Brian P. Brooks

2.7k total citations
73 papers, 1.4k citations indexed

About

Brian P. Brooks is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Brian P. Brooks has authored 73 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 25 papers in Genetics and 19 papers in Ophthalmology. Recurrent topics in Brian P. Brooks's work include Retinal Development and Disorders (23 papers), Ocular Disorders and Treatments (15 papers) and melanin and skin pigmentation (14 papers). Brian P. Brooks is often cited by papers focused on Retinal Development and Disorders (23 papers), Ocular Disorders and Treatments (15 papers) and melanin and skin pigmentation (14 papers). Brian P. Brooks collaborates with scholars based in United States, United Kingdom and Netherlands. Brian P. Brooks's co-authors include Delphine Blain, Yuri V. Sergeev, Kapil Bharti, Stefano Bertuzzi, Robert B. Hufnagel, Monika B. Dolinska, Wadih M. Zein, Aman George, Joan Z. Balog and Paul T. Wingfield and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Brian P. Brooks

72 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brian P. Brooks United States 22 884 390 360 253 203 73 1.4k
Robert B. Hufnagel United States 20 848 1.0× 199 0.5× 247 0.7× 307 1.2× 138 0.7× 97 1.3k
Maria A. Musarella Canada 22 1.4k 1.5× 375 1.0× 434 1.2× 407 1.6× 132 0.7× 45 1.8k
Jacoline B. ten Brink Netherlands 22 1.3k 1.4× 480 1.2× 608 1.7× 682 2.7× 282 1.4× 49 2.0k
Tamar Ben‐Yosef Israel 30 2.2k 2.5× 325 0.8× 426 1.2× 474 1.9× 109 0.5× 82 2.8k
Janine Davis United States 17 959 1.1× 114 0.3× 245 0.7× 113 0.4× 300 1.5× 23 1.6k
Arnold Munnich France 25 1.6k 1.8× 196 0.5× 580 1.6× 237 0.9× 88 0.4× 55 2.3k
Lijin Dong United States 24 1.4k 1.5× 176 0.5× 239 0.7× 313 1.2× 161 0.8× 64 2.0k
Christian Hamel France 20 1.2k 1.4× 203 0.5× 265 0.7× 323 1.3× 87 0.4× 39 1.5k
Panagiotis I. Sergouniotis United Kingdom 30 1.8k 2.0× 273 0.7× 579 1.6× 1.1k 4.4× 325 1.6× 83 2.3k
Mirella Bruttini Italy 22 1.0k 1.2× 234 0.6× 777 2.2× 78 0.3× 34 0.2× 40 1.6k

Countries citing papers authored by Brian P. Brooks

Since Specialization
Citations

This map shows the geographic impact of Brian P. Brooks'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 Brian P. Brooks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian P. Brooks more than expected).

Fields of papers citing papers by Brian P. Brooks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian P. Brooks. 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 Brian P. Brooks. The network helps show where Brian P. Brooks may publish in the future.

