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K. Seburn · SciRah

Researcher profile · Semantic Scholar

K. Seburn

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K. Seburn — researcher profile on SciRah

h-index: 23
Works: 55
Citations: 2,535

Most-cited papers

The harlequin mouse mutation downregulates apoptosis-inducing factor
Jeffrey A Klein, C. Longo-Guess, M. Rossmann, K. Seburn +4 more
2002Nature628 citations
Semantic Scholar
An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model.
K. Seburn, L. Nangle, G. Cox, P. Schimmel +1 more
2006Neuron212 citations Open access
Semantic Scholar
A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations.
R. Maue, R. Burgess, Bing Wang, Christine M. Wooley +15 more
2012Human Molecular Genetics125 citations Open access
Semantic Scholar
Charcot-Marie-Tooth–Linked Mutant GARS Is Toxic to Peripheral Neurons Independent of Wild-Type GARS Levels
W. Motley, K. Seburn, M. Nawaz, Kathy E. Miers +7 more
2011PLoS Genetics117 citations Open access
Semantic Scholar
Auditory brainstem responses in 10 inbred strains of mice.
Xiaoming Zhou, P. Jen, K. Seburn, W. Frankel +1 more
2006Brain Research117 citations Open access
Semantic Scholar
Mutations in a P-Type ATPase Gene Cause Axonal Degeneration
Xian-Jun Zhu, R. Libby, W. D. de Vries, Richard S. Smith +4 more
2012PLoS Genetics108 citations Open access
Semantic Scholar
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy
Francesca Achilli, Virginie Bros-Facer, Hazel P. Williams, G. Banks +17 more
2009Disease Models & Mechanisms104 citations Open access
Semantic Scholar
Alteration of the unfolded protein response modifies neurodegeneration in a mouse model of Marinesco–Sjögren syndrome
Lihong Zhao, C. Rosales, K. Seburn, D. Ron +1 more
2009Human Molecular Genetics99 citations Open access
Semantic Scholar
Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice
Dorothy Concepcion, K. Seburn, Gen Wen, W. Frankel +1 more
2004Genetics99 citations
Semantic Scholar
Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot–Marie–Tooth Type 2d
E. Spaulding, J. N. Sleigh, K. H. Morelli, M. Pinter +2 more
2016Journal of Neuroscience72 citations Open access
Semantic Scholar
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations
M. Stum, H. Mclaughlin, Erica L. Kleinbrink, Kathy E. Miers +4 more
2010Molecular and cellular neurosciences69 citations Open access
Semantic Scholar
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination
B. Patton, Bing Wang, Yukie S. Tarumi, K. Seburn +1 more
2008Journal of Cell Science67 citations Open access
Semantic Scholar
Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease
L. Bogdanik, J. N. Sleigh, C. Tian, M. Samuels +3 more
2013Disease Models & Mechanisms56 citations Open access
Semantic Scholar
Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
Kimberly A Huebsch, E. Kudryashova, Christine M. Wooley, R. Sher +3 more
2005Human Molecular Genetics56 citations Open access
Semantic Scholar
Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6.
M. Strokin, K. Seburn, G. Cox, Kimberly Martens +1 more
2012Human Molecular Genetics48 citations Open access
Semantic Scholar
Age, experience and genetic background influence treadmill walking in mice
Christine M. Wooley, Shu-Qin Xing, R. Burgess, G. Cox +1 more
2008Physiology and Behavior48 citations Open access
Semantic Scholar
Defective carbohydrate metabolism in mice homozygous for the tubby mutation.
Yun Wang, K. Seburn, L. Bechtel, Bruce Y. Lee +3 more
2006Physiological Genomics43 citations
Semantic Scholar
Altered terminal Schwann cell morphology precedes denervation in SOD1 mice
D. Carrasco, K. Seburn, M. Pinter
2015Experimental Neurology40 citations Open access
Semantic Scholar
Neuromuscular disease models and analysis.
R. Burgess, G. Cox, K. Seburn
2010Methods in molecular biology39 citations
Semantic Scholar
Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes
K. H. Morelli, K. Seburn, D. Schroeder, E. Spaulding +3 more
2017Cell Reports36 citations Open access
Semantic Scholar
Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25
F. Runkel, H. Büssow, K. Seburn, G. Cox +3 more
2006Mammalian Genome30 citations
Semantic Scholar
Short-Term Afferent Axotomy Increases Both Strength and Depression at Ia–Motoneuron Synapses in Rat
K. Seburn, Timothy C. Cope
1998Journal of Neuroscience27 citations Open access
Semantic Scholar
Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Nav1.6) and a genetically linkedretinal mutation, rd13
David A. Buchner, K. Seburn, W. Frankel, M. Meisler
2004Mammalian Genome25 citations Open access
Semantic Scholar
Lack of Neuropathy-Related Phenotypes in Hint1 Knockout Mice
K. Seburn, K. H. Morelli, A. Jordanova, R. Burgess
2014Journal of Neuropathology and Experimental Neurology23 citations Open access
Semantic Scholar
Effects of altered muscle activation on oxidative enzyme activity in rat alpha-motoneurons.
K. Seburn, C. Coicou, P. Gardiner
1994Journal of applied physiology21 citations
Semantic Scholar
Motoneurons innervating two regions of rat medial gastrocnemius muscle with differing contractile and histochemical properties.
S. Vanden Noven, P. Gardiner, K. Seburn
1994Acta Anatomica21 citations
Semantic Scholar
Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron disease
