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Kshitiz Singh
Kshitiz Singh
Primary: Queen's University, Canada. Other affiliations: The Children's Hospital of Philadelphia
Verified email at queensu.ca - Homepage
Title
Cited by
Cited by
Year
In utero CRISPR-mediated therapeutic editing of metabolic genes
AC Rossidis, JD Stratigis, AC Chadwick, HA Hartman, NJ Ahn, H Li, ...
Nature medicine 24 (10), 1513-1518, 2018
2002018
In utero gene editing for monogenic lung disease
D Alapati, WJ Zacharias, HA Hartman, AC Rossidis, JD Stratigis, NJ Ahn, ...
Science translational medicine 11 (488), eaav8375, 2019
882019
Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells
S Dastidar, S Ardui, K Singh, D Majumdar, N Nair, Y Fu, D Reyon, ...
Nucleic acids research 46 (16), 8275-8298, 2018
882018
Efficient in vivo liver-directed gene editing using CRISPR/Cas9
K Singh, H Evens, N Nair, MY Rincón, S Sarcar, E Samara-Kuko, ...
Molecular Therapy 26 (5), 1241-1254, 2018
762018
In Utero Adenine Base Editing Corrects Multi-Organ Pathology in a Lethal Lysosomal Storage Disease
KS Sourav K., Brandon M. White, Meghana V. Kashyap, Apeksha Dave, Felix R ...
Nature Communications 12 (1), 2021
432021
Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytes
S Dastidar, D Majumdar, J Tipanee, K Singh, AF Klein, D Furling, ...
Molecular Therapy 30 (1), 75-91, 2022
132022
Combined targeting of EGFR/HER promotes anti-tumor efficacy in subsets of KRAS mutant lung cancer resistant to single EGFR blockade
IA Umelo, O De Wever, P Kronenberger, J Van Deun, A Noor, K Singh, ...
Oncotarget 6 (24), 20132, 2015
102015
Hemophilia gene therapy: the end of the beginning?
D De Wolf, K Singh, MK Chuah, T VandenDriessche
Human Gene Therapy 34 (17-18), 782-792, 2023
62023
In utero gene editing for monogenic lung disease. Sci Transl Med 11
D Alapati, WJ Zacharias, HA Hartman, AC Rossidis, JD Stratigis, NJ Ahn, ...
52019
AZ-3102 significantly increases survival and decreases neuroinflammation in a mouse model of Sandhoff disease
K Landskroner, K Singh, M Mitchell, J Walia
Molecular Genetics and Metabolism 138 (2), 107193, 2023
12023
Gene Expression Profile in the Sandhoff Mouse Brain with Progression of Age
K Singh, BM Quinville, M Mitchell, Z Chen, JS Walia
Genes 13 (11), 2020, 2022
12022
CRISPR/Cas9-mediated editing for dominant genetic disorders: efficient excision of trinucleotide repeat expansion in myotonic dystrophy
S Dastidar, S Ardui, K Singh, N Nair, Y Fu, D Reyon, E Samara, MFM Gerli, ...
Human Gene Therapy 28 (12), A7-A7, 2017
12017
Prenatal Interventions for the Treatment of Congenital Disorders
K Singh
Regenerative Medicine, 259–268, 2023
2023
Liver-directed gene editing with crispr-cas9: Comprehensive on-target and off-target analyses
K Singh
2023
Efficient In utero RNA lipid nanoparticle-mediated gene editing for correction of type 1 tyrosinemia without the AAV-associated genotoxicity
K Singh, R Riley, M Kashyap, B White, S Bose, H Li, A Dave, R Palanki, ...
HUMAN GENE THERAPY 32 (19-20), A68-A68, 2021
2021
In Utero Lipid Nanoparticle Delivery of CRISPR Technology to Correct Hereditary Tyrosinemia Type 1
K Singh, RS Riley, MVV Kashyap, B White, SK Bose, H Li, R Palanki, ...
MOLECULAR THERAPY 29 (4), 10-10, 2021
2021
Molecular Tools for Editing Globin Genes
K Singh
Fetal Hemoglobin: The Panacea for Major β-Hemoglobinopathies, 2020
2020
IN UTERO GENE EDITING FOR MONOGENIC LUNG DISEASE
WJ ZACHARIAS, S ZHOU, J KATZEN, Y TOMER, AC CHADWICK, ...
SCIENCE TRANSLATIONAL MEDICINE 11 (488), 2019
2019
Truncated gRNAs result in efficient in vivo liver-directed gene inactivation using CRISPR/Cas9
K Singh, H Evens, N Nair, MY Rincon, S Sarcar, E Samara, MK Chuah, ...
Human Gene Therapy 29 (12), A112-A112, 2018
2018
CRISPR/Cas9-Mediated Editing of Trinucleotide Repeat Expansion in Myotonic Dystrophy
S Dastidar, K Singh, N Nair, Y Fu, D Reyon, E Samara, MFM Gerli, ...
Molecular Therapy 25 (5), 85-85, 2017
2017
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