Ronald Cohn - Publications

Affiliations: 
Human Genetics Johns Hopkins University, Baltimore, MD 
Area:
Genetics, Molecular Biology, Cell Biology

36/74 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Cohn RD, Dubowitz V. Duchenne muscular dystrophy: Ringo to the rescue? Neuromuscular Disorders : Nmd. 26: 5-6. PMID 26801251 DOI: 10.1016/j.nmd.2015.12.001  0.4
2015 Wojtal D, Kemaladewi DU, Malam Z, Abdullah S, Wong TW, Hyatt E, Baghestani Z, Pereira S, Stavropoulos J, Mouly V, Mamchaoui K, Muntoni F, Voit T, Gonorazky HD, Dowling JJ, ... ... Cohn RD, et al. Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders. American Journal of Human Genetics. PMID 26686765 DOI: 10.1016/j.ajhg.2015.11.012  0.4
2015 Fleming L, Lemmon M, Beck N, Johnson M, Mu W, Murdock D, Bodurtha J, Hoover-Fong J, Cohn R, Bosemani T, Barañano K, Hamosh A. Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy. American Journal of Medical Genetics. Part A. PMID 26394714 DOI: 10.1002/ajmg.a.37369  0.4
2015 Oskoui M, Gazzellone MJ, Thiruvahindrapuram B, Zarrei M, Andersen J, Wei J, Wang Z, Wintle RF, Marshall CR, Cohn RD, Weksberg R, Stavropoulos DJ, Fehlings D, Shevell MI, Scherer SW. Clinically relevant copy number variations detected in cerebral palsy. Nature Communications. 6: 7949. PMID 26236009 DOI: 10.1038/ncomms8949  0.4
2015 Marshall CR, Farrell SA, Cushing D, Paton T, Stockley TL, Stavropoulos DJ, Ray PN, Szego M, Lau L, Pereira SL, Cohn RD, Wintle RF, Abuzenadah AM, Abu-Elmagd M, Scherer SW. 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. PMID 25923536 DOI: 10.1186/1471-2164-16-S1-S12  0.4
2015 Dubowitz V, Cohn RD. Dystrophin and Duchenne dystrophy. Neuromuscular Disorders : Nmd. 25: 361-2. PMID 25890834 DOI: 10.1016/j.nmd.2015.03.013  0.4
2014 Malam Z, Cohn RD. Stem cells on alert: priming quiescent stem cells after remote injury. Cell Stem Cell. 15: 7-8. PMID 24996163 DOI: 10.1016/j.stem.2014.06.012  0.4
2014 Bowdin S, Ray PN, Cohn RD, Meyn MS. The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical care. Human Mutation. 35: 513-9. PMID 24599881 DOI: 10.1002/humu.22536  0.4
2014 Auer DR, Sysa-Shah P, Bedja D, Simmers JL, Pak E, Dutra A, Cohn R, Gabrielson KL, Chakravarti A, Kapoor A. Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse. Biotechnology Letters. 36: 1179-85. PMID 24563304 DOI: 10.1007/s10529-014-1473-x  0.4
2014 MacDonald EM, Andres-Mateos E, Mejias R, Simmers JL, Mi R, Park JS, Ying S, Hoke A, Lee SJ, Cohn RD. Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition. Disease Models & Mechanisms. 7: 471-81. PMID 24504412 DOI: 10.1242/dmm.014126  0.4
2014 Ivakine EA, Cohn RD. Maintaining skeletal muscle mass: lessons learned from hibernation. Experimental Physiology. 99: 632-7. PMID 24443348 DOI: 10.1113/expphysiol.2013.074344  0.4
2013 Xu R, Andres-Mateos E, Mejias R, MacDonald EM, Leinwand LA, Merriman DK, Fink RH, Cohn RD. Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilization. Experimental Neurology. 247: 392-401. PMID 23333568 DOI: 10.1016/j.expneurol.2013.01.005  0.4
