T. P. Dryja

471 total citations
10 papers, 371 citations indexed

About

T. P. Dryja is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, T. P. Dryja has authored 10 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Ophthalmology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in T. P. Dryja's work include Retinal Development and Disorders (6 papers), Advanced biosensing and bioanalysis techniques (3 papers) and Photoreceptor and optogenetics research (2 papers). T. P. Dryja is often cited by papers focused on Retinal Development and Disorders (6 papers), Advanced biosensing and bioanalysis techniques (3 papers) and Photoreceptor and optogenetics research (2 papers). T. P. Dryja collaborates with scholars based in United States, Switzerland and France. T. P. Dryja's co-authors include Eliot L. Berson, Terri L. McGee, Michael A. Sandberg, Meredith O. Sweeney, Dror Sharon, Eliot L. Berson, Carol Weigel-DiFranco, G.A.P. Bruns, Joyce M. Rapaport and Daniel M. Albert and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Documenta Ophthalmologica.

In The Last Decade

T. P. Dryja

10 papers receiving 362 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. P. Dryja United States	7	320	147	78	64	57	10	371
Esther Pomares Spain	14	413 1.3×	176 1.2×	61 0.8×	70 1.1×	89 1.6×	30	489
Katsuhiro Hosono Japan	13	407 1.3×	197 1.3×	47 0.6×	68 1.1×	132 2.3×	45	507
Lisette Hetterschijt Netherlands	10	339 1.1×	51 0.3×	34 0.4×	92 1.4×	95 1.7×	12	381
María Isabel López-Molina Spain	12	287 0.9×	130 0.9×	45 0.6×	41 0.6×	70 1.2×	18	351
Imad Ghazi France	10	618 1.9×	366 2.5×	81 1.0×	86 1.3×	120 2.1×	15	688
Ascensión Giménez Spain	9	335 1.0×	183 1.2×	53 0.7×	34 0.5×	64 1.1×	14	363
Shreyasi Choudhury United States	11	328 1.0×	130 0.9×	80 1.0×	79 1.2×	87 1.5×	13	376
F.P.M. Cremers Netherlands	8	377 1.2×	243 1.7×	44 0.6×	45 0.7×	83 1.5×	10	443
Christelle Michiels France	14	532 1.7×	279 1.9×	203 2.6×	57 0.9×	74 1.3×	28	641
Peter Humphries Ireland	5	430 1.3×	131 0.9×	118 1.5×	106 1.7×	88 1.5×	8	481

Countries citing papers authored by T. P. Dryja

Since Specialization

Citations

This map shows the geographic impact of T. P. Dryja'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 T. P. Dryja with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. P. Dryja more than expected).

Fields of papers citing papers by T. P. Dryja

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. P. Dryja

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

McGee, Terri L., et al.. (2010). Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa. Journal of Medical Genetics. 47(7). 499–506. 127 indexed citations

Neuner‐Jehle, Martin, et al.. (2009). Clinical Pharmacogenetic Analysis of Patients With Neovascular AMD Treated With Ranibizumab in the EXCITE Trial. 50(13). 722–722. 2 indexed citations

Rivolta, Carlo, Radha Ayyagari, Paul A. Sieving, Eliot L. Berson, & T. P. Dryja. (2003). Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. PubMed. 9. 49–51. 9 indexed citations

Sharon, Dror, et al.. (2001). The mutation spectrum of RPGR-ORF15 in North American patients with X-linked retinitis pigmentosa. 42(4). 642. 6 indexed citations

Sharon, Dror, G.A.P. Bruns, Terri L. McGee, et al.. (2000). X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.. PubMed. 41(9). 2712–21. 92 indexed citations

Dryja, T. P., et al.. (1997). Quantification of the paternal allele bias for new germline mutations in the retinoblastoma gene. Human Genetics. 100(3-4). 446–449. 42 indexed citations

Hahn, Lauri B., et al.. (1996). Missense mutation in the gene encoding the α subunit of rod transducin cosegregates with Nougaret's congenital night blindness. 37(3). 1 indexed citations

Sandberg, Michael A., Carol Weigel-DiFranco, T. P. Dryja, & Eliot L. Berson. (1995). Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa.. PubMed. 36(9). 1934–42. 61 indexed citations

Jacobson, Samuel G., Indra Mohindra, Richard Held, T. P. Dryja, & Daniel M. Albert. (1984). Visual acuity development in tyrosinase negative oculocutaneous albinism. Documenta Ophthalmologica. 56(4). 337–344. 19 indexed citations

10.

Dryja, T. P. & Daniel M. Albert. (1980). Lack of Adrenergic Influence on the Pigmentation of Iris Nevus Cells. Archives of Ophthalmology. 98(11). 1996–1996. 12 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.

Explore authors with similar magnitude of impact