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Results:
1-19
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Results: 19
Authors:
Curran, S
Mill, J
Tahir, E
Kent, L
Richards, S
Gould, A
Huckett, L
Sharp, J
Batten, C
Fernando, S
Ozbay, F
Yazgan, Y
Simonoff, E
Thompson, M
Taylor, E
Asherson, P
Citation: S. Curran et al., Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples, MOL PSYCHI, 6(4), 2001, pp. 425-428
Authors:
Mill, J
Curran, S
Kent, L
Richards, S
Gould, A
Virdee, V
Huckett, L
Sharp, J
Batten, C
Fernando, S
Simanoff, E
Thompson, M
Zhao, J
Sham, P
Taylor, E
Asherson, P
Citation: J. Mill et al., Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample, MOL PSYCHI, 6(4), 2001, pp. 440-444
Authors:
Wickham, H
Walsh, C
Asherson, P
Taylor, C
Sigmundson, T
Gill, M
Owen, MJ
McGuffin, P
Murray, R
Sham, P
Citation: H. Wickham et al., Familiality of symptom dimensions in schizophrenia, SCHIZOPHR R, 47(2-3), 2001, pp. 223-232
Authors:
Moore, T
Hecquet, S
McLellann, A
Ville, D
Grid, D
Picard, F
Moulard, B
Asherson, P
Makoff, AJ
McCormick, D
Nasef, L
Froguel, P
Arzimanoglou, A
LeGuern, E
Bailleul, B
Citation: T. Moore et al., Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME, EPILEPSY R, 46(2), 2001, pp. 157-167
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
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
Authors:
Curran, S
Mill, J
Sham, P
Rijsdijk, F
Marusic, K
Taylor, E
Asherson, P
Citation: S. Curran et al., QTL association analysis of the DRD4 exon 3 VNTR polymorphism in a population sample of children screened with a parent rating scale for ADHD symptoms, AM J MED G, 105(4), 2001, pp. 387-393
Authors:
Asherson, P
Barr, C
Biederman, J
Buitelaar, J
Castellanos, X
Curran, S
Doyle, A
Ebstein, R
Eisenberg, J
Faraone, SV
Gill, M
Hay, D
Holmes, J
Hudziak, J
Kennedy, J
Kent, L
Levy, F
Manor, I
Mick, E
Price, T
Rohde, LA
Rowe, D
Sargeant, J
Simonoff, E
Spencer, T
Swanson, J
Taylor, E
Todd, R
Waldman, I
Yazgan, Y
Citation: P. Asherson et al., Report from the Second International Meeting of the Attention Deficit Hyperactivity Disorder Molecular Genetics Network, AM J MED G, 105(3), 2001, pp. 255-258
Authors:
Chioza, B
Wilkie, H
Nashef, L
Blower, J
McCormick, D
Sham, P
Asherson, P
Makoff, AJ
Citation: B. Chioza et al., Association between the alpha(1a) calcium channel gene CACNA1A and idiopathic generalized epilepsy, NEUROLOGY, 56(9), 2001, pp. 1245-1246
Authors:
Collier, DA
Curran, S
Asherson, P
Citation: Da. Collier et al., Mission: Not impossible? Candidate gene studies in child psychiatric disorders, MOL PSYCHI, 5(5), 2000, pp. 457-460
Authors:
Goodwin, H
Curran, N
Chioza, B
Blower, J
Nashef, L
Asherson, P
Makoff, AJ
Citation: H. Goodwin et al., No association found between polymorphisms in genes encoding mGluR7 and mGluR8 and idiopathic generalised epilepsy in a case control study, EPILEPSY R, 39(1), 2000, pp. 27-31
Authors:
Chioza, B
Goodwin, H
Blower, J
McCormick, D
Nashef, L
Asherson, P
Makoff, AJ
Citation: B. Chioza et al., Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and IGE, AM J MED G, 96(6), 2000, pp. 814-816
Authors:
Curran, S
Newman, S
Taylor, E
Asherson, P
Citation: S. Curran et al., Hypescheme: An operational criteria checklist and minimum data set for molecular genetic studies of attention deficit and hyperactivity disorders, AM J MED G, 96(3), 2000, pp. 244-250
Authors:
Asherson, P
Barkley, R
Barr, C
Berg, K
Biederman, J
Castellanos, X
Comings, D
Curran, S
Doyle, A
Ebstein, R
Eisenberg, J
Ergelen, E
Faraone, S
Freund, L
Geller, D
Gill, M
Holmes, J
Hudziak, J
Kennedy, J
Kent, L
Manor, I
Mick, E
Mitchell, H
Navia, B
Pato, C
Pato, M
Price, T
Sargeant, J
Simonoff, E
Smalley, S
Spencer, T
Swanson, J
Waldman, I
Wilens, T
Yazgan, Y
Citation: P. Asherson et al., Collaborative possibilities for molecular genetic studies of attention deficit hyperactivity disorder: Report from an international conference, AM J MED G, 96(3), 2000, pp. 251-257
Authors:
Asherson, P
Curran, S
Citation: P. Asherson et S. Curran, Approaches to gene identification in neuro-psychiatric and other complex disorders, ACT NEUR SC, 102, 2000, pp. 20-22
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
Authors:
Fisher, PJ
Turic, D
Williams, NM
McGuffin, P
Asherson, P
Ball, D
Craig, I
Eley, T
Hill, L
Chorney, K
Chorney, MJ
Benbow, CP
Lubinski, D
Plomin, R
Owen, MJ
Citation: Pj. Fisher et al., DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children, HUM MOL GEN, 8(5), 1999, pp. 915-922
Authors:
Hill, L
Craig, IW
Asherson, P
Ball, D
Eley, T
Ninomiya, T
Fisher, PJ
Turic, D
McGuffin, P
Owen, MJ
Chorney, K
Chorney, MJ
Benbow, CP
Lubinski, D
Thompson, LA
Plomin, R
Citation: L. Hill et al., DNA pooling and dense marker maps: a systematic search for genes for cognitive ability, NEUROREPORT, 10(4), 1999, pp. 843-848
Authors:
Cardno, AG
Jones, LA
Murphy, KC
Sanders, RD
Asherson, P
Owen, MJ
McGuffin, P
Citation: Ag. Cardno et al., Dimensions of psychosis in affected sibling pairs, SCHIZO BULL, 25(4), 1999, pp. 841-850
Risultati:
1-19
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