| Role of peroxisome proliferator-activated receptor-α (PPARα) in bezafibrate-induced hepatocarcinogenesis and cholestasis T Hays, I Rusyn, AM Burns, MJ Kennett, JM Ward, FJ Gonzalez, JM Peters Carcinogenesis 26 (1), 219-227, 2005 | 161 | 2005 |
| Virological synapses allow HIV-1 uptake and gene expression in renal tubular epithelial cells P Chen, BK Chen, A Mosoian, T Hays, MJ Ross, PE Klotman, ME Klotman Journal of the American Society of Nephrology 22 (3), 496-507, 2011 | 105 | 2011 |
| Yeast nuclear envelope subdomains with distinct abilities to resist membrane expansion JL Campbell, A Lorenz, KL Witkin, T Hays, J Loidl, O Cohen-Fix Molecular biology of the cell 17 (4), 1768-1778, 2006 | 101 | 2006 |
| Genomic identification of potential risk factors during acetaminophen-induced liver disease in susceptible and resistant strains of mice KD Welch, TP Reilly, M Bourdi, T Hays, CA Pise-Masison, MF Radonovich, ... Chemical research in toxicology 19 (2), 223-233, 2006 | 61 | 2006 |
| Genetic testing for kidney disease of unknown etiology T Hays, EE Groopman, AG Gharavi Kidney international 98 (3), 590-600, 2020 | 56 | 2020 |
| Components of the Spindle Assembly Checkpoint Regulate the Anaphase-Promoting Complex During Meiosis in Caenorhabditis elegans KK Stein, ES Davis, T Hays, A Golden Genetics 175 (1), 107-123, 2007 | 52 | 2007 |
| Brc1-mediated rescue of Smc5/6 deficiency: requirement for multiple nucleases and a novel Rad18 function KM Lee, S Nizza, T Hayes, KL Bass, A Irmisch, JM Murray, MJ O'Connell Genetics 175 (4), 1585-1595, 2007 | 45 | 2007 |
| The prevalence and clinical significance of congenital anomalies of the kidney and urinary tract in preterm infants T Hays, MV Thompson, DA Bateman, R Sahni, VN Tolia, RH Clark, ... JAMA Network Open 5 (9), e2231626-e2231626, 2022 | 23 | 2022 |
| Glomerular MYH9 expression is reduced by HIV-1 T Hays, VD D’Agati, JA Garellek, T Warren, ME Trubin, DP Hyink, JC He, ... Aids 26 (7), 797-803, 2012 | 21 | 2012 |
| Proteomics analysis of the non-muscle myosin heavy chain IIa-enriched actin-myosin complex reveals multiple functions within the podocyte T Hays, A Ma’ayan, NR Clark, CM Tan, A Teixeira, A Teixeira, JW Choi, ... PLoS One 9 (6), e100660, 2014 | 18 | 2014 |
| Genetic testing for unexplained perinatal disorders T Hays, RJ Wapner Current opinion in pediatrics 33 (2), 195-202, 2021 | 17 | 2021 |
| APOL1 variants in HIV-associated nephropathy: just one piece of the puzzle T Hays, CM Wyatt Kidney international 82 (3), 259-260, 2012 | 15 | 2012 |
| Implementation of rapid genome sequencing for critically ill infants with complex congenital heart disease T Hays, R Hernan, M Disco, EL Griffin, N Goldshtrom, D Vargas, ... Circulation: Genomic and Precision Medicine 16 (5), 415-420, 2023 | 7 | 2023 |
| The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction BK Brar, K Blakemore, C Hertenstein, JL Miller, KA Miller, H Shamseldin, ... Prenatal Diagnosis 44 (2), 196-204, 2024 | 5 | 2024 |
| Rare single nucleotide and copy number variants and the etiology of congenital obstructive uropathy: implications for genetic diagnosis DF Ahram, TY Lim, J Ke, G Jin, M Verbitsky, M Bodria, BH Kil, ... Journal of the American Society of Nephrology 34 (6), 1105-1119, 2023 | 5 | 2023 |
| Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study EH Leow, JH Lee, CP Hornik, YH Ng, T Hays, RH Clark, VN Tolia, ... Pediatric Nephrology 38 (1), 161-172, 2023 | 5 | 2023 |
| Learning the Language of Medical Device Innovation: A Longitudinal Interdisciplinary Elective for Medical Students LM Maloney, M Hakimi, T Hays, J Adachi, A Chau, BS Esper, V Koulouris, ... Academic Medicine 97 (9), 1341-1345, 2022 | 3 | 2022 |
| The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease E Zhao, M Bomback, A Khan, S Krishna Murthy, D Solowiejczyk, NL Vora, ... Prenatal Diagnosis, 2024 | 1 | 2024 |
| A deep intronic PKHD1 variant identified by SpliceAI in a deceased neonate with autosomal recessive polycystic kidney disease F Richter, KD Rutherford, AJ Cooke, M Meshkati, V Eddy-Abrams, ... American Journal of Kidney Diseases, 2024 | 1 | 2024 |
| Nine is the New Ten of Apgar Scores: An Observational Retrospective Cohort Study SS Everett, M Bomback, P Roth, N Goldshtrom, RA Polin, A Lyford, T Hays The Journal of Pediatrics, 114150, 2024 | | 2024 |
Amanda M Burns MSPH DABTSenior Managing Health Scientist, Stantec在 stantec.com 的电子邮件经过验证
