Validation of an obstetric comorbidity index in an external population von Metcalfe, A, Lix, LM, Johnson, J‐A, Currie, G, Lyon, AW, Bernier, F, Tough, SC

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Geohydromechanical processes in the Excavation Damaged Zone in crystalline rock, rock salt, and indurated and plastic clays—in the context of radioactive waste disposal von Tsang, Chin-Fu, Bernier, F., Davies, C.

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Public health policy research: making the case for a political science approach von BERNIER, NICOLE F., CLAVIER, CAROLE

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Diagnostic criteria for respiratory chain disorders in adults and children von BERNIER, F. P, BONEH, A, DENNETT, X, CHOW, C. W, CLEARY, M. A, THORBURN, D. R

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Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing von Balci, T.B., Hartley, T., Xi, Y., Dyment, D.A., Beaulieu, C.L., Bernier, F.P., Dupuis, L., Horvath, G.A., Mendoza‐Londono, R., Prasad, C., Richer, J., Yang, X.‐R., Armour, C.M., Bareke, E., Fernandez, B.A., McMillan, H.J., Lamont, R.E., Majewski, J., Parboosingh, J.S., Prasad, A.N., Rupar, C.A., Schwartzentruber, J., Smith, A.C., Tétreault, M., Innes, A.M., Boycott, K.M.

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“Ectomycorrhizal exploration type” could be a functional trait explaining the spatial distribution of tree symbiotic fungi as a function of forest humus forms von F, Khalfallah, L, Bon, M, El Mazlouzi, M R, Bakker, N, Fanin, R, Bellanger, F, Bernier, A, De Schrijver, C, Ducatillon, M N, Fotelli, G, Gateble, M J, Gundale, M, Larsson, A, Legout, W L, Mason, A, Nordin, A, Smolander, G, Spyroglou, E I, Vanguelova, K, Verheyen, L, Vesterdal, B, Zeller, L, Augusto, D, Derrien, M, Buée

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Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition von Davey, K M, Parboosingh, J S, McLeod, D R, Chan, A, Casey, R, Ferreira, P, Snyder, F F, Bridge, P J, Bernier, F P

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Large-scale vibrating coil magnetometer for the magnetic characterization of bulk superconductors von Arsenault, A., Charpentier-Pépin, B., Forcier, A., Nassiri, N., Bellemare, J., Lacroix, C., Ménard, D., Sirois, F., Bernier, F., Lamarre, J.-M.

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Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1‐related ciliopathy spectrum von Gillesse, E., Wade, A., Parboosingh, J. S., Au, P. Y. B., Bernier, F. P., Lamont, R. E., Innes, A. M.

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Maternal pre-pregnancy BMI influences the associations between bisphenol and phthalate exposures and maternal weight changes and fat accumulation von Irvine, Nathalie, Bell, Rhonda C., Subhan, Fatheema B., Field, Catherine J., Liu, Jiaying, MacDonald, Amy M., Kinniburgh, David W., Martin, Jonathan W., Dewey, Deborah, England-Mason, Gillian, Kaplan, B.J., Field, C.J., Bell, R.C., Bernier, F.P., Cantell, M., Casey, L.M., Eliasziw, M., Farmer, A., Gagnon, L., Giesbrecht, G.F., Goonewardene, L., Johnston, D., Kooistra, L., Letourneau, N., Manca, D.P., Martin, J.W., McCargar, L.J., O'Beirne, M., Pop, V.J., Deane, A.J., Singhal, N., Letourneau (current Pi), N., Dewey, D., Forbes, L., Giesbrecht, G., Lebel, C., Leung, B., McMorris, C., Ross, K.

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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care von Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.

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MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement von Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.

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HSP27 Multimerization Mediated by Phosphorylation-sensitive Intermolecular Interactions at the Amino Terminus von Lambert, H, Charette, S J, Bernier, A F, Guimond, A, Landry, J

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Evaluation of a method estimating real-time individual lysine requirements in two lines of growing–finishing pigs von Cloutier, L., Pomar, C., Létourneau Montminy, M. P., Bernier, J. F., Pomar, J.

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High resolution pore size analysis in metallic powders by X-ray tomography von Heim, K., Bernier, F., Pelletier, R., Lefebvre, L.-P.

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Expansion of the GLE1‐associated arthrogryposis multiplex congenita clinical spectrum von Smith, C., Parboosingh, J.S., Boycott, K.M., Bönnemann, C.G., Mah, J.K., Lamont, R.E., Micheil Innes, A., Bernier, F.P.

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Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families von Hartley, T., Wagner, J.D., Warman‐Chardon, J., Tétreault, M., Brady, L., Baker, S., Tarnopolsky, M., Bourque, P.R., Parboosingh, J.S., Smith, C., McInnes, B., Innes, A.M., Bernier, F., Curry, C.J., Yoon, G., Horvath, G.A., Bareke, E., Gillespie, M., Majewski, J., Bulman, D.E., Dyment, D.A., Boycott, K.M.

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Germins and germin-like proteins: Plant do-all proteins. But what do they do exactly? von Bernier, François, Berna, Anne

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Mutations in the novel protocadherin PCDH15 cause usher syndrome type 1F von ALAGRAMAM, Kumar N, HUIJUN YUAN, SCHWARTZ, Stuart, LEE, Charles, MORTON, Cynthia C, MULLINS, Robert F, RAMESH, Arabandi, VAN CAMP, Guy, HAGEMEN, Gregory S, WOYCHIK, Richard P, SMITH, Richard J. H, KUEHN, Markus H, MURCIA, Crystal L, WAYNE, Sigrid, SRIKUMARI SRISAILPATHY, C. R, LOWRY, R. Brian, KNAUS, Russell, VAN LAER, Lut, BERNIER, F. P

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Differences in splanchnic metabolism between late gestation and early lactation dairy cows von Doepel, L., Lobley, G.E., Bernier, J.F., Dubreuil, P., Lapierre, H.

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