| Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity K Hopp, CJ Ward, CJ Hommerding, SH Nasr, HF Tuan, VG Gainullin, ... The Journal of clinical investigation 122 (11), 4257-4273, 2012 | 394 | 2012 |
| Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3 R Tammachote, CJ Hommerding, RM Sinders, CA Miller, PG Czarnecki, ... Human molecular genetics 18 (17), 3311-3323, 2009 | 154 | 2009 |
| Polycystin-1 maturation requires polycystin-2 in a dose-dependent manner VG Gainullin, K Hopp, CJ Ward, CJ Hommerding, PC Harris The Journal of clinical investigation 125 (2), 607-620, 2015 | 140 | 2015 |
| Tolvaptan plus pasireotide shows enhanced efficacy in a PKD1 model K Hopp, CJ Hommerding, X Wang, H Ye, PC Harris, VE Torres Journal of the American Society of Nephrology 26 (1), 39-47, 2015 | 129 | 2015 |
| B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis K Hopp, CM Heyer, CJ Hommerding, SA Henke, JL Sundsbak, S Patel, ... Human molecular genetics 20 (13), 2524-2534, 2011 | 96 | 2011 |
| Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3 MB Consugar, VJ Kubly, DJ Lager, CJ Hommerding, WC Wong, E Bakker, ... Human genetics 121, 591-599, 2007 | 91 | 2007 |
| The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity AC Leightner, CJ Hommerding, Y Peng, JL Salisbury, VG Gainullin, ... Human molecular genetics 22 (10), 2024-2040, 2013 | 63 | 2013 |
| The Role of Stem Cell Genomic Instability in Aging CJ Hommerding, BG Childs, DJ Baker Current Stem Cell Reports 1, 151-161, 2015 | 1 | 2015 |
| PC1-PC2 complex assembly across ER-Plasma Membrane junctions is disrupted in ADPKD. VG Gainullin, CJ Ward, CJ Hommerding, K Hopp, PC Harris MOLECULAR BIOLOGY OF THE CELL 24, 2013 | | 2013 |
