Thomas W. Glover

Biochemistry, Genetics and Molecular Biology · University of Michigan

Established · publishing since 1978

Genetics and Neurodevelopmental Disorders Genomic variations and chromosomal abnormalities DNA Repair Mechanisms Epigenetics and DNA Methylation Neurofibromatosis and Schwannoma Cases

Publications

194

Citations

20,164

Est. group size

Recurring co-author estimate

Active years

Publishing since 1978

In context

Among 1,668 established Biochemistry, Genetics and Molecular Biology PIs within our index

Citations: 20,164cohort median 3,422

Publications / year (recent): 2.0cohort median 4.8

Typically publishes in teams of ~6 · 17% small-team papers (≤3 authors) · across 16 venues

Publication cadence

Publications per year over the last 10 years — averaging 2.0/year recently

Collaborators per year

Distinct co-authors at University of Michigan each year — a rough indication of whether the group around this researcher has been growing or contracting. An estimate from co-authorship, not a roster: collaborators are not necessarily lab members, and recent years can be under-counted while indexing catches up.

Recent publications

High-fidelity rare structural variant detection with HiFiRE3 reduced representation via restriction enzyme ends
bioRxiv (Cold Spring Harbor Laboratory) · 2026
A CDK1 phospho-switch reprograms TRAIP to unload replisomes in mitosis
Science · 2026
Replication stress induces POLQ-mediated structural variant formation throughout common fragile sites after entry into mitosis
Nature Communications · 2024
POLQ mediates replication-stress induced structural variant formation throughout common fragile sites during mitosis
bioRxiv (Cold Spring Harbor Laboratory) · 2024
svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
NAR Genomics and Bioinformatics · 2022
Diagnosis and management of acute pancreatitis
Clinical Radiology · 2022
Stephen T. Warren, Ph.D. (1953–2021): A remembrance
The American Journal of Human Genetics · 2022
svCapture: Efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
bioRxiv (Cold Spring Harbor Laboratory) · 2022
Locus-specific transcription silencing at the <i>FHIT</i> gene suppresses replication stress-induced copy number variant formation and associated replication delay
Nucleic Acids Research · 2021
Twin peaks: finding fragile sites with MiDAS-seq
Cell Research · 2020
34. De novo constitutional PATRR-mediated t(3;8) balanced translocation associated with clear cell renal cell carcinoma
Cancer Genetics · 2020
Effects of hydroxyurea on CNV induction in the mouse germline
Environmental and Molecular Mutagenesis · 2018
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations
Human Genetics · 2018
Fragile sites in cancer: more than meets the eye
Nature reviews. Cancer · 2017
Abstract 491: Elucidating <i>de novo</i> PATRR-mediated t(3;8) balanced translocation and clear cell renal cell carcinoma
Cancer Research · 2017

Publishes in

bioRxiv (Cold Spring Harbor Laboratory)×3
Nature reviews. Cancer×1
JIMD Reports×1
Nature Communications×1
Head & Neck×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 25, 2026.

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