Catherine E. Cottrell
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
178
Citations
2,540
Est. group size
~23
Recurring co-author estimate
Active years
55
Publishing since 1972
Catherine E. Cottrell's work focuses on molecular diagnostics for pediatric cancers and rare genetic disorders, including brain tumors, sarcomas, and vascular malformations. Her research often involves using genetic sequencing techniques (such as cell-free DNA analysis and single-cell long-read sequencing) to identify tumor-specific mutations and inform targeted treatments. She also contributes to large-scale collaborative initiatives that characterize the molecular features of rare childhood tumors.
Publication output grew notably from 2017 to a peak around 2021-2022, then has moderated somewhat but remained steady in recent years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Cell-Free DNA Uncovered Tumor Heterogeneity and Informed Targeted Therapy in a Pediatric Rhabdomyosarcoma
JCO Precision Oncology · 2026
- Integrated molecular characterization of pediatric soft tissue sarcomas: A report from the COG and CCDI molecular characterization initiative.
Journal of Clinical Oncology · 2025
- Understanding the molecular landscape of rare tumors through the CCDI-COG Molecular Characterization Initiative.
Journal of Clinical Oncology · 2025
- 275PMagnetic resonance imaging based radiomic feature extraction for bone quality assessment in corticosteroid treated boys of Duchenne muscular dystrophy
Neuromuscular Disorders · 2025
- HGG-25. Brainstem high-grade astrocytoma with piloid feature (HGAP) with an NTRK fusion: durable disease response to targeted therapy with larotrectinib
Neuro-Oncology Pediatrics · 2025
- Defining the transcriptome of PIK3CA-altered cells in a human capillary malformation using single cell long-read sequencing
Scientific Reports · 2024
- Structural and Dynamic Analyses of Pathogenic Variants in PIK3R1 Reveal a Shared Mechanism Associated among Cancer, Undergrowth, and Overgrowth Syndromes
Life · 2024
- Cover Image, Volume 50, Issue 1
Neuropathology and Applied Neurobiology · 2024
- 398P Magnetic resonance imaging detects bone alterations in corticosteroid treated boys with DMD
Neuromuscular Disorders · 2024
- WNT‐activated, <i>MYC</i> ‐amplified medulloblastoma displaying intratumoural heterogeneity
Neuropathology and Applied Neurobiology · 2023
- Enhancing the didactic learning experience for Laboratory Genetics and Genomics fellows through a multi‐institutional lecture series
Journal of Genetic Counseling · 2023
- A LINE-1 mediated deletion resulting in germline retinoblastoma predisposition
Neuro-Oncology Advances · 2023
- Author response for "WNT‐activated, <i>MYC</i>‐amplified medulloblastoma displaying intratumoural heterogeneity"
2023
- Author response for "WNT‐activated, <i>MYC</i>‐amplified medulloblastoma displaying intratumoural heterogeneity"
2023
- Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines
Journal of Molecular Diagnostics · 2022
- Neuro-Oncology×10
- Genetics in Medicine Open×10
- Cancer Genetics×9
- Molecular Case Studies×8
- Molecular Genetics and Metabolism×7
- Marco L. Leung
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Kristy Lee
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Daniel C. Koboldt
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Alex H. Wagner
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Yassmine Akkari
Biochemistry, Genetics and Molecular Biology · The Ohio State 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.
Claim or correct this profile