Ronald Cohn

Human Genetics Johns Hopkins University, Baltimore, MD 
Genetics, Molecular Biology, Cell Biology
"Ronald Cohn"
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...