| The long and short isoforms of Ret function as independent signaling complexes BA Tsui-Pierchala, RC Ahrens, RJ Crowder, J Milbrandt, EM Johnson Journal of Biological Chemistry 277 (37), 34618-34625, 2002 | 142 | 2002 |
| Modulation of the GABAA‐gated chloride channel
by reactive oxygen species R Sah, F Galeffi, R Ahrens, G Jordan, RD Schwartz‐Bloom Journal of neurochemistry 80 (3), 383-391, 2002 | 105 | 2002 |
| NMDA receptor blockade and hippocampal neuronal loss impair fear conditioning and position habit reversal in C57Bl/6 mice ME Bardgett, R Boeckman, D Krochmal, H Fernando, R Ahrens, ... Brain research bulletin 60 (1-2), 131-142, 2003 | 89 | 2003 |
| Stimulation of entorhinal cortex–dentate gyrus circuitry is antidepressive S Yun, RP Reynolds, I Petrof, A White, PD Rivera, A Segev, AD Gibson, ... Nature medicine 24 (5), 658-666, 2018 | 87 | 2018 |
| Nerve growth factor promotes the survival of sympathetic neurons through the cooperative function of the protein kinase C and phosphatidylinositol 3-kinase pathways BA Pierchala, RC Ahrens, AJ Paden, EM Johnson Journal of Biological Chemistry 279 (27), 27986-27993, 2004 | 72 | 2004 |
| Chloride transport inhibitors influence recovery from oxygen–glucose deprivation-induced cellular injury in adult hippocampus BB Pond, F Galeffi, R Ahrens, RD Schwartz-Bloom Neuropharmacology 47 (2), 253-262, 2004 | 55 | 2004 |
| Precision therapy for a new disorder of AMPA receptor recycling due to mutations in ATAD1 RC Ahrens-Nicklas, GKE Umanah, N Sondheimer, MA Deardorff, ... Neurology: Genetics 3 (1), e130, 2017 | 48 | 2017 |
| Brain branched-chain amino acids in maple syrup urine disease: implications for neurological disorders J Xu, Y Jakher, RC Ahrens-Nicklas International Journal of Molecular Sciences 21 (20), 7490, 2020 | 47 | 2020 |
| Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit RC Ahrens‐Nicklas, S Khan, J Garbarini, S Woyciechowski, ... American journal of medical genetics Part A 170 (12), 3090-3097, 2016 | 44 | 2016 |
| Multiple sulfatase deficiency: a disease comprising mucopolysaccharidosis, sphingolipidosis, and more caused by a defect in posttranslational modification L Schlotawa, LA Adang, K Radhakrishnan, RC Ahrens-Nicklas International journal of molecular sciences 21 (10), 3448, 2020 | 39 | 2020 |
| Re-evaluating the efficacy of β-adrenergic agonists and antagonists in long QT-3 syndrome through computational modelling RC Ahrens-Nicklas, CE Clancy, DJ Christini Cardiovascular research 82 (3), 439-447, 2009 | 39 | 2009 |
| Disruption of cardiac thin filament assembly arising from a mutation in LMOD2: A novel mechanism of neonatal dilated cardiomyopathy RC Ahrens-Nicklas, CT Pappas, GP Farman, RM Mayfield, TM Larrinaga, ... Science advances 5 (9), eaax2066, 2019 | 38 | 2019 |
| Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement R Ahrens-Nicklas, L Schlotawa, A Ballabio, N Brunetti-Pierri, M De Castro, ... Molecular genetics and metabolism 123 (3), 337-346, 2018 | 38 | 2018 |
| Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With … EJ Bhoj, M Li, R Ahrens-Nicklas, LC Pyle, J Wang, VW Zhang, C Clarke, ... JIMD Reports, Volume 19, 59-66, 2015 | 36 | 2015 |
| Newborn screening for Pompe disease: Pennsylvania experience C Ficicioglu, RC Ahrens-Nicklas, J Barch, SR Cuddapah, BS DiBoscio, ... International Journal of Neonatal Screening 6 (4), 89, 2020 | 34 | 2020 |
| ECHS1 deficiency as a cause of severe neonatal lactic acidosis RD Ganetzky, K Bloom, R Ahrens-Nicklas, A Edmondson, MA Deardorff, ... JIMD Reports, Volume 30, 33-37, 2016 | 34 | 2016 |
| Molecular annotation of integrative feeding neural circuits CA Pérez, SA Stanley, RW Wysocki, J Havranova, R Ahrens-Nicklas, ... Cell metabolism 13 (2), 222-232, 2011 | 29 | 2011 |
| Anthropomorphizing the mouse cardiac action potential via a novel dynamic clamp method RC Ahrens-Nicklas, DJ Christini Biophysical Journal 97 (10), 2684-2692, 2009 | 27 | 2009 |
| Adolescent presentations of inborn errors of metabolism RC Ahrens-Nicklas, G Slap, C Ficicioglu Journal of Adolescent Health 56 (5), 477-482, 2015 | 26 | 2015 |
| Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease LA Adang, L Schlotawa, S Groeschel, C Kehrer, K Harzer, ... Journal of inherited metabolic disease 43 (6), 1298-1309, 2020 | 25 | 2020 |
