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Results: 1-25 | 26-36
Results: 1-25/36
An in-frame deletion in the alpha(2C) adrenergic receptor is common in African-Americans
Authors: Feng, J Zheng, J Gelernter, J Kranzler, H Cook, E Goldman, D Jones, IR Craddock, N Heston, LL Delisi, L Peltonen, L Bennett, WP Sommer, SS
Citation: J. Feng et al., An in-frame deletion in the alpha(2C) adrenergic receptor is common in African-Americans, MOL PSYCHI, 6(2), 2001, pp. 168-172
Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibilitygene for bipolar disorder
Authors: Jacobsen, NJO Franks, EKE Elvidge, G Jones, I McCandless, F O'Donovan, MC Owen, MJ Craddock, N
Citation: Njo. Jacobsen et al., Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibilitygene for bipolar disorder, MOL PSYCHI, 6(1), 2001, pp. 92-97
Candidate gene studies of bipolar disorder
Authors: Jones, I Craddock, N
Citation: I. Jones et N. Craddock, Candidate gene studies of bipolar disorder, ANN MED, 33(4), 2001, pp. 248-256
Susceptibility gene(s) forAlzheimer's disease on chromosome 10
Authors: Lendon, C Craddock, N
Citation: C. Lendon et N. Craddock, Susceptibility gene(s) forAlzheimer's disease on chromosome 10, TRENDS NEUR, 24(10), 2001, pp. 557-559
No association between CHRNA7 microsatellite markers and attention-deficithyperactivity disorder
Authors: Kent, L Green, E Holmes, J Thapar, A Gill, M Hawi, Z Fitzgerald, M Asherson, P Curran, S Mills, J Payton, A Craddock, N
Citation: L. Kent et al., No association between CHRNA7 microsatellite markers and attention-deficithyperactivity disorder, AM J MED G, 105(8), 2001, pp. 686-689
Allelic variation of a BalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis
Authors: Elvidge, G Jones, I McCandless, F Asherson, P Owen, MJ Craddock, N
Citation: G. Elvidge et al., Allelic variation of a BalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis, AM J MED G, 105(4), 2001, pp. 307-311
Scanning of estrogen receptor alpha (ER alpha) and thyroid hormone receptor alpha (TR alpha) genes in patients with psychiatric diseases: Four missense mutations identified in ER alpha gene
Authors: Feng, JN Yan, J Michaud, S Craddock, N Jones, IR Cook, EH Goldman, D Heston, LL Peltonen, L Delisi, LE Sommer, SS
Citation: Jn. Feng et al., Scanning of estrogen receptor alpha (ER alpha) and thyroid hormone receptor alpha (TR alpha) genes in patients with psychiatric diseases: Four missense mutations identified in ER alpha gene, AM J MED G, 105(4), 2001, pp. 369-374
CUX2, a potential regulator of NCAM expression: Genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder
Authors: Jacobsen, NJO Elvidge, G Franks, EKE O'Donovan, MC Craddock, N Owen, MJ
Citation: Njo. Jacobsen et al., CUX2, a potential regulator of NCAM expression: Genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder, AM J MED G, 105(3), 2001, pp. 295-300
Is LBP-1c/CP2/LSF a disease-modifying gene for Alzheimer's disease?
