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Robert H. Baloh
Robert H. Baloh
Novartis Institutes for Biomedical Research
Verified email at novartis.com
Title
Cited by
Cited by
Year
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
9842015
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
8072009
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
7532008
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
7531998
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
7502013
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
6852010
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
6532013
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
6411998
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
5932000
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
5752016
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
5712009
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), 1268-1283. e6, 2018
5702018
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
5462007
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
5122014
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
4471997
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
4102000
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
3212015
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
2752014
Neurturin shares receptors and signal transduction pathways with glial cell line-derived neurotrophic factor in sympathetic neurons
DJ Creedon, MG Tansey, RH Baloh, PA Osborne, PA Lampe, TJ Fahrner, ...
Proceedings of the National Academy of Sciences 94 (13), 7018-7023, 1997
2671997
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
2652021
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