Brian P. Brooks

3.9k total citations
55 papers, 1.9k 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 55 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 21 papers in Genetics and 15 papers in Ophthalmology. Recurrent topics in Brian P. Brooks's work include Retinal Diseases and Treatments (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Ocular Disorders and Treatments (8 papers). Brian P. Brooks is often cited by papers focused on Retinal Diseases and Treatments (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Ocular Disorders and Treatments (8 papers). Brian P. Brooks collaborates with scholars based in United States, United Kingdom and Canada. Brian P. Brooks's co-authors include John J. DiGiovanna, Deborah Tamura, Kenneth H. Kraemer, George Battaglia, Errol B. De Souza, Kenneth H. Fischbeck, N J Patronas, Raphael Schiffmann, James Eberwine and Scott A. Mackler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and SHILAP Revista de lepidopterología.

In The Last Decade

Brian P. Brooks

53 papers receiving 1.9k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	O03: Hydroxocobalamin (OHCbl) dose intensification can prevent visual deterioration and improve neurological and biochemical outcomes in CBLC deficiency 2025 ·Genetics in Medicine Open ·Charles P. Venditti, Jennifer L. Sloan, Wadih M. Zein, Audrey Thurm, (unknown), Carol Van Ryzin, Susan Ferry, (unknown), (unknown), Laryssa A. Huryn, Brian P. Brooks, Irini Manoli	0
2	Retina and RPE lipid profile changes linked with ABCA4 associated Stargardt's maculopathy 2023 ·Pharmacology & Therapeutics ·Mitra Farnoodian, (unknown), Francesca Barone, (unknown), (unknown), Bokkyoo Jun, Khanh Do, William C. Gordon, (unknown), (unknown), (unknown), Tiziana Cogliati, Ruchi Sharma, Brian P. Brooks, Nicolás G. Bazán, Kapil Bharti	9
3	Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease 2022 ·PLoS Genetics ·Jana Zernant, Winston Lee, Jun Wang, Kerry Goetz, Ehsan Ullah, Takayuki Nagasaki, (unknown), Gerald A. Fishman, Stephen H. Tsang, Santa J. Tumminia, Brian P. Brooks, Robert B. Hufnagel, Rui Chen, Rando Allikmets	9
4	Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlates 2022 ·JCI Insight ·Maximilian Pfau, Catherine A. Cukras, Laryssa A. Huryn, Wadih M. Zein, Ehsan Ullah, (unknown), Amy Turriff, Michelle A. Chen, (unknown), (unknown), Robert B. Hufnagel, (unknown), Brian P. Brooks	15
5	A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung disease 2020 ·American Journal of Medical Genetics Part A ·Elizabeth A. Burke, (unknown), Lynne A. Wolfe, Brian P. Brooks, John J. DiGiovanna, Donald W. Hadley, Tanya Lehky, Andrea Gropman, Cynthia J. Tifft, William A. Gahl, Camilo Toro, David R. Adams	7
6	Elucidating the genotypic spectrum of nanophthalmos and high hyperopia 2020 ·Investigative Ophthalmology & Visual Science ·Lev Prasov, Bin Guan, Ehsan Ullah, Sayoko E. Moroi, Steven M. Archer, (unknown), (unknown), (unknown), (unknown), Laryssa A. Huryn, Hemant Pawar, Brian P. Brooks, Julia E. Richards, Robert B. Hufnagel	0
7	Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center 2018 ·Ophthalmology ·Brian P. Brooks, Wadih M. Zein, A. Thompson, (unknown), Dan Doherty, Melissa A. Parisi, Ian A. Glass, May Christine V. Malicdan, Thierry Vilboux, Meghana Vemulapalli, James C. Mullikin, William A. Gahl, Meral Gunay‐Aygun	41
