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발행년	- (예 : 2010-2015)

전체선택

Parent–child exome sequencing identifiesa de novo truncating mutation in TCF4 in non-syndromic intellectual disability

Academic Journal

Hamdan, F F; Daoud, H; Patry, L; Dionne-Laporte, A; Spiegelman, D; Dobrzeniecka, S; Rouleau, G A; Michaud, J L

Clinical Genetics. Feb 01, 2013 83(2):198-200

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Academic Journal

Addington, A M; Gauthier, J; Piton, A; Hamdan, F F; Raymond, A; Gogtay, N; Miller, R; Tossell, J; Bakalar, J; Germain, G; Gochman, P; Long, R; Rapoport, J L; Rouleau, G A

Molecular Psychiatry. Apr 01, 2012 17(4):468-468

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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Academic Journal

Piton, A; Gauthier, J; Hamdan, F F; Lafrenière, R G; Yang, Y; Henrion, E; Laurent, S; Noreau, A; Thibodeau, P; Karemera, L; Spiegelman, D; Kuku, F; Duguay, J; Destroismaisons, L; Jolivet, P; Côté, M; Lachapelle, K; Diallo, O; Raymond, A; Marineau, C; Champagne, N; Xiong, L; Gaspar, C; Rivière, J -B; Tarabeux, J; Cossette, P; Krebs, M -O; Rapoport, J L; Addington, A; DeLisi, L E; Mottron, L; Joober, R; Fombonne, E; Drapeau, P; Rouleau, G A

Molecular Psychiatry. Aug 01, 2011 16(8):867-880

EBSCOHost PDF Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Academic Journal

Addington, A M; Gauthier, J; Piton, A; Hamdan, F F; Raymond, A; Gogtay, N; Miller, R; Tossell, J; Bakalar, J; Germain, G; Gochman, P; Long, R; Rapoport, J L; Rouleau, G A

Molecular Psychiatry. Mar 01, 2011 16(3):238-239

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Characterization of a stable form of tryptophan hydroxylase from the human parasite Schistosoma mansoni.

Periodical

Hamdan, F F; Ribeiro, P

Journal of Biological Chemistry; July 1999, Vol. 274 Issue: 31 p21746-54, 9p

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Erratum: A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Academic Journal

Addington, A M; Gauthier, J; Piton, A; Hamdan, F F; Raymond, A; Gogtay, N; Miller, R; Tossell, J; Bakalar, J; Germain, G; Gochman, P; Long, R; Rapoport, J L; Rouleau, G A

Molecular Psychiatry. 17(4):468-468

EBSCOHost PDF Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

Rare Mutations in N-methyl-D-aspartate Glutamate Receptors in Autism Spectrum Disorders and Schizophrenia

Academic Journal

Tarabeux, J; Kebir, O; Hamdan, F F; Piton, A; Henrion, É; Millet, B; Fathalli, F; Joober, R; Rapoport, J L; Fombonne, É; Mottron, L; Forget-Dubois, N; Boivin, M; Michaud, J L; Drapeau, P; Lafrenière, R G; Rouleau, G A; Krebs, M-O; Gauthier, J.; DeLisi, Lynn E; Xiong, L.; Spiegelman, D.

Tarabeux, J., O. Kebir, J. Gauthier, F. F. Hamdan, L. Xiong, A. Piton, D. Spiegelman, et al. 2011. Rare mutations in n-methyl-d-aspartate glutamate receptors in autism spectrum disorders and schizophrenia. Translational Psychiatry 1(11): e55.

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