Megan R. Glassford

Biochemistry, Genetics and Molecular Biology · University of Michigan

Established · publishing since 1993

Genomic variations and chromosomal abnormalities Genomics and Rare Diseases Congenital heart defects research Hereditary Neurological Disorders Epilepsy research and treatment

Publications

Citations

227

Est. group size

—

Recurring co-author estimate

Active years

Publishing since 1993

In context

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

Citations: 227cohort median 3,422

Publications / year (recent): 0.6cohort median 4.8

Typically publishes in teams of ~7 · 11% small-team papers (≤3 authors) · across 8 venues

Publication cadence

Publications per year over the last 10 years — averaging 0.6/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

P354: Mosaic FBXW7-related neurodevelopmental disorder presenting with developmental delay, hypotonia, expressive language delay, anorectal malformation, and proximal aorta dilation
Genetics in Medicine Open · 2026
Refining the phenotype of SINO syndrome: A comprehensive cohort report of 14 novel cases
Genetics in Medicine · 2024
De novo variants in <i>EMC1</i> lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in <i>Drosophila</i>
Human Molecular Genetics · 2022
Caregiver Perspectives on a Child's Diagnosis of 3q29 Deletion: “We Can't Just Wish This Thing Away”
Journal of Developmental & Behavioral Pediatrics · 2021
Bone tissue and osteoblasts from X-linked type XVIII OI with defects in regulated intramembrane proteolysis have distinct features
Bone Reports · 2021
The Use of B-Cell Polysome Profiling to Validate Novel RPL5 (uL18) and RPL26 (uL24) Variants in Diamond-Blackfan Anemia
Journal of Pediatric Hematology/Oncology · 2020
“We can’t just wish this thing away”: Caregiver perspectives on a child’s diagnosis of 3q29 deletion
medRxiv · 2020
Novel features of 3q29 deletion syndrome: Results from the 3q29 registry
American Journal of Medical Genetics Part A · 2016
Table 1. [Genomic Testing Used in the 3q29 Recurrent Deletion].
2016

Publishes in

American Journal of Medical Genetics Part A×1
Pediatric Research×1
Pediatric Neurology×1
Human Molecular Genetics×1
Genetics in Medicine×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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