Daniel Navarro-Gomez

1.2k total citations
19 papers, 621 citations indexed

About

Daniel Navarro-Gomez is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Daniel Navarro-Gomez has authored 19 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Ophthalmology. Recurrent topics in Daniel Navarro-Gomez's work include Retinal Development and Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Retinal Diseases and Treatments (3 papers). Daniel Navarro-Gomez is often cited by papers focused on Retinal Development and Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Retinal Diseases and Treatments (3 papers). Daniel Navarro-Gomez collaborates with scholars based in United States, Netherlands and Italy. Daniel Navarro-Gomez's co-authors include Eric A. Pierce, Emily Place, Kinga M. Bujakowska, Xiaowu Gai, Qin Liu, Mark Consugar, Janey L. Wiggs, Maria E Sousa, Daniel G. Taub and Dan Yi Wang and has published in prestigious journals such as Nature Biotechnology, Bioinformatics and The American Journal of Human Genetics.

In The Last Decade

Daniel Navarro-Gomez

18 papers receiving 611 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Navarro-Gomez United States 13 495 204 178 51 38 19 621
Travis Cossette United States 11 327 0.7× 175 0.9× 87 0.5× 51 1.0× 67 1.8× 14 451
Roberta Tammaro Italy 11 515 1.0× 180 0.9× 87 0.5× 70 1.4× 20 0.5× 12 615
Yanrong Shi United States 10 485 1.0× 97 0.5× 104 0.6× 53 1.0× 50 1.3× 14 594
David McGaughey United States 14 433 0.9× 145 0.7× 58 0.3× 28 0.5× 18 0.5× 20 587
Anne Louise Askou Denmark 17 490 1.0× 145 0.7× 247 1.4× 28 0.5× 63 1.7× 31 661
Rajeshwari D. Koilkonda United States 13 818 1.7× 155 0.8× 172 1.0× 101 2.0× 23 0.6× 21 889
Silvio Alessandro Di Gioia Switzerland 10 333 0.7× 126 0.6× 83 0.5× 44 0.9× 12 0.3× 14 425
Patcharee Lertrit Thailand 17 625 1.3× 131 0.6× 87 0.5× 67 1.3× 29 0.8× 41 770
Béatrice Bocquet France 16 527 1.1× 80 0.4× 264 1.5× 87 1.7× 31 0.8× 37 607
Rebecca McGreal United States 10 537 1.1× 55 0.3× 87 0.5× 18 0.4× 66 1.7× 13 680

Countries citing papers authored by Daniel Navarro-Gomez

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Navarro-Gomez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Navarro-Gomez. 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 Daniel Navarro-Gomez. The network helps show where Daniel Navarro-Gomez may publish in the future.

Co-authorship network of co-authors of Daniel Navarro-Gomez

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Navarro-Gomez. A scholar is included among the top collaborators of Daniel Navarro-Gomez 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 Daniel Navarro-Gomez. Daniel Navarro-Gomez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Zaslavsky, Kirill, et al.. (2025). Low population penetrance of variants associated with inherited retinal degenerations. The American Journal of Human Genetics. 113(1). 71–82.
2.
Bronstein, Revital, Elizabeth E. Capowski, Sudeep Mehrotra, et al.. (2020). A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. Human Molecular Genetics. 29(6). 967–979. 18 indexed citations
3.
Kinde, Benyam, Emily Place, Daniel Navarro-Gomez, et al.. (2020). Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations. Genetics in Medicine. 22(6). 1079–1087. 66 indexed citations
4.
Place, Emily, Katherine R. Chao, Stephanie DiTroia, et al.. (2020). Expanding the phenotypic spectrum in RDH12-associated retinal disease. Molecular Case Studies. 6(1). a004754–a004754. 20 indexed citations
5.
Jamshidi, Farzad, Emily Place, Sudeep Mehrotra, et al.. (2018). Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration. Genetics in Medicine. 21(3). 694–704. 17 indexed citations
6.
Kleinstiver, Benjamin P., Michelle S. Prew, Daniel Navarro-Gomez, et al.. (2018). Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis Pigmentosa. The CRISPR Journal. 1(1). 55–64. 90 indexed citations
7.
Davoudi, Samaneh, Victoria Chang, Daniel Navarro-Gomez, et al.. (2018). Association of genetic variants in RAB23 and ANXA11 with uveitis in sarcoidosis.. PubMed. 24. 59–74. 15 indexed citations
8.
Pierce, Eric A., et al.. (2017). The Effect Of Vitamin A On Progression Of Retinitis Pigmentosa Is Not Determined By The Underlying Genetic Cause Of Disease. Investigative Ophthalmology & Visual Science. 58(8). 2011–2011. 2 indexed citations
9.
Bretón‐Romero, Rosa, J. L. Herraiz, Abel Suárez‐Fueyo, et al.. (2017). International mentoring as a new educational approach to alleviate brain drain, empower young talent, and internationalize higher education. Nature Biotechnology. 35(3). 285–288. 2 indexed citations
10.
Ung, Cindy, Li Shen, Samaneh Davoudi, et al.. (2017). Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy. Vision Research. 139. 168–176. 32 indexed citations
11.
Comander, Jason, Carol Weigel-DiFranco, Matthew Maher, et al.. (2017). The Genetic Basis of Pericentral Retinitis Pigmentosa—A Form of Mild Retinitis Pigmentosa. Genes. 8(10). 256–256. 32 indexed citations
12.
Nakata, Isao, et al.. (2016). Inherited optic atrophy gene discovery using whole exome sequencing.. Investigative Ophthalmology & Visual Science. 57(12). 5063–5063. 1 indexed citations
13.
Bujakowska, Kinga M., Rosario Fernández‐Godino, Emily Place, et al.. (2016). Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. Genetics in Medicine. 19(6). 643–651. 40 indexed citations
14.
Davoudi, Samaneh, Daniel Navarro-Gomez, Li Shen, et al.. (2016). NOD2 genetic variants and sarcoidosis-associated uveitis. American Journal of Ophthalmology Case Reports. 3. 39–42. 8 indexed citations
15.
Shen, Li, Maria Angela Diroma, Michael Gonzalez, et al.. (2016). MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease. Human Mutation. 37(6). 540–548. 31 indexed citations
16.
Consugar, Mark, Daniel Navarro-Gomez, Emily Place, et al.. (2014). Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. Genetics in Medicine. 17(4). 253–261. 179 indexed citations
17.
Bujakowska, Kinga M., Mark Consugar, Emily Place, et al.. (2014). Targeted Exon Sequencing in Usher Syndrome Type I. Investigative Ophthalmology & Visual Science. 55(12). 8488–8496. 12 indexed citations
18.
Navarro-Gomez, Daniel, Jeremy Leipzig, Li Shen, et al.. (2014). Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier. Bioinformatics. 31(8). 1310–1312. 45 indexed citations
19.
Pérez-Porro, Alicia, Daniel Navarro-Gomez, María Jesús Uriz, & Gonzalo Giribet. (2013). A NGS approach to the encrusting Mediterranean sponge Crella elegans (Porifera, Demospongiae, Poecilosclerida): transcriptome sequencing, characterization and overview of the gene expression along three life cycle stages. Molecular Ecology Resources. 13(3). 494–509. 11 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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