LabCompass

Piotr Hadaczek

Biochemistry, Genetics and Molecular Biology · The Ohio State University

Established · publishing since 1993Rising activity

Publications

104

Citations

3,792

Est. group size

~4

Recurring co-author estimate

Active years

33

Publishing since 1993

Research summary
AI-generated

Piotr Hadaczek's work focuses on gene therapy approaches for neurological diseases, particularly using engineered viral vectors (like AAV) to deliver therapeutic genes directly into the brain and spinal fluid. Their research spans preclinical studies in non-human primates for conditions such as Huntington's disease, Niemann-Pick disease, and Parkinson's disease, as well as drug delivery methods for pediatric brain tumors like diffuse intrinsic pontine glioma. Recent work also touches on CRISPR-based genome editing for cholesterol-related therapies.

Viral vector gene therapy (AAV-based)CNS drug and gene delivery methodsNeurodegenerative disease models (Huntington's, Parkinson's, Niemann-Pick)Pediatric brain tumor treatment (DIPG)Genome editing (CRISPR) for disease treatment

Publication output was low and intermittent from 2017-2022, with a large but likely anomalous spike in 2023, followed by a return to modest activity in 2024-2025.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026

Publication cadence
Publications per year over the last 10 years — averaging 4.6/year recently
2017: 1 publication172018: 3 publications182019: 2 publications192020: 1 publication2021222023: 20 publications20232024: 2 publications242025: 1 publication2526
Recent publications
Publishes in
  • Molecular Therapy — Methods & Clinical Development×2
  • Molecular Therapy×2
  • Zenodo (CERN European Organization for Nuclear Research)×2
  • Movement Disorders×1
  • Gene Therapy×1
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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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