Authors: Lendon, C Craddock, N
Citation: C. Lendon et N. Craddock, Is LBP-1c/CP2/LSF a disease-modifying gene for Alzheimer's disease?, LANCET, 358(9287), 2001, pp. 1029-1030
Cigarette smoking and psychotic symptoms in bipolar affective disorder
Authors: Corvin, A O'Mahony, E O'Regan, M Comerford, C O'Connell, R Craddock, N Gill, M
Citation: A. Corvin et al., Cigarette smoking and psychotic symptoms in bipolar affective disorder, BR J PSYCHI, 179, 2001, pp. 35-38
Molecular genetics of bipolar disorder
Authors: Craddock, N Jones, I
Citation: N. Craddock et I. Jones, Molecular genetics of bipolar disorder, BR J PSYCHI, 178, 2001, pp. S128-S133
Familiality of the puerperal trigger in bipolar disorder: Results of a family study
Authors: Jones, I Craddock, N
Citation: I. Jones et N. Craddock, Familiality of the puerperal trigger in bipolar disorder: Results of a family study, AM J PSYCHI, 158(6), 2001, pp. 913-917
No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder
Authors: Bowen, T Ashworth, L Kirov, G Guy, CA Jones, IR McCandless, F Craddock, N O-Donovan, MC Owen, MJ
Citation: T. Bowen et al., No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder, BIPOL DIS, 2(4), 2000, pp. 328-331
Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder
Authors: Speight, G Turic, D Austin, J Hoogendoorn, B Cardno, AG Jones, L Murphy, KC Sanders, R McCarthy, G Jones, I McCandless, F McGuffin, P Craddock, N Owen, MJ Buckland, P O'Donovan, MC
Citation: G. Speight et al., Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder, MOL PSYCHI, 5(3), 2000, pp. 327-331
Pooled genotyping of microsatellite markers in parent-offspring trios
Authors: Kirov, G Williams, N Sham, P Craddock, N Owen, MJ
Citation: G. Kirov et al., Pooled genotyping of microsatellite markers in parent-offspring trios, GENOME RES, 10(1), 2000, pp. 105-115
Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population
Authors: Harris, JM Cumming, AM Craddock, N St Clair, D Lendon, CL
Citation: Jm. Harris et al., Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population, NEUROSCI L, 294(1), 2000, pp. 37-40
Molecular genetic studies of bipolar disorder and puerperal psychosis at two polymorphisms in the estrogen receptor at gene (ESR 1)
Authors: Jones, I Middle, F McCandless, F Coyle, N Robertson, E Brockington, I Lendon, C Craddock, N
Citation: I. Jones et al., Molecular genetic studies of bipolar disorder and puerperal psychosis at two polymorphisms in the estrogen receptor at gene (ESR 1), AM J MED G, 96(6), 2000, pp. 850-853
Five missense variants in the amino-terminal domain of the glucocorticoid receptor: No association with puerperal psychosis or schizophrenia
Authors: Feng, JO Zheng, J Bennett, WP Heston, LL Jones, IR Craddock, N Sommer, SS
Citation: Jo. Feng et al., Five missense variants in the amino-terminal domain of the glucocorticoid receptor: No association with puerperal psychosis or schizophrenia, AM J MED G, 96(3), 2000, pp. 412-417
Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene
Authors: Middle, F Jones, I McCandless, F Barrett, T Khanim, F Owen, MJ Lendon, C Craddock, N
Citation: F. Middle et al., Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene, AM J MED G, 96(2), 2000, pp. 154-157
Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis
Authors: Coyle, N Jones, I Roberson, E Lendon, C Craddock, N
Citation: N. Coyle et al., Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis, LANCET, 356(9240), 2000, pp. 1490-1491
Psychiatric genetics
Authors: Craddock, N
Citation: N. Craddock, Psychiatric genetics, BR J PSYCHI, 177, 2000, pp. 571-571
Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5
Authors: Kirov, G Jones, I McCandless, F Craddock, N Owen, MJ
Citation: G. Kirov et al., Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5, MOL PSYCHI, 4(6), 1999, pp. 558-565
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
Authors: Nothen, MM Cichon, S Rohleder, H Hemmer, S Franzek, E Fritze, J Albus, M Borrmann-Hassenbach, M Kreiner, R Weigelt, B Minges, J Lichtermann, D Maier, W Craddock, N Fimmers, R Holler, T Baur, MP Rietschel, M Propping, P
Citation: Mm. Nothen et al., Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families, MOL PSYCHI, 4(1), 1999, pp. 76-84
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
Authors: Sakuntabhai, A Ruiz-Perez, V Carter, S Jacobsen, N Burge, S Monk, S Smith, M Munro, CS O'Donovan, M Craddock, N Kucherlapati, R Rees, JL Owen, M Lathrop, GM Monaco, AP Strachan, T Hovnanian, A
Citation: A. Sakuntabhai et al., Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease, NAT GENET, 21(3), 1999, pp. 271-277
CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder
Authors: Guy, CA Bowen, T Jones, I McCandless, F Owen, MJ Craddock, N O'Donovan, MC
Citation: Ca. Guy et al., CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder, NEUROBIOL D, 6(4), 1999, pp. 302-307
Risultati: 1-25 | 26-36