Schofield PR - Search Results

1

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, Postmus I, Smith AV, Smith JA, Thalamuthu A, Thomson R, Vitart V, Wang J, Yu L, Zgaga L, Zhao W, Boxall R, Harris SE, Hill WD, Liewald DC, Luciano M, Adams H, Ames D, Amin N, Amouyel P, Assareh AA, Au R, Becker JT, Beiser A, Berr C, Bertram L, Boerwinkle E, Buckley BM, Campbell H, Corley J, De Jager PL, Dufouil C, Eriksson JG, Espeseth T, Faul JD, Ford I; Generation Scotland; Gottesman RF, Griswold ME, Gudnason V, Harris TB, Heiss G, Hofman A, Holliday EG, Huffman J, Kardia SL, Kochan N, Knopman DS, Kwok JB, Lambert JC, Lee T, Li G, Li SC, Loitfelder M, Lopez OL, Lundervold AJ, Lundqvist A, Mather KA, Mirza SS, Nyberg L, Oostra BA, Palotie A, Papenberg G, Pattie A, Petrovic K, Polasek O, Psaty BM, Redmond P, Reppermund S, Rotter JI, Schmidt H, Schuur M, Schofield PW, Scott RJ, Steen VM, Stott DJ, van Swieten JC, Taylor KD, Trollor J, Trompet S, Uitterlinden AG, Weinstein G, Widen E, Windham BG, Jukema JW, Wright AF, Wright MJ, Yang Q, Amieva H, Attia JR, Bennett DA, Brodaty H, de Craen AJ, Hayward C,… See abstract for full author list ➔ Davies G, et al. Among authors: schofield pw, schofield pr. Mol Psychiatry. 2015 Feb;20(2):183-92. doi: 10.1038/mp.2014.188. Epub 2015 Feb 3. Mol Psychiatry. 2015. PMID: 25644384 Free PMC article.

2

Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.

Kwok JB, Taddei K, Hallupp M, Fisher C, Brooks WS, Broe GA, Hardy J, Fulham MJ, Nicholson GA, Stell R, St George Hyslop PH, Fraser PE, Kakulas B, Clarnette R, Relkin N, Gandy SE, Schofield PR, Martins RN. Kwok JB, et al. Among authors: schofield pr. Neuroreport. 1997 Apr 14;8(6):1537-42. doi: 10.1097/00001756-199704140-00043. Neuroreport. 1997. PMID: 9172170

3

Nonparametric simulation-based statistical analyses for bipolar affective disorder locus on chromosome 21q22.3.

Kwok JB, Adams LJ, Salmon JA, Donald JA, Mitchell PB, Schofield PR. Kwok JB, et al. Among authors: schofield pr. Am J Med Genet. 1999 Feb 5;88(1):99-102. doi: 10.1002/(sici)1096-8628(19990205)88:1<99::aid-ajmg18>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10050976

4

Novel Leu723Pro amyloid precursor protein mutation increases amyloid beta42(43) peptide levels and induces apoptosis.

Kwok JB, Li QX, Hallupp M, Whyte S, Ames D, Beyreuther K, Masters CL, Schofield PR. Kwok JB, et al. Among authors: schofield pr. Ann Neurol. 2000 Feb;47(2):249-53. doi: 10.1002/1531-8249(200002)47:2<249::aid-ana18>3.0.co;2-8. Ann Neurol. 2000. PMID: 10665499

5

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

Stanford PM, Halliday GM, Brooks WS, Kwok JB, Storey CE, Creasey H, Morris JG, Fulham MJ, Schofield PR. Stanford PM, et al. Among authors: schofield pr. Brain. 2000 May;123 ( Pt 5):880-93. doi: 10.1093/brain/123.5.880. Brain. 2000. PMID: 10775534

6

Variable phenotype of Alzheimer's disease with spastic paraparesis.

Smith MJ, Kwok JB, McLean CA, Kril JJ, Broe GA, Nicholson GA, Cappai R, Hallupp M, Cotton RG, Masters CL, Schofield PR, Brooks WS. Smith MJ, et al. Among authors: schofield pr. Ann Neurol. 2001 Jan;49(1):125-9. doi: 10.1002/1531-8249(200101)49:1<125::aid-ana21>3.0.co;2-1. Ann Neurol. 2001. PMID: 11198283

7

A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q.

Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen KR, Rosso A, Donald JA, Adams LJ, Schofield PR. Badenhop RF, et al. Among authors: schofield pr. Mol Psychiatry. 2001 Jul;6(4):396-403. doi: 10.1038/sj.mp.4000887. Mol Psychiatry. 2001. PMID: 11443523

8

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB).

Rees MI, Lewis TM, Kwok JB, Mortier GR, Govaert P, Snell RG, Schofield PR, Owen MJ. Rees MI, et al. Among authors: schofield pr. Hum Mol Genet. 2002 Apr 1;11(7):853-60. doi: 10.1093/hmg/11.7.853. Hum Mol Genet. 2002. PMID: 11929858

9

A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.

Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR. Badenhop RF, et al. Among authors: schofield pr. Mol Psychiatry. 2002;7(6):594-603. doi: 10.1038/sj.mp.4001025. Mol Psychiatry. 2002. PMID: 12140782

10

Stylized transcript map of chromosome 4q35 encompassing the locus for a bipolar disorder susceptibility gene.

Blair IP, Adam LJ, Badenhop RF, Moses MJ, Scimone A, Morris JA, Ma L, Austin CP, Donald JA, Mitchell PB, Schofield PR. Blair IP, et al. Among authors: schofield pr. Mol Psychiatry. 2002;7(7):669. doi: 10.1038/sj.mp.4001154. Mol Psychiatry. 2002. PMID: 12192607 No abstract available.

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