Eric Weh
Biochemistry, Genetics and Molecular Biology · University of Michigan
Publications
48
Citations
746
Est. group size
~14
Recurring co-author estimate
Active years
17
Publishing since 2010
Typically publishes in teams of ~5 · 8% small-team papers (≤3 authors) · across 10 venues
- Deletions of distant regulatory sequences upstream of zebrafish <i>pitx2</i> result in a range of ocular phenotypes
bioRxiv (Cold Spring Harbor Laboratory) · 2019
- Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Human Molecular Genetics · 2017
- Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome
PLoS ONE · 2017
- An in vivo investigation of the upstream regulatory elements of PITX2/pitx2 through generation of large deletions of conserved enhancer elements in zebrafish
Investigative Ophthalmology & Visual Science · 2017
- Genes and regulation of eye development
Acta Ophthalmologica · 2017
- 8q21.11 microdeletion in two patients with syndromic peters anomaly
American Journal of Medical Genetics Part A · 2016
- Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
Clinical Genetics · 2016
- Analysis of <i>CYP1B1</i> in pediatric and adult glaucoma and other ocular phenotypes.
PubMed · 2016
- Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
BMC Medical Genetics · 2016
- Genetic Analysis of Developmental Ocular Disorders
Investigative Ophthalmology & Visual Science · 2016
- Additional file 1: Table S1. of Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
Figshare · 2016
- Additional file 1: Table S1. of Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
Figshare · 2016
- Investigative Ophthalmology & Visual Science×9
- bioRxiv (Cold Spring Harbor Laboratory)×5
- eLife×4
- Experimental Eye Research×2
- Figshare×2
- Heather Hager
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Thomas J. Wubben
Biochemistry, Genetics and Molecular Biology · University of Michigan
- John Y.S. Han
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Abigail T. Fahim
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Athanasios J. Karoukis
Biochemistry, Genetics and Molecular Biology · University of Michigan
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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