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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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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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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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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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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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A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. M., Maas, S. M., Henneman, P., Lip, K. v. d., Venema, A., Baranano, K., Chassevent, A., Aref-Eshghi, E., van Essen, A. J., Fukuda, T., Ikeda, H., Jacquemont, M., Kim, H.-G., Labalme, A., Lewis, S. M. E., Lesca, G., Madrigal, I., Mahida, S., Matsumoto, N., Rabionet, R., Rajcan-Separovic, E., Qiao, Y., Sadikovic, B., Saitsu, H., Sweetser, D. A., Alders, M., Mannens, M. M. A. M.
Published in Clinical epigenetics (04.11.2019)
Published in Clinical epigenetics (04.11.2019)
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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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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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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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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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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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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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High-resolution human genome scanning using whole-genome BAC arrays
Li, J, Jiang, T, Bejjani, B, Rajcan-Separovic, E, Cai, W W
Published in Cold Spring Harbor Symposia on Quantitative Biology (2003)
Published in Cold Spring Harbor Symposia on Quantitative Biology (2003)
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The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review
Lopes, Fátima, Torres, Fátima, Soares, Gabriela, van Karnebeek, Clara D., Martins, Cecília, Antunes, Diana, Silva, João, Muttucomaroe, Lauren, Botelho, Luís Filipe, Sousa, Susana, Rendeiro, Paula, Tavares, Purificação, Van Esch, Hilde, Rajcan-Separovic, Evica, Maciel, Patrícia
Published in Frontiers in genetics (2019)
Published in Frontiers in genetics (2019)
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FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13
RAJCAN-SEPAROVIC, E, MAHADEVAN, M. S, LEFEBVRE, C, BESNER-JOHNSTON, A, IKEDA, J.-E, KORNELUK, R. G, MACKENZIE, A
Published in Cytogenetic and genome research (01.01.1996)
Published in Cytogenetic and genome research (01.01.1996)
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Non-muscle myosin heavy chain (MYH9): A new partner fused to ALK in anaplastic large cell lymphoma
Lamant, Laurence, Gascoyne, Randy D., Duplantier, Marie Michèle, Armstrong, Florence, Raghab, Ashraf, Chhanabhai, Mukesh, Rajcan-Separovic, Evica, Raghab, Janie, Delsol, Georges, Espinos, Estelle
Published in Genes chromosomes & cancer (01.08.2003)
Published in Genes chromosomes & cancer (01.08.2003)
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