Robert B. Hufnagel

3.5k total citations
97 papers, 1.3k citations indexed

About

Robert B. Hufnagel is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Robert B. Hufnagel has authored 97 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 31 papers in Genetics and 29 papers in Ophthalmology. Recurrent topics in Robert B. Hufnagel's work include Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (22 papers) and Ocular Disorders and Treatments (14 papers). Robert B. Hufnagel is often cited by papers focused on Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (22 papers) and Ocular Disorders and Treatments (14 papers). Robert B. Hufnagel collaborates with scholars based in United States, United Kingdom and Germany. Robert B. Hufnagel's co-authors include Nadean L. Brown, Zubair M. Ahmed, Brian P. Brooks, Howard M. Saal, Wadih M. Zein, Tien Le, Robert A. Sisk, Robert J. Hopkin, Laryssa A. Huryn and Temesgen Fufa and has published in prestigious journals such as Genes & Development, SHILAP Revista de lepidopterología and Ophthalmology.

In The Last Decade

Robert B. Hufnagel

91 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert B. Hufnagel United States 20 848 307 247 199 138 97 1.3k
Wadih M. Zein United States 21 762 0.9× 288 0.9× 369 1.5× 246 1.2× 144 1.0× 86 1.4k
Shuhei Kameya Japan 18 968 1.1× 347 1.1× 164 0.7× 135 0.7× 120 0.9× 56 1.1k
Brian P. Brooks United States 22 884 1.0× 253 0.8× 360 1.5× 390 2.0× 203 1.5× 73 1.4k
Felix Tonagel Germany 14 772 0.9× 347 1.1× 119 0.5× 97 0.5× 124 0.9× 33 1.0k
Emin Cumhur Şener Türkiye 15 395 0.5× 289 0.9× 184 0.7× 82 0.4× 94 0.7× 38 1.0k
Maria A. Musarella Canada 22 1.4k 1.6× 407 1.3× 434 1.8× 375 1.9× 132 1.0× 45 1.8k
Shunbin Xu United States 18 1.4k 1.7× 308 1.0× 113 0.5× 91 0.5× 267 1.9× 37 2.2k
Jacoline B. ten Brink Netherlands 22 1.3k 1.5× 682 2.2× 608 2.5× 480 2.4× 282 2.0× 49 2.0k
Janine Davis United States 17 959 1.1× 113 0.4× 245 1.0× 114 0.6× 300 2.2× 23 1.6k
Samuel McLenachan Australia 20 575 0.7× 374 1.2× 78 0.3× 78 0.4× 203 1.5× 77 1.1k

Countries citing papers authored by Robert B. Hufnagel

Since Specialization
Citations

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

Fields of papers citing papers by Robert B. Hufnagel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert B. Hufnagel. 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 Robert B. Hufnagel. The network helps show where Robert B. Hufnagel may publish in the future.

Co-authorship network of co-authors of Robert B. Hufnagel

This figure shows the co-authorship network connecting the top 25 collaborators of Robert B. Hufnagel. A scholar is included among the top collaborators of Robert B. Hufnagel 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 Robert B. Hufnagel. Robert B. Hufnagel 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.
Ullah, Ehsan, et al.. (2025). Genotype–Phenotype Spectrum of eyeGENE Patients With Familial Exudative Vitreoretinopathy: Novel Variants in Norrin/β-Catenin Signaling Pathway Genes. Investigative Ophthalmology & Visual Science. 66(2). 9–9. 1 indexed citations
2.
Sánchez, A.I., et al.. (2023). Prenatal and infantile diagnosis of craniosynostosis in individuals with RASopathies. American Journal of Medical Genetics Part A. 194(2). 195–202. 2 indexed citations
3.
Cornelis, Stéphanie S., Miriam Bauwens, Lonneke Haer‐Wigman, et al.. (2023). Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework. Human Mutation. 2023. 1–12. 7 indexed citations
4.
Hufnagel, Robert B., et al.. (2023). A Comprehensive Report of Intrinsically Disordered Regions in Inherited Retinal Diseases. Genes. 14(8). 1601–1601. 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.
Zernant, Jana, Winston Lee, Jun Wang, et al.. (2022). Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease. PLoS Genetics. 18(3). e1010129–e1010129. 9 indexed citations
7.
Guan, Bin, Ehsan Ullah, Amy Turriff, et al.. (2022). Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder. Genes. 13(4). 675–675. 3 indexed citations
8.
Iannaccone, Alessandro, Carmen C. Brewer, Peiyao Cheng, et al.. (2021). Auditory and olfactory findings in patients with USH2A‐related retinal degeneration—Findings at baseline from the rate of progression in USH2A‐related retinal degeneration natural history study (RUSH2A). American Journal of Medical Genetics Part A. 185(12). 3717–3727. 5 indexed citations
9.
Fufa, Temesgen, et al.. (2021). Building the mega single-cell transcriptome ocular meta-atlas. GigaScience. 10(10). 21 indexed citations
10.
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
11.
Venkatesh, Aditya, Mansoor Ali Syed, Raymond Oh, et al.. (2021). Antisense oligonucleotide mediated increase in OPA1 improves mitochondrial function in fibroblasts derived from patients with autosomal dominant optic atrophy (ADOA). Investigative Ophthalmology & Visual Science. 62(8). 1482–1482. 1 indexed citations
12.
Liu, Jianfei, Catherine A. Cukras, Robert B. Hufnagel, et al.. (2021). Active Cell Appearance Model Induced Generative Adversarial Networks for Annotation-Efficient Cell Segmentation and Identification on Adaptive Optics Retinal Images. IEEE Transactions on Medical Imaging. 40(10). 2820–2831. 14 indexed citations
13.
Prasov, Lev, Bin Guan, Ehsan Ullah, et al.. (2020). Elucidating the genotypic spectrum of nanophthalmos and high hyperopia. Investigative Ophthalmology & Visual Science. 61(7). 1251–1251.
14.
Liu, James, et al.. (2020). Loss of uba2 function in zebrafish phenocopies a rare human disorder. Investigative Ophthalmology & Visual Science. 61(7). 2790–2790. 1 indexed citations
15.
Richardson, Rudy J., John K. Fink, Paul Glynn, et al.. (2020). Neuropathy target esterase (NTE/PNPLA6) and organophosphorus compound-induced delayed neurotoxicity (OPIDN). PubMed. 4. 1–78. 33 indexed citations
16.
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
17.
Valencia, C. Alexander, et al.. (2020). An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(4). 996–1008. 8 indexed citations
18.
Venkatesh, Aditya, Zhiyu Li, Anne Christiansen, et al.. (2020). Antisense oligonucleotide mediated increase of OPA1 expression using TANGO technology for the treatment of autosomal dominant optic atrophy. Investigative Ophthalmology & Visual Science. 61(7). 2755–2755. 3 indexed citations
19.
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
20.
Hufnagel, Robert B., et al.. (2007). Conserved regulation of Math5 and Math1 revealed by Math5-GFP transgenes. Molecular and Cellular Neuroscience. 36(4). 435–448. 27 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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