Thomas W. Prior

Johnson & Johnson (United States) — United States

Medicine · Health Sciences

61h-index19.7kcitations243works7.02yr avg
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Research Topics

Neurogenetic and Muscular Disorders Research(91), RNA modifications and cancer(56), Muscle Physiology and Disorders(40), Congenital Anomalies and Fetal Surgery(30), RNA Research and Splicing(21)

Publications242 total

10 Year Follow-up of CALGB 10603/Ratify: Midostaurin Versus Placebo Plus Intensive Chemotherapy in Newly Diagnosed <i>FLT3</i> Mutant Acute Myeloid Leukemia Patients Aged 18-60 Years
Blood·2024· 8 citedOpen Access
<scp>Gerstmann‐Sträussler‐Scheinker</scp> Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology
Movement Disorders Clinical Practice·2024· 6 citedOpen Access
Clinical SMN1 and SMN2 Gene-Specific Sequencing to Enhance the Clinical Sensitivity of Spinal Muscular Atrophy Diagnostic Testing
Human Mutation·2023· 1 citedOpen Access
P17.04.B A PHASE 2 STUDY OF NIRAPARIB CONCOMITANT WITH TUMOR TREATING FIELDS (TTFIELDS) IN PATIENTS WITH RECURRENT HIGH-GRADE GLIOMA (HGG)
Neuro-Oncology·2023· 2 citedOpen Access
Supplementary Table 1 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
Data from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
Supplementary Table 2 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
Data from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
Supplementary Table 1 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
Supplementary Table 2 from Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients
2023Open Access
P423: SMN1 SMN2 gene-specific sequencing enhances the clinical sensitivity of spinal muscular atrophy diagnostic testing
Genetics in Medicine Open·2023Open Access
Genomic landscape of patients with FLT3-mutated acute myeloid leukemia (AML) treated within the CALGB 10603/RATIFY trial
Leukemia·2022· 32 citedOpen Access
eP366: A comprehensive study of E200K genetic Creutzfeldt Jakob disease cases; effects of codon 129 polymorphism
Genetics in Medicine·2022
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion
Viruses·2021· 6 citedOpen Access
Molecular landscape and prognostic impact of FLT3-ITD insertion site in acute myeloid leukemia: RATIFY study results
Leukemia·2021· 85 citedOpen Access
Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative
JCO Precision Oncology·2021· 64 citedOpen Access
Ein burgenländisches Leben
Böhlau Verlag eBooks·2021
New CFTR variant testing standards promote identification of infrequent and novel variants, which may have important therapeutic and fertility implications
Molecular Genetics and Metabolism·2021
Midostaurin reduces relapse in FLT3-mutant acute myeloid leukemia: the Alliance CALGB 10603/RATIFY trial
Leukemia·2021· 91 citedOpen Access
Spinal Muscular Atrophy: Mutations, Testing, and Clinical Relevance
The Application of Clinical Genetics·2021· 148 citedOpen Access
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Frequent Co-authors

Kathryn J. Swoboda(11), John T. Kissel(10), Arthur H.M. Burghes(10), Pamela J. Snyder(9), Thomas O. Crawford(8), Jerry R. Mendell(6), Kristin J. Krosschell(6), Sandra P. Reyna(6), W. David Arnold(5), Albert de la Chapelle(5), Richard S. Finkel(5), Richard Shell(4), Clara D. Bloomfield(4), Guido Marcucci(4), Richard A. Larson(4), Heather Hampel(4), Wendy L. Frankel(4), Kaisa Sotamaa(4), Judith A. Westman(4), Jenny Panescu(4)