Arranz M - Search Results

1

Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32.

Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M, et al. Lin MW, et al. Among authors: arranz m. Psychiatr Genet. 1995 Fall;5(3):117-26. doi: 10.1097/00041444-199505030-00004. Psychiatr Genet. 1995. PMID: 8746410

2

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Collier DA, Barrett TG, Curtis D, Macleod A, Arranz MJ, Maassen JA, Bundey S. Collier DA, et al. Among authors: arranz mj. Am J Hum Genet. 1996 Oct;59(4):855-63. Am J Hum Genet. 1996. PMID: 8808601 Free PMC article.

3

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families.

Kunugi H, Vallada HP, Sham PC, Hoda F, Arranz MJ, Li T, Nanko S, Murray RM, McGuffin P, Owen M, Gill M, Collier DA. Kunugi H, et al. Among authors: arranz mj. Psychiatr Genet. 1997 Autumn;7(3):97-101. doi: 10.1097/00041444-199723000-00001. Psychiatr Genet. 1997. PMID: 9323320

4

Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families.

Arranz M, Sharma T, Sham P, Kerwin R, Nanko S, Owen M, Gill M, Collier D. Arranz M, et al. Am J Med Genet. 1995 Oct 9;60(5):377-81. doi: 10.1002/ajmg.1320600506. Am J Med Genet. 1995. PMID: 8546149

5

No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene.

Kunugi H, Vallada HP, Hoda F, Kirov G, Gill M, Aitchison KJ, Ball D, Arranz MJ, Murray RM, Collier DA. Kunugi H, et al. Among authors: arranz mj. Biol Psychiatry. 1997 Aug 15;42(4):282-5. doi: 10.1016/S0006-3223(96)00366-6. Biol Psychiatry. 1997. PMID: 9270905 Clinical Trial.

6

Catechol-O-methyltransferase Val158Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder.

Li T, Vallada H, Curtis D, Arranz M, Xu K, Cai G, Deng H, Liu J, Murray R, Liu X, Collier DA. Li T, et al. Among authors: arranz m. Pharmacogenetics. 1997 Oct;7(5):349-53. doi: 10.1097/00008571-199710000-00002. Pharmacogenetics. 1997. PMID: 9352569

7

Case-control, haplotype relative risk and transmission disequilibrium analysis of a dopamine D2 receptor functional promoter polymorphism in schizophrenia.

Li T, Arranz M, Aitchison KJ, Bryant C, Liu X, Kerwin RW, Murray R, Sham P, Collier DA. Li T, et al. Among authors: arranz m. Schizophr Res. 1998 Jul 27;32(2):87-92. doi: 10.1016/s0920-9964(98)00024-3. Schizophr Res. 1998. PMID: 9713903

8

Mapping genomic loci implicates genes and synaptic biology in schizophrenia.

Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, Koopmans F, Magnusson S, Richards AL, Sidorenko J, Wu Y, Zeng J, Grove J, Kim M, Li Z, Voloudakis G, Zhang W, Adams M, Agartz I, Atkinson EG, Agerbo E, Al Eissa M, Albus M, Alexander M, Alizadeh BZ, Alptekin K, Als TD, Amin F, Arolt V, Arrojo M, Athanasiu L, Azevedo MH, Bacanu SA, Bass NJ, Begemann M, Belliveau RA, Bene J, Benyamin B, Bergen SE, Blasi G, Bobes J, Bonassi S, Braun A, Bressan RA, Bromet EJ, Bruggeman R, Buckley PF, Buckner RL, Bybjerg-Grauholm J, Cahn W, Cairns MJ, Calkins ME, Carr VJ, Castle D, Catts SV, Chambert KD, Chan RCK, Chaumette B, Cheng W, Cheung EFC, Chong SA, Cohen D, Consoli A, Cordeiro Q, Costas J, Curtis C, Davidson M, Davis KL, de Haan L, Degenhardt F, DeLisi LE, Demontis D, Dickerson F, Dikeos D, Dinan T, Djurovic S, Duan J, Ducci G, Dudbridge F, Eriksson JG, Fañanás L, Faraone SV, Fiorentino A, Forstner A, Frank J, Freimer NB, Fromer M, Frustaci A, Gadelha A, Genovese G, Gershon ES, Giannitelli M, Giegling I, Giusti-Rodríguez P, Godard S, Goldstein JI, González Peñas J, González-Pinto A, … See abstract for full author list ➔ Trubetskoy V, et al. Nature. 2022 Apr;604(7906):502-508. doi: 10.1038/s41586-022-04434-5. Epub 2022 Apr 8. Nature. 2022. PMID: 35396580 Free PMC article.

9

Association between clozapine response and allelic variation in the 5-HT2C receptor gene.

Sodhi MS, Arranz MJ, Curtis D, Ball DM, Sham P, Roberts GW, Price J, Collier DA, Kerwin RW. Sodhi MS, et al. Among authors: arranz mj. Neuroreport. 1995 Dec 29;7(1):169-72. Neuroreport. 1995. PMID: 8742444

10

Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine.

Arranz MJ, Munro J, Owen MJ, Spurlock G, Sham PC, Zhao J, Kirov G, Collier DA, Kerwin RW. Arranz MJ, et al. Mol Psychiatry. 1998 Jan;3(1):61-6. doi: 10.1038/sj.mp.4000348. Mol Psychiatry. 1998. PMID: 9491814

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