Brian P. Brooks

Also affiliated with National Eye Institute

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.5Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia

Ophthalmology(2022)10.1016/j.ophtha.2022.02.010

Top 14%

1.5DataRank

Top 14%74 citations

Gail Maconachie, Jinu Han, Line Kessel, Maria M. van Genderen, Rebecca J. McLean +34 more

Papers

Driven by 21 papers — median percentile 86. Top paper: “Genotypic and Phenotypic Spectrum of Foveal Hypoplasia”.

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia

Ophthalmology(2022)10.1016/j.ophtha.2022.02.010

Top 14%

1.5DataRank

Top 14%74 citations

Gail Maconachie, Jinu Han, Line Kessel, Maria M. van Genderen, Rebecca J. McLean +34 more

Atypical and ultra-rare Usher syndrome: a review

Ophthalmic Genetics(2020)10.1080/13816810.2020.1747090

N/A

0.538DataRank · unranked

35 citations

Robert B. Hufnagel, Thomas B. Friedman, Amy Turriff, Carmen C. Brewer, Christopher Zalewski +6 more

Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease

PLoS Genetics(2022)10.1371/journal.pgen.1010129

N/A

0.425DataRank · unranked

16 citations

Winston Lee, Jun Wang, Kerry Goetz, Ehsan Ullah, Takayuki Nagasaki +9 more

ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease

Investigative Ophthalmology & Visual Science(2022)10.1167/iovs.63.4.20

N/A

0.312DataRank · unranked

7 citations

Manar Salameh, Mubeen Khan, Elise Héon, Ketan Mishra, Rebekkah J. Hitti‐Malin +12 more

Clinical diagnosis of presumed SOX2 gonadosomatic mosaicism

Ophthalmic Genetics(2021)10.1080/13816810.2021.1888127

N/A

0DataRank · unranked

4 citations

Robert B. Hufnagel, Bin Guan, Delphine Blain, Julie C. Sapp, Andrea Gropman +5 more

Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB–Mediated Autoinflammatory Disease with Retinal Dystrophy

Ophthalmology(2022)10.1016/j.ophtha.2022.10.026

N/A

0DataRank · unranked

35 citations

Christina Torres Kozycki, Jasmine Y. Serpen, Wadih M. Zein, Ehsan Ullah, Alessandro Iannaccone +8 more

Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.31966

N/A

0DataRank · unranked

4 citations

Melissa A. Parisi, Burak Altintas, May Christine V. Malicdan, Thierry Vilboux, Jasmine Knoll +6 more

Transcriptional mapping of the macaque retina and RPE-choroid reveals conserved inter-tissue transcription drivers and signaling pathways

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.01.21.477280

N/A

0DataRank · unranked

0 citations

David McGaughey, Congxiao Zhang, Sairah Yousaf, James H. Liu, Brian P. Brooks +4 more

Retina and RPE lipid profile changes linked with ABCA4 associated Stargardt's maculopathy

Pharmacology & Therapeutics(2023)10.1016/j.pharmthera.2023.108482

N/A

0DataRank · unranked

20 citations

Devika Bose, Francesca Barone, Luke Mathew Nelson, Marisa Boyle, Bokkyoo Jun +11 more

Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome

medRxiv(2024)10.1101/2024.11.09.24316578

N/A

0DataRank · unranked

2 citations

Ehsan Ullah, Aman George, Mara I Maftei, Elangovan Elangovan, Daniel Sanchez-Mendoza +18 more

Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans

Translational Vision Science & Technology(2024)10.1167/tvst.13.9.4

N/A

0DataRank · unranked

0 citations

Raisa Ionin, Laryssa A. Huryn, Catherine A. Cukras, Delphine Blain, Aime Agather +5 more

Systematic phenotype and genotype characterization of Moebius syndrome

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103437

N/A

0DataRank · unranked

1 citations

Julie A. Jurgens, Narisu Narisu, Zhongyang Zhang, Brenda J. Barry, Carol Van Ryzin +37 more

TYROSINASE-Deficient Human Retinal Pigment Epithelium Exhibits Melanosome Maturation Defects

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.13.4

N/A

0DataRank · unranked

1 citations

Tyler Pfister, Charles DeYoung, Ruchi Sharma, Mones Abu‐Asab, Jizhong Zou +3 more

A zebrafish model of crim1 loss of function has small and misshapen lenses with dysregulated clic4 and fgf1b expression

Frontiers in Cell and Developmental Biology(2025)10.3389/fcell.2025.1522094

N/A

0DataRank · unranked

1 citations

Stephanie Htun, Manoj K. Pandey, Yihui Sun, Albert Frank Magnusen, Ehsan Ullah +9 more

Ampyrone (4-Aminoantipyrine) is a Direct Agonist of Human Tyrosinase and Potential Therapeutic for Oculocutaneous Albinism and Disorders of Hypopigmentation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.682036

N/A

0DataRank · unranked

1 citations

Yuhong Wang, Nathan P. Coussens, Vijay K. Kalaskar, Zuhal Eraslan, Samuel Grondin +21 more

Case Report: Association of Ocular Colobomas With a Novel Missense Variant in CDC42, a Member of the Rho Family of Small GTPases

Clinical Genetics(2025)10.1111/cge.14768

N/A

0DataRank · unranked

0 citations

Nawaal Shinwari, Aleksey Porollo, Eniolami O. Dosunmu, Ehsan Ullah, Bin Guan +7 more

Retinoschisis associated with Kearns-Sayre syndrome

Ophthalmic Genetics(2020)10.1080/13816810.2020.1799416

N/A

0DataRank · unranked

8 citations

Robert B. Hufnagel, Delphine Blain, Andrea Gropman, Brian P. Brooks, Julia Chertkof

Transgene-Induced Chromosomal Rearrangement With Aberrant Human Vascular Endothelial Growth Factor at the Optic Fissure Leads to Uveal Coloboma in Mice

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.13.7

N/A

0DataRank · unranked

0 citations

Ramakrishna P. Alur, Vijay K. Kalaskar, Aman George, Elangovan Boobalan, David McGaughey +11 more

Reply

Journal of American Association for Pediatric Ophthalmology and Strabismus(2020)10.1016/j.jaapos.2019.10.009

N/A

0DataRank · unranked

0 citations

Catherine A. Cukras, Brian P. Brooks, Laryssa A. Huryn, Amy Turriff

In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7

medRxiv(2020)10.1101/2020.10.05.20207340

N/A

0DataRank · unranked

0 citations

Shabbir Hussain I. Merchant, Sanaz Attaripour-Isfahani, Hyun Joo Cho, Patrick Mcgurrin, Brian P. Brooks +5 more

In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7

NeuroImage Clinical(2021)10.1016/j.nicl.2021.102561

N/A

0DataRank · unranked

6 citations

Shabbir Hussain I. Merchant, Sanaz Attaripour-Isfahani, Hyun Joo Cho, Patrick Mcgurrin, Brian P. Brooks +5 more

Brian P. Brooks

Indexed papers

Top data-sharing exemplar

Papers