry. 1998 Jan;3(1):42-9. doi: 10.1038/sj.mp.4000342. Mol Psychiatry. 1998. PMID: 9491812

5

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia.

Williams J, Spurlock G, Holmans P, Mant R, Murphy K, Jones L, Cardno A, Asherson P, Blackwood D, Muir W, Meszaros K, Aschauer H, Mallet J, Laurent C, Pekkarinen P, Seppala J, Stefanis CN, Papadimitriou GN, Macciardi F, Verga M, Pato C, Azevedo H, Crocq MA, Gurling H, Owen MJ, et al. Williams J, et al. Mol Psychiatry. 1998 Mar;3(2):141-9. doi: 10.1038/sj.mp.4000376. Mol Psychiatry. 1998. PMID: 9577838

6

Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia.

Bowen T, Guy CA, Craddock N, Cardno AG, Williams NM, Spurlock G, Murphy KC, Jones LA, Gray M, Sanders RD, McCarthy G, Chandy KG, Fantino E, Kalman K, Gutman GA, Gargus JJ, Williams J, McGuffin P, Owen MJ, O'Donovan MC. Bowen T, et al. Among authors: williams j, williams nm. Mol Psychiatry. 1998 May;3(3):266-9. doi: 10.1038/sj.mp.4000400. Mol Psychiatry. 1998. PMID: 9672903

7

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Turic D, et al. Among authors: williams n, williams j. Mol Psychiatry. 2003 Feb;8(2):176-85. doi: 10.1038/sj.mp.4001216. Mol Psychiatry. 2003. PMID: 12610650

8

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Harold D, et al. Among authors: williams j. Mol Psychiatry. 2006 Dec;11(12):1085-91, 1061. doi: 10.1038/sj.mp.4001904. Epub 2006 Oct 10. Mol Psychiatry. 2006. PMID: 17033633 Clinical Trial.

9

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.

Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, Hopkin E, Pound K, Fernando S, Easton M, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Morris DW, et al. Among authors: williams n, williams j. Hum Mol Genet. 2000 Mar 22;9(5):843-8. doi: 10.1093/hmg/9.5.843. Hum Mol Genet. 2000. PMID: 10749993

10

Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability.

Morris DW, Ivanov D, Robinson L, Williams N, Stevenson J, Owen MJ, Williams J, O'Donovan MC. Morris DW, et al. Among authors: williams n, williams j. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):97-103. doi: 10.1002/ajmg.b.30033. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274049

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