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Results: 1-14 |
Results: 14
Mutation screening of the KCNN3 gene reveals a rare frameshift mutation
Authors: Bowen, T Williams, N Norton, N Spurlock, G Wittekindt, OH Morris-Rosendahl, DJ Williams, H Brzustowicz, L Hoogendoorn, B Zammit, S Jones, G Sanders, RD Jones, LA McCarthy, G Jones, S Bassett, A Cardno, AG Owen, MJ O'Donovan, MC
Citation: T. Bowen et al., Mutation screening of the KCNN3 gene reveals a rare frameshift mutation, MOL PSYCHI, 6(3), 2001, pp. 259-260
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls
Authors: Sklar, P Schwab, SG Williams, NM Daly, M Schaffner, S Maier, W Albus, M Trixler, M Eichhammer, P Lerer, B Hallmayer, J Norton, N Williams, H Zammit, S Cardno, AG Jones, S McCarthy, G Milanova, V Kirov, G O'Donovan, MC Lander, ES Owen, MJ Wildenauer, DB
Citation: P. Sklar et al., Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls, NAT GENET, 28(2), 2001, pp. 126-128
A genomewide linkage study of age at onset in schizophrenia
Authors: 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
Citation: Ag. Cardno et al., A genomewide linkage study of age at onset in schizophrenia, AM J MED G, 105(5), 2001, pp. 439-445
Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype
Authors: 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
Citation: G. Jones et al., Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype, BR J PSYCHI, 179, 2001, pp. 351-355
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14
Authors: McEntagart, M Norton, N Williams, H Teare, MD Dunstan, M Baker, P Houlden, H Reilly, M Wood, N Harper, PS Futreal, PA Williams, N Rahman, N
Citation: M. Mcentagart et al., Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14, AM J HU GEN, 68(5), 2001, pp. 1270-1276
Cheap, accurate and rapid allele frequency estimation of single nucleotidepolymorphisms by primer extension and DHPLC in DNA pools
Authors: Hoogendoorn, B Norton, N Kirov, G Williams, N Hamshere, ML Spurlock, G Austin, J Stephens, MK Buckland, PR Owen, MJ O'Donovan, MC
Citation: B. Hoogendoorn et al., Cheap, accurate and rapid allele frequency estimation of single nucleotidepolymorphisms by primer extension and DHPLC in DNA pools, HUM GENET, 107(5), 2000, pp. 488-493
A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers
Authors: Jonsson, EG Norton, N Gustavsson, JF Oreland, L Owen, MJ Sedvall, GC
Citation: Eg. Jonsson et al., A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers, J PSYCH RES, 34(3), 2000, pp. 239-244
APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome
Authors: Deb, S Braganza, J Norton, N Williams, H Kehoe, PG Williams, J Owen, MJ
Citation: S. Deb et al., APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome, BR J PSYCHI, 176, 2000, pp. 468-472
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III
Authors: Levinson, DF Holmans, P Straub, RE Owen, MJ Wildenauer, DB Gejman, PV Pulver, AE Laurent, C Kendler, KS Walsh, D Norton, N Williams, NM Schwab, SG Lerer, B Mowry, BJ Sanders, AR Antonarakis, SE Blouin, JL DeLeuze, JF Mallet, J
Citation: Df. Levinson et al., Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III, AM J HU GEN, 67(3), 2000, pp. 652-663
Autosome search for schizophrenia susceptibility genes in multiply affected families
Authors: Rees, MI Fenton, I Williams, NM Holmans, P Norton, N Cardno, A Asherson, P Spurlock, G Roberts, E Parfitt, E Mant, P Vallada, H Dawson, E Li, MW Collier, DA Powell, JF Nanko, S Gill, M McGuffin, P Owen, MJ
Citation: Mi. Rees et al., Autosome search for schizophrenia susceptibility genes in multiply affected families, MOL PSYCHI, 4(4), 1999, pp. 353-359
A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs
Authors: Williams, NM Rees, MI Holmans, P Norton, N Cardno, AG Jones, LA Murphy, KC Sanders, RD McCarthy, G Gray, MY Fenton, I McGuffin, P Owen, MJ
Citation: Nm. Williams et al., A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs, HUM MOL GEN, 8(9), 1999, pp. 1729-1739
A full genome scan for late onset Alzheimer's disease
Authors: Kehoe, P Wavrant-De Vrieze, F Crook, R Wu, WS Holmans, P Fenton, I Spurlock, G Norton, N Williams, H Williams, N Lovestone, S Perez-Tur, J Hutton, M Chartier-Harlin, MC Shears, S Roehl, K Booth, J Van Voorst, W Ramic, D Williams, J Goate, A Hardy, J Owen, MJ
Citation: P. Kehoe et al., A full genome scan for late onset Alzheimer's disease, HUM MOL GEN, 8(2), 1999, pp. 237-245
Sixth World Congress of Psychiatric Genetics X Chromosome Workshop
Authors: Paterson, AD DeLisi, L Faraone, SV Gejman, PV Goossens, D Hovatta, I Kaufmann, CA Klauck, SM Kunugi, H Levinson, DF Mors, O Norton, N Smalley, SL
Citation: Ad. Paterson et al., Sixth World Congress of Psychiatric Genetics X Chromosome Workshop, AM J MED G, 88(3), 1999, pp. 279-286
No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome
Authors: Deb, S Braganza, J Owen, M Kehoe, P Williams, H Norton, N
Citation: S. Deb et al., No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome, ALZHEIM REP, 1(6), 1998, pp. 365-368
Risultati: 1-14 |