| Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ... Science 347 (6229), 1436-1441, 2015 | 1022 | 2015 |
| TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration I Wegorzewska, S Bell, NJ Cairns, TM Miller, RH Baloh Proceedings of the National Academy of Sciences 106 (44), 18809-18814, 2009 | 827 | 2009 |
| Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion D Sareen, JG O’Rourke, P Meera, A Muhammad, S Grant, M Simpkinson, ... Science translational medicine 5 (208), 208ra149-208ra149, 2013 | 786 | 2013 |
| TDP‐43 A315T mutation in familial motor neuron disease MA Gitcho, RH Baloh, S Chakraverty, K Mayo, JB Norton, D Levitch, ... Annals of Neurology: Official Journal of the American Neurological …, 2008 | 762 | 2008 |
| Artemin, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRα3–RET receptor complex RH Baloh, MG Tansey, PA Lampe, TJ Fahrner, H Enomoto, KS Simburger, ... Neuron 21 (6), 1291-1302, 1998 | 759 | 1998 |
| Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex A Misko, S Jiang, I Wegorzewska, J Milbrandt, RH Baloh Journal of Neuroscience 30 (12), 4232-4240, 2010 | 707 | 2010 |
| Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration C Lagier-Tourenne, M Baughn, F Rigo, S Sun, P Liu, HR Li, J Jiang, ... Proceedings of the National Academy of Sciences 110 (47), E4530-E4539, 2013 | 685 | 2013 |
| Persephin, a novel neurotrophic factor related to GDNF and neurturin J Milbrandt, FJ De Sauvage, TJ Fahrner, RH Baloh, ML Leitner, ... Neuron 20 (2), 245-253, 1998 | 643 | 1998 |
| Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 623 | 2018 |
| C9orf72 is required for proper macrophage and microglial function in mice JG O’rourke, L Bogdanik, A Yáñez, D Lall, AJ Wolf, A Muhammad, R Ho, ... Science 351 (6279), 1324-1329, 2016 | 610 | 2016 |
| The GDNF family ligands and receptors—implications for neural development RH Baloh, H Enomoto, EM Johnson Jr, J Milbrandt Current opinion in neurobiology 10 (1), 103-110, 2000 | 596 | 2000 |
| Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease JS Ju, RA Fuentealba, SE Miller, E Jackson, D Piwnica-Worms, RH Baloh, ... Journal of Cell Biology 187 (6), 875-888, 2009 | 593 | 2009 |
| Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations RH Baloh, RE Schmidt, A Pestronk, J Milbrandt Journal of Neuroscience 27 (2), 422-430, 2007 | 551 | 2007 |
| Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ... Nature neuroscience 17 (5), 664-666, 2014 | 543 | 2014 |
| TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret RH Baloh, MG Tansey, JP Golden, DJ Creedon, RO Heuckeroth, CL Keck, ... Neuron 18 (5), 793-802, 1997 | 449 | 1997 |
| GFRα-mediated localization of RET to lipid rafts is required for effective downstream signaling, differentiation, and neuronal survival MG Tansey, RH Baloh, J Milbrandt, EM Johnson Neuron 25 (3), 611-623, 2000 | 412 | 2000 |
| C9orf72 BAC transgenic mice display typical pathologic features of ALS/FTD JG O’Rourke, L Bogdanik, A Muhammad, TF Gendron, KJ Kim, A Austin, ... Neuron 88 (5), 892-901, 2015 | 341 | 2015 |
| Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ... Nature genetics 53 (12), 1636-1648, 2021 | 332 | 2021 |
| Inflammation in ALS/FTD pathogenesis ME McCauley, RH Baloh Acta neuropathologica 137 (5), 715-730, 2019 | 288 | 2019 |
| TREM2 variant p. R47H as a risk factor for sporadic amyotrophic lateral sclerosis J Cady, ED Koval, BA Benitez, C Zaidman, J Jockel-Balsarotti, P Allred, ... JAMA neurology 71 (4), 449-453, 2014 | 285 | 2014 |
