Eva Lenassi

1.2k total citations
29 papers, 859 citations indexed

About

Eva Lenassi is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Eva Lenassi has authored 29 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Ophthalmology and 8 papers in Genetics. Recurrent topics in Eva Lenassi's work include Retinal Development and Disorders (14 papers), Retinal Diseases and Treatments (12 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Eva Lenassi is often cited by papers focused on Retinal Development and Disorders (14 papers), Retinal Diseases and Treatments (12 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Eva Lenassi collaborates with scholars based in United Kingdom, Slovenia and United States. Eva Lenassi's co-authors include Glen Jeffery, Jaimie Hoh Kam, Andrew R. Webster, Panagiotis I. Sergouniotis, Anthony T. Moore, Marko Hawlina, Maria Bitner‐Glindzicz, Zubin Saihan, Linda Luxon and Anthony G. Robson and has published in prestigious journals such as PLoS ONE, Journal of Applied Physiology and Ophthalmology.

In The Last Decade

Eva Lenassi

29 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Lenassi United Kingdom 17 595 436 168 141 77 29 859
Ajoy Vincent Canada 18 757 1.3× 462 1.1× 188 1.1× 216 1.5× 45 0.6× 68 1.0k
Bernard Puech France 17 699 1.2× 514 1.2× 149 0.9× 189 1.3× 27 0.4× 42 965
Antje Bernd Germany 11 601 1.0× 420 1.0× 174 1.0× 167 1.2× 122 1.6× 22 821
Blanca Garcı́a-Sandoval Spain 21 1.0k 1.7× 549 1.3× 158 0.9× 187 1.3× 118 1.5× 56 1.2k
Karmen M Trzupek United States 12 420 0.7× 278 0.6× 41 0.2× 76 0.5× 122 1.6× 16 617
Sten Kjellström United States 14 909 1.5× 416 1.0× 320 1.9× 248 1.8× 40 0.5× 23 1.0k
Genevieve Wright United Kingdom 18 1.2k 2.1× 822 1.9× 215 1.3× 214 1.5× 66 0.9× 35 1.4k
Dominique Ducroq France 17 1.2k 1.9× 756 1.7× 181 1.1× 246 1.7× 54 0.7× 20 1.3k
Samer Khateb Israel 16 525 0.9× 178 0.4× 56 0.3× 147 1.0× 67 0.9× 43 662
Yukiko Makiyama Japan 17 515 0.9× 572 1.3× 182 1.1× 55 0.4× 19 0.2× 24 758

Countries citing papers authored by Eva Lenassi

Since Specialization
Citations

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

Fields of papers citing papers by Eva Lenassi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Lenassi

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Lenassi. A scholar is included among the top collaborators of Eva Lenassi 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 Eva Lenassi. Eva Lenassi 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.
Lenassi, Eva, Ana Carolina de Carvalho, Anja Thormann, et al.. (2023). EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders. Journal of Medical Genetics. 60(8). 810–818. 3 indexed citations
2.
Chan, Hwei Wuen, José S. Pulido, Gavin Arno, et al.. (2020). Clinical and Genetic Findings in CTNNA1-Associated Macular Pattern Dystrophy. Ophthalmology. 128(6). 952–955. 10 indexed citations
3.
Lenassi, Eva, Jamie M. Ellingford, Panagiotis I. Sergouniotis, et al.. (2020). Establishing Genotype–phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and Rehabilitation. Otology & Neurotology. 41(4). 431–437. 12 indexed citations
4.
Lenassi, Eva, Jill Clayton‐Smith, Sofia Douzgou, et al.. (2019). Clinical utility of genetic testing in 201 preschool children with inherited eye disorders. Genetics in Medicine. 22(4). 745–751. 40 indexed citations
5.
Lenassi, Eva, et al.. (2017). Craniofacial linear scleroderma associated with retinal telangiectasia and exudative retinal detachment. Journal of American Association for Pediatric Ophthalmology and Strabismus. 21(3). 251–254. 9 indexed citations
6.
Lenassi, Eva, Maja Kojović, Polona Jaki Mekjavič, Saša Šega, & Nataša Vidović Valentinčič. (2016). Persistent Placoid Maculopathy Complicated by Cerebral Vasculitis. Journal of Neuro-Ophthalmology. 37(3). 273–275. 7 indexed citations
7.
Lenassi, Eva, Ajoy Vincent, Zheng Li, et al.. (2015). A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants. European Journal of Human Genetics. 23(10). 1318–1327. 85 indexed citations
8.
Lenassi, Eva, Zubin Saihan, Maria Bitner‐Glindzicz, & Andrew R. Webster. (2014). The effect of the common c.2299delG mutation in USH2A on RNA splicing. Experimental Eye Research. 122. 9–12. 23 indexed citations
9.
Kam, Jaimie Hoh, Eva Lenassi, Talat H. Malik, Matthew C. Pickering, & Glen Jeffery. (2013). Complement Component C3 Plays a Critical Role in Protecting the Aging Retina in a Murine Model of Age-Related Macular Degeneration. American Journal Of Pathology. 183(2). 480–492. 67 indexed citations
10.
Lenassi, Eva, Zubin Saihan, Zheng Li, et al.. (2013). A comprehensive screen of the USH2A gene in 185 patients with autosomal recessive retinal disease. Investigative Ophthalmology & Visual Science. 54(15). 677–677. 1 indexed citations
11.
Lenassi, Eva, Zubin Saihan, Valentina Cipriani, et al.. (2013). Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation. Ophthalmology. 121(2). 580–587. 27 indexed citations
12.
Steele-Stallard, Heather B., Polona Le Quesne Stabej, Eva Lenassi, et al.. (2013). Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing. Orphanet Journal of Rare Diseases. 8(1). 122–122. 44 indexed citations
13.
Lenassi, Eva, Robert Wilke, Adnan Tufail, et al.. (2012). Laser Clearance of Drusen Deposit in Patients With Autosomal Dominant Drusen (p.Arg345Trp in EFEMP1). American Journal of Ophthalmology. 155(1). 190–198. 9 indexed citations
14.
Golding, Matt, et al.. (2011). Distorting The Mosaic: The Effect of Melanin on Ageing RPE. Investigative Ophthalmology & Visual Science. 52(14). 3208–3208. 1 indexed citations
15.
Sergouniotis, Panagiotis I., Alice E. Davidson, Donna S. Mackay, et al.. (2011). Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina. The American Journal of Human Genetics. 89(6). 782–791. 34 indexed citations
16.
Sergouniotis, Panagiotis I., Alice E. Davidson, Eva Lenassi, et al.. (2011). Retinal Structure, Function, and Molecular Pathologic Features in Gyrate Atrophy. Ophthalmology. 119(3). 596–605. 77 indexed citations
17.
Lenassi, Eva, Anthony G. Robson, Marko Hawlina, & Graham E. Holder. (2011). THE VALUE OF TWO-FIELD PATTERN ELECTRORETINOGRAM IN ROUTINE CLINICAL ELECTROPHYSIOLOGIC PRACTICE. Retina. 32(3). 588–599. 18 indexed citations
18.
Kam, Jaimie Hoh, Eva Lenassi, & Glen Jeffery. (2010). Viewing Ageing Eyes: Diverse Sites of Amyloid Beta Accumulation in the Ageing Mouse Retina and the Up-Regulation of Macrophages. PLoS ONE. 5(10). e13127–e13127. 110 indexed citations
19.
20.
Lenassi, Eva, et al.. (2008). VEP maturation and visual acuity in infants and preschool children. Documenta Ophthalmologica. 117(2). 111–120. 42 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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