Jenina Capasso

581 total citations
36 papers, 316 citations indexed

About

Jenina Capasso is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Jenina Capasso has authored 36 papers receiving a total of 316 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Genetics and 13 papers in Ophthalmology. Recurrent topics in Jenina Capasso's work include Retinal Development and Disorders (19 papers), Ocular Disorders and Treatments (12 papers) and Retinal Diseases and Treatments (8 papers). Jenina Capasso is often cited by papers focused on Retinal Development and Disorders (19 papers), Ocular Disorders and Treatments (12 papers) and Retinal Diseases and Treatments (8 papers). Jenina Capasso collaborates with scholars based in United States, Thailand and India. Jenina Capasso's co-authors include Alex V. Levin, Mai Tsukikawa, Reuven Sharony, Chris F. Inglehearn, Yu‐Hung Lai, Tamar Ben‐Yosef, Claire E. L. Smith, Alan J. Mighell, Steven J. Brookes and William G. Newman and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Ophthalmology.

In The Last Decade

Jenina Capasso

34 papers receiving 308 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jenina Capasso United States	12	238	113	103	45	28	36	316
Jan-Willem R. Pott Netherlands	8	293 1.2×	176 1.6×	71 0.7×	48 1.1×	38 1.4×	9	336
Elena Schiff United Kingdom	10	300 1.3×	134 1.2×	107 1.0×	40 0.9×	38 1.4×	29	418
Hannah Verdin Belgium	14	317 1.3×	69 0.6×	268 2.6×	23 0.5×	34 1.2×	29	467
Jan Liebelt Australia	10	291 1.2×	61 0.5×	156 1.5×	24 0.5×	27 1.0×	20	449
Leen Abu Safieh Saudi Arabia	11	428 1.8×	144 1.3×	197 1.9×	36 0.8×	54 1.9×	21	527
Ana Arteche‐López Spain	9	172 0.7×	58 0.5×	95 0.9×	20 0.4×	28 1.0×	23	262
Weining Rong China	10	246 1.0×	133 1.2×	56 0.5×	69 1.5×	31 1.1×	26	348
Gaoen Ma China	9	275 1.2×	135 1.2×	61 0.6×	79 1.8×	14 0.5×	19	357
Anh-Chi N. Le United States	6	436 1.8×	61 0.5×	70 0.7×	31 0.7×	19 0.7×	6	489

Countries citing papers authored by Jenina Capasso

Since Specialization

Citations

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

Fields of papers citing papers by Jenina Capasso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jenina Capasso. 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 Jenina Capasso. The network helps show where Jenina Capasso may publish in the future.

Co-authorship network of co-authors of Jenina Capasso

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

All Works

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20 of 20 papers shown

Capasso, Jenina, et al.. (2023). Mutations in AGBL5 associated with Retinitis pigmentosa. Ophthalmic Genetics. 45(3). 275–280. 1 indexed citations

Capasso, Jenina, et al.. (2023). Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis. American Journal of Medical Genetics Part A. 191(4). 1007–1012.

Capasso, Jenina, et al.. (2023). Genetics of the anterior segment dysgenesis. Taiwan Journal of Ophthalmology. 13(4). 500–504. 3 indexed citations

Capasso, Jenina, et al.. (2022). Experiences of genetic testing among individuals with retinitis pigmentosa. Ophthalmic Genetics. 43(5). 633–640. 7 indexed citations

Jiang, Ming‐Ming, Xiaohui Li, Ronit Marom, et al.. (2021). A novel de novo intronic variant in ITPR1 causes Gillespie syndrome. American Journal of Medical Genetics Part A. 185(8). 2315–2324. 5 indexed citations

Guimarães, Thales A. C. de, Jenina Capasso, & Alex V. Levin. (2019). Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces. Ophthalmic Genetics. 40(3). 213–218. 1 indexed citations

Pefkianaki, Maria, Adele Schneider, Jenina Capasso, et al.. (2018). Ocular manifestations of PACS1 mutation. Journal of American Association for Pediatric Ophthalmology and Strabismus. 22(4). 323–325. 10 indexed citations

Tsukikawa, Mai, Avrey Thau, Jenina Capasso, et al.. (2018). Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations. Ophthalmic Genetics. 39(3). 384–390. 14 indexed citations

Petersen‐Jones, Simon M., Laurence M. Occelli, Paige A. Winkler, et al.. (2017). Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach. Journal of Clinical Investigation. 128(1). 190–206. 46 indexed citations

10.

Lai, Yu‐Hung, et al.. (2017). Autoimmune retinopathy associated with systemic lupus erythematosus: A diagnostic dilemma. Taiwan Journal of Ophthalmology. 7(3). 172–172. 8 indexed citations

11.

Smith, Claire E. L., James A. Poulter, Alex V. Levin, et al.. (2016). Spectrum of PEX1 and PEX6 variants in Heimler syndrome. European Journal of Human Genetics. 24(11). 1565–1571. 43 indexed citations

12.

Lai, Yu‐Hung, Jenina Capasso, Richard Kaiser, & Alex V. Levin. (2016). Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene. Ophthalmic Genetics. 37(4). 424–426. 7 indexed citations

13.

Capasso, Jenina, et al.. (2015). Anirdia‐like phenotype caused by 6p25 dosage aberrations. American Journal of Medical Genetics Part A. 167(3). 524–528. 11 indexed citations

14.

Hope, William C., et al.. (2015). Peters anomaly in cri-du-chat syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 19(3). 277–279. 2 indexed citations

15.

Zhang, Li, Yu‐Hung Lai, Jenina Capasso, Stella Han, & Alex V. Levin. (2015). Early onset ectopia lentis due to a FBN1 mutation with non‐penetrance. American Journal of Medical Genetics Part A. 167(6). 1365–1368. 11 indexed citations

16.

Capasso, Jenina. (2014). The cost of genetic testing for ocular disease. Current Opinion in Ophthalmology. 25(5). 394–399. 19 indexed citations

17.

Battista, Robert A., et al.. (2013). Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son. Ophthalmic Genetics. 36(2). 156–159. 13 indexed citations

18.

Capasso, Jenina, et al.. (2013). Lyonization in ophthalmology. Current Opinion in Ophthalmology. 24(5). 389–397. 11 indexed citations

19.

Capasso, Jenina, et al.. (2013). Ocular Manifestations of 22q11.2 Microduplication. Ophthalmology. 121(1). 392–398. 19 indexed citations

20.

Capasso, Jenina, et al.. (2012). Genetics for the ophthalmologist. SHILAP Revista de lepidopterología. 5(3). 144–144. 4 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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