Hamshere ML - Search Results

1

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.

Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, Heun R, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J. Harold D, et al. Among authors: hamshere ml. Nat Genet. 2009 Oct;41(10):1088-93. doi: 10.1038/ng.440. Epub 2009 Sep 6. Nat Genet. 2009. PMID: 19734902 Free PMC article.

2

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. Hum Mol Genet. 2000 Mar 22;9(5):843-8. doi: 10.1093/hmg/9.5.843. Hum Mol Genet. 2000. PMID: 10749993

3

Susceptibility locus for Alzheimer's disease on chromosome 10.

Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R, Hamshere M, Abraham R, Tunstall N, Rice F, Carty S, Lillystone S, Kehoe P, Rudrasingham V, Jones L, Lovestone S, Perez-Tur J, Williams J, Owen MJ, Hardy J, Goate AM. Myers A, et al. Science. 2000 Dec 22;290(5500):2304-5. doi: 10.1126/science.290.5500.2304. Science. 2000. PMID: 11125144

4

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools.

Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, Austin J, Stephens MK, Buckland PR, Owen MJ, O'Donovan MC. Hoogendoorn B, et al. Among authors: hamshere ml. Hum Genet. 2000 Nov;107(5):488-93. doi: 10.1007/s004390000397. Hum Genet. 2000. PMID: 11140947

5

A genomewide linkage study of age at onset in schizophrenia.

Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ. Cardno AG, et al. Among authors: hamshere ml. Am J Med Genet. 2001 Jul 8;105(5):439-45. doi: 10.1002/ajmg.1404. Am J Med Genet. 2001. PMID: 11449396

6

Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype.

Jones G, Zammit S, Norton N, Hamshere ML, Jones SJ, Milham C, Sanders RD, McCarthy GM, Jones LA, Cardno AG, Gray M, Murphy KC, Owen MJ. Jones G, et al. Among authors: hamshere ml. Br J Psychiatry. 2001 Oct;179:351-5. doi: 10.1192/bjp.179.4.351. Br J Psychiatry. 2001. PMID: 11581117

7

Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.

Abraham R, Myers A, Wavrant-DeVrieze F, Hamshere ML, Thomas HV, Marshall H, Compton D, Spurlock G, Turic D, Hoogendoorn B, Kwon JM, Petersen RC, Tangalos E, Norton J, Morris JC, Bullock R, Liolitsa D, Lovestone S, Hardy J, Goate A, O'Donovan M, Williams J, Owen MJ, Jones L. Abraham R, et al. Among authors: hamshere ml. Hum Genet. 2001 Dec;109(6):646-52. doi: 10.1007/s00439-001-0614-1. Epub 2001 Nov 1. Hum Genet. 2001. PMID: 11810277

8

Full genome screen for Alzheimer disease: stage II analysis.

Myers A, Wavrant De-Vrieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstall N, Jones L, Lovestone S, Williams J, Owen MJ, Hardy J, Goate A. Myers A, et al. Am J Med Genet. 2002 Mar 8;114(2):235-44. doi: 10.1002/ajmg.10183. Am J Med Genet. 2002. PMID: 11857588

9

Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios.

West A, Langley K, Hamshere ML, Kent L, Craddock N, Owen MJ, O'Donovan M, Thapar A. West A, et al. Among authors: hamshere ml. Mol Psychiatry. 2002;7(9):962-6. doi: 10.1038/sj.mp.4001129. Mol Psychiatry. 2002. PMID: 12399949

10

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.

Williams NM, Spurlock G, Norton N, Williams HJ, Hamshere ML, Krawczak M, Kirov G, Nikolov I, Georgieva L, Jones S, Cardno AG, O'Donovan MC, Owen MJ. Williams NM, et al. Among authors: hamshere ml. Mol Psychiatry. 2002;7(10):1092-100. doi: 10.1038/sj.mp.4001188. Mol Psychiatry. 2002. PMID: 12476324

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