Follow
Richard T Wang
Title
Cited by
Cited by
Year
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
H Lee, AY Huang, L Wang, AJ Yoon, G Renteria, A Eskin, RH Signer, ...
Genetics in Medicine 22 (3), 490-499, 2020
1492020
Achieving effective treatment of patients with chronic psychotic illness and comorbid substance dependence
AP Ho, JW Tsuang, RP Liberman, R Wang, JN Wilkins, TA Eckman, ...
American Journal of Psychiatry 156 (11), 1765-1770, 1999
1431999
Dantrolene enhances antisense-mediated exon skipping in human and mouse models of Duchenne muscular dystrophy
GC Kendall, EI Mokhonova, M Moran, NE Sejbuk, DW Wang, O Silva, ...
Science translational medicine 4 (164), 164ra160-164ra160, 2012
1192012
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
H Barseghyan, W Tang, RT Wang, M Almalvez, E Segura, MS Bramble, ...
Genome medicine 9 (1), 1-11, 2017
1052017
A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes
A Lin, RT Wang, S Ahn, CC Park, DJ Smith
Genome research 20 (8), 1122-1132, 2010
1002010
DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation …
RT Wang, F Barthelemy, AS Martin, ED Douine, A Eskin, A Lucas, ...
Human mutation 39 (9), 1193-1202, 2018
772018
Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids
CC Park, S Ahn, JS Bloom, A Lin, RT Wang, T Wu, A Sekar, AH Khan, ...
Nature genetics 40 (4), 421, 2008
412008
Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids
CC Park, S Ahn, JS Bloom, A Lin, RT Wang, T Wu, A Sekar, AH Khan, ...
Nature genetics 40 (4), 421, 2008
412008
Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids
CC Park, S Ahn, JS Bloom, A Lin, RT Wang, T Wu, A Sekar, AH Khan, ...
Nature genetics 40 (4), 421, 2008
412008
Online Self-Report Data for Duchenne Muscular Dystrophy Confirms Natural History and Can Be Used to Assess for Therapeutic Benefits
RT Wang, CAS Fadlon, JW Ulm, I Jankovic, A Eskin, A Lu, VR Miller, ...
Plos Currents Muscular Dystrophy, 2014
402014
Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factors
KJ Counterman, P Furlong, RT Wang, AS Martin
Muscle & Nerve 61 (1), 36-43, 2020
292020
Directed mammalian gene regulatory networks using expression and comparative genomic hybridization microarray data from radiation hybrids
S Ahn, RT Wang, CC Park, A Lin, RM Leahy, K Lange, DJ Smith
PLoS computational biology 5 (6), e1000407, 2009
242009
A well‐tolerated core needle muscle biopsy process suitable for children and adults
F Barthelemy, JD Woods, S Nieves‐Rodriguez, ED Douine, R Wang, ...
Muscle & Nerve 62 (6), 688-698, 2020
222020
Effects of genome-wide copy number variation on expression in mammalian cells
RT Wang, S Ahn, CC Park, AH Khan, K Lange, DJ Smith
BMC genomics 12, 1-15, 2011
182011
Targeting RyR Activity Boosts Antisense Exon 44 and 45 Skipping in Human DMD Skeletal or Cardiac Muscle Culture Models
F Barthélémy, RT Wang, C Hsu, ED Douine, EE Marcantonio, SF Nelson, ...
Molecular Therapy-Nucleic Acids 18, 580-589, 2019
172019
Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue
DD Scripture-Adams, KN Chesmore, F Barthélémy, RT Wang, ...
Communications Biology 5 (1), 989, 2022
152022
What Can DuchenneConnect Teach Us About Treating Duchenne Muscular Dystrophy?
RT Wang, SF Nelson
Current opinion in neurology 28 (5), 535, 2015
112015
Undiagnosed Diseases Network. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
H Lee, AY Huang, LK Wang, AJ Yoon, G Renteria, A Eskin, RH Signer, ...
Genet Med 22 (3), 490-499, 2020
102020
Undiagnosed Diseases Network, Palmer CGS, Martinez-Agosto JA, Nelson SF. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
H Lee, AY Huang, LK Wang, AJ Yoon, G Renteria, A Eskin, RH Signer, ...
Genet Med 22 (3), 490-499, 2020
102020
Evaluating genetic modifiers of Duchenne muscular dystrophy disease progression using modeling and MRI
AM Barnard, DW Hammers, WT Triplett, S Kim, SC Forbes, RJ Willcocks, ...
Neurology 99 (21), e2406-e2416, 2022
62022
The system can't perform the operation now. Try again later.
Articles 1–20