C. Godfrey

Harvard University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

5h-index582citations20works9.52yr avg
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Research Topics

Muscle Physiology and Disorders(12), Ubiquitin and proteasome pathways(5), Neurogenetic and Muscular Disorders Research(3), Cellular Mechanics and Interactions(2), Bacterial biofilms and quorum sensing(2)

Publications20 total

Pseudomonas aeruginosa aggregates elicit neutrophil swarming
iScience·2025Open Access
Self-extinguishing relay waves enable homeostatic control of human neutrophil swarming
Developmental Cell·2024· 19 citedOpen Access
identification of genetic variation within populations of the woolly apple aphid (<i>Hemiptera</i>:<i> Aphididae</i>) in the United Kingdom using microsatellite markers
Acta Horticulturae·2023
Self-extinguishing relay waves enable homeostatic control of human neutrophil swarming
2023· 7 citedOpen Access
The physiological consequences of different levels of dystrophin following antisense based exon-skipping in the mdx mouse
Neuromuscular Disorders·2015
P1 Peptide-conjugated phosphodiamidate morpholino treatment in mdx mice: cardiac dystrophin restoration and function
Neuromuscular Disorders·2014
Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008
Neuromuscular Disorders·2012· 63 cited
P04 Advancing the potential of peptide-PMO compounds in exon skipping therapy for DMD
Neuromuscular Disorders·2012
Refining the genetics of muscular dystrophies with defective glycosylation of dystroglycan
UCL Discovery (University College London)·2010
Expression analysis of alpha-dystroglycan glycosyltransferases during myoblast-myotube differentiation
UCL Discovery (University College London)·2009
An investigation of candidate genes in dystroglycanopathy patients
UCL Discovery (University College London)·2009
EM.P.2.03 An investigation of candidate genes in dystroglycanopathy patients
Neuromuscular Disorders·2009
EM.P.2.01 Expression analysis of α-dystroglycan glycosyltransferases during myoblast-myotube differentiation
Neuromuscular Disorders·2009· 1 cited
Muscular dystrophies due to defective glycosylation of dystroglycan.
PubMed·2007· 52 citedOpen Access
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Brain·2007· 433 citedOpen Access
C.P.3.06 Spectrum of brain changes and genotype-phenotype correlations in secondary dystroglycanopathies
Neuromuscular Disorders·2007· 1 cited
C.P.3.04 Mild POMGnT1 mutations underlie a novel limb girdle muscular dystrophy variant
Neuromuscular Disorders·2007
P.O.1 Molecular genetic analysis of 6 glycosyltransferases in a large population of dystroglycanopathy patients significantly widens the spectrum of phenotypes resulting from POMT1, POMGnT1 and Fukutin mutations
Neuromuscular Disorders·2006· 1 cited
The identification of compound heterozygous mutations in the Fukutin gene in two non Japanese patients with Limb girdle muscular dystrphy.
UCL Discovery (University College London)·2006
Identification of Rat Enamel Organ RNA Transcripts Using Differential-Display
Connective Tissue Research·1998· 5 cited

Frequent Co-authors

Martin Brockington(9), Emma Clement(7), Silvia Torelli(7), Stephen Abbs(7), R. Mein(5), Volker Straub(4), Francesco Muntoni(4), F. Muntoni(4), S. Robb(3), L. Feng(3), C. Jimenez‐Mallebrera(3), Maria Kinali(3), S. Brown(3), Haluk Topaloğlu(3), Kathryn N. North(3), Eugenio Mercuri(3), Alex Hopke(3), Daniel Irimia(3), Graham McClorey(3), Michael J. Gait(3)