O. Nahum

发表

Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders

V. Jobanputra, Preti Jain, M. Mansukhani, 2016, Oncotarget.

Genomic alterations in pulmonary adenocarcinoma in situ in an adolescent patient.

A. Borczuk, M. Mansukhani, B. Levy, 2014, Archives of pathology & laboratory medicine.

Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?

K. Hirschhorn, L. Ala‐Kokko, P. Warburton, 2012, Genetics in Medicine.

The proximal chromosome 14q microdeletion syndrome: Delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature

V. Jobanputra, D. Warburton, B. Levy, 2011, American journal of medical genetics. Part A.

Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis.

W. Chung, B. Levy, P. Ullner, 2010, Molecular genetics and metabolism.

Chromosomal microarray versus karyotyping for prenatal diagnosis.

D. Ledbetter, L. Shaffer, Ankita Patel, 2012, The New England journal of medicine.

The genetic landscape of dural marginal zone lymphomas

V. Jobanputra, E. Jaffe, L. Cascione, 2016, Oncotarget.

Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behavior.

Dimitris Kletsas, Jiri Bartek, Vassilis G Gorgoulis, 2007, Cancer research.

Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration

A. Borczuk, J. Testa, B. Levy, 2016, Cancer biology & therapy.

Chromosomal microarray versus karyotyping for prenatal diagnosis

D. Ledbetter, L. Shaffer, Ankita Patel, 2013 .

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study

V. Jobanputra, D. Goldstein, S. Petrovski, 2019, The Lancet.

DNA Extraction from Various Types of Prenatal Specimens.

B. Levy, O. Nahum, Amanda L Thomas, 2018, Methods in molecular biology.

One SHOX Can Make You Short

M. Shohat, O. Nahum, C. Legum, 2002 .

Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA

D. L. Coppock, B. Levy, A. Shanske, 2010, American journal of medical genetics. Part A.

Fetal DNA fingerprinting of DNA isolated from the peripheral maternal circulation at 9 gestational weeks allows precise identification of which embryos implanted following multiple embryo transfer

B. Levy, N. Treff, O. Nahum, 2008 .

Prenatal Diagnosis Using Chromosomal SNP Microarrays.

B. Levy, M. Ganapathi, O. Nahum, 2018, Methods in molecular biology.

Rapid Nanopore Sequencing-Based Screen for Aneuploidy in Reproductive Care.

B. Levy, C. Cinnioğlu, R. Kayali, 2022, New England Journal of Medicine.

Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR).

Christie M. Buchovecky, B. Levy, O. Nahum, 2018, Methods in molecular biology.