| Proteomic analysis of cisplatin-induced cochlear damage: Methods and early changes in protein expression DE Coling, D Ding, R Young, M Lis, E Stofko, KM Blumenthal, RJ Salvi Hearing research 226 (1-2), 140-156, 2007 | 53 | 2007 |
| mRNA transcript diversity creates new opportunities for pharmacological intervention ES Barrie, RM Smith, JC Sanford, W Sadee Molecular pharmacology 81 (5), 620-630, 2012 | 46 | 2012 |
| Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies NC Rose, ES Barrie, J Malinowski, GP Jenkins, MR McClain, D LaGrave, ... Genetics in Medicine 24 (7), 1379-1391, 2022 | 35 | 2022 |
| Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity ES Barrie, D Weinshenker, A Verma, S Pendergrass, L Lange, MD Ritchie, ... Circulation research, CIRCRESAHA. 114.304398, 2014 | 32 | 2014 |
| The CHRNA5/CHRNA3/CHRNB4 Nicotinic Receptor Regulome: Genomic Architecture, Regulatory Variants, and Clinical Associations ES Barrie, K Hartmann, SH Lee, JT Frater, M Seweryn, D Wang, W Sadee Human Mutation 38 (1), 112-119, 2017 | 29 | 2017 |
| Regulatory effects of genomic translocations at the human carboxylesterase-1 (CES1) gene locus JC Sanford, X Wang, J Shi, ES Barrie, D Wang, HJ Zhu, W Sadee Pharmacogenetics and genomics 26 (5), 197-207, 2016 | 25 | 2016 |
| De novo loss-of-function variants in NSD2 (WHSC1) associate with a subset of Wolf–Hirschhorn syndrome ES Barrie, MP Alfaro, RB Pfau, MJ Goff, KL McBride, K Manickam, ... Molecular Case Studies 5 (4), a004044, 2019 | 24 | 2019 |
| Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene ES Barrie, CE Cottrell, J Gastier-Foster, SE Hickey, AD Patel, SL Santoro, ... European journal of medical genetics 63 (3), 103735, 2020 | 12 | 2020 |
| Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHD ES Barrie, JK Pinsonneault, W Sadee, JA Hollway, BL Handen, T Smith, ... Journal of developmental and physical disabilities 30 (3), 355-371, 2018 | 11 | 2018 |
| Glycerol concentrations required for the successful vitrification of cocktail conditions in a high-throughput crystallization screen R Kempkes, E Stofko, K Lam, EH Snell Acta Crystallographica Section D: Biological Crystallography 64 (3), 287-301, 2008 | 11 | 2008 |
| Human bacterial artificial chromosome (BAC) transgenesis fully rescues noradrenergic function in dopamine β-hydroxylase knockout mice JF Cubells, JP Schroeder, ES Barrie, DF Manvich, W Sadee, T Berg, ... PLoS One 11 (5), e0154864, 2016 | 10 | 2016 |
| ACMG Professional Practice and Guidelines Committee. Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk … NC Rose, ES Barrie, J Malinowski, GP Jenkins, MR McClain, D LaGrave, ... Genet. Med 24 (7), 1379-91, 2022 | 9 | 2022 |
| Expanding the spectrum of CEP55‐associated disease to viable phenotypes ES Barrie, E Overwater, MM van Haelst, MM Motazacker, KV Truxal, ... American Journal of Medical Genetics Part A 182 (5), 1201-1208, 2020 | 8 | 2020 |
| Alpha‐synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3ʹUTR ES Barrie, SH Lee, JT Frater, M Kataki, DW Scharre, W Sadee Molecular genetics & genomic medicine 6 (4), 565-574, 2018 | 7 | 2018 |
| Role of ITGAE in the development of autoimmune diabetes in non-obese diabetic mice ES Barrie, M Lodder, PH Weinreb, J Buss, A Rajab, C Adin, QS Mi, ... Journal of Endocrinology 224 (3), 235-243, 2015 | 5 | 2015 |
| Advances in Cell-Free DNA ES Barrie, A Ferreira-Gonzalez Advances in Molecular Pathology 5 (1), 141-148, 2022 | 2 | 2022 |
| Acute megakaryoblastic leukemia with trisomy 3 and CBFA2T3::GLIS2: A case report J Gillam, A Catic, P Paulraj, J Dalton, G Lai, C Jackson‐Cook, S Turner, ... Genes, Chromosomes and Cancer 61 (8), 491-496, 2022 | 1 | 2022 |
| Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant ES Barrie, Y Li, D Lamb-Thrush, S Hashimoto, T Matthews, D Mouhlas, ... European journal of medical genetics 61 (7), 416-420, 2018 | 1 | 2018 |
| A Collaborative Translational Autism Research Program for the Military GE Herman, E Hansen-Kiss, W Sadee, E Barrie, ... | 1 | 2016 |
| Optical genome mapping reveals balanced and unbalanced genetic changes associated with tumor‐forming potential in an early‐stage prostate cancer epithelial subline (M2205) P Paulraj, E Barrie, C Jackson‐Cook Molecular Genetics & Genomic Medicine 12 (1), e2307, 2024 | | 2024 |
