Bohu Pan Data-verified

Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.

Researcher

Last publication 2025 Last refreshed 2026-05-16

faculty

16 h-index 54 pubs 1,408 cited

Biography and Research Information

OverviewAI-generated summary

Bohu Pan's research focuses on the application of high-throughput sequencing technologies, particularly whole-genome sequencing (WGS) and targeted RNA sequencing (RNA-seq), to investigate genetic variation, mutagenicity, and disease mechanisms. Pan has studied the reproducibility of inherited variants detected using short-read WGS and explored biases in germline structural variant detection. This work includes evaluating the mutagenicity of substances like silver nanoparticles using WGS in mouse lymphoma cells. Additionally, Pan has investigated interactions between SARS-CoV-2 and the ACE2 receptor using computational modeling and has analyzed SARS-CoV-2 sequences to identify epidemiological traits. The researcher also focuses on augmenting precision medicine through targeted RNA-seq for detecting expressed mutations. Pan has published 53 papers, with an h-index of 15 and over 1,200 citations, and collaborates frequently with researchers at the National Center for Toxicological Research, including Joe Meehan and Weigong Ge.

Metrics

  • h-index: 16
  • Publications: 54
  • Citations: 1,408

Selected Publications

  • Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations (2025)
    4 citations DOI OpenAlex
  • Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing (2024)
    7 citations DOI OpenAlex
  • Clonal hematopoiesis driven by mutated DNMT3A promotes inflammatory bone loss (2024)
    89 citations DOI OpenAlex
  • Evaluation of mutagenic susceptibility of different stages in germ cell development of Caenorhabditis elegans using whole genome sequencing (2023)
    2 citations DOI OpenAlex
  • Additional file 3 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 13 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 5 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 15 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 10 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 9 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 11 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 1 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 6 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 12 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)
  • Additional file 7 of Assessing reproducibility of inherited variants detected with short-read whole genome sequencing (2022)

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Collaboration Network

96 Collaborators 43 Institutions 7 Countries

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