Ying‐Chen Claire Hou
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
44
Citations
1,184
Est. group size
~5
Recurring co-author estimate
Active years
19
Publishing since 2008
This researcher works in clinical genomics, focusing on using DNA and RNA sequencing technologies to diagnose genetic diseases, including cancers, chromosomal syndromes, and vascular anomalies, especially in pediatric patients. Much of the work involves interpreting complex genetic test results (like copy number changes and mosaic variants) to improve diagnostic accuracy and guide patient care. The research bridges laboratory genomic testing with real-world clinical decision-making.
Publication output has grown substantially over the last decade, rising from about 1 paper per year in 2017-2019 to 7-8 papers per year in 2025-2026.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- P572: Lessons learned from clinical use of the ACMG/CGC technical standards for somatic copy number alterations: Challenges and improvement*
Genetics in Medicine Open · 2026
- P612: Diagnostic utility of genomic testing in a challenging vascular anomaly: A case report
Genetics in Medicine Open · 2026
- O13: Prevalence of cancer predisposition variants in a pediatric pineoblastoma cohort
Genetics in Medicine Open · 2026
- Generation and Single-cell Transcriptomic Analysis of Hepatocellular Carcinoma Organoids following Drug Treatment
Journal of Visualized Experiments · 2026
- ID #1000 Radiation-induced high-grade glioma with molecularly distinct metachronous recurrence in a pediatric leukemia survivor
Neuro-Oncology Pediatrics · 2026
- Next-Generation Sequencing in Pediatric Leukemia
2026
- Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes
Genome Medicine · 2025
- Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes
medRxiv · 2025
- Novel t(14;19)(q32.2;p13.12) structural variant identified by genome sequencing in a myeloid neoplasm post cytotoxic therapy: a case report
Journal of Laboratory and Precision Medicine · 2025
- 34. Best practices for testing low-level mosaic variants:Recommendations from CGC somatic overgrowth and vascular anomalies working group
Cancer Genetics · 2025
- Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome
European Journal of Human Genetics · 2024
- Clinical whole‐genome sequencing in cancer diagnosis
Human Mutation · 2022
- Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations
Frontiers in Pediatrics · 2022
- eP362: Mosaic RAS family in-frame insertion variants in patients with hemangiomas and vascular malformations
Genetics in Medicine · 2022
- 25. Genetic spectrum of RAS Alterations-A Highlight of in-frame insertion variants in association with vascular anomalies
Cancer Genetics · 2022
- Genetics in Medicine Open×10
- Cancer Genetics×4
- The American Journal of Human Genetics×2
- Proceedings of the National Academy of Sciences×2
- Genetics in Medicine×2
- Marco L. Leung
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Danielle Mouhlas
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
- 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