2013 Andres-Mateos E, Brinkmeier H, Burks TN, Mejias R, Files DC, Steinberger M, Soleimani A, Marx R, Simmers JL, Lin B, Finanger Hedderick E, Marr TG, Lin BM, Hourdé C, Leinwand LA, ... ... Cohn RD, et al. Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy. Embo Molecular Medicine. 5: 80-91. PMID 23161797 DOI: 10.1002/emmm.201201443  0.4
2012 Cohn RD. Stem cells in severe infantile spinal muscular atrophy (SMA1). Neuromuscular Disorders : Nmd. 22: 1106-7. PMID 23206851 DOI: 10.1016/j.nmd.2012.10.023  0.4
2012 Andres-Mateos E, Mejias R, Soleimani A, Lin BM, Burks TN, Marx R, Lin B, Zellars RC, Zhang Y, Huso DL, Marr TG, Leinwand LA, Merriman DK, Cohn RD. Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels. Plos One. 7: e48884. PMID 23155423 DOI: 10.1371/journal.pone.0048884  0.4
2012 MacDonald EM, Cohn RD. TGFβ signaling: its role in fibrosis formation and myopathies. Current Opinion in Rheumatology. 24: 628-34. PMID 22918531 DOI: 10.1097/BOR.0b013e328358df34  0.4
2012 Files DC, D'Alessio FR, Johnston LF, Kesari P, Aggarwal NR, Garibaldi BT, Mock JR, Simmers JL, DeGorordo A, Murdoch J, Willis MS, Patterson C, Tankersley CG, Messi ML, Liu C, ... ... Cohn RD, et al. A critical role for muscle ring finger-1 in acute lung injury-associated skeletal muscle wasting. American Journal of Respiratory and Critical Care Medicine. 185: 825-34. PMID 22312013 DOI: 10.1164/rccm.201106-1150OC  0.4
2011 Burks TN, Cohn RD. One size may not fit all: anti-aging therapies and sarcopenia. Aging. 3: 1142-53. PMID 22184279  0.4
2011 Abadir PM, Foster DB, Crow M, Cooke CA, Rucker JJ, Jain A, Smith BJ, Burks TN, Cohn RD, Fedarko NS, Carey RM, O'Rourke B, Walston JD. Identification and characterization of a functional mitochondrial angiotensin system. Proceedings of the National Academy of Sciences of the United States of America. 108: 14849-54. PMID 21852574 DOI: 10.1073/pnas.1101507108  0.4
2011 Burks TN, Cohn RD. Role of TGF-β signaling in inherited and acquired myopathies. Skeletal Muscle. 1: 19. PMID 21798096 DOI: 10.1186/2044-5040-1-19  0.4
2011 Burks TN, Andres-Mateos E, Marx R, Mejias R, Van Erp C, Simmers JL, Walston JD, Ward CW, Cohn RD. Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia. Science Translational Medicine. 3: 82ra37. PMID 21562229 DOI: 10.1126/scitranslmed.3002227  0.4
2011 Holm TM, Habashi JP, Doyle JJ, Bedja D, Chen Y, van Erp C, Lindsay ME, Kim D, Schoenhoff F, Cohn RD, Loeys BL, Thomas CJ, Patnaik S, Marugan JJ, Judge DP, et al. Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice. Science (New York, N.Y.). 332: 358-61. PMID 21493862 DOI: 10.1126/science.1192149  0.4
2011 Lisi EC, Cohn RD. Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature. Developmental Medicine and Child Neurology. 53: 586-99. PMID 21418198 DOI: 10.1111/j.1469-8749.2011.03918.x  0.4
2011 Finanger Hedderick EL, Simmers JL, Soleimani A, Andres-Mateos E, Marx R, Files DC, King L, Crawford TO, Corse AM, Cohn RD. Loss of sarcolemmal nNOS is common in acquired and inherited neuromuscular disorders. Neurology. 76: 960-7. PMID 21403107 DOI: 10.1212/WNL.0b013e31821043c8  0.4
