John R. Heckenlively
Biochemistry, Genetics and Molecular Biology · University of Michigan
Publications
419
Citations
24,205
Est. group size
—
Recurring co-author estimate
Active years
49
Publishing since 1977
Typically publishes in teams of ~13 · 0% small-team papers (≤3 authors) · across 4 venues
- Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy
Journal of Clinical Investigation · 2018
- Mutations in the novel gene IFT88 are involved in causing non-syndromic inherited retinal degeneration (IRD)
2018
- GPR98
2018
- CLRN1
2018
- Progressive Loss of Rod Sensitivity in Patients with Autosomal Dominant Retinitis Pigmentosa (adRP) due to RHO Pro23His Mutation
Investigative Ophthalmology & Visual Science · 2017
- Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing
PLoS ONE · 2016
- De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy
Scientific Reports · 2016
- Investigative Ophthalmology & Visual Science×10
- American Journal of Ophthalmology×4
- Ophthalmic Genetics×4
- Translational Vision Science & Technology×3
- Human Mutation×3
- Naheed W. Khan
Biochemistry, Genetics and Molecular Biology · University of Michigan
- John Y.S. Han
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Kari Branham
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Dana Schlegel
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Sanae S. Imanishi
Biochemistry, Genetics and Molecular Biology · Indiana 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 25, 2026.
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