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Analysis of genetic variations of protein tyrosine kinase fyn and their association with alcohol dependence in two independent cohorts.
Schumann G, Rujescu D, Kissling C, Soyka M, Dahmen N, Preuss UW, Wieman S, Depner M, Wellek S, Lascorz J, Bondy B, Giegling I, Anghelescu I, Cowen MS, Poustka A, Spanagel R, Mann K, Henn FA, Szegedi A. Schumann G, et al. Among authors: poustka a. Biol Psychiatry. 2003 Dec 15;54(12):1422-6. doi: 10.1016/s0006-3223(03)00635-8. Biol Psychiatry. 2003. PMID: 14675807
Point mutation analysis of the FMR-1 gene in autism.
Vincent JB, Konecki DS, Munstermann E, Bolton P, Poustka A, Poustka F, Gurling HM. Vincent JB, et al. Among authors: poustka a, poustka f. Mol Psychiatry. 1996 Jul;1(3):227-31. Mol Psychiatry. 1996. PMID: 9118347
A genome-wide scan for common alleles affecting risk for autism.
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter … See abstract for full author list ➔ Anney R, et al. Among authors: poustka a, poustka f. Hum Mol Genet. 2010 Oct 15;19(20):4072-82. doi: 10.1093/hmg/ddq307. Epub 2010 Jul 27. Hum Mol Genet. 2010. PMID: 20663923 Free PMC article.
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.
Bacchelli E, Blasi F, Biondolillo M, Lamb JA, Bonora E, Barnby G, Parr J, Beyer KS, Klauck SM, Poustka A, Bailey AJ, Monaco AP, Maestrini E; International Molecular Genetic Study of Autism Consortium (IMGSAC). Bacchelli E, et al. Among authors: poustka a. Mol Psychiatry. 2003 Nov;8(11):916-24. doi: 10.1038/sj.mp.4001340. Mol Psychiatry. 2003. PMID: 14593429
Analysis of reelin as a candidate gene for autism.
Bonora E, Beyer KS, Lamb JA, Parr JR, Klauck SM, Benner A, Paolucci M, Abbott A, Ragoussis I, Poustka A, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism (IMGSAC). Bonora E, et al. Among authors: poustka a. Mol Psychiatry. 2003 Oct;8(10):885-92. doi: 10.1038/sj.mp.4001310. Mol Psychiatry. 2003. PMID: 14515139
Alternative splicing in the fragile X gene FMR1.
Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al. Verkerk AJ, et al. Among authors: poustka a. Hum Mol Genet. 1993 Aug;2(8):1348. doi: 10.1093/hmg/2.8.1348. Hum Mol Genet. 1993. PMID: 8401531 No abstract available.
Alternative splicing in the fragile X gene FMR1.
Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al. Verkerk AJ, et al. Among authors: poustka a. Hum Mol Genet. 1993 Apr;2(4):399-404. doi: 10.1093/hmg/2.4.399. Hum Mol Genet. 1993. PMID: 8504300
308 results