Targeting BTK with Ibrutinib in Relapsed or Refractory Mantle-Cell Lymphoma
Wang, Michael L, Rule, Simon, Martin, Peter, Goy, Andre, Auer, Rebecca, Kahl, Brad S, Jurczak, Wojciech, Advani, Ranjana H, Romaguera, Jorge E, Williams, Michael E, Barrientos, Jacqueline C, Chmielowska, Ewa, Radford, John, Stilgenbauer, Stephan, Dreyling, Martin, Jedrzejczak, Wieslaw Wiktor, Johnson, Peter, Spurgeon, Stephen E, Li, Lei, Zhang, Liang, Newberry, Kate, Ou, Zhishuo, Cheng, Nancy, Fang, Bingliang, McGreivy, Jesse, Clow, Fong, Buggy, Joseph J, Chang, Betty Y, Beaupre, Darrin M, Kunkel, Lori A, Blum, Kristie A
Published in The New England journal of medicine (08.08.2013)
Published in The New England journal of medicine (08.08.2013)
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Journal Article
Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder
Szafranski, Przemyslaw, Dharmadhikari, Avinash V, Brosens, Erwin, Gurha, Priyatansh, Kolodziejska, Katarzyna E, Zhishuo, Ou, Dittwald, Piotr, Majewski, Tadeusz, Mohan, K Naga, Chen, Bo, Person, Richard E, Tibboel, Dick, de Klein, Annelies, Pinner, Jason, Chopra, Maya, Malcolm, Girvan, Peters, Gregory, Arbuckle, Susan, Guiang, 3rd, Sixto F, Hustead, Virginia A, Jessurun, Jose, Hirsch, Russel, Witte, David P, Maystadt, Isabelle, Sebire, Neil, Fisher, Richard, Langston, Claire, Sen, Partha, Stankiewicz, Paweł
Published in Genome research (01.01.2013)
Published in Genome research (01.01.2013)
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Journal Article
Novel selective inhibitors of nuclear export CRM1 antagonists for therapy in mantle cell lymphoma
Zhang, Kejie, Wang, Michael, Tamayo, Archito T, Shacham, Sharon, Kauffman, Michael, Lee, John, Zhang, Liang, Ou, Zhishuo, Li, Changping, Sun, Luhong, Ford, Richard J, Pham, Lan V
Published in Experimental hematology (2013)
Published in Experimental hematology (2013)
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Journal Article
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
Celestino-Soper, Patricia B.S., Shaw, Chad A., Sanders, Stephan J., Li, Jian, Murtha, Michael T., Ercan-Sencicek, A. Gulhan, Davis, Lea, Thomson, Susanne, Gambin, Tomasz, Chinault, A. Craig, Ou, Zhishuo, German, Jennifer R., Milosavljevic, Aleksandar, Sutcliffe, James S., Cook, Edwin H., Stankiewicz, Pawel, State, Matthew W., Beaudet, Arthur L.
Published in Human molecular genetics (15.11.2011)
Published in Human molecular genetics (15.11.2011)
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Journal Article
Partial 5p Deletion and Partial 5q Duplication in a Patient with Multiple Congenital Anomalies: A Two-Step Mechanism in Chromosomal Rearrangement Mediated by Non-Allelic Homologous Recombination
Ou, Zhishuo Z, Kochmar, Sally, Yatsenko, Svetlana A, Woerner, Audrey C, Acquaro, Roxanne, Ortiz, Damara, Surti, Urvashi, Hu, Jie
Published in Cytogenetic and genome research (01.01.2018)
Published in Cytogenetic and genome research (01.01.2018)
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Journal Article
22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome
Ben-Shachar, Shay, Ou, Zhishuo, Shaw, Chad A., Belmont, John W., Patel, Millan S., Hummel, Marybeth, Amato, Stephen, Tartaglia, Nicole, Berg, Jonathan, Sutton, V. Reid, Lalani, Seema R., Chinault, A. Craig, Cheung, Sau W., Lupski, James R., Patel, Ankita
Published in American journal of human genetics (01.01.2008)
Published in American journal of human genetics (01.01.2008)
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Journal Article
Development and validation of a CGH microarray for clinical cytogenetic diagnosis
Cheung, Sau W., Shaw, Chad A., Yu, Wei, Li, Jiangzham, Ou, Zhishuo, Patel, Ankita, Yatsenko, Svetlana A., Cooper, Mitchell L., Furman, Patti, Stankiewicz, Pawal, Lupski, James R., Chinault, A Craig, Beaudet, Arthur L.
