Kari Branham

Biochemistry, Genetics and Molecular Biology · University of Michigan

Mid career · publishing since 2004

Retinal Development and Disorders Retinal Diseases and Treatments Photoreceptor and optogenetics research Retinal Imaging and Analysis RNA regulation and disease

Publications

208

Citations

12,366

Est. group size

Recurring co-author estimate

Active years

Publishing since 2004

In context

Among 1,692 mid career Biochemistry, Genetics and Molecular Biology PIs within our index

Citations: 12,366cohort median 809

Publications / year (recent): 3.0cohort median 3.2

Typically publishes in teams of ~7 · 0% small-team papers (≤3 authors) · across 12 venues

Publication cadence

Publications per year over the last 10 years — averaging 3.0/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

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
medRxiv · 2025
Clinical sequencing of the retinitis pigmentosa gene RPGR in over 1,000 cases of vision loss
Molecular vision · 2024
Clinical sequencing of the retinitis pigmentosa gene RPGR in over 1,000 cases of vision loss.
PubMed · 2024
Tissue‐specific genotype–phenotype correlations among USH2A‐related disorders in the RUSH2A study
Human Mutation · 2022
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy
Proceedings of the National Academy of Sciences · 2022
Readability, Content, and Accountability Assessment of Online Health Information for Retinitis Pigmentosa & Retinitis Pigmentosa Treatment Options
Ophthalmic Genetics · 2022
RUSH2A: systematic cohort variant modeling reveals phenotypic correlates
Investigative Ophthalmology & Visual Science · 2020
Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation
Human Mutation · 2019
BBS5
2018
PDE6B
2018
BBS9
2018
BBS10
2018
BBS7
2018
BBS12
2018
BBS1
2018

Publishes in

Investigative Ophthalmology & Visual Science×12
Ophthalmic Genetics×6
BMC Ophthalmology×3
Human Mutation×3
American Journal of Ophthalmology×3

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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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