C. DiDonato

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Aliases
C Didonato, Christine Didonato, Christine J Didonato, Christine J. Didonato
Publication record
53 papers · 2,565 citations · H-index 29

PAPERS

Longitudinal Assessment of Timed Function Tests in Ambulatory Individuals with SMA Treated with Nusinersen
20233 citationsauthor #10
Identifying Biomarkers of Spinal Muscular Atrophy for Further Development
202319 citationsauthor #6
In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy
202126 citationsauthor #3
Dysphagia Phenotypes in Spinal Muscular Atrophy: The Past, Present, and Promise for the Future
202134 citationsauthor #3
Combination molecular therapies for type 1 spinal muscular atrophy
202070 citationsauthor #5
Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn2B/- mouse model of spinal muscular atrophy.
202010 citationsauthor #5
Permittivity of ex vivo healthy and diseased murine skeletal muscle from 10 kHz to 1 MHz
201935 citationsauthor #3
Hyperexcitability precedes motoneuron loss in the Smn2B/-mouse model of spinal muscular atrophy.
201915 citationsauthor #7
Permittivity of ex vivo healthy and diseased murine skeletal muscle from 10 kHz to 1 MHz
201935 citationsauthor #2
Friedreich's Ataxia: Clinical Presentation of a Compound Heterozygote Child with a Rare Nonsense Mutation and Comparison with Previously Published Cases
20185 citationsauthor #2
Mammalian Models of Spinal Muscular Atrophy
20177 citationsauthor #2
In vitro and in vivo effects of 2,4 diaminoquinazoline inhibitors of the decapping scavenger enzyme DcpS: Context-specific modulation of SMN transcript levels
201714 citationsauthor #2
Absence of UCHL 1 function leads to selective motor neuropathy
201639 citationsauthor #12
Oscillations in Hb9-Expressing Interneurons Sensory Modulation of Locomotor-Like Membrane
20150 citationsauthor #5
Mechanistic principles of antisense targets for the treatment of spinal muscular atrophy.
201559 citationsauthor #3
ECG in neonate mice with spinal muscular atrophy allows assessment of drug efficacy.
20158 citationsauthor #2
A Short Antisense Oligonucleotide Ameliorates Symptoms of Severe Mouse Models of Spinal Muscular Atrophy
201461 citationsauthor #6
Dissociation of hepatic insulin resistance from susceptibility of nonalcoholic fatty liver disease induced by a high-fat and high-carbohydrate diet in mice.
201442 citationsauthor #7
Behavioral Phenotyping for neonates: Righting reflex
20142 citationsauthor #1
Antisense oligonucleotide mediated therapy of spinal muscular atrophy
201349 citationsauthor #3
The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models.
201389 citationsauthor #17
ANTISENSE OLIGONUCLEOTIDE MEDIATED THERAPY OF SPINAL
20130 citationsauthor #4
Motor Neuron Rescue in Spinal Muscular Atrophy Mice Demonstrates That Sensory-Motor Defects Are a Consequence, Not a Cause, of Motor Neuron Dysfunction
2012184 citationsauthor #6
Protein Profiling In Mouse Models Of Spinal Muscular Atrophy
20120 citationsauthor #5
Genotyping protocols for commonly used SMA model mice
20110 citationsauthor #1
Characterization of a commonly used mouse model of SMA reveals increased seizure susceptibility and heightened fear response in FVB/N mice.
201121 citationsauthor #6
Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice.
2010195 citationsauthor #4
Development of electrocardiogram intervals during growth of FVB/N neonate mice
201029 citationsauthor #4
Molecular and phenotypic reassessment of an infrequently used mouse model for spinal muscular atrophy.
201056 citationsauthor #4
Mouse Survival Motor Neuron Alleles That Mimic SMN2 Splicing and Are Inducible Rescue Embryonic Lethality Early in Development but Not Late
201079 citationsauthor #6
Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo.
2009122 citationsauthor #2
Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect.
2008217 citationsauthor #6
G.P.4.12 Translational readthrough modulates SMN stability: Potential for aminoglycosides as an SMA therapy
20080 citationsauthor #4
Association between Ag I -CA Alleles and Severity of Autosomal Recessive Proximal Spinal Muscular Atrophy
20070 citationsauthor #1
SMN Transcript Stability: Could Modulation of Messenger RNA Degradation Provide a Novel Therapy for Spinal Muscular Atrophy?
200731 citationsauthor #3
Spinal Muscular Atrophy: Classification, Diagnosis, Management, Pathogenesis, and Future Research Directions
200755 citationsauthor #5
Development of a Gene Therapy Strategy for the Restoration of Survival Motor Neuron Protein Expression: Implications for Spinal Muscular Atrophy Therapy
200339 citationsauthor #1
SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTra2 beta 1.
2002138 citationsauthor #2
Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing.
200155 citationsauthor #1
Complete nucleotide sequence, genomic organization, and promoter analysis of the murine survival motor neuron gene (Smn)
19994 citationsauthor #1
The mouse neuronal apoptosis inhibitory protein gene maps to a conserved syntenic region of mouse chromosome 13
19971 citationsauthor #1
Deletion and conversion in spinal muscular atrophy patients: Is there a relationship to severity?
1997107 citationsauthor #1
Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene.
1997125 citationsauthor #1
Genetic and physical mapping of the mouse host resistance locus Lgn1
19979 citationsauthor #4
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs.
1995106 citationsauthor #4
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients
199583 citationsauthor #2
A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.
199452 citationsauthor #8
A YAC contig of the region containing the spinal muscular atrophy gene (SMA): identification of an unstable region.
199443 citationsauthor #2
Linkage mapping of the spinal muscular atrophy gene
199426 citationsauthor #7
Identification of strong allele association and candidate cDNAs for the Spinal Muscular Atrophy gene
19941 citationsauthor #1
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.
199482 citationsauthor #1
Molecular studies of carnitine palmitoyltransferase cpt from human liver
19900 citationsauthor #4
Animal Models: Why Are They so Important? Animal Models of Spinal Muscular Atrophy
year unknown84 citationsauthor #2

TIMELINE

1990 0 citations

1994 204 citations

1995 189 citations

1997 242 citations

1999 4 citations

2001 55 citations

2002 138 citations

2003 39 citations

2007 86 citations

2008 217 citations

2009 122 citations

2010 359 citations

2011 21 citations

2012 184 citations

2013 138 citations

2014 105 citations

2015 67 citations

2016 39 citations

2017 21 citations

2018 5 citations

2019 50 citations

2020 80 citations

2021 60 citations

2023 22 citations

Unknown 84 citations

C. DiDonato

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