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P. Trifillis · SciRah

Researcher profile · Semantic Scholar

P. Trifillis

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P. Trifillis — researcher profile on SciRah

h-index: 19
Works: 62
Citations: 3,050

Most-cited papers

PTC124 targets genetic disorders caused by nonsense mutations
E. Welch, E. R. Barton, Jin Zhuo, Y. Tomizawa +38 more
2007Nature1,159 citations
Semantic Scholar
SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy
N. Naryshkin, M. Weetall, A. Dakka, J. Narasimhan +44 more
2014Science455 citations
Semantic Scholar
An mRNA Stability Complex Functions with Poly(A)-Binding Protein To Stabilize mRNA In Vitro
Zuo-Ren Wang, N. Day, P. Trifillis, M. Kiledjian
1999Molecular and Cellular Biology286 citations Open access
Semantic Scholar
Characterization of the biochemical properties of the human Upf1 gene product that is involved in nonsense-mediated mRNA decay.
A. Bhattacharya, K. Czaplinski, P. Trifillis, F. He +2 more
2000RNA: A publication of the RNA Society196 citations Open access
Semantic Scholar
Natural History and Real‐World Data in Rare Diseases: Applications, Limitations, and Future Perspectives
Jing Liu, Jeffrey S. Barrett, Efthimia Leonardi, L. Lee +3 more
2022Journal of clinical pharmacology127 citations Open access
Semantic Scholar
Identification of Target Messenger RNA Substrates for the Murine Deleted in Azoospermia-Like RNA-Binding Protein1
Xinfu Jiao, P. Trifillis, M. Kiledjian
2002Biology of Reproduction100 citations
Semantic Scholar
Safety and effectiveness of ataluren: comparison of results from the STRIDE Registry and CINRG DMD Natural History Study
E. Mercuri, F. Muntoni, A. N. Osorio, M. Tulinius +11 more
2020Journal of Comparative Effectiveness Research94 citations Open access
Semantic Scholar
Deflazacort versus prednisone/prednisolone for maintaining motor function and delaying loss of ambulation: A post HOC analysis from the ACT DMD trial
P. Shieh, J. Mcintosh, Fengbin Jin, Marcio Souza +6 more
2018Muscle and Nerve57 citations Open access
Semantic Scholar
Ataluren delays loss of ambulation and respiratory decline in nonsense mutation Duchenne muscular dystrophy patients
C. McDonald, F. Muntoni, V. Penematsa, Joel Jiang +10 more
2021Journal of Comparative Effectiveness Research55 citations Open access
Semantic Scholar
Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy.
C. Campbell, R. Barohn, E. Bertini, B. Chabrol +31 more
2020Journal of Comparative Effectiveness Research55 citations Open access
Semantic Scholar
Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis.
P. Trifillis, P. Ioannou, E. Schwartz, Saul Surrey
1991Blood52 citations Open access
Semantic Scholar
Finding the right RNA: identification of cellular mRNA substrates for RNA-binding proteins.
P. Trifillis, N. Day, M. Kiledjian
1999RNA: A publication of the RNA Society50 citations Open access
Semantic Scholar
Different hematological phenotypes caused by the interaction of triplicated α‐globin genes and heterozygous β‐thalassemia
C. Camaschella, A. Kattamis, D. Petroni, A. Roetto +7 more
199749 citations Open access
Semantic Scholar
Safety and effectiveness of ataluren in patients with nonsense mutation DMD in the STRIDE Registry compared with the CINRG Duchenne Natural History Study (2015–2022): 2022 interim analysis
E. Mercuri, A. N. Osorio, F. Muntoni, F. Buccella +12 more
2023Journal of Neurology48 citations Open access
Semantic Scholar
Ataluren use in patients with nonsense mutation Duchenne muscular dystrophy: patient demographics and characteristics from the STRIDE Registry.
F. Muntoni, I. Desguerre, M. Guglieri, A. N. Osorio +11 more
2019Journal of Comparative Effectiveness Research35 citations Open access
Semantic Scholar
Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.
C. Camaschella, A. Kattamis, D. Petroni, A. Roetto +7 more
1997American journal of hematology/oncology26 citations
