Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia
Harris, Rachel A., Stevens, Jadd. M., Pickering, Diane L., Althof, Pamela A., Smith, Lynette M., Sanmann, Jennifer N., Dave, Bhavana J.
Published in Leukemia research (01.11.2021)
Published in Leukemia research (01.11.2021)
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Journal Article
Genetic drivers of oncogenic pathways in molecular subgroups of peripheral T-cell lymphoma
Heavican, Tayla B., Bouska, Alyssa, Yu, Jiayu, Lone, Waseem, Amador, Catalina, Gong, Qiang, Zhang, Weiwei, Li, Yuping, Dave, Bhavana J., Nairismägi, Maarja-Liisa, Greiner, Timothy C., Vose, Julie, Weisenburger, Dennis D., Lachel, Cynthia, Wang, Chao, Fu, Kai, Stevens, Jadd M., Lim, Soon Thye, Ong, Choon Kiat, Gascoyne, Randy D., Missiaglia, Edoardo, Lemonnier, Francois, Haioun, Corinne, Hartmann, Sylvia, Pedersen, Martin Bjerregård, Laginestra, Maria Antonella, Wilcox, Ryan A., Teh, Bin Tean, Yoshida, Noriaki, Ohshima, Koichi, Seto, Masao, Rosenwald, Andreas, Ott, German, Campo, Elias, Rimsza, Lisa M., Jaffe, Elaine S., Braziel, Rita M., d'Amore, Francesco, Inghirami, Giorgio, Bertoni, Francesco, de Leval, Laurence, Gaulard, Philippe, Staudt, Louis M., McKeithan, Timothy W., Pileri, Stefano, Chan, Wing C., Iqbal, Javeed
Published in Blood (11.04.2019)
Published in Blood (11.04.2019)
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Journal Article
Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray
Sanmann, Jennifer N., Pickering, Diane L., Golden, Denae M., Stevens, Jadd M., Hempel, Thomas E., Althof, Pamela A., Wiggins, Michele L., Starr, Lois J., Davé, Bhavana J., Sanger, Warren G.
Published in Genetics in medicine (01.11.2015)
Published in Genetics in medicine (01.11.2015)
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Journal Article
Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: Review of distal 7q deletions
Rush, Eric T., Stevens, Jadd M., Sanger, Warren G., Olney, Ann H.
Published in American journal of medical genetics. Part A (01.07.2013)
Published in American journal of medical genetics. Part A (01.07.2013)
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Journal Article
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome
Sanmann, Jennifer N., Bishay, Danielle L., Starr, Lois J., Bell, Carla A., Pickering, Diane L., Stevens, Jadd M., Kahler, Stephen G., Olney, Ann Haskins, Schaefer, G. Bradley, Sanger, Warren G.
Published in American journal of medical genetics. Part A (01.06.2012)
Published in American journal of medical genetics. Part A (01.06.2012)
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Journal Article
Microdeletion in distal 17p13.1: A recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability
Zeesman, Susan, Kjaergaard, Susanne, Hove, Hanne D., Kirchhoff, Maria, Stevens, Jadd M., Nowaczyk, Małgorzata J.M.
Published in American journal of medical genetics. Part A (01.08.2012)
Published in American journal of medical genetics. Part A (01.08.2012)
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Journal Article
Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL
Utter, Rachel A, Pickering, Diane L, Stevens, Jadd M, Althof, Pamela A, Sanger, Warren G, Dave, Bhavana J
Published in Cancer genetics (01.06.2014)
Published in Cancer genetics (01.06.2014)
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Journal Article
Microarray Studies in Pediatric T-Cell Acute Lymphoblastic Leukemia/Lymphoma: A Report of Four Cases
Sanmann, Jennifer N, Pickering, Diane L, Stevens, Jadd M, Sanger, Warren G
Published in Cancer genetics (01.05.2013)
Published in Cancer genetics (01.05.2013)
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Journal Article