2011 Cohn RD. Muscle cramps and coffee Neuromuscular Disorders. 21: 311. PMID 21377365 DOI: 10.1016/j.nmd.2011.02.011  0.4
2010 Wang CH, Bonnemann CG, Rutkowski A, Sejersen T, Bellini J, Battista V, Florence JM, Schara U, Schuler PM, Wahbi K, Aloysius A, Bash RO, Béroud C, Bertini E, Bushby K, ... Cohn RD, et al. Consensus statement on standard of care for congenital muscular dystrophies. Journal of Child Neurology. 25: 1559-81. PMID 21078917 DOI: 10.1177/0883073810381924  0.4
2010 Lee SJ, Lee YS, Zimmers TA, Soleimani A, Matzuk MM, Tsuchida K, Cohn RD, Barton ER. Regulation of muscle mass by follistatin and activins. Molecular Endocrinology (Baltimore, Md.). 24: 1998-2008. PMID 20810712 DOI: 10.1210/me.2010-0127  0.4
2008 Cheng TL, Cohn RD, Dover GJ. The genetics revolution and primary care pediatrics. Jama. 299: 451-3. PMID 18230784 DOI: 10.1001/jama.299.4.451  0.4
2007 Cohn RD, van Erp C, Habashi JP, Soleimani AA, Klein EC, Lisi MT, Gamradt M, ap Rhys CM, Holm TM, Loeys BL, Ramirez F, Judge DP, Ward CW, Dietz HC. Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states. Nature Medicine. 13: 204-10. PMID 17237794 DOI: 10.1038/nm1536  0.4
2006 Cohn RD, Eklund E, Bergner AL, Casella JF, Woods SL, Althaus J, Blakemore KJ, Fox HE, Hoover-Fong JE, Hamosh A, Braverman NE, Freeze HH, Boyadjiev SA. Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation. Pediatrics. 118: e514-21. PMID 16816004 DOI: 10.1542/peds.2005-1307  0.4
2006 Habashi JP, Judge DP, Holm TM, Cohn RD, Loeys BL, Cooper TK, Myers L, Klein EC, Liu G, Calvi C, Podowski M, Neptune ER, Halushka MK, Bedja D, Gabrielson K, et al. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome. Science (New York, N.Y.). 312: 117-21. PMID 16601194 DOI: 10.1126/science.1124287  0.4
2004 Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nature Medicine. 10: 696-703. PMID 15184894 DOI: 10.1038/nm1059  0.4
2003 Saito F, Moore SA, Barresi R, Henry MD, Messing A, Ross-Barta SE, Cohn RD, Williamson RA, Sluka KA, Sherman DL, Brophy PJ, Schmelzer JD, Low PA, Wrabetz L, Feltri ML, et al. Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization. Neuron. 38: 747-58. PMID 12797959 DOI: 10.1016/S0896-6273(03)00301-5  0.4
2002 Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP. Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration. Cell. 110: 639-48. PMID 12230980 DOI: 10.1016/S0092-8674(02)00907-8  0.4
2002 Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature. 418: 422-5. PMID 12140559 DOI: 10.1038/nature00838  0.4
2002 Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature. 418: 417-22. PMID 12140558 DOI: 10.1038/nature00837  0.4
Low-probability matches
2019 Erwood S, Brewer RA, Bily TMI, Maino E, Zhou L, Cohn RD, Ivakine EA. Modeling Niemann-Pick disease type C in a human haploid cell line allows for patient variant characterization and clinical interpretation. Genome Research. 29: 2010-2019. PMID 31754021 DOI: 10.1101/gr.250720.119  0.01
2019 Wang Y, Gallant RC, Neves MAD, Lei X, Gupta S, Coelho R, Wong T, Cohn RD, Campbell KP, Ni H. Alpha-Dystroglycan Supports Platelet Aggregation and Thrombus Formation. Blood. 134: 11. PMID 31724005 DOI: 10.1182/blood-2019-131521  0.01
