| Most non-parotid “acinic cell carcinomas” represent mammary analoge secretory carcinomas JA Bishop, R Yonescu, D Batista, DW Eisele, WH Westra Am J Surg Pathol 37 (7), 1053-1057, 2013 | 197 | 2013 |
| Utility of mammaglobin immunohistochemistry as a proxy marker for the ETV6-NTRK3 translocation in the diagnosis of salivary mammary analogue secretory carcinoma JA Bishop, R Yonescu, D Batista, S Begum, DW Eisele, WH Westra Human pathology 44 (10), 1982-1988, 2013 | 170 | 2013 |
| Acute bilineal leukemia: a rare disease with poor outcome EG Weir, MA Ansari-Lari, DAS Batista, CA Griffin, S Fuller, BD Smith, ... Leukemia 21 (11), 2264-2270, 2007 | 155 | 2007 |
| Topography, clinical, and genomic correlates of 5q myeloid malignancies revisited A Jerez, LP Gondek, AM Jankowska, H Makishima, B Przychodzen, ... Journal of Clinical Oncology 30 (12), 1343-1349, 2012 | 134 | 2012 |
| Molecular analysis of a complex chromosomal rearrangement and a review of familial cases DAS Batista, GS Pai, G Stetten American Journal of Medical Genetics Part A 53 (3), 255-263, 1994 | 132 | 1994 |
| Cytopathologic features of mammary analogue secretory carcinoma JA Bishop, R Yonescu, DAS Batista, WH Westra, SZ Ali Cancer cytopathology 121 (5), 228-233, 2013 | 112 | 2013 |
| Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature CM Tuck-Muller, H Chen, JE Martínez, CC Shen, S Li, C Kusyk, ... Human genetics 96 (1), 119-129, 1995 | 103 | 1995 |
| 3q29 interstitial microduplication: A new syndrome in a three‐generation family EC Lisi, A Hamosh, KF Doheny, E Squibb, B Jackson, R Galczynski, ... American Journal of Medical Genetics Part A 146 (5), 601-609, 2008 | 93 | 2008 |
| The impact of chromosomal microarray on clinical management: a retrospective analysis LB Henderson, CD Applegate, E Wohler, MB Sheridan, J Hoover-Fong, ... Genetics in Medicine 16 (9), 657-664, 2014 | 86 | 2014 |
| Mutations in Alström protein impair terminal differentiation of cardiomyocytes LT Shenje, P Andersen, MK Halushka, C Lui, L Fernandez, GB Collin, ... Nature communications 5, 3416, 2014 | 84 | 2014 |
| Interstitial microduplication of Xp22. 31: Causative of intellectual disability or benign copy number variant? F Li, Y Shen, U Köhler, FH Sharkey, D Menon, L Coulleaux, V Malan, ... European journal of medical genetics 53 (2), 93-99, 2010 | 84 | 2010 |
| A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21 Y Kazuki, FJ Gao, Y Li, AJ Moyer, B Devenney, K Hiramatsu, ... eLife 9, e56223, 2020 | 72 | 2020 |
| Glandular odontogenic cysts (GOCs) lack MAML2 rearrangements: a finding to discredit the putative nature of GOC as a precursor to central mucoepidermoid carcinoma JA Bishop, R Yonescu, D Batista, GR Warnock, WH Westra Head and neck pathology 8 (3), 287-290, 2014 | 64 | 2014 |
| Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: search for recurrent chromosome abnormalities DAS Batista, EC Vonderheid, A Hawkins, L Morsberger, P Long, ... Genes, Chromosomes and Cancer 45 (4), 383-391, 2006 | 62 | 2006 |
| A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization DAS Batista, CM Tuck-Muller, JE Martinez, WG Kearns, PL Pearson, ... Human genetics 92 (2), 117-121, 1993 | 50 | 1993 |
| Mutations in FARS2 and non‐fatal mitochondrial dysfunction in two siblings HJ Vernon, R McClellan, DAS Batista, S Naidu American Journal of Medical Genetics Part A 167 (5), 1147-1151, 2015 | 45 | 2015 |
| Loss of the mismatched human leukocyte antigen haplotype in two acute myelogenous leukemia relapses after haploidentical bone marrow transplantation with posttransplantation … SR McCurdy, BS Iglehart, DA Batista, CD Gocke, Y Ning, HA Knaus, ... Leukemia 30 (10), 2102, 2016 | 44 | 2016 |
| Creation and characterization of an airway epithelial cell line for stable expression of CFTR variants LB Gottschalk, B Vecchio-Pagan, N Sharma, ST Han, A Franca, ... Journal of Cystic Fibrosis 15 (3), 285-294, 2016 | 40 | 2016 |
| Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot K Weiss, C Applegate, T Wang, DAS Batista American Journal of Medical Genetics Part A 167 (11), 2702-2706, 2015 | 39 | 2015 |
| Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy? MJM Nowaczyk, BA Thompson, S Zeesman, U Moog, PA Sanchez‐Lara, ... Clinical genetics 85 (2), 138-146, 2014 | 39 | 2014 |
