| Preemptive pharmacogenomic testing for precision medicine: a comprehensive analysis of five actionable pharmacogenomic genes using next-generation DNA sequencing and a … Y Ji, JM Skierka, JH Blommel, BE Moore, DL VanCuyk, JK Bruflat, ... The Journal of Molecular Diagnostics 18 (3), 438-445, 2016 | 177 | 2016 |
| Confirming variants in next-generation sequencing panel testing by Sanger sequencing LM Baudhuin, SA Lagerstedt, EW Klee, N Fadra, D Oglesbee, MJ Ferber The Journal of Molecular Diagnostics 17 (4), 456-461, 2015 | 144 | 2015 |
| Uterine inflammatory myofibroblastic tumors in pregnant women with and without involvement of the placenta: a study of 6 cases with identification of a novel TIMP3-RET fusion EH Cheek, N Fadra, RA Jackson, JI Davila, WR Sukov, MT Uckerman, ... Human Pathology 97, 29-39, 2020 | 47 | 2020 |
| Development and verification of an RNA sequencing (RNA-Seq) assay for the detection of gene fusions in tumors JL Winters, JI Davila, AM McDonald, AA Nair, N Fadra, RN Wehrs, ... The Journal of Molecular Diagnostics 20 (4), 495-511, 2018 | 40 | 2018 |
| Impact of RNA degradation on fusion detection by RNA-seq JI Davila, NM Fadra, X Wang, AM McDonald, AA Nair, BR Crusan, X Wu, ... BMC genomics 17, 1-9, 2016 | 40 | 2016 |
| RNA sequencing identifies a novel USP9X‐USP6 promoter swap gene fusion in a primary aneurysmal bone cyst PR Blackburn, JI Davila, RA Jackson, N Fadra, MA Atiq, BA Pitel, AA Nair, ... Genes, Chromosomes and Cancer 58 (8), 589-594, 2019 | 33 | 2019 |
| RNA-seq reveals differences in expressed tumor mutation burden in colorectal and endometrial cancers with and without defective DNA-mismatch repair MA DiGuardo, JI Davila, RA Jackson, AA Nair, N Fadra, KT Minn, MA Atiq, ... The Journal of Molecular Diagnostics 23 (5), 555-564, 2021 | 19 | 2021 |
| Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): molecular profiling confirms frequent MAPK pathway activation CM Ida, DR Johnson, AA Nair, J Davila, TM Kollmeyer, K Minn, NM Fadra, ... Journal of Neuropathology & Experimental Neurology 80 (9), 821-829, 2021 | 15 | 2021 |
| LPCAT1-TERT fusions are uniquely recurrent in epithelioid trophoblastic tumors and positively regulate cell growth GR Oliver, S Marcano-Bonilla, J Quist, EJ Tolosa, E Iguchi, AA Swanson, ... PloS one 16 (5), e0250518, 2021 | 5 | 2021 |
| Clinical validation of a next generation sequencing panel test for hereditary colorectal cancer MJ Ferber, LM Peterson, JH Blommel, NM Fadra, BC Thomas J Med Diagn Meth 5 (210), 2, 2016 | 5 | 2016 |
| Multiple isodicentric Y chromosomes in myeloid malignancies: a unique cytogenetic entity and potential therapeutic target AA Mangaonkar, MM Patnaik, GR Oliver, KW Rao, K Kaiser-Rogers, ... Leukemia & Lymphoma 60 (3), 821-824, 2019 | 3 | 2019 |
| Transcriptomic and immunophenotypic characterization of two cases of adamantinoma‐like Ewing sarcoma of the thyroid gland K Chatzopoulos, JI Davila, N Fadra, RA Jackson, KT Minn, S Sotiriou, ... Histopathology 83 (3), 426-434, 2023 | 1 | 2023 |
| Deletion of the Vitamin D Receptor in Skeletal Muscle is Associated with Improved Glucose Tolerance and Reduced Muscle Function L Losbanos, T Craig, N Fadra, A Nair, A Matveyenko, R Kumar The FASEB Journal 36, 2022 | 1 | 2022 |
| Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease N Fadra, LE Schultz-Rogers, P Chanana, MA Cousin, EL Macke, A Ferrer, ... BMC genomics 25 (1), 371, 2024 | | 2024 |
| Clinical Validation of Tagmentation-Based Genome Sequencing for Germline Disorders W Shen, HL Sellers, LA Choate, MI Stein, PP Tandale, J Tan, R Setlem, ... The Journal of Molecular Diagnostics 25 (7), 524-531, 2023 | | 2023 |
| 101. Development of an analytical pipeline for detecting fusions of clinical relevance in liver cancer C McCabe, N Fadra, D O'Brien, A Nair, R Smoot, L Roberts, M Torbenson, ... Cancer Genetics 268, 32, 2022 | | 2022 |
| OP040: Clinical validation of tagmentation-based genome sequencing for germline disorders H Sellers, M Stein, P Tandale, J Tan, R Setlem, Y Sakai, N Fadra, C Sosa, ... Genetics in Medicine 24 (3), S366, 2022 | | 2022 |
| 35. Atypical FISH patterns clarified by RNAseq in solid tumor specimens B Pitel, R Meyer, K Minn, N Fadra, A Nair, J Davila, K Pearce, J Voss, ... Cancer Genetics 260, 12, 2022 | | 2022 |
| 42. Genomic gymnastics: Using RNAseq and mate pair sequencing to collaboratively decipher structural variation B Pitel, N Fadra, J Davila, P Greipp, N Hoppman, R Jackson, R Jenkins, ... Cancer Genetics 244, 16, 2020 | | 2020 |
| Oncogenic Fusion Detection Using RNA-seq in a Cohort of 158 Sarcomas MA Atiq, K Fritchie, JI Davila, RB Jenkins, AL Folpe, BR Kipp, CY Inwards, ... JOURNAL OF MOLECULAR DIAGNOSTICS 21 (6), 1216-1216, 2019 | | 2019 |
Eric KleeMayo ClinicVerified email at mayo.edu
