Ronald Cohn

Affiliations: 
Human Genetics Johns Hopkins University, Baltimore, MD 
Area:
Genetics, Molecular Biology, Cell Biology
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"Ronald Cohn"
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Publications

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Cohn RD, Dubowitz V. (2016) Duchenne muscular dystrophy: Ringo to the rescue? Neuromuscular Disorders : Nmd. 26: 5-6
Wojtal D, Kemaladewi DU, Malam Z, et al. (2015) Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders. American Journal of Human Genetics
Fleming L, Lemmon M, Beck N, et al. (2015) Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy. American Journal of Medical Genetics. Part A
Oskoui M, Gazzellone MJ, Thiruvahindrapuram B, et al. (2015) Clinically relevant copy number variations detected in cerebral palsy. Nature Communications. 6: 7949
Marshall CR, Farrell SA, Cushing D, et al. (2015) Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. Bmc Genomics. 16: S12
Dubowitz V, Cohn RD. (2015) Dystrophin and Duchenne dystrophy. Neuromuscular Disorders : Nmd. 25: 361-2
Malam Z, Cohn RD. (2014) Stem cells on alert: priming quiescent stem cells after remote injury. Cell Stem Cell. 15: 7-8
Bowdin S, Ray PN, Cohn RD, et al. (2014) The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical care. Human Mutation. 35: 513-9
Auer DR, Sysa-Shah P, Bedja D, et al. (2014) Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse. Biotechnology Letters. 36: 1179-85
MacDonald EM, Andres-Mateos E, Mejias R, et al. (2014) Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition. Disease Models & Mechanisms. 7: 471-81
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