Kari Branham

12.1k total citations
66 papers, 3.2k citations indexed

About

Kari Branham is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Kari Branham has authored 66 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 43 papers in Ophthalmology and 13 papers in Genetics. Recurrent topics in Kari Branham's work include Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (37 papers) and Glaucoma and retinal disorders (10 papers). Kari Branham is often cited by papers focused on Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (37 papers) and Glaucoma and retinal disorders (10 papers). Kari Branham collaborates with scholars based in United States, Canada and United Kingdom. Kari Branham's co-authors include Anand Swaroop, Gonçalo R. Abecasis, Mohammad Othman, John R. Heckenlively, Sepideh Zareparsi, Mingyao Li, Ritu Khanna, Atsuhiro Kanda, Thiran Jayasundera and Shirley He and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Kari Branham

66 papers receiving 3.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kari Branham United States 26 2.2k 1.6k 1.3k 412 340 66 3.2k
Eranga N. Vithana Singapore 32 1.8k 0.8× 1.6k 1.0× 1.6k 1.2× 385 0.9× 156 0.5× 82 3.4k
B. Jeroen Klevering Netherlands 38 3.4k 1.5× 3.3k 2.0× 1.5k 1.1× 435 1.1× 248 0.7× 102 4.9k
Jana Zernant United States 33 2.8k 1.3× 2.8k 1.7× 1.0k 0.8× 259 0.6× 497 1.5× 75 3.8k
Camiel J. F. Boon Netherlands 32 3.6k 1.6× 1.7k 1.0× 2.1k 1.6× 224 0.5× 93 0.3× 140 4.6k
Yi Yu United States 19 1.0k 0.5× 608 0.4× 656 0.5× 261 0.6× 349 1.0× 37 1.8k
Michael P. Fautsch United States 32 2.3k 1.0× 1.3k 0.8× 1.3k 1.0× 185 0.4× 119 0.3× 122 3.5k
Bärbel Rohrer United States 31 1.3k 0.6× 1.5k 0.9× 463 0.4× 109 0.3× 591 1.7× 88 2.6k
Xueshan Xiao China 34 1.8k 0.8× 2.6k 1.6× 845 0.6× 754 1.8× 83 0.2× 147 3.6k
David G. Charteris United Kingdom 40 3.3k 1.5× 1.0k 0.6× 3.1k 2.3× 243 0.6× 55 0.2× 92 4.1k
M Uyama Japan 28 2.3k 1.0× 1.3k 0.8× 1.2k 0.9× 137 0.3× 88 0.3× 135 3.0k

Countries citing papers authored by Kari Branham

Since Specialization
Citations

This map shows the geographic impact of Kari Branham's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kari Branham with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kari Branham more than expected).

Fields of papers citing papers by Kari Branham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kari Branham. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kari Branham. The network helps show where Kari Branham may publish in the future.

Co-authorship network of co-authors of Kari Branham

This figure shows the co-authorship network connecting the top 25 collaborators of Kari Branham. A scholar is included among the top collaborators of Kari Branham based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kari Branham. Kari Branham is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Branham, Kari, et al.. (2020). Genetic testing for inherited retinal degenerations: Triumphs and tribulations. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(3). 571–577. 10 indexed citations
3.
Ratnapriya, Rinki, İlhan E. Acar, Maartje J. Geerlings, et al.. (2020). Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. Human Molecular Genetics. 29(12). 2022–2034. 24 indexed citations
4.
Hufnagel, Robert B., Bin Guan, Ehsan Ullah, et al.. (2020). RUSH2A: systematic cohort variant modeling reveals phenotypic correlates. Investigative Ophthalmology & Visual Science. 61(7). 836–836. 1 indexed citations
5.
Fahim, Abigail T., Kari Branham, Neruban Kumaran, et al.. (2019). Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration. British Journal of Ophthalmology. 103(12). bjophthalmol–2018. 23 indexed citations
6.
Fahim, Abigail T., Lori S. Sullivan, Sara J. Bowne, et al.. (2019). X-Chromosome Inactivation is a Biomarker of Clinical Severity in Female Carriers of X-linked Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 60(9). 2961–2961. 1 indexed citations
7.
Branham, Kari, Igor Kozak, Pooja Biswas, et al.. (2018). Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two Pedigrees. Advances in experimental medicine and biology. 1074. 229–236. 2 indexed citations
8.
Sullivan, Lori S., Sara J. Bowne, Daniel C. Koboldt, et al.. (2017). A Novel Dominant Mutation in SAG , the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States. Investigative Ophthalmology & Visual Science. 58(5). 2774–2774. 26 indexed citations
9.
Thompson, Debra A., Robin R. Ali, Eyal Banin, et al.. (2015). Advancing Therapeutic Strategies for Inherited Retinal Degeneration: Recommendations From the Monaciano Symposium. Investigative Ophthalmology & Visual Science. 56(2). 918–931. 79 indexed citations
10.
Wang, Chaolong, Xiaowei Zhan, Jennifer L. Bragg‐Gresham, et al.. (2014). Ancestry estimation and control of population stratification for sequence-based association studies. Nature Genetics. 46(4). 409–415. 89 indexed citations
11.
Zahid, Sarwar, Naheed Khan, Kari Branham, et al.. (2013). Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused byRPGRMutations. JAMA Ophthalmology. 131(8). 1016–1016. 30 indexed citations
12.
Fahim, Abigail T., Naheed Khan, Sarwar Zahid, et al.. (2013). Diagnostic Fundus Autofluorescence Patterns in Achromatopsia. American Journal of Ophthalmology. 156(6). 1211–1219.e2. 35 indexed citations
13.
Oliver, Verity F., Maria Franchina, Andrew E. Jaffe, et al.. (2013). Hypomethylation of the IL17RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration. Cell Reports. 5(6). 1527–1535. 37 indexed citations
14.
Bowne, Sara J., Lori S. Sullivan, Jennifer D. Churchill, et al.. (2012). Genome-Wide Linkage Analysis For Gene Discovery In Autosomal Dominant Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 53(14). 4528–4528. 1 indexed citations
15.
Branham, Kari, Mohammad Othman, Richard G. Weleber, et al.. (2010). X-Linked Recessive Mutations in Simplex Males With Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 51(13). 1399–1399. 1 indexed citations
16.
Wu, David M., Pelin Atmaca-Sönmez, Paul A. Sieving, et al.. (2009). Long-term follow-up of a family with dominant X-linked retinitis pigmentosa. Eye. 24(5). 764–774. 26 indexed citations
17.
Iannaccone, Alessandro, et al.. (2007). Retinal Phenotype of an X-Linked Pseudo-usher Syndrome in Association with the G173R Mutation in the RPGR Gene. Advances in experimental medicine and biology. 613. 221–227. 3 indexed citations
18.
Trager, Edward H., et al.. (2007). Madeline 2.0 PDE: a new program for local and web-based pedigree drawing. Bioinformatics. 23(14). 1854–1856. 19 indexed citations
19.
Zareparsi, Sepideh, Monika Buraczyńska, Kari Branham, et al.. (2005). Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration. Human Molecular Genetics. 14(11). 1449–1455. 154 indexed citations
20.
Abecasis, Gonçalo R., Beverly M. Yashar, Yu Zhao, et al.. (2004). Age-Related Macular Degeneration: A High-Resolution Genome Scan for Susceptibility Loci in a Population Enriched for Late-Stage Disease. The American Journal of Human Genetics. 74(3). 482–494. 116 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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