Adam P. DeLuca

3.6k total citations
46 papers, 2.1k citations indexed

About

Adam P. DeLuca is a scholar working on Molecular Biology, Ophthalmology and Sensory Systems. According to data from OpenAlex, Adam P. DeLuca has authored 46 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 17 papers in Ophthalmology and 10 papers in Sensory Systems. Recurrent topics in Adam P. DeLuca's work include Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (10 papers). Adam P. DeLuca is often cited by papers focused on Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (10 papers). Adam P. DeLuca collaborates with scholars based in United States, Netherlands and Japan. Adam P. DeLuca's co-authors include Todd E. Scheetz, Edwin M. Stone, Robert F. Mullins, Budd A. Tucker, Val C. Sheffield, Terry A. Braun, Richard J. Smith, Michael S. Hildebrand, S. Scott Whitmore and A. Eliot Shearer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Adam P. DeLuca

45 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adam P. DeLuca United States 23 1.4k 643 551 366 260 46 2.1k
Elena Aller Spain 26 1.8k 1.3× 321 0.5× 863 1.6× 243 0.7× 88 0.3× 55 2.3k
Yvette J.M. de Kok Netherlands 9 981 0.7× 321 0.5× 329 0.6× 225 0.6× 109 0.4× 12 1.3k
Teresa Jaijo Spain 22 984 0.7× 201 0.3× 597 1.1× 151 0.4× 63 0.2× 58 1.4k
A. Pinckers Netherlands 24 1.7k 1.2× 990 1.5× 158 0.3× 357 1.0× 296 1.1× 133 2.6k
Karen Grønskov Denmark 27 1.6k 1.1× 252 0.4× 188 0.3× 925 2.5× 107 0.4× 90 2.3k
Daniel Gibbs United States 26 1.3k 0.9× 940 1.5× 139 0.3× 345 0.9× 480 1.8× 51 2.4k
Nahid G. Robertson United States 22 616 0.4× 154 0.2× 1.1k 2.0× 82 0.2× 36 0.1× 31 1.7k
Gema García‐García Spain 17 764 0.5× 145 0.2× 366 0.7× 146 0.4× 43 0.2× 48 983
Stéphane Blanchard France 20 1.9k 1.3× 82 0.1× 1.4k 2.5× 370 1.0× 26 0.1× 32 2.9k
Isabelle Schrauwen United States 25 690 0.5× 56 0.1× 525 1.0× 336 0.9× 31 0.1× 105 1.8k

Countries citing papers authored by Adam P. DeLuca

Since Specialization
Citations

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

Fields of papers citing papers by Adam P. DeLuca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adam P. DeLuca. 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 Adam P. DeLuca. The network helps show where Adam P. DeLuca may publish in the future.

Co-authorship network of co-authors of Adam P. DeLuca

This figure shows the co-authorship network connecting the top 25 collaborators of Adam P. DeLuca. A scholar is included among the top collaborators of Adam P. DeLuca 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 Adam P. DeLuca. Adam P. DeLuca 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.
Voigt, Andrew P., Michael A. Collingwood, S. Scott Whitmore, et al.. (2023). Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement. Stem Cells Translational Medicine. 12(6). 365–378. 12 indexed citations
2.
Whitmore, S. Scott, Adam P. DeLuca, Jeaneen L. Andorf, et al.. (2023). Modeling rod and cone photoreceptor cell survival in vivo using optical coherence tomography. Scientific Reports. 13(1). 6896–6896. 2 indexed citations
3.
DeLuca, Adam P., S. Scott Whitmore, Jeaneen L. Andorf, et al.. (2023). Using Goldmann Visual Field Volume to Track Disease Progression in Choroideremia. SHILAP Revista de lepidopterología. 3(4). 100397–100397.
4.
Raj, Abhishek, Katherine Young, Adam P. DeLuca, et al.. (2021). Label-free microfluidic enrichment of cancer cells from non-cancer cells in ascites. Scientific Reports. 11(1). 18032–18032. 8 indexed citations
5.
Whitmore, S. Scott, Adam P. DeLuca, D. Brice Critser, et al.. (2020). Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease. Scientific Reports. 10(1). 16576–16576. 14 indexed citations
6.
Voigt, Andrew P., S. Scott Whitmore, Adam P. DeLuca, et al.. (2020). Spectacle: An interactive resource for ocular single-cell RNA sequencing data analysis. Experimental Eye Research. 200. 108204–108204. 67 indexed citations
7.
Han, Ian C., S. Scott Whitmore, D. Brice Critser, et al.. (2018). Wide-Field Swept-Source OCT and Angiography in X-Linked Retinoschisis. Ophthalmology Retina. 3(2). 178–185. 30 indexed citations
8.
Hedberg‐Buenz, Adam, et al.. (2017). Primary congenital and developmental glaucomas. Human Molecular Genetics. 26(R1). R28–R36. 71 indexed citations
9.
Stone, Edwin M., Jeaneen L. Andorf, S. Scott Whitmore, et al.. (2017). Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease. Ophthalmology. 124(9). 1314–1331. 299 indexed citations
10.
Burnight, Erin R., Luke A. Wiley, Adam P. DeLuca, et al.. (2016). CRISPR/Cas9-mediated genome editing for correction of inherited retinal disease mutations.. Investigative Ophthalmology & Visual Science. 57(12). 1157–1157. 2 indexed citations
11.
Gaynor, Sophia C., Eric T. Monson, Adam P. DeLuca, et al.. (2016). A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1080–1087. 13 indexed citations
12.
DeLuca, Adam P., S. Scott Whitmore, Tasneem P. Sharma, et al.. (2015). Hypomorphic mutations inTRNT1cause retinitis pigmentosa with erythrocytic microcytosis. Human Molecular Genetics. 25(1). 44–56. 56 indexed citations
13.
DeLuca, Adam P., Joseph C. Giacalone, Luke A. Wiley, et al.. (2014). RPGR, a common source of missed variants in exome sequencing experiments. Investigative Ophthalmology & Visual Science. 55(13). 3262–3262. 1 indexed citations
14.
Whitmore, S. Scott, Alex H. Wagner, Adam P. DeLuca, et al.. (2014). Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-Seq. Experimental Eye Research. 129. 93–106. 89 indexed citations
15.
Braun, Terry A., Alex H. Wagner, Adam P. DeLuca, et al.. (2013). The Ocular Tissue Database. Investigative Ophthalmology & Visual Science. 54(15). 3383–3383. 3 indexed citations
16.
DeLuca, Adam P., et al.. (2013). Vision Variation Database (VVD). Investigative Ophthalmology & Visual Science. 54(15). 3382–3382. 2 indexed citations
17.
Wagner, Alex H., Kyle R. Taylor, Adam P. DeLuca, et al.. (2013). Prioritization of Retinal Disease Genes: An Integrative Approach. Human Mutation. 34(6). 853–859. 6 indexed citations
18.
Wagner, Alex H., Vijay Anand, Jon E. Chatterton, et al.. (2013). Exon-level expression profiling of ocular tissues. Experimental Eye Research. 111. 105–111. 68 indexed citations
19.
Eppsteiner, Robert W., A. Eliot Shearer, Michael S. Hildebrand, et al.. (2012). Prediction of cochlear implant performance by genetic mutation: The spiral ganglion hypothesis. Hearing Research. 292(1-2). 51–58. 108 indexed citations
20.
Hildebrand, Michael S., Adam P. DeLuca, Kyle R. Taylor, et al.. (2009). A Contemporary Review of AudioGene audioprofiling: A machine‐based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss. The Laryngoscope. 119(11). 2211–2215. 29 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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