F. Gonzalez–Fernandez

1.1k total citations
23 papers, 800 citations indexed

About

F. Gonzalez–Fernandez is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, F. Gonzalez–Fernandez has authored 23 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Ophthalmology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in F. Gonzalez–Fernandez's work include Retinal Development and Disorders (16 papers), Retinoids in leukemia and cellular processes (12 papers) and Retinal Diseases and Treatments (8 papers). F. Gonzalez–Fernandez is often cited by papers focused on Retinal Development and Disorders (16 papers), Retinoids in leukemia and cellular processes (12 papers) and Retinal Diseases and Treatments (8 papers). F. Gonzalez–Fernandez collaborates with scholars based in United States and Spain. F. Gonzalez–Fernandez's co-authors include C.D.B. Bridges, S.–L. Fong, G. I. Liou, Richard Alvarez, James I. Healy, Robert A. Landers, D. Lam, Dominic Man-Kit Lam, Scott R. VandenBerg and Bao Yang and has published in prestigious journals such as The Journal of Cell Biology, Journal of Neurochemistry and Vision Research.

In The Last Decade

F. Gonzalez–Fernandez

22 papers receiving 772 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F. Gonzalez–Fernandez United States 15 686 356 159 103 85 23 800
Robert A. Landers United States 18 747 1.1× 309 0.9× 200 1.3× 157 1.5× 83 1.0× 27 844
Walid Moghrabi Saudi Arabia 10 618 0.9× 226 0.6× 144 0.9× 95 0.9× 54 0.6× 17 682
Marcia Lloyd United States 15 987 1.4× 620 1.7× 182 1.1× 154 1.5× 174 2.0× 18 1.2k
Sassan M. Azarian United States 10 1.1k 1.7× 575 1.6× 237 1.5× 206 2.0× 154 1.8× 16 1.3k
Michael H. Chaitin United States 15 627 0.9× 224 0.6× 202 1.3× 222 2.2× 109 1.3× 17 747
James S. Friedman United States 14 793 1.2× 257 0.7× 255 1.6× 131 1.3× 68 0.8× 20 935
F. P. M. Cremers Netherlands 7 804 1.2× 482 1.4× 93 0.6× 132 1.3× 119 1.4× 8 879
Melanie M. Sohocki United States 14 1.0k 1.5× 501 1.4× 267 1.7× 160 1.6× 93 1.1× 18 1.1k
Thanh Hoang United States 13 707 1.0× 151 0.4× 113 0.7× 79 0.8× 72 0.8× 20 805
Lynette Feeney United States 13 416 0.6× 314 0.9× 94 0.6× 134 1.3× 151 1.8× 20 687

Countries citing papers authored by F. Gonzalez–Fernandez

Since Specialization
Citations

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

Fields of papers citing papers by F. Gonzalez–Fernandez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. Gonzalez–Fernandez. 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 F. Gonzalez–Fernandez. The network helps show where F. Gonzalez–Fernandez may publish in the future.

Co-authorship network of co-authors of F. Gonzalez–Fernandez

This figure shows the co-authorship network connecting the top 25 collaborators of F. Gonzalez–Fernandez. A scholar is included among the top collaborators of F. Gonzalez–Fernandez 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 F. Gonzalez–Fernandez. F. Gonzalez–Fernandez 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.
Mendiola, Andrew S., et al.. (2016). TGFβ induces BIGH3 expression and human retinal pericyte apoptosis: a novel pathway of diabetic retinopathy. Eye. 30(12). 1639–1647. 20 indexed citations
2.
Garlipp, Mary Alice & F. Gonzalez–Fernandez. (2010). Light-Dependent Interaction of Interphotoreceptor Retinoid-Binding Protein (IRBP) With Xenopus Cone Outer Segments. 51(13). 1896–1896. 2 indexed citations
3.
Griswold, Jennifer, et al.. (2009). Bovine IRBP Functions in vitro as a Thiol-Based Antioxidant. 50(13). 4504–4504.
4.
Gonzalez–Fernandez, F., et al.. (2005). The interphotoreceptor retinoid-binding protein (IRBP) of the chicken (Gallus gallus domesticus).. PubMed. 11. 833–45. 14 indexed citations
5.
Gonzalez–Fernandez, F.. (2002). Evolution of the visual cycle: the role of retinoid-binding proteins. Journal of Endocrinology. 175(1). 75–88. 29 indexed citations
6.
Gonzalez–Fernandez, F., et al.. (1999). 11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.. PubMed. 5. 41–41. 70 indexed citations
7.
Cunningham, Lisa L., et al.. (1999). Interphotoreceptor Retinoid-Binding Protein (IRBP) is Rapidly Cleared From theXenopusInterphotoreceptor Matrix. Experimental Eye Research. 68(4). 399–410. 9 indexed citations
8.
Sherman, Nicholas E., et al.. (1998). Arginine to glutamine substitutions in the fourth module of Xenopus interphotoreceptor retinoid-binding protein.. PubMed. 4. 30–30. 7 indexed citations
9.
10.
Gonzalez–Fernandez, F., et al.. (1998). Ultrastructural changes in rabbit ciliary body after extraocular mitomycin C.. PubMed. 39(10). 1971–5. 21 indexed citations
11.
Braiman, Mark S., et al.. (1997). Truncational mutagenesis of the fourth module of xenopus irbp. Investigative Ophthalmology & Visual Science. 38(4). 4 indexed citations
12.
Gonzalez–Fernandez, F., et al.. (1993). Differential Expression of Interphotoreceptor Retinoid-binding Protein, Opsin, Cellular Retinaldehyde-binding Protein, and Basic Fibroblastic Growth Factor. Experimental Eye Research. 56(4). 411–427. 33 indexed citations
13.
Gonzalez–Fernandez, F., et al.. (1993). Differential Expression of Retinal Proteins in a Pineal Parenchymal Tumor. Journal of Neuropathology & Experimental Neurology. 52(5). 516–524. 20 indexed citations
14.
Gonzalez–Fernandez, F., M. Beatriz S. Lopes, José M. Garcı́a-Fernández, et al.. (1992). Expression of developmentally defined retinal phenotypes in the histogenesis of retinoblastoma.. PubMed. 141(2). 363–75. 40 indexed citations
15.
16.
LaVail, Matthew M., David S. Papermaster, C.D.B. Bridges, et al.. (1987). Absence of an inherited retinal degeneration in the WAG/Rij rat. Experimental Eye Research. 44(3). 465–469. 5 indexed citations
17.
Gonzalez–Fernandez, F., et al.. (1985). Interstitial retinol-binding protein in the interphotoreceptor matrix of normal and dystrophic rats.. PubMed. 190. 213–29. 6 indexed citations
18.
Bridges, C.D.B., Richard Alvarez, S.–L. Fong, et al.. (1984). Visual cycle in the mammalian eye. Vision Research. 24(11). 1581–1594. 56 indexed citations
19.
Fong, S.–L., G. I. Liou, Robert A. Landers, et al.. (1984). Characterization, Localization, and Biosynthesis of an Interstitial Retinol‐Binding Glycoprotein in the Human Eye. Journal of Neurochemistry. 42(6). 1667–1676. 88 indexed citations
20.
Liou, G. I., C.D.B. Bridges, S.–L. Fong, Richard Alvarez, & F. Gonzalez–Fernandez. (1982). Vitamin a transport between retina and pigment epithelium—an interstitial protein carrying endogenous retinol (interstitial retinol-binding protein). Vision Research. 22(12). 1457–1467. 183 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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