8	Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center 2017 ·Genetics in Medicine ·Thierry Vilboux, Dan Doherty, Ian A. Glass, Melissa A. Parisi, Ian G. Phelps, Andrew R. Cullinane, Wadih M. Zein, Brian P. Brooks, Theo Heller, Ariane Soldatos, Neal L. Oden, (unknown), Meghana Vemulapalli, James C. Mullikin, May Christine V. Malicdan, William A. Gahl, Meral Gunay‐Aygun	88
9	In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations 2017 ·Cell Reports ·Hiroko Shimada, Quanlong Lü, (unknown), Kunio Nagashima, Milton A. English, Elizabeth M. Semler, (unknown), Artur V. Cideciyan, Tiansen Li, Brian P. Brooks, Meral Gunay‐Aygun, Samuel G. Jacobson, Tiziana Cogliati, Christopher J. Westlake, Anand Swaroop	109
10	Modeling ciliogenesis in Leber congenital amaurosis using fibroblasts from patients with CEP290 mutations 2016 ·Investigative Ophthalmology & Visual Science ·(unknown), (unknown), Milton A. English, (unknown), (unknown), Tiziana Cogliati, Brian P. Brooks, Samuel G. Jacobson, Anand Swaroop	3
11	Ophthalmic Manifestations and Long-Term Visual Outcomes in Patients with Cobalamin C Deficiency 2016 ·Ophthalmology ·Brian P. Brooks, A. Thompson, Jennifer L. Sloan, Irini Manoli, Nuria Carrillo, Wadih M. Zein, Charles P. Venditti	30
12	eyeGENE(R) 2012 ·Current Opinion in Ophthalmology ·Kerry Goetz, (unknown), Santa J. Tumminia, Brian P. Brooks	16
13	Ophthalmic Manifestations and Histopathology of Xeroderma Pigmentosum: Two Clinicopathological Cases and a Review of the Literature 2011 ·Survey of Ophthalmology ·Hema L. Ramkumar, Brian P. Brooks, Xiaoguang Cao, Deborah Tamura, John J. DiGiovanna, Kenneth H. Kraemer, Chi‐Chao Chan	50
14	Congenital Aniridia Variant: Minimally Abnormal Irides with Severe Limbal Stem Cell Deficiency 2011 ·Ophthalmology ·(unknown), Brian P. Brooks, Edward J. Holland	45
15	Ocular Manifestations of Trichothiodystrophy 2011 ·Ophthalmology ·Brian P. Brooks, A. Thompson, Janine A. Clayton, Chi‐Chao Chan, Deborah Tamura, Wadih M. Zein, Delphine Blain, (unknown), John Rowan, (unknown), Sikandar G. Khan, Takahiro Ueda, (unknown), Kyu‐Seon Oh, John J. DiGiovanna, Kenneth H. Kraemer	21
16	Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL 2010 ·Human Mutation ·(unknown), (unknown), Elangovan Boobalan, Yuri V. Sergeev, Rafael C. Caruso, Edwin M. Stone, Anand Swaroop, Mary A. Johnson, Brian P. Brooks	47
17	Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: A complex genotype–phenotype relationship 2007 ·Neuroscience ·Kenneth H. Kraemer, N J Patronas, Raphael Schiffmann, Brian P. Brooks, Deborah Tamura, John J. DiGiovanna	310
18	A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome 2004 ·Ophthalmic Genetics ·Brian P. Brooks, Sayoko E. Moroi, Catherine A. Downs, (unknown), Mohammad Othman, Elena V. Semina, Julia E. Richards	24
19	Characterization of an Expanded Glutamine Repeat Androgen Receptor in a Neuronal Cell Culture System 1997 ·Neurobiology of Disease ·Brian P. Brooks, Henry L. Paulson, Diane E. Merry, Edgar F. Salazar‐Grueso, Albert O. Brinkmann, Elizabeth M. Wilson, Kenneth H. Fischbeck	69
20	Pharmacologic profile of MDMA (3,4-methylenedioxymethamphetamine) at various brain recognition sites 1988 ·European Journal of Pharmacology ·George Battaglia, Brian P. Brooks, (unknown), Errol B. De Souza	228

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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