D. Carrasco, B. Bahr, K. Seburn, M. Pinter
2016Experimental Neurology19 citations Open access
Semantic Scholar
Nerve Terminal Degeneration Is Independent of Muscle Fiber Genotype in SOD1G93A Mice
D. Carrasco, E. Bichler, K. Seburn, M. Pinter
2010PLoS ONE19 citations Open access
Semantic Scholar
Adaptations of rat lateral gastrocnemius motor units in response to voluntary running.
K. Seburn, P. Gardiner
1995Journal of applied physiology19 citations
Semantic Scholar
A Spontaneous Mutation in Contactin 1 in the Mouse
M. Davisson, R. Bronson, A. Tadenev, W. Motley +3 more
2011PLoS ONE18 citations Open access
Semantic Scholar
Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit
M. Traka, K. Seburn, B. Popko
2006Mammalian Genome16 citations
Semantic Scholar
Clenbuterol has a greater influence on untrained than on previously trained skeletal muscle in rats
R. Murphy, L. Béliveau, K. Seburn, P. Gardiner
2006European Journal of Applied Physiology and Occupational Physiology15 citations
Semantic Scholar
Genetic analysis of Pycr1 and Pycr2 in mice.
M. Stum, A. Tadenev, K. Seburn, Kathy E. Miers +10 more
2021Genetics14 citations Open access
Semantic Scholar
Decline in spontaneous activity of group Aalphabeta sensory afferents after sciatic nerve axotomy in rat.
K. Seburn, P. Catlin, J. F. Dixon, Ming-Hsie Lee +2 more
1999Neuroscience Letters12 citations
Semantic Scholar
Effect of manipulation of plasma lactate on integrated EMG during cycling.
K. Seburn, D. J. Sanderson, Angelo N. Belcastro, D. Mckenzie
1992Medicine & Science in Sports & Exercise12 citations Open access
Semantic Scholar
Motor terminal degeneration unaffected by activity changes in SOD1G93A mice; a possible role for glycolysis
D. Carrasco, E. Bichler, M. Rich, Xue-Yong Wang +2 more
2012Neurobiology of Disease11 citations Open access
Semantic Scholar
Severe disturbance in the Ca 2 1 signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla 2 g 6
M. Strokin, K. Seburn, G. Cox, Kimberly Martens +1 more
201211 citations
Semantic Scholar
A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy
T. Hines, J. Bailey, Hedi Liu, A. Guntur +5 more
2023Biology8 citations Open access
Semantic Scholar
Enhancing the versatility of wireless biopotential acquisition for myoelectric prosthetic control
Rebecca A. Bercich, Zhi Wang, Henry Mei, L. Hammer +3 more
2016Journal of Neural Engineering8 citations Open access
Semantic Scholar
Metabolite profile of a mouse model of Charcot–Marie–Tooth type 2D neuropathy: implications for disease mechanisms and interventions
P. Bais, K. Beebe, K. H. Morelli, M. Currie +9 more
2016Biology Open8 citations Open access
Semantic Scholar
Strain-Specific Hyperkyphosis and Megaesophagus in Add1 null mice
R. F. Robledo, K. Seburn, A. Nicholson, Luanne L. Peters
2012Genesis5 citations Open access
Semantic Scholar
Similar age‐related changes in two regions of muscle with different properties
S. Noven, K. Seburn, N. Latham, P. Gardiner
1996NeuroReport5 citations
Semantic Scholar
Neuromuscular Disease Models and Analysis.
R. Burgess, G. Cox, K. Seburn
2016Methods in molecular biology3 citations
Semantic Scholar
How Does Injury Strengthen Ia-Motoneuron Synapses?
Timothy C. Cope, K. Seburn, C. Buck
20011 citations
Semantic Scholar
Effect of cadence on the EMG of vastus lateralis and oxygen uptake during steady-state submaximal cycling
B. Reimer, D. Sanderson, K. Seburn
19891 citations
Semantic Scholar
P 1-A-4 Comparison of intrinsic discharge characteristics and contractile properties of rat triceps surae motoneurons
K. Seburn, J. Sleigh, Emily Spaulding, R. Burgess +6 more
20140 citations
Semantic Scholar
Implantable Sensor for Longitudinal Recording of Spontaneous and Voluntary-Evoked EMG and NAP in Untethered Animals
Rebecca A. Bercich, K. Seburn, P. Irazoqui
20130 citations
Semantic Scholar
Toward an Optogenetic Autonomous Nerve Control (OANC) System
Malika S. Datta, Matthew P. Ward, Steven T. Lee, K. Seburn +1 more
20130 citations
Semantic Scholar
Screening for Ocular Mutants in the Neuroscience Mutagenesis Facility (NMF) at The Jackson Laboratory
P. Nishina, K. Seburn, Nmf Staff, W. Frankel
20030 citations
Semantic Scholar
An algorithm for detecting phenotypic mutants for the JAX neuroscience mutagenesis facility
Ś. Sen, K. Seburn
20000 citations
Semantic Scholar

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R. Burgess×17
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W. Frankel×5
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M. Pinter×5
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P. Gardiner — researcher profile on SciRah

Kathy E. Miers×4

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Kathy E. Miers — researcher profile on SciRah

K. H. Morelli×4

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K. H. Morelli — researcher profile on SciRah

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D. Carrasco — researcher profile on SciRah

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R. Bronson — researcher profile on SciRah

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S. Ackerman — researcher profile on SciRah

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Christine M. Wooley — researcher profile on SciRah

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Timothy C. Cope — researcher profile on SciRah