Semantic Scholar
Analysis of delta-globin gene mutations in Greek cypriots.
P. Trifillis, A. Kyrri, E. Kalogirou, A. Kokkofitou +3 more
1993Blood23 citations Open access
Semantic Scholar
Analysis of 5' flanking regions of the gamma globin genes from major African haplotype backgrounds associated with sickle cell disease.
S. Month, R. Wood, P. Trifillis, P. Orchowski +4 more
1990Journal of Clinical Investigation23 citations Open access
Semantic Scholar
Purification and RNA Binding Properties of the Polycytidylate-Binding Proteins αCP1 and αCP2
M. Kiledjian, N. Day, P. Trifillis
199922 citations
Semantic Scholar
Discovery of Novel Small Molecule Inhibitors of VEGF Expression in Tumor Cells Using a Cell-Based High Throughput Screening Platform
Liang-Xian Cao, M. Weetall, J. Bombard, H. Qi +14 more
2016PLoS ONE19 citations Open access
Semantic Scholar
Longitudinal Evaluation of Working Memory in Duchenne Muscular Dystrophy
M. Thangarajh, G. Elfring, P. Trifillis
2020Journal of Clinical Medicine17 citations Open access
Semantic Scholar
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy.
P. Shieh, G. Elfring, P. Trifillis, Claudio L Santos +6 more
2021Journal of Comparative Effectiveness Research13 citations Open access
Semantic Scholar
The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy
M. Thangarajh, G. Elfring, P. Trifillis, J. Mcintosh +1 more
2018Neurology12 citations Open access
Semantic Scholar
Disease progression rates in ambulatory Duchenne muscular dystrophy by steroid type, patient age and functional status
C. McDonald, J. Marden, P. Shieh, Brenda Wong +7 more
2023Journal of Comparative Effectiveness Research11 citations Open access
Semantic Scholar
Polymerization of Three Hemoglobin A2 Variants Containing Valδ6 and Inhibition of Hemoglobin S Polymerization by Hemoglobin A2*
K. Adachi, J. Pang, L. R. Reddy, Lorelle E. Bradley +4 more
1996Journal of Biological Chemistry11 citations Open access
Semantic Scholar
Functional and Clinical Outcomes Associated with Steroid Treatment among Non-ambulatory Patients with Duchenne Muscular Dystrophy
C. McDonald, O. Mayer, K. Hor, Debra Miller +10 more
2022Journal of Neuromuscular Diseases7 citations Open access
Semantic Scholar
Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment
C. McDonald, Lee-Jen Wei, K. Flanigan, G. Elfring +2 more
2021Muscle and Nerve7 citations Open access
Semantic Scholar
T.P.7 Small molecule compounds correct alternative splicing of the SMN2 gene and restore SMN protein expression and function
N. Naryshkin, J. Narasimhan, A. Dakka, V. Gabbeta +38 more
20116 citations
Semantic Scholar
Purification and RNA binding properties of the polycytidylate-binding proteins alphaCP1 and alphaCP2.
M. Kiledjian, N. Day, P. Trifillis
1999Methods6 citations
Semantic Scholar
Expression Studies of δ-Globin Gene Alleles Associated with Reduced Hemoglobin A2 Levels in Greek Cypriots*
P. Trifillis, K. Adachi, T. Yamaguchi, E. Schwartz +1 more
1996Journal of Biological Chemistry6 citations Open access
Semantic Scholar
Safety and Efficacy of Ataluren in nmDMD Patients from Study 041, a Phase 3, Randomized, Double-Blind, Placebo-Controlled Trial (PL5.001)
C. McDonald, Shiwen Wu, S. Gulati, Hirofumi Komaki +17 more
2023Tuesday, April 254 citations
Semantic Scholar
Ataluren Preserves Upper Limb Function in nmDMD Patients from Study 041, a Phase 3 Placebo-Controlled Trial, and the STRIDE Registry (S34.008)
C. McDonald, E. Mercuri, F. Muntoni, H. Gordish-Dressman +15 more
2023Wednesday, April 263 citations
Semantic Scholar
Use of a ≥5-second threshold in baseline time to stand from supine to predict disease progression in Duchenne muscular dystrophy
Craig M. McDonald, Marcio Souza, G. Elfring, J. Mcintosh +4 more
20183 citations
Semantic Scholar
P.22 Age at loss of ambulation in patients with DMD from the STRIDE registry and the CINRG natural history study: A matched cohort analysis
