Richard K. Wilson
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
677
Citations
250,276
Est. group size
~20
Recurring co-author estimate
Active years
56
Publishing since 1970
Richard K. Wilson's work centers on genomic sequencing and its application to understanding cancer and genetic disease, including large-scale studies of cancer genomes, pediatric and congenital cancers, and rare genetic disorders. His research uses DNA sequencing technologies to identify mutations, structural genome changes, and inherited (germline) risk factors that contribute to disease. Much of this work involves large international consortia analyzing thousands of cancer genomes to catalog patterns of mutation and genome rearrangement.
Publication output was high and relatively steady from 2017 to 2023 (often 30-50+ papers/year) but dropped sharply in 2024-2025, suggesting a recent slowdown in output.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Tracing the evolution of sequencing into the era of genomic medicine
Nature Reviews Genetics · 2025
- Comprehensive Genomic Characterization of Congenital and Infantile Cancers Reveals High Yield of Medically Meaningful Findings
JCO Precision Oncology · 2025
- A Splice‐Region Variant Causes an Atypical Presentation of <scp>GNAS</scp> Inactivation Disorder
American Journal of Medical Genetics Part A · 2025
- POS0716 DYSREGULATED LIPID AND METABOLIC PATHWAYS MAY CONTRIBUTE TO UNDERLYING DISEASE MECHANISMS IN PATIENTS WITH HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
Annals of the Rheumatic Diseases · 2025
- Germline susceptibility from broad genomic profiling of pediatric brain cancers
Neuro-Oncology Advances · 2024
- Optical Genome Mapping (<scp>OGM</scp>) Identifies Multiple Structural Variants in a Case With Atypical Phelan‐<scp>McDermid</scp> Syndrome
American Journal of Medical Genetics Part A · 2024
- Author Correction: Pan-cancer analysis of whole genomes
Nature · 2023
- Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Nature · 2023
- Author Correction: The repertoire of mutational signatures in human cancer
Nature · 2023
- Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Nature Genetics · 2023
- Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Nature Genetics · 2023
- Author Correction: Patterns of somatic structural variation in human cancer genomes
Nature · 2023
- Author Correction: Genomic basis for RNA alterations in cancer
Nature · 2023
- Author Correction: The landscape of viral associations in human cancers
Nature Genetics · 2023
- Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Nature Genetics · 2023
- Figshare×31
- Nature Communications×28
- Nature×16
- bioRxiv (Cold Spring Harbor Laboratory)×16
- Nature Genetics×15
- S. Cenk Şahinalp
Biochemistry, Genetics and Molecular Biology · Indiana University
- Keiko Akagi
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- David E. Symer
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Deloris Veney
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Nawal Kassem
Biochemistry, Genetics and Molecular Biology · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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