Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia von 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

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Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype von D'Amours, G, Kibar, Z, Mathonnet, G, Fetni, R, Tihy, F, Désilets, V, Nizard, S, Michaud, JL, Lemyre, E

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Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures von Mahmud, A.A., Nahid, N.A., Nassif, C., Sayeed, M.S.B., Ahmed, M.U., Parveen, M., Khalil, M.I., Islam, M.M., Nahar, Z., Rypens, F., Hamdan, F.F., Rouleau, G.A., Hasnat, A., Michaud, J.L.

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Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus von MICHAUD, Jacques L, BOUCHER, Francine, MELNYK, Anna, GAUTHIER, France, GOSHU, Eleni, LEVY, Emile, MITCHELL, Grant A, HIMMS-HAGEN, Jean, FAN, Chen-Ming

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A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly von Srour, M., Hamdan, F. F., Gan-Or, Z., Labuda, D., Nassif, C., Oskoui, M., Gana-Weisz, M., Orr-Urtreger, A., Rouleau, G.A., Michaud, J.L.

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Polymicrogyria with dysmorphic basal ganglia? Think tubulin von Amrom, D., Tanyalçin, I., Verhelst, H., Deconinck, N., Brouhard, G.J., Décarie, J.-C., Vanderhasselt, T., Das, S., Hamdan, F.F., Lissens, W., Michaud, J.L., Jansen, A.C.

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FSGS-associated α-actinin-4 (K256E) impairs cytoskeletal dynamics in podocytes von Michaud, J.-L.R., Chaisson, K.M., Parks, R.J., Kennedy, C.R.J.

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Refining the phenotype associated with biallelic DNAJC21 mutations von D'Amours, G., Lopes, Fátima Daniela Teixeira, Gauthier, J., Saillour, V., Nassif, C., Wynn, R., Alos, N., Leblanc, T., Capri, Y., Nizard, S., Lemyre, E., Michaud, J. L., Pelletier, V-A, Pastore, Y. D., Soucy, J-F

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The developmental program of the hypothalamus and its disorders von Michaud, JL

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Closure of the bronchial stump by manual suture and incidence of bronchopleural fistula in a series of 209 pneumonectomies for lung cancer von Hubaut, J.-J., Baron, O., Al Habash, O., Despins, Ph, Duveau, D., Michaud, J.L.

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G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex von Piao, Xianhua, Hill, R. Sean, Bodell, Adria, Chang, Bernard S., Basel-Vanagaite, Lina, Straussberg, Rachel, Dobyns, William B., Qasrawi, Bassam, Winter, Robin M., Innes, A. Micheil, Voit, Thomas, Ross, M. Elizabeth, Michaud, Jacques L., Déscarie, Jean-Claude, Barkovich, A. James, Walsh, Christopher A.

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Early and late outcome after elective cardiac surgery in patients with cirrhosis von Bizouarn, Philippe, Ausseur, Antoine, Desseigne, Pascal, Le Teurnier, Yann, Nougarede, Bertrand, Train, Michel, Michaud, Jean Luc

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MYOD1 involvement in myopathy von Lopes, Fátima Daniela Teixeira, Miguet, M., Mucha, B. E., Gauthier, J., Saillour, V., Nguyen, C.-T. É., Vanasse, M., Ellezam, B., Michaud, J. L., Soucy, J.-F., Campeau, P. M.

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Fat chance: genetic syndromes with obesity von Delrue, M-A, Michaud, JL

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Isolated mitral valve replacement with St Jude Medical prosthesis: Long-term results : A follow-up of 19 years von REMADI, J. P, BARON, O, ROUSSEL, C, BIZOUARN, P, HABASCH, Al, DESPINS, P, MICHAUD, J. L, DUVEAU, D

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Aggressive surgical management in localized pulmonary mycotic and nonmycotic infections for neutropenic patients with acute leukemia: Report of eighteen cases von Baron, O., Guillaumé, B., Moreau, P., Germaud, P., Despins, P., De Lajartre, A.Y., Michaud, J.L.

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Parent-child exome sequencing identifiesa de novo truncating mutation in TCF4 in non-syndromic intellectual disability von Hamdan, F F, Daoud, H, Patry, L, Dionne-Laporte, A, Spiegelman, D, Dobrzeniecka, S, Rouleau, G A, Michaud, J L

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Association between injury indices and outcome after severe traumatic brain injury in children von Massagli, Teresa L., Michaud, Linda J., Rivara, Frederick P.

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Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1 von Michaud, J L, Rosenquist, T, May, N R, Fan, C M

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Members of the bHLH-PAS family regulate Shh transcription in forebrain regions of the mouse CNS von Epstein, D J, Martinu, L, Michaud, J L, Losos, K M, Fan, C, Joyner, A L

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