Author

Mark R. Wilkinson

St. Jude Children's Research HospitalORCID 0000-0001-9135-3394Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:variant effect prediction· 3 Assay:whole-exome sequencing· 3

Frequent Co-Authors

Jeffery M. KlcoiD· 2 shared Kim E. NicholsiD· 2 shared Mohammad K. EldomeryiD· 2 shared Patrick R. BlackburniD· 2 shared Aman PateliD· 1 shared Cai LiiD· 1 shared Chih-Hsuan Wu· 1 shared Chimene A. KesserwaniD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Jeffery M. KlcoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 8, 2026

Prevalence and Clinical Significance of Adult-Onset Cancer Predisposition Variants in Pediatric Oncology

Jamie L. Maciaszek, Victor Pastor Loyola, Taylor Cain…·Mohammad K. Eldomery

The paper examines the prevalence and clinical significance of adult-onset cancer predisposition variants in pediatric cancer patients, finding most variants are secondary rather than directly related to the tumor.

DOI 10.64898/2026.06.07.26354365

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 20, 2025

Analysis and Interpretation of Somatic NMD-Escaping Variants in Oncogenes and Dual-Function Genes across Adult and Pediatric Cancer Cohorts

Mohammad K. Eldomery, Karissa M. Dieseldorff Jones, Maria Namwanje…·Patrick R. Blackburn

The paper analyzes somatic NMDe variants in oncogenes and dual-function genes across cancer cohorts, identifying two distinct patterns with different functional consequences.

DOI 10.1101/2025.11.20.25340490

humanwhole-exome sequencing

𝕏 PostBluesky

BioinformaticsGenome ResearchPeer-reviewedSep 1, 2019

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): A Cloud-based Platform for Curating and Classifying Germline Variants

Michael N. Edmonson, Aman Patel, Dale J. Hedges…·Jinghui Zhang

PeCanPIE is a cloud-based platform for annotating and classifying germline variants in pediatric cancer, using ACMG guidelines to rank and classify variants from VCF files.

49 citations

humanwhole-exome sequencing

𝕏 PostBluesky