| Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions VG Gorgoulis, LVF Vassiliou, P Karakaidos, P Zacharatos, A Kotsinas, ... Nature 434 (7035), 907-913, 2005 | 2434 | 2005 |
| Chromosomal microarray versus karyotyping for prenatal diagnosis RJ Wapner, CL Martin, B Levy, BC Ballif, CM Eng, JM Zachary, M Savage, ... New England Journal of Medicine 367 (23), 2175-2184, 2012 | 1620 | 2012 |
| In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial EJ Forman, KH Hong, KM Ferry, X Tao, D Taylor, B Levy, NR Treff, ... Fertility and sterility 100 (1), 100-107. e1, 2013 | 600 | 2013 |
| Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study S Petrovski, V Aggarwal, JL Giordano, M Stosic, K Wou, L Bier, E Spiegel, ... The Lancet 393 (10173), 758-767, 2019 | 557 | 2019 |
| Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci B Zimmermann, M Hill, G Gemelos, Z Demko, M Banjevic, J Baner, ... Prenatal diagnosis 32 (13), 1233-1241, 2012 | 500 | 2012 |
| Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes RJ Wapner, JE Babiarz, B Levy, M Stosic, B Zimmermann, S Sigurjonsson, ... American journal of obstetrics and gynecology 212 (3), 332. e1-332. e9, 2015 | 402 | 2015 |
| Restoration of replication fork stability in BRCA1-and BRCA2-deficient cells by inactivation of SNF2-family fork remodelers A Taglialatela, S Alvarez, G Leuzzi, V Sannino, L Ranjha, JW Huang, ... Molecular cell 68 (2), 414-430. e8, 2017 | 401 | 2017 |
| Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study J Menasha, B Levy, K Hirschhorn, NB Kardon Genetics in Medicine 7 (4), 251-263, 2005 | 384 | 2005 |
| The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ... Nature genetics 49 (1), 36-45, 2017 | 334 | 2017 |
| Prenatal diagnosis by chromosomal microarray analysis B Levy, R Wapner Fertility and sterility 109 (2), 201-212, 2018 | 318 | 2018 |
| Karyotype versus microarray testing for genetic abnormalities after stillbirth UM Reddy, GP Page, GR Saade, RM Silver, VR Thorsten, CB Parker, ... New England journal of medicine 367 (23), 2185-2193, 2012 | 296 | 2012 |
| First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy D Wells, T Escudero, B Levy, K Hirschhorn, JDA Delhanty, S Munne Fertility and sterility 78 (3), 543-549, 2002 | 281 | 2002 |
| Evidence for a Niemann–Pick C (NPC) gene family: identification and characterization of NPC1L1 JP Davies, B Levy, YA Ioannou Genomics 65 (2), 137-145, 2000 | 279 | 2000 |
| Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays NR Treff, J Su, X Tao, B Levy, RT Scott Jr Fertility and sterility 94 (6), 2017-2021, 2010 | 274 | 2010 |
| Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis B Levy, S Sigurjonsson, B Pettersen, MK Maisenbacher, MP Hall, ... Obstetrics & Gynecology 124 (2 PART 1), 202-209, 2014 | 254 | 2014 |
| SNP microarray-based 24 chromosome aneuploidy screening demonstrates that cleavage-stage FISH poorly predicts aneuploidy in embryos that develop to morphologically normal … LE Northrop, NR Treff, B Levy, RT Scott MHR: Basic science of reproductive medicine 16 (8), 590-600, 2010 | 253 | 2010 |
| Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behavior M Liontos, M Koutsami, M Sideridou, K Evangelou, D Kletsas, B Levy, ... Cancer research 67 (22), 10899-10909, 2007 | 250 | 2007 |
| Noninvasive prenatal testing: the future is now ER Norwitz, B Levy Reviews in obstetrics and gynecology 6 (2), 48, 2013 | 232 | 2013 |
| The copy number variation landscape of congenital anomalies of the kidney and urinary tract M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ... Nature genetics 51 (1), 117-127, 2019 | 220 | 2019 |
| Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome RL Collins, H Brand, CE Redin, C Hanscom, C Antolik, MR Stone, ... Genome biology 18, 1-21, 2017 | 207 | 2017 |