Co-authorship network of co-authors of Brian P. Brooks

This figure shows the co-authorship network connecting the top 25 collaborators of Brian P. Brooks. A scholar is included among the top collaborators of Brian P. Brooks 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 Brian P. Brooks. Brian P. Brooks 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.
Li, Joanne, Jianfei Liu, Vineeta Das, et al.. (2025). Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopy. Communications Medicine. 5(1). 105–105. 1 indexed citations
2.
Brooks, Brian P., et al.. (2025). Advances in machine learning for ABCA4-related retinopathy: segmentation and phenotyping. International Ophthalmology. 45(1). 314–314. 1 indexed citations
3.
Swaroop, Anand, et al.. (2025). Cone Rod Homeobox ( CRX ): literature review and new insights. Ophthalmic Genetics. 46(4). 338–346. 1 indexed citations
4.
Benson, Matthew D., Delphine Blain, Denise Cunningham, et al.. (2023). RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3′-end of ORF15. Investigative Ophthalmology & Visual Science. 64(12). 19–19. 3 indexed citations
5.
Huryn, Laryssa A., Lev Prasov, Wadih M. Zein, et al.. (2022). Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome. British Journal of Ophthalmology. 107(10). 1554–1559. 3 indexed citations
6.
Liu, Tao, Andrew J. Bower, Jianfei Liu, et al.. (2021). High-resolution imaging of cone photoreceptors and retinal pigment epithelial cells in Chediak-Higashi Syndrome. Investigative Ophthalmology & Visual Science. 62(8). 1903–1903. 1 indexed citations
7.
Soleilhavoup, Clément, Marco Travaglio, Pedro Garção, et al.. (2020). Nolz1 expression is required in dopaminergic axon guidance and striatal innervation. Nature Communications. 11(1). 3111–3111. 8 indexed citations
8.
Liu, Jianfei, Tao Liu, Aman George, et al.. (2019). Longitudinal adaptive optics fluorescence microscopy reveals cellular mosaicism in patients. JCI Insight. 4(6). 22 indexed citations
9.
Prendergast, James, Aara Patel, Sunit Dutta, et al.. (2019). Detailed analysis of chick optic fissure closure reveals Netrin-1 as an essential mediator of epithelial fusion. eLife. 8. 32 indexed citations
10.
Huryn, Laryssa A., et al.. (2018). Comprehensive Review of the Genetics of Albinism. Journal of Visual Impairment & Blindness. 112(6). 683–700. 1 indexed citations
11.
Velez, Gabriel, Alexander G. Bassuk, Kellie A. Schaefer, et al.. (2018). A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay. Molecular Case Studies. 4(3). a002519–a002519. 21 indexed citations
12.
Jeffrey, Brett G., Amy Turriff, Laryssa A. Huryn, et al.. (2016). The National Eye Institute Prospective ABCA4 Retinopathy Natural History Study: Fundus Guided Retinal Sensitivity Over 1 Year. Investigative Ophthalmology & Visual Science. 57(12). 141–141. 1 indexed citations
13.
George, Aman, Dina J. Zand, Robert B. Hufnagel, et al.. (2016). Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness. The American Journal of Human Genetics. 99(6). 1388–1394. 70 indexed citations
14.
Johnston, Jennifer J., Katie L. Lewis, David Ng, et al.. (2015). Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations. The American Journal of Human Genetics. 96(6). 913–925. 43 indexed citations
15.
Jeffrey, Brett G., et al.. (2014). Quantitative Measurement of Color Discrimination with a Low Vision Color Test in Patients with Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 55(13). 1399–1399. 2 indexed citations
16.
Sergeev, Yuri V., Katherine Pogrebniak, Wadih M. Zein, et al.. (2013). Molecular modeling of functional domain of ABCA4: towards understanding the genotype-to-phenotype relationships in Stargardt’s disease. Investigative Ophthalmology & Visual Science. 54(15). 1325–1325. 1 indexed citations
17.
Simeonov, Dimitre R., Xinjing Wang, Chen Wang, et al.. (2013). DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics. Human Mutation. 34(6). 827–835. 102 indexed citations
18.
Solomon, Benjamin D., Daniel Pineda‐Alvarez, Joan Z. Balog, et al.. (2009). Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia. American Journal of Medical Genetics Part A. 149A(11). 2543–2546. 73 indexed citations
19.
Gradstein, Libe, E. J. Fitzgibbon, J. Fielding Hejtmancik, et al.. (2006). Atypical Phenotype and Genotype in a Family With Suspected X–Linked Ocular Albinism. Investigative Ophthalmology & Visual Science. 47(13). 2508–2508. 1 indexed citations
20.
Tang, Johnny, Parag A. Gokhale, Steven E. Brooks, Delphine Blain, & Brian P. Brooks. (2006). Increased Corneal Thickness In Patients With Ocular Coloboma. Journal of American Association for Pediatric Ophthalmology and Strabismus. 10(2). 175–177. 7 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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