Schofield PR - Search Results

1

Genetic architecture of subcortical brain structures in 38,851 individuals.

Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, Teumer A, van der Lee SJ, Yang J, Yanek LR, Lee TV, Li S, Hu Y, Koh JY, Eicher JD, Desrivières S, Arias-Vasquez A, Chauhan G, Athanasiu L, Rentería ME, Kim S, Hoehn D, Armstrong NJ, Chen Q, Holmes AJ, den Braber A, Kloszewska I, Andersson M, Espeseth T, Grimm O, Abramovic L, Alhusaini S, Milaneschi Y, Papmeyer M, Axelsson T, Ehrlich S, Roiz-Santiañez R, Kraemer B, Håberg AK, Jones HJ, Pike GB, Stein DJ, Stevens A, Bralten J, Vernooij MW, Harris TB, Filippi I, Witte AV, Guadalupe T, Wittfeld K, Mosley TH, Becker JT, Doan NT, Hagenaars SP, Saba Y, Cuellar-Partida G, Amin N, Hilal S, Nho K, Mirza-Schreiber N, Arfanakis K, Becker DM, Ames D, Goldman AL, Lee PH, Boomsma DI, Lovestone S, Giddaluru S, Le Hellard S, Mattheisen M, Bohlken MM, Kasperaviciute D, Schmaal L, Lawrie SM, Agartz I, Walton E, Tordesillas-Gutierrez D, Davies GE, Shin J, Ipser JC, Vinke LN, Hoogman M, Jia T, Burkhardt R, Klein M, Crivello F, Janowitz D, Carmichael O, Haukvik UK, Aribisala BS, Schmidt H, Strike LT, Cheng CY, Risacher SL, Pütz B, Fleisch… See abstract for full author list ➔ Satizabal CL, et al. Among authors: schofield pr. Nat Genet. 2019 Nov;51(11):1624-1636. doi: 10.1038/s41588-019-0511-y. Epub 2019 Oct 21. Nat Genet. 2019. PMID: 31636452 Free PMC article.

2

Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia.

Deckert J, Nöthen MM, Rietschel M, Wildenauer D, Bondy B, Ertl MA, Knapp M, Schofield PR, Albus M, Maier W, Propping P. Deckert J, et al. Among authors: schofield pr. J Neural Transm (Vienna). 1996;103(12):1447-55. doi: 10.1007/BF01271259. J Neural Transm (Vienna). 1996. PMID: 9029412 Clinical Trial.

3

Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region.

Deckert J, Nöthen MM, Bryant SP, Schuffenhauer S, Schofield PR, Spurr NK, Propping P. Deckert J, et al. Among authors: schofield pr. Hum Genet. 1997 Mar;99(3):326-8. doi: 10.1007/s004390050366. Hum Genet. 1997. PMID: 9050917

4

Exclusion of linkage between bipolar affective disorder and chromosome 16 in 12 Australian pedigrees.

Adams LJ, Salmon JA, Kwok JB, Vivero C, Donald JA, Mitchell PB, Schofield PR. Adams LJ, et al. Among authors: schofield pr. Am J Med Genet. 1997 May 31;74(3):304-10. doi: 10.1002/(sici)1096-8628(19970531)74:3<304::aid-ajmg12>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9184315

5

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

6

Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q.

Brodaty H, Mitchell P, Luscombe G, Kwok JJ, Badenhop RF, McKenzie R, Schofield PR. Brodaty H, et al. Among authors: schofield pr. Hum Genet. 2002 Jan;110(1):8-14. doi: 10.1007/s00439-001-0650-x. Epub 2001 Dec 4. Hum Genet. 2002. PMID: 11810290

7

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

8

Intraneuronal advanced glycation endproducts in presenilin-1 Alzheimer's disease.

Münch G, Shepherd CE, McCann H, Brooks WS, Kwok JB, Arendt T, Hallupp M, Schofield PR, Martins RN, Halliday GM. Münch G, et al. Among authors: schofield pr. Neuroreport. 2002 Apr 16;13(5):601-4. doi: 10.1097/00001756-200204160-00013. Neuroreport. 2002. PMID: 11973454

9

Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35.

Badenhop RF, Moses MJ, Scimone A, Adams LJ, Kwok JB, Jones AM, Davison G, Evans MR, Kirkby KC, Hewitt JE, Donald JA, Mitchell PB, Schofield PR. Badenhop RF, et al. Among authors: schofield pr. Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):23-32. doi: 10.1002/ajmg.b.10023. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12555231

10

Alzheimer's disease with spastic paraparesis and 'cotton wool' plaques: two pedigrees with PS-1 exon 9 deletions.

Brooks WS, Kwok JB, Kril JJ, Broe GA, Blumbergs PC, Tannenberg AE, Lamont PJ, Hedges P, Schofield PR. Brooks WS, et al. Among authors: schofield pr. Brain. 2003 Apr;126(Pt 4):783-91. doi: 10.1093/brain/awg084. Brain. 2003. PMID: 12615638

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