Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study by Petrovski, Slavé, Aggarwal, Vimla, Giordano, Jessica L, Stosic, Melissa, Wou, Karen, Bier, Louise, Spiegel, Erica, Brennan, Kelly, Stong, Nicholas, Jobanputra, Vaidehi, Ren, Zhong, Zhu, Xiaolin, Mebane, Caroline, Nahum, Odelia, Wang, Quanli, Kamalakaran, Sitharthan, Malone, Colin, Anyane-Yeboa, Kwame, Miller, Russell, Levy, Brynn, Goldstein, David B, Wapner, Ronald J

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Deregulated Overexpression of hCdt1 and hCdc6 Promotes Malignant Behavior by LIONTOS, Michalis, KOUTSAMI, Marilena, LYGEROU, Zoi, TARAVIRAS, Stavros, KITTAS, Christos, BARTKOVA, Jirina, PAPAVASSILIOU, Athanasios G, BARTEK, Jiri, HALAZONETIS, Thanos D, GORGOULIS, Vassilis G, SIDERIDOU, Maria, EVANGELOU, Konstantinos, KLETSAS, Dimitris, LEVY, Brynn, KOTSINAS, Athanassios, NAHUM, Odelia, ZOUMPOURLIS, Vassilis, KOULOUKOUSSA, Mirsini

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The genetic landscape of dural marginal zone lymphomas by Ganapathi, Karthik A, Jobanputra, Vaidehi, Iwamoto, Fabio, Jain, Preti, Chen, Jinli, Cascione, Luciano, Nahum, Odelia, Levy, Brynn, Xie, Yi, Khattar, Pallavi, Hoehn, Daniela, Bertoni, Francesco, Murty, Vundavalli V, Pittaluga, Stefania, Jaffe, Elaine S, Alobeid, Bachir, Mansukhani, Mahesh M, Bhagat, Govind

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Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration by Borczuk, Alain C., Pei, Jianming, Taub, Robert N., Levy, Brynn, Nahum, Odelia, Chen, Jinli, Chen, Katherine, Testa, Joseph R.

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Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders by Margolskee, Elizabeth, Jobanputra, Vaidehi, Jain, Preti, Chen, Jinli, Ganapathi, Karthik, Nahum, Odelia, Levy, Brynn, Morscio, Julie, Murty, Vundavalli, Tousseyn, Thomas, Alobeid, Bachir, Mansukhani, Mahesh, Bhagat, Govind

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Genomic and Targeted Mutational Analysis of T/NK-Cell Post-Transplant Lymphoproliferative Disorders Provides Insight into Disease Biology by Margolskee, Elizabeth Michelle, Jobanputra, Vaidehi, Jain, Preti, Chen, Jinli, Nahum, Odelia, Levy, Brynn, Ganapathi, Karthik A, Murty, Vundavalli, Tousseyn, Thomas, Alobeid, Bachir, Manuskhani, Mahesh, Bhagat, Govind

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The proximal chromosome 14q microdeletion syndrome: Delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature by Torgyekes, Edina, Shanske, Alan L., Anyane-Yeboa, Kwame, Nahum, Odelia, Pirzadeh, Sara, Blumfield, Einat, Jobanputra, Vaidehi, Warburton, Dorothy, Levy, Brynn

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Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis by Levy, Brynn, Wang, Dong, Ullner, Paivi M., Engelstad, Kristin, Yang, Hong, Nahum, Odelia, Chung, Wendy K., De Vivo, Darryl C.

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Molecular Inversion Probes for Detection of Copy Number Alterations and Loss of Heterozygosity in Renal Cell Carcinoma by Jobanputra, Vaidehi, Nahum, Odelia, Northop, Lesley E, Monzon, Federico A, Levy, Brynn

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