Ronald D Cohn (Ronald Cohn)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Histone Deacetylase

Muscular Dystrophy

Top Venues

Nature medicine

European journal of human genetics : EJHG

Nature biotechnology

Genome research

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaona Lu, Kim Ng, Filippo Pinto E Vairo, James Collins, Ronald D Cohn, Kacie Riley, Katherine Agre, Ralitza Gavrilova, Eric W Klee, Jill Anne Rosenfeld, Yong-Hui Jiang
Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European journal of human genetics : EJHG (2024)
Xiaona Lu, Kim Ng, Filippo Pinto E Vairo, James Collins, Ronald D Cohn, Kacie Riley, Katherine Agre, Ralitza Gavrilova, Eric W Klee, Jill Anne Rosenfeld, Yong-Hui Jiang
Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European journal of human genetics : EJHG 32 (7) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Xiaona Lu, Kim Ng, Filippo Pinto E Vairo, James Collins, Ronald D Cohn, Kacie Riley, Katherine Agre, Ralitza Gavrilova, Eric W Klee, Jill Anne Rosenfeld, Yong-Hui Jiang
Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European journal of human genetics : EJHG 32 (7) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Ryan M Marks, Ori Scott, Evgueni A Ivakine, Ronald D Cohn
An optimized toolkit for prime editing. Nature biotechnology (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Ryan M Marks, Ori Scott, Evgueni A Ivakine, Ronald D Cohn
An optimized toolkit for prime editing. Nature biotechnology 42 (2) (2024)
Lucie O M Perillat, Tatianna W Y Wong, Eleonora Maino, Abdalla Ahmed, Ori Scott, Elzbieta Hyatt, Paul Delgado-Olguin, Shagana Visuvanathan, Evgueni A Ivakine, Ronald D Cohn
Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55. Disease models & mechanisms (2024)
Ryan M Marks, Ori Scott, Evgueni A Ivakine, Ronald D Cohn
An optimized toolkit for prime editing. Nature biotechnology 42 (2) (2024)
Xiaona Lu, Kim Ng, Filippo Pinto E Vairo, James Collins, Ronald D Cohn, Kacie Riley, Katherine Agre, Ralitza Gavrilova, Eric W Klee, Jill Anne Rosenfeld, Yong-Hui Jiang
Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European journal of human genetics : EJHG 32 (7) (2024)
Xiaona Lu, Kim Ng, Filippo Pinto E Vairo, James Collins, Ronald D Cohn, Kacie Riley, Katherine Agre, Ralitza Gavrilova, Eric W Klee, Jill Anne Rosenfeld, Yong-Hui Jiang
Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European journal of human genetics : EJHG 32 (7) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine (2024)
Eleonora Maino, Daria Wojtal, Sonia L Evagelou, Aiman Farheen, Tatianna W Y Wong, Kyle Lindsay, Ori Scott, Samar Z Rizvi, Elzbieta Hyatt, Matthew Rok, Shagana Visuvanathan, Amanda Chiodo, Michelle Schneeweiss, Evgueni A Ivakine, Ronald D Cohn
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression. EMBO molecular medicine 13 (5) (2021)
Steven Erwood, Reid A Brewer, Teija M I Bily, Eleonora Maino, Liangchi Zhou, Ronald D Cohn, Evgueni A Ivakine
Modeling Niemann-Pick disease type C in a human haploid cell line allows for patient variant characterization and clinical interpretation. Genome research 29 (12) (2019)