Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss
Rajcan-Separovic, E., Diego-Alvarez, D., Robinson, W.P., Tyson, C., Qiao, Y., Harvard, C., Fawcett, C., Kalousek, D., Philipp, T., Somerville, M.J., Stephenson, M.D.
Published in Human reproduction (Oxford) (01.11.2010)
Published in Human reproduction (Oxford) (01.11.2010)
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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
Rajcan-Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Published in Journal of medical genetics (01.04.2007)
Published in Journal of medical genetics (01.04.2007)
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Journal Article
Autism-associated familial microdeletion of Xp11.22
Qiao, Y, Liu, X, Harvard, C, Hildebrand, MJ, Rajcan-Separovic, E, Holden, JJA, Lewis, MES
Published in Clinical genetics (01.08.2008)
Published in Clinical genetics (01.08.2008)
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Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability
Qiao, Y, Tyson, C, Hrynchak, M, Lopez-Rangel, E, Hildebrand, J, Martell, S, Fawcett, C, Kasmara, L, Calli, K, Harvard, C, Liu, X, Holden, JJA, Lewis, SME, Rajcan-Separovic, E
Published in Clinical genetics (01.02.2013)
Published in Clinical genetics (01.02.2013)
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Genomic changes detected by array CGH in human embryos with developmental defects
Rajcan-Separovic, E., Qiao, Y., Tyson, C., Harvard, C., Fawcett, C., Kalousek, D., Stephenson, M., Philipp, T.
Published in Molecular human reproduction (01.02.2010)
Published in Molecular human reproduction (01.02.2010)
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Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics
Qiao, Y, Harvard, C, Tyson, C, Liu, X, Fawcett, C, Pavlidis, P, Holden, J. J. A, Lewis, M. E. S, Rajcan-Separovic, E
Published in Human genetics (01.08.2010)
Published in Human genetics (01.08.2010)
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Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH
Tyson, C., Harvard, C., Locker, R., Friedman, J.M., Langlois, S., Lewis, M.E.S., Van Allen, M., Somerville, M., Arbour, L., Clarke, L., McGilivray, B., Yong, S.L., Siegel-Bartel, J., Rajcan-Separovic, E.
Published in American journal of medical genetics. Part A (15.12.2005)
Published in American journal of medical genetics. Part A (15.12.2005)
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15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH
Koochek, M, Harvard, C, Hildebrand, MJ, Van Allen, M, Wingert, H, Mickelson, E, Holden, JJA, Rajcan-Separovic, E, Lewis, MES
Published in Clinical genetics (01.02.2006)
Published in Clinical genetics (01.02.2006)
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A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH
Harvard, C, Malenfant, P, Koochek, M, Creighton, S, Mickelson, ECR, Holden, JJA, Lewis, MES, Rajcan-Separovic, E
Published in Clinical genetics (01.04.2005)
Published in Clinical genetics (01.04.2005)
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Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability
Tyson, C., Dawson, A.J., Bal, S., Tomiuk, M., Anderson, T., Tucker, D., Riordan, D., Chudoba, I., Morash, B., Mhanni, A., Chudley, A.E., McGillivray, B., Parslow, M., Rappold, G., Roeth, R., Fawcett, C., Qiao, Y., Harvard, C., Rajcan‐Separovic, E.
Published in American journal of medical genetics. Part A (01.03.2009)
Published in American journal of medical genetics. Part A (01.03.2009)
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Journal Article
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability
Qiao, Y., Harvard, C., Riendeau, N., Fawcett, C., Liu, X., Holden, J.J.A., Lewis, M.E.S., Rajcan-Separovic, E.
Published in Cytogenetic and genome research (01.01.2008)
Published in Cytogenetic and genome research (01.01.2008)
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A comparison of video and static photo lineups with child and adolescent witnesses
Havard, Catriona, Memon, Amina, Clifford, Brian, Gabbert, Fiona
Published in Applied cognitive psychology (01.12.2010)
Published in Applied cognitive psychology (01.12.2010)
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Phenomic determinants of genomic variation in autism spectrum disorders
Qiao, Y, Riendeau, N, Koochek, M, Liu, X, Harvard, Chansonette, Hildebrand, M J, Holden, J J A, Rajcan-Separovic, E, Lewis, M E S
Published in Journal of medical genetics (01.10.2009)
Published in Journal of medical genetics (01.10.2009)
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Original Article: 15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH
Koochek, M, Harvard, C, Hildebrand, MJ, M Van Allen, Wingert, H, Mickelson, E, Holden, JJA, Rajcan-Separovic, E, MES Lewis
Published in Clinical genetics (01.02.2006)
Published in Clinical genetics (01.02.2006)
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Journal Article
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGG
HARVARD, C, MALENFANT, P, KOOCHEK, M, CREIGHTON, S, MICKELSON, E. C. R, HOLDEN, J. J. A, LEWIS, M. E. S, RAJCAN-SEPAROVIC, E
Published in Clinical genetics (2005)
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Published in Clinical genetics (2005)
Journal Article
Observational Constraints on the Nature of Dark Energy: First Cosmological Results from the ESSENCE Supernova Survey
Wood-Vasey, W. M, Miknaitis, G, Stubbs, C. W, Jha, S, Riess, A. G, Garnavich, P. M, Kirshner, R. P, Aguilera, C, Becker, A. C, Blackman, J. W, Blondin, S, Challis, P, Clocchiatti, A, Conley, A, Covarrubias, R, Davis, T. M, Filippenko, A. V, Foley, R. J, Garg, A, Hicken, M, Krisciunas, K, Leibundgut, B, Li, W, Matheson, T, Miceli, A, Narayan, G, Pignata, G, Prieto, J. L, Rest, A, Salvo, M. E, Schmidt, B. P, Smith, R. C, Sollerman, J, Spyromilio, J, Tonry, J. L, Suntzeff, N. B, Zenteno, A
Published in The Astrophysical journal (10.09.2007)
Published in The Astrophysical journal (10.09.2007)
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