2019 Garcia B, Lee J, Edraki A, Hidalgo-Reyes Y, Erwood S, Mir A, Trost CN, Seroussi U, Stanley SY, Cohn RD, Claycomb JM, Sontheimer EJ, Maxwell KL, Davidson AR. Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing. Cell Reports. 29: 1739-1746.e5. PMID 31722192 DOI: 10.1016/j.celrep.2019.10.017  0.01
2019 Kemaladewi DU, Bassi PS, Erwood S, Al-Basha D, Gawlik KI, Lindsay K, Hyatt E, Kember R, Place KM, Marks RM, Durbeej M, Prescott SA, Ivakine EA, Cohn RD. A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene. Nature. PMID 31341277 DOI: 10.1038/s41586-019-1430-x  0.01
2019 Gonorazky HD, Naumenko S, Ramani AK, Nelakuditi V, Mashouri P, Wang P, Kao D, Ohri K, Viththiyapaskaran S, Tarnopolsky MA, Mathews KD, Moore SA, Osorio AN, Villanova D, Kemaladewi DU, ... Cohn RD, et al. Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease. American Journal of Human Genetics. 104: 1007. PMID 31051109 DOI: 10.1016/j.ajhg.2019.04.004  0.01
2019 Borlot F, Whitney R, Cohn RD, Weiss SK. MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature review. Seizure. PMID 30922778 DOI: 10.1016/j.seizure.2019.03.015  0.01
2019 Gonorazky HD, Naumenko S, Ramani AK, Nelakuditi V, Mashouri P, Wang P, Kao D, Ohri K, Viththiyapaskaran S, Tarnopolsky MA, Mathews KD, Moore SA, Osorio AN, Villanova D, Kemaladewi DU, ... Cohn RD, et al. Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease. American Journal of Human Genetics. PMID 30827497 DOI: 10.1016/j.ajhg.2019.01.012  0.01
2019 Cohn RD. Letter to the Editor. Forensic Science International. PMID 30665690 DOI: 10.1016/j.forsciint.2019.01.002  0.01
2018 Cordeiro D, Bullivant G, Siriwardena K, Evans A, Kobayashi J, Cohn RD, Mercimek-Andrews S. Genetic landscape of pediatric movement disorders and management implications. Neurology. Genetics. 4: e265. PMID 30283815 DOI: 10.1212/NXG.0000000000000265  0.01
2018 Cordeiro D, Bullivant G, Cohn RD, Raiman J, Mercimek-Andrews S. Outcome of Patients With Inherited Neurotransmitter Disorders. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-6. PMID 30109838 DOI: 10.1017/cjn.2018.266  0.01
2018 Cohn I, Cohn RD, Ito S. Professional opportunity for pharmacists to integrate pharmacogenomics in medication therapy. Canadian Pharmacists Journal : Cpj = Revue Des Pharmaciens Du Canada : Rpc. 151: 167-169. PMID 29796128 DOI: 10.1177/1715163518766376  0.01
2018 Shabanova I, Cohen E, Cada M, Vincent A, Cohn RD, Dror Y. ERCC6L2-associated inherited bone marrow failure syndrome. Molecular Genetics & Genomic Medicine. PMID 29633571 DOI: 10.1002/mgg3.388  0.01
2018 Costain G, Jobling R, Walker S, Reuter MS, Snell M, Bowdin S, Cohn RD, Dupuis L, Hewson S, Mercimek-Andrews S, Shuman C, Sondheimer N, Weksberg R, Yoon G, Meyn MS, et al. Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing. European Journal of Human Genetics : Ejhg. PMID 29453418 DOI: 10.1038/s41431-018-0114-6  0.01
2018 Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, ... ... Cohn RD, et al. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 190: E126-E136. PMID 29431110 DOI: 10.1503/cmaj.171151  0.01