E. Mercuri, F. Muntoni, F. Buccella, I. Desguerre +12 more
2022Neuromuscular Disorders2 citations
Semantic Scholar
Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial
C. Werner, H. Kroger, X. Luo, J. Mcintosh +7 more
2017Neuropediatrics2 citations
Semantic Scholar
urification and RNA Binding Properties of the olycytidylate-Binding Proteins a CP 1 and a CP 2
egerditch Kiledjian, N. Day, P. Trifillis
19992 citations
Semantic Scholar
Correction to: Safety and effectiveness of ataluren in patients with nonsense mutation DMD in the STRIDE Registry compared with the CINRG Duchenne Natural History Study (2015–2022): 2022 interim analysis
E. Mercuri, A. N. Osorio, F. Muntoni, F. Buccella +12 more
2023Journal of Neurology1 citations Open access
Semantic Scholar
Ataluren Delays Loss of Ambulation and Decline in Pulmonary Function in Patients with Nonsense Mutation Duchenne Muscular Dystrophy (2553)
Craig M. McDonald, F. Muntoni, Mark Rance, Joel Jiang +9 more
2021Neurology1 citations
Semantic Scholar
Ataluren in Patients Aged  2 to < 5 Years with Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD): 28-week Results from a Phase 2 Study
C. Werner, C. Tian, R. Kong, E. O'Mara +4 more
2019Neuropediatrics1 citations
Semantic Scholar
Preservation of Function over time as Measured by North Star Ambulatory Assessment in Ambulatory Boys with Nonsense Mutation Muscular Dystrophy Treated with Ataluren (S51.004)
C. McDonald, Lee-Jen Wei, G. Elfring, T. Schilling +5 more
2019Neurology1 citations
Semantic Scholar
Effect of Ataluren on Age at Loss of Ambulation in Nonsense Mutation Duchenne Muscular Dystrophy: Observational Data from the STRIDE Registry
C. Werner, A. Delage, F. Buccella, I. Desguerre +8 more
2019Neuropediatrics1 citations
Semantic Scholar
Meta-Analysis of Deflazacort vs Prednisone/Prednisolone in Patients with Duchenne Muscular Dystrophy (P2.325)
B. Darras, P. Riebling, E. O'Mara, G. Elfring +9 more
2018Neurology1 citations
Semantic Scholar
P198 Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE registry
F. Muntoni, F. Buccella, I. Desguerre, J. Kirschner +10 more
2023Neuromuscular Disorders0 citations
Semantic Scholar
P196 Age at loss of ambulation in patients with DMD from the STRIDE registry and the CINRG natural history study: a matched cohort analysis
E. Mercuri, F. Muntoni, F. Buccella, I. Desguerre +13 more
2023Neuromuscular Disorders0 citations
Semantic Scholar
P197 Pulmonary function in patients with Duchenne muscular dystrophy from the STRIDE registry and CINRG natural history study: a matched cohort analysis
M. Tulinius, F. Buccella, I. Desguerre, J. Kirschner +13 more
2023Neuromuscular Disorders0 citations
Semantic Scholar
Evaluation of the Biodistribution, Efficacy, and Side-Effect Profile of Deflazacort, Prednisolone and Vamorolone in a DMD Mouse Model (S34.010)
Grace Liu, P. Lipari, A. Mollin, Stephen Jung +14 more
2023Wednesday, April 260 citations
Semantic Scholar
P.19 Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE Registry
F. Muntoni, F. Buccella, I. Desguerre, J. Kirschner +9 more
2022Neuromuscular Disorders0 citations
Semantic Scholar
P.23 Pulmonary function in patients with Duchenne muscular dystrophy from the STRIDE Registry and CINRG Natural History Study: a matched cohort analysis
M. Tulinius, F. Buccella, I. Desguerre, J. Kirschner +12 more
2022Neuromuscular Disorders0 citations
Semantic Scholar
Pulmonary Function in Nonambulatory Patients with nmDMD from the STRIDE Registry and CINRG Duchenne Natural History Study: A Matched Cohort Analysis
A. Bernert, O. Nascimento, M. Tulinius, F. Buccella +9 more
2021Neuropediatrics0 citations
Semantic Scholar
DMD - TREATMENT
M. Tulinius, F. Buccella, I. Desguerre, J. Kirschner +11 more
2021Neuromuscular Disorders0 citations
Semantic Scholar

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E. Mercuri×16
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