De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder von Hamilton, P J, Campbell, N G, Sharma, S, Erreger, K, Herborg Hansen, F, Saunders, C, Belovich, A N, Sahai, M A, Cook, E H, Gether, U, Mchaourab, H S, Matthies, H J G, Sutcliffe, J S, Galli, A

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Influence of gender on working and spatial memory in the novel object recognition task in the rat von Sutcliffe, J.S., Marshall, K.M., Neill, J.C.

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Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism von Delahanty, R J, Kang, J Q, Brune, C W, Kistner, E O, Courchesne, E, Cox, N J, Cook, E H, Macdonald, R L, Sutcliffe, J S

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Characterizing sleep disorders in an autism-specific collection of electronic health records von Singer, E.V., Niarchou, M., Maxwell-Horn, A., Hucks, D., Johnston, R., Sutcliffe, J.S., Davis, L.K., Malow, B.A.

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Analysis of the RELN gene as a genetic risk factor for autism von Skaar, D A, Shao, Y, Haines, J L, Stenger, J E, Jaworski, J, Martin, E R, DeLong, G R, Moore, J H, McCauley, J L, Sutcliffe, J S, Ashley-Koch, A E, Cuccaro, M L, Folstein, S E, Gilbert, J R, Pericak-Vance, M A

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Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation von ABOU-KHALIL, B, GE, Q, DESAI, R, RYTHER, R, BAZYK, A, BAILEY, R, HAINES, J. L, SUTCLIFFE, J. S, GEORGE, A. L

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Abnormal connexin expression in human chronic wounds von Sutcliffe, J.E.S., Chin, K.Y., Thrasivoulou, C., Serena, T.E., O'Neil, S., Hu, R., White, A.M., Madden, L., Richards, T., Phillips, A.R.J., Becker, D.L.

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene ( UBE3A ) in Angelman syndrome von Matsuura, Toshinobu, Sutcliffe, James S, Fang, Ping, Galjaard, Robert-Jan, Jiang, Yong-hui, Benton, Claudia S, Rommens, Johanna M, Beaudet, Arthur L

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Imprinted expression of the murine Angelman syndrome gene, Ube3a , in hippocampal and Purkinje neurons von Albrecht, Urs, Sutcliffe, James S, Cattanach, Bruce M, Beechey, Colin V, Armstrong, Dawna, Eichele, Gregor, Beaudet, Arthur L

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Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism von McCauley, J.L., Olson, L.M., Dowd, M., Amin, T., Steele, A., Blakely, R.D., Folstein, S.E., Haines, J.L., Sutcliffe, J.S.

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Oestradiol attenuates the cognitive deficit induced by acute phencyclidine treatment in mature female hooded-Lister rats von Sutcliffe, JS, Rhaman, F., Marshall, KM, Neill, JC

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Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism von Nurmi, E L, Amin, T, Olson, L M, Jacobs, M M, McCauley, J L, Lam, A Y, Organ, E L, Folstein, S E, Haines, J L, Sutcliffe, J S

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Brain and peripheral pharmacokinetics of levodopa in the cynomolgus monkey following administration of opicapone, a third generation nitrocatechol COMT inhibitor von Bonifácio, M.J., Sutcliffe, J.S., Torrão, L., Wright, L.C., Soares-da-Silva, P.

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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region von Sutcliffe, James S, Nakao, Mitsuyoshi, Christian, Susan, Örstavik, Karen H, Tommerup, Niels, Ledbetter, David H, Beaudet, Arthur L

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Allelic Heterogeneity at the Serotonin Transporter Locus ( SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors von Sutcliffe, James S., Delahanty, Ryan J., Prasad, Harish C., McCauley, Jacob L., Han, Qiao, Jiang, Lan, Li, Chun, Folstein, Susan E., Blakely, Randy D.

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox von Fu, Ying-Hui, Kuhl, Derek P.A., Pizzuti, Antonio, Pieretti, Maura, Sutcliffe, James S., Richards, Stephen, Verkert, Annemieke J.M.H., Holden, Jeanette J.A., Fenwick, Raymond G., Warren, Stephen T., Oostra, Ben A., Nelson, David L., Caskey, C.Thomas

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The spectrum of mutations in UBE3A causing Angelman syndrome von PING FANG, LEV-LEHMAN, E, LANGLOIS, S, GRAHAM, J. M, BEUTEN, J, WILLEMS, P. J, LEDBETTER, D. H, BEAUDET, A. L, TSAI, T.-F, MATSUURA, T, BENTON, C. S, SUTCLIFFE, J. S, CHRISTIAN, S. L, KUBOTA, T, HALLEY, D. J, MEIJERS-HEIJBOER, H

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Incidence of coronary heart disease in a health authority in London: review of a community register von Sutcliffe, Steven J, Fox, Kevin F, Wood, David A, Sutcliffe, Angela, Stock, Kathryn, Wright, Melissa, Akhras, Fawaz, Langford, Ed

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0028 SHORTER SLEEP DURATION IS ASSOCIATED WITH SOCIAL IMPAIRMENT AND PSYCHIATRIC COMORBIDITIES IN AUTISM von Veatch, OJ, Sutcliffe, JS, Warren, ZE, Keenan, BT, Potter, MH, Pack, AI, Malow, BA

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The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region von Sutcliffe, J S, Jiang, Y H, Galijaard, R J, Matsuura, T, Fang, P, Kubota, T, Christian, S L, Bressler, J, Cattanach, B, Ledbetter, D H, Beaudet, A L

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