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Behavioural phenotypes: From models to intervention

Heussler, H.S and Oliver, C (2011) Behavioural phenotypes: From models to intervention. Journal Of Intellectual Disability Research, 55. pp. 945-947.

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Type of Work:Article
Date:2011 (Publication)
School/Faculty:Colleges (2008 onwards) > College of Life & Environmental Sciences
Department:School of Psychology

Brendel C, Belakhov V, Werner H, Wegener E, Gärtner J, Nudelman I, Baasov T, Huppke P. Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. J Mol
Med (Berl). 2011 Apr;89(4):389-98.

Cornish, K. and Hocking, D.R. (2011). Carriers of the FMR1 gene: Does size matter? Journal of Intellectual Disability Research, 55, XX –XX.

Dykens EM, Roof E, Bittel D, Butler MG.TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome. J Child Psychol Psychiatry. 2011 May;52(5):580-7.

Ehninger D, Silva AJ. Rapamycin for treating Tuberous sclerosis and Autism spectrum disorders. Trends Mol Med. 2011 Feb;17(2):78-87. Epub 2010 Nov 4.

Glaze DG, Percy AK, Motil KJ et al A Study of the Treatment of Rett Syndrome With Folate and Betaine J Child Neurol. 2009 May; 24(5): 551–556. Holland, A.J. (2011). The evolving nature of research into intellectual disabilities: Priorities and possibilities. Journal of Intellectual Disability Research, 55, XX –XX.

Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ. Distinct phenotypes distinguish the molecular classes of Angelman syndrome. J Med Genet. 2001 Dec;38(12):834-45.

Kates WR, Antshel KM, Faraone SV, Fremont WP, Higgins AM, Shprintzen RJ, Botti JA, Kelchner L, McCarthy C.Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.Biol Psychiatry. 2011 May 15;69(10):945-52.

Krueger DA, Care MM, Holland K, Agricola K, Tudor C, Mangeshkar P, Wilson KA, Byars A, Sahmoud T, Franz DN. Everolimus for Subependymal Giant-Cell Astrocytomas in Tuberous Sclerosis. N Engl J Med 2010; 363:1801-1811

Krueger DD, Bear MF. Toward fulfilling the promise of molecular medicine in fragile X syndrome. Annu Rev Med. 2011 Feb 18;62:411-29.

Mari F, Azimonti S, Bertani I, Bolognese F, Colombo E, Caselli R, Scala E, Longo I, Grosso S, Pescucci C, Ariani F, Hayek G, Balestri P, Bergo A, Badaracco G, Zappella M, Broccoli V, Renieri A, Kilstrup-Nielsen C, Landsberger N. CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome. Hum Mol Genet. 2005 Jul 15;14(14):1935-46.

Moore, D. and George, R. (2011). A tool for the visualisation and modelling of typical and atypical development: ACORNS an Accessible Cause-Outcome Representation and Notation System. Journal of Intellectual Disability Research, 55, XX –XX.

Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA. Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid. Am J Med Genet A. 2010 Aug;152A(8)

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, PHum Mol Genet. ustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. 2007 Jan 1;16(1):83-91.

Rawas, S. A., Delamont, R. S., Engerström, I. W., Hansen, S., Apartopoulos, F., Smeets, E.E.J., Curfs, L.M.G., Pini, G. and Julu, P.O.O. (2011). The modification of apneustic breathing in Rett Syndrome with a 5-HT1-A agonist. Journal of Intellectual Disability Research, 55, XX –XX.

Weaving LS, Christodoulou J, Williamson SL, Friend KL, McKenzie OL, Archer H, Evans J, Clarke A, Pelka GJ, Tam PP, Watson C, Lahooti H, Ellaway CJ, Bennetts B, Leonard H, Gécz J. Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. Am J Hum Genet. 2004 Dec;75(6):1079-93.

Winarni, T.I., Chanchaiya, W., Au, J., Adams, E., Mu, Y., Nguyen, D.V. and Hagerman R.J. (2011). Sertraline improves the developmental trajectory for language in young children with Fragile X syndrome. Journal of Intellectual Disability Research, 55, XX –XX.

Wong, H.T., McCartney, D.L., Lewis, J., Sampson, J.R., Howe, C.J. and de Vries, P.J. (2011). Individuals with TSC1 and TSC2 mutations show distinct patterns of intellectual abilities. Journal of Intellectual Disability Research, 55, XX –XX.

Subjects:BF Psychology
Institution:University of Birmingham
Copyright Holders:Christopher Oliver
ID Code:1429
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