Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors
Cruceanu, C, Schmouth, J-F, Torres-Platas, S G, Lopez, J P, Ambalavanan, A, Darcq, E, Gross, F, Breton, B, Spiegelman, D, Rochefort, D, Hince, P, Petite, J M, Gauthier, J, Lafrenière, R G, Dion, P A, Greenwood, C M, Kieffer, B L, Alda, M, Turecki, G, Rouleau, G A
Published in Molecular psychiatry (01.10.2018)
Published in Molecular psychiatry (01.10.2018)
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Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia
Tarabeux, J, Kebir, O, Gauthier, J, Hamdan, F F, Xiong, L, Piton, A, Spiegelman, D, Henrion, É, Millet, B, Fathalli, F, Joober, R, Rapoport, J L, DeLisi, L E, Fombonne, É, Mottron, L, Forget-Dubois, N, Boivin, M, Michaud, J L, Drapeau, P, Lafrenière, R G, Rouleau, G A, Krebs, M-O
Published in Translational psychiatry (15.11.2011)
Published in Translational psychiatry (15.11.2011)
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The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
Brown, Carolyn J., Hendrich, Brian D., Rupert, Jim L., Lafrenière, Ronald G., Xing, Yigong, Lawrence, Jeanne, Willard, Huntington F.
Published in Cell (30.10.1992)
Published in Cell (30.10.1992)
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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
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
Published in Molecular psychiatry (01.08.2011)
Published in Molecular psychiatry (01.08.2011)
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A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
Brown, Carolyn J, Ballabio, Andrea, Rupert, James L, Lafreniere, Ronald G, Grompe, Markus, Tonlorenzi, Rossana, Willard, Huntington F
Published in Nature (London) (03.01.1991)
Published in Nature (London) (03.01.1991)
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Instability of the EPM1 Minisatellite
Larson, Garry P., Ding, Shaofeng, Lafrenière, Ronald G., Rouleau, Guy A., Krontiris, Theodore G.
Published in Human molecular genetics (01.10.1999)
Published in Human molecular genetics (01.10.1999)
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Localization of the X inactivation centre on the human X chromosome in Xq13
Brown, Carolyn J, Lafreniere, Ronald G, Powers, Vicki E, Sebastio, Gianfranco, Ballabio, Andrea, Pettigrew, Anjana L, Ledbetter, David H, Levy, Elaine, Craig, Ian W, Willard, Huntington F
Published in Nature (London) (03.01.1991)
Published in Nature (London) (03.01.1991)
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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
Rouleau, Guy A, Nohira, Osamu, Mathieu, Jean, Heutink, Peter, Duranceau, André, Codère, Francois, Fardeau, Michel, Brais, Bernard, Korcyn, Amos D, Chrétien, Nathalie, Rochefort, Daniel L, Tomé, Fernando M.S, Xie, Ya-Gang, Rommens, Johanna M, Blumen, Segiu, Lafrentére, Ronald G, Uyama, Eichiro, Bouchard, Jean-Pierre
Published in Nature genetics (01.02.1998)
Published in Nature genetics (01.02.1998)
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Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia
Rack, K A, Chelly, J, Gibbons, R J, Rider, S, Benjamin, D, Lafreniére, R G, Oscier, D, Hendriks, R W, Craig, I W, Willard, H F
Published in Human molecular genetics (01.07.1994)
Published in Human molecular genetics (01.07.1994)
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A Radiation Hybrid Map of 48 Loci Including the Clouston Hidrotic Ectodermal Dysplasia Locus in the Pericentromeric Region of Chromosome 13q
Kibar, Zoha, Lafrenière, Ronald G., Chakravarti, Aravinda, Wang, Jia-Chi, Chevrette, Mario, Der Kaloustian, Vazken M., Rouleau, Guy A.
Published in Genomics (San Diego, Calif.) (15.02.1999)
Published in Genomics (San Diego, Calif.) (15.02.1999)
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2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes
Lafrenière, R G, Brown, C J, Rider, S, Chelly, J, Taillon-Miller, P, Chinault, A C, Monaco, A P, Willard, H F
Published in Human molecular genetics (01.08.1993)
Published in Human molecular genetics (01.08.1993)
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Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status
Quigley, C A, Friedman, K J, Johnson, A, Lafreniere, R G, Silverman, L M, Lubahn, D B, Brown, T R, Wilson, E M, Willard, H F, French, F S
Published in The journal of clinical endocrinology and metabolism (01.04.1992)
Published in The journal of clinical endocrinology and metabolism (01.04.1992)
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Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3
LAFRENIERE, R. G, ROCHEFORT, D. L, ROMMENS, J. M, ROULEAU, G. A, KIBAR, Z, FON, E. A, HAN, F.-Y, COCHIUS, J, KANG, X, BAIRD, S, KORNELUK, R. G, ANDERMANN, E
Published in Genomics (San Diego, Calif.) (15.12.1996)
Published in Genomics (San Diego, Calif.) (15.12.1996)
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Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
Cochius, Jeffrey I, Rouleau, Guy A, Lafreniére, Ronald G, Chrétien, Nathalie, Cossio, Otto Hernandez, Pouliot, Marc A, Andermann, Eva, Farrell, Kevin, Pranzatelli, Michael R, Patry, George, Söderfeldt, Birgitta, Hale, Bradford R, Rochefort, Daniel L, Rommens, Johanna M, Federico, Antonio, Andermann, Frederick, Nousiainen, Unto, Janszky, József, Kmiec, Tomasz, Kälviäinen, Reetta, Sørensen, Troels, Uldall, Peter
Published in Nature genetics (01.03.1997)
Published in Nature genetics (01.03.1997)
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Mechanisms of uptake and resistance to troxacitabine, a novel deoxycytidine nucleoside analogue, in human leukemic and solid tumor cell lines
GOURDEAU, Henriette, CLARKE, Marilyn L, LAFRENIERE, Ronald G, CASS, Carol E, OUELLET, France, MOWLES, Delores, SELNER, Milada, RICHARD, Annie, LEE, Nola, MACKEY, John R, YOUNG, James D, JOLIVET, Jacques
Published in Cancer research (Chicago, Ill.) (01.10.2001)
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Published in Cancer research (Chicago, Ill.) (01.10.2001)
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Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3
Lafrenière, R G, Rochefort, D L, Chrétien, N, Neville, C E, Korneluk, R G, Zuo, L, Wei, Y, Lichter, J, Rouleau, G A
Published in Genome research (01.12.1996)
Published in Genome research (01.12.1996)
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