Published in Genetics in medicine (01.07.2005)
Published in Genetics in medicine (01.07.2005)
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Journal Article
Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes
Ou, Zhishuo, Stankiewicz, Paweł, Xia, Zhilian, Breman, Amy M, Dawson, Brian, Wiszniewska, Joanna, Szafranski, Przemyslaw, Cooper, M Lance, Rao, Mitchell, Shao, Lina, South, Sarah T, Coleman, Karlene, Fernhoff, Paul M, Deray, Marcel J, Rosengren, Sally, Roeder, Elizabeth R, Enciso, Victoria B, Chinault, A Craig, Patel, Ankita, Kang, Sung-Hae L, Shaw, Chad A, Lupski, James R, Cheung, Sau W
Published in Genome research (01.01.2011)
Published in Genome research (01.01.2011)
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Journal Article
Neuronal expression of peroxisome proliferator-activated receptor-gamma (PPARγ) and 15d-prostaglandin J2 : Mediated protection of brain after experimental cerebral ischemia in rat
ZHISHUO OU, XIURONG ZHAO, LABICHE, Lise A, STRONG, Roger, GROTTA, James C, HERRMANN, Oliver, ARONOWSKI, Jaroslaw
Published in Brain research (22.06.2006)
Published in Brain research (22.06.2006)
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Journal Article
The Genomic Landscape of PAX5, IKZF1, and CDKN2A/B Alterations in B-Cell Precursor Acute Lymphoblastic Leukemia
Ou, Zhishuo, Sherer, Maureen, Casey, Jane, Bakos, Heather A, Vitullo, Kathleen, Hu, Jie, Friehling, Erika, Gollin, Susanne M, Surti, Urvashi, Yatsenko, Svetlana A
Published in Cytogenetic and genome research (01.01.2016)
Published in Cytogenetic and genome research (01.01.2016)
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Journal Article
Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results
Kang, Sung-Hae L., Shaw, Chad, Ou, Zhishuo, Eng, Patricia A., Cooper, M. Lance, Pursley, Amber N., Sahoo, Trilochan, Bacino, Carlos A., Chinault, A. Craig, Stankiewicz, Pawel, Patel, Ankita, Lupski, James R., Cheung, Sau Wai
Published in American journal of medical genetics. Part A (01.05.2010)
Published in American journal of medical genetics. Part A (01.05.2010)
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Journal Article
Chromosome 12q13.13q13.13 microduplication and microdeletion: a case report and literature review
Hu, Jie, Ou, Zhishuo, Infante, Elena, Kochmar, Sally J, Madan-Khetarpal, Suneeta, Hoffner, Lori, Parsazad, Shafagh, Surti, Urvashi
Published in Molecular cytogenetics (19.06.2017)
Published in Molecular cytogenetics (19.06.2017)
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Journal Article
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping
El-Hattab, Ayman W, Smolarek, Teresa A, Walker, Martha E, Schorry, Elizabeth K, Immken, LaDonna L, Patel, Gayle, Abbott, Mary-Alice, Lanpher, Brendan C, Ou, Zhishuo, Kang, Sung-Hae L, Patel, Ankita, Scaglia, Fernando, Lupski, James R, Cheung, Sau Wai, Stankiewicz, Pawel
Published in Human genetics (01.10.2009)
Published in Human genetics (01.10.2009)
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Journal Article
Lenalidomide in relapsed or refractory mantle cell lymphoma: overview and perspective
Desai, Madhav, Newberry, Kate, Ou, Zhishuo, Wang, Michael, Zhang, Liang
Published in Therapeutic Advances in Hematology (01.06.2014)
Published in Therapeutic Advances in Hematology (01.06.2014)
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Book Review
Journal Article
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement
Ou, Zhishuo, Martin, Donna M., Bedoyan, Jirair K., Cooper, M. Lance, Chinault, A. Craig, Stankiewicz, Pawel, Cheung, Sau W.
Published in American journal of medical genetics. Part A (01.10.2008)
Published in American journal of medical genetics. Part A (01.10.2008)
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Journal Article
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation
Probst, Frank J., Roeder, Elizabeth R., Enciso, Victoria B., Ou, Zhishuo, Cooper, M. Lance, Eng, Patricia, Li, Jiangzhen, Gu, Yanghong, Stratton, Robert F., Chinault, A. Craig, Shaw, Chad A., Sutton, V. Reid, Cheung, Sau Wai, Nelson, David L.
Published in American journal of medical genetics. Part A (15.06.2007)
Published in American journal of medical genetics. Part A (15.06.2007)
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Journal Article
Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay
Gu, Jun, Sreenath Nagamani, Sandesh C., Hopwood, Vicki L., Sanchez, Beatriz, Saeidinejad, Yasaman, Ou, Zhishuo, Peacock, Sandra, Grange, Dorothy K., Stankiewicz, Pawel, Cheung, Sau Wai
Published in American journal of medical genetics. Part A (01.10.2011)
Published in American journal of medical genetics. Part A (01.10.2011)
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Journal Article
De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently “balanced” paracentric inversion of 14(q21q23)
Jiang, Yong‐Hui, Martinez, Jose E., Ou, Zhishuo, Cooper, M. Lance, Kang, Sung‐Hae L., Pursley, Amber, Cheung, Sau W.
Published in American journal of medical genetics. Part A (01.08.2008)
Published in American journal of medical genetics. Part A (01.08.2008)
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Journal Article
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations
ZHISHUO OU, JARMUZ, Malgorzata, LUPSKI, James R, CHINAULT, A. Craig, CHEUNG, Sau W, STANKIEWICZ, Pawel, SPARAGANA, Steven P, MICHAUD, Jacques, DECARIE, Jean-Claude, YATSENKO, Svetlana A, NOWAKOWSKA, Beata, FURINAN, Patti, SHAW, Chad A, SHAFFER, Lisa G
Published in Human genetics (01.09.2006)
Published in Human genetics (01.09.2006)
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Journal Article
Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement
Shchelochkov, Oleg A, Cooper, M Lance, Ou, Zhishuo, Peacock, Sandra, Yatsenko, Svetlana A, Brown, Chester W, Fang, Ping, Stankiewicz, Pawel, Cheung, Sau Wai
Published in Molecular cytogenetics (25.07.2008)
Published in Molecular cytogenetics (25.07.2008)
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Journal Article