2017 Cohn I, Paton TA, Marshall CR, Basran R, Stavropoulos DJ, Ray PN, Monfared N, Hayeems RZ, Meyn MS, Bowdin S, Scherer SW, Cohn RD, Ito S. Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study. Npj Genomic Medicine. 2: 19. PMID 29263831 DOI: 10.1038/s41525-017-0021-8  0.01
2017 Wong TWY, Cohn RD. Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy. Current Gene Therapy. PMID 29173172 DOI: 10.2174/1566523217666171121165046  0.01
2017 Hayeems RZ, Bhawra J, Tsiplova K, Meyn MS, Monfared N, Bowdin S, Stavropoulos DJ, Marshall CR, Basran R, Shuman C, Ito S, Cohn I, Hum C, Girdea M, Brudno M, ... Cohn RD, et al. Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. European Journal of Human Genetics : Ejhg. PMID 29158552 DOI: 10.1038/s41431-017-0020-3  0.01
2017 Dowling JJ, D Gonorazky H, Cohn RD, Campbell C. Treating pediatric neuromuscular disorders: The future is now. American Journal of Medical Genetics. Part A. PMID 28889642 DOI: 10.1002/ajmg.a.38418  0.01
2017 Reijnders MRF, Ansor NM, Kousi M, Yue WW, Tan PL, Clarkson K, Clayton-Smith J, Corning K, Jones JR, Lam WWK, Mancini GMS, Marcelis C, Mohammed S, Pfundt R, Roifman M, ... Cohn R, et al. RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. American Journal of Human Genetics. 101: 466-477. PMID 28886345 DOI: 10.1016/j.ajhg.2017.08.007  0.01
2017 Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, Thiruvahindrapuram B, Merico D, Jobling R, Nalpathamkalam T, Pellecchia G, Sung WWL, Wang Z, Bikangaga P, Boelman C, ... ... Cohn RD, et al. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28771251 DOI: 10.1038/gim.2017.119  0.01
2017 Kemaladewi DU, Maino E, Hyatt E, Hou H, Ding M, Place KM, Zhu X, Bassi P, Baghestani Z, Deshwar AG, Merico D, Xiong HY, Frey BJ, Wilson MD, Ivakine EA, ... Cohn RD, et al. Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism. Nature Medicine. PMID 28714989 DOI: 10.1038/nm.4367  0.01
2017 Oei K, Hayeems RZ, Ungar WJ, Cohn RD, Cohen E. Genetic Testing among Children in a Complex Care Program. Children (Basel, Switzerland). 4. PMID 28531152 DOI: 10.3390/children4050042  0.01
2017 Zou Y, Donkervoort S, Salo AM, Reghan Foley A, Barnes AM, Hu Y, Makareeva E, Leach ME, Mohassel P, Dastgir J, Deardorff MA, Cohn RD, DiNonno WO, Malfait F, Lek M, et al. P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye. Human Molecular Genetics. PMID 28419360 DOI: 10.1093/hmg/ddx110  0.01
2017 Schoch K, Meng L, Szelinger S, Bearden DR, Stray-Pedersen A, Busk OL, Stong N, Liston E, Cohn RD, Scaglia F, Rosenfeld JA, Tarpinian J, Skraban CM, Deardorff MA, Friedman JN, et al. A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay. American Journal of Human Genetics. PMID 28132692 DOI: 10.1016/j.ajhg.2016.12.013  0.01
2017 Al Teneiji A, Bruun TU, Sidky S, Cordeiro D, Cohn RD, Mendoza-Londono R, Moharir M, Raiman J, Siriwardena K, Kyriakopoulou L, Mercimek-Mahmutoglu S. Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II. Molecular Genetics and Metabolism. PMID 28122681 DOI: 10.1016/j.ymgme.2016.12.014  0.01
2016 Stavropoulos DJ, Merico D, Jobling R, Bowdin S, Monfared N, Thiruvahindrapuram B, Nalpathamkalam T, Pellecchia G, Yuen RKC, Szego MJ, Hayeems RZ, Shaul RZ, Brudno M, Girdea M, Frey B, ... ... Cohn RD, et al. Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine. Npj Genomic Medicine. 1. PMID 28567303 DOI: 10.1038/npjgenmed.2015.12  0.01
2016 Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, ... ... Cohn RD, et al. Recommendations for the integration of genomics into clinical practice. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27171546 DOI: 10.1038/gim.2016.17  0.01
2016 Kemaladewi DU, Cohn RD. Exon Snipping in Duchenne Muscular Dystrophy. Trends in Molecular Medicine. 22: 187-9. PMID 26856237 DOI: 10.1016/j.molmed.2016.01.007  0.01
2016 Yoon G, Malam Z, Paton T, Marshall CR, Hyatt E, Ivakine Z, Scherer SW, Lee KS, Hawkins C, Cohn RD. Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L. The Journal of Pediatrics. PMID 26825290 DOI: 10.1016/j.jpeds.2015.12.060  0.01
2016 Gonorazky H, Liang M, Cummings B, Lek M, Micallef J, Hawkins C, Basran R, Cohn R, Wilson MD, MacArthur D, Marshall CR, Ray PN, Dowling JJ. RNAseq analysis for the diagnosis of muscular dystrophy. Annals of Clinical and Translational Neurology. 3: 55-60. PMID 26783550 DOI: 10.1002/acn3.267  0.01
2012 Gupta A, Bembea M, Brown A, Robertson C, Romer L, Cohn RD. Respiratory failure secondary to human metapneumovirus requiring extracorporeal membrane oxygenation in a 32-month-old child. Case Reports in Pediatrics. 2012: 268074. PMID 22675646 DOI: 10.1155/2012/268074  0.01
2010 Cohn RD. Best practice in Duchenne dystrophy. Neuromuscular Disorders : Nmd. 20: 292. PMID 20371092 DOI: 10.1016/j.nmd.2010.03.012  0.01
2009 Goo MJ, Ki MR, Lee HR, Yang HJ, Yuan DW, Hong IH, Park JK, Hong KS, Han JY, Hwang OK, Kim DH, Do SH, Cohn RD, Jeong KS. Helicobacter pylori promotes hepatic fibrosis in the animal model. Laboratory Investigation; a Journal of Technical Methods and Pathology. 89: 1291-303. PMID 19736546 DOI: 10.1038/labinvest.2009.90  0.01
2009 Fontana S, Cohn RD. SP-litting the satellite niche to repopulate muscle. Cell Stem Cell. 4: 194-5. PMID 19265654 DOI: 10.1016/j.stem.2009.02.002  0.01
2007 Cohn RD, Liang HY, Shetty R, Abraham T, Wagner KR. Myostatin does not regulate cardiac hypertrophy or fibrosis. Neuromuscular Disorders : Nmd. 17: 290-6. PMID 17336525 DOI: 10.1016/j.nmd.2007.01.011  0.01
2007 Lisi MT, Cohn RD. Congenital muscular dystrophies: new aspects of an expanding group of disorders. Biochimica Et Biophysica Acta. 1772: 159-72. PMID 17097859 DOI: 10.1016/j.bbadis.2006.09.006  0.01
2006 Peddy SB, Vricella LA, Crosson JE, Oswald GL, Cohn RD, Cameron DE, Valle D, Loeys BL. Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene. Pediatrics. 117: 1830-3. PMID 16651346 DOI: 10.1542/peds.2005-2301  0.01
2005 Cohn RD. Dystroglycan: important player in skeletal muscle and beyond. Neuromuscular Disorders : Nmd. 15: 207-17. PMID 15725582 DOI: 10.1016/j.nmd.2004.11.005  0.01
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