Eva Lenassi

1.2k citations

29 papers · 859 indexed · h-index 17

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
- Retinal and Optic Conditions
Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in ⓘ

Ophthalmology 14
- Retinal Diseases and Treatments 12
- Retinal and Optic Conditions 4
Sensory Systems 4
- Hearing, Cochlea, Tinnitus, Genetics 4

Co-authors: Glen Jeffery (5 shared papers)Jaimie Hoh Kam (3 shared papers)Andrew R. Webster (13 shared papers)Anthony T. Moore (6 shared papers)Panagiotis I. Sergouniotis (8 shared papers)Marko Hawlina (7 shared papers)Maria Bitner‐Glindzicz (5 shared papers)Zubin Saihan (5 shared papers)
Journals: Investigative Ophthalmology & Visual Science (5 papers)Ophthalmology (3 papers)European Journal of Human Genetics (2 papers)Acta Ophthalmologica (2 papers)The American Journal of Human Genetics (2 papers)
Partner nations: United Kingdom Slovenia United States

In The Last Decade

Eva Lenassi

29 papers receiving 844 citations

Peers

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-authors

The 25 scholars most cited alongside Eva Lenassi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eva Lenassi Line = papers co-authored together Eva Lenassi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Viewing Ageing Eyes: Diverse Sites of Amyloid Beta Accumulation in the Ageing Mouse Retina and the Up-Regulation of Macrophages PLoS ONE ·Jaimie Hoh Kam, Eva Lenassi, Glen Jeffery	2010	110
2	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 ·Eva Lenassi, Ajoy Vincent, Zheng Li, Zubin Saihan, Alison J. Coffey, Heather B. Steele-Stallard, Anthony T. Moore, Karen P. Steel, Linda Luxon, Elise Héon, Maria Bitner‐Glindzicz, Andrew R. Webster	2015	85
3	Retinal Structure, Function, and Molecular Pathologic Features in Gyrate Atrophy Ophthalmology ·Panagiotis I. Sergouniotis, Alice E. Davidson, Eva Lenassi, Sophie Devery, Anthony T. Moore, Andrew R. Webster	2011	77
4	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 ·Jaimie Hoh Kam, Eva Lenassi, Talat H. Malik, Matthew C. Pickering, Glen Jeffery	2013	67
5	Biallelic Variants in TTLL5, Encoding a Tubulin Glutamylase, Cause Retinal Dystrophy The American Journal of Human Genetics ·Panagiotis I. Sergouniotis, Christina Chakarova, Cian Murphy, Mirjana M Becker, Eva Lenassi, Gavin Arno, Monkol Lek, Daniel G. MacArthur, Shomi S. Bhattacharya, Anthony T. Moore, Graham E. Holder, Anthony G. Robson, Uwe Wolfrum, Andrew R. Webster, Vincent Plagnol	2014	64
6	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 ·Heather B. Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi, Linda Luxon, Mireille Claustres, Anne‐Françoise Roux, Andrew R. Webster, Maria Bitner‐Glindzicz	2013	44
7	VEP maturation and visual acuity in infants and preschool children Documenta Ophthalmologica ·Eva Lenassi, Katarina Likar, Branka Stirn-Kranjc, Jelka Brecelj	2008	42
8	Clinical utility of genetic testing in 201 preschool children with inherited eye disorders Genetics in Medicine ·Eva Lenassi, Jill Clayton‐Smith, Sofia Douzgou, Simon Ramsden, Stuart Ingram, Georgina Hall, Claire Hardcastle, Tracy Fletcher, Rachel L. Taylor, Jamie M. Ellingford, William Newman, Cecilia Fenerty, Vinod Sharma, Iva Lloyd, Susmito Biswas, Jane Ashworth, Graeme C. Black, Panagiotis I. Sergouniotis	2019	40
9	Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina The American Journal of Human Genetics ·Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay, Eva Lenassi, Zheng Li, Anthony G. Robson, Xu Yang, Jaimie Hoh Kam, Timothy Isaacs, Graham E. Holder, Glen Jeffery, Jonathan Beck, Anthony T. Moore, Vincent Plagnol, Andrew R. Webster	2011	34
10	Correlation between Macular Morphology and Sensitivity in Patients with Retinitis Pigmentosa and Hyperautofluorescent Ring Investigative Ophthalmology & Visual Science ·Eva Lenassi, Eric Troeger, Robert Wilke, Marko Hawlina	2011	34
11	An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data Genes ·Valentina Cipriani, Nikolas Pontikos, Gavin Arno, Panagiotis I. Sergouniotis, Eva Lenassi, Penpitcha Thawong, Daniel Daniš, Michel Michaelides, Andrew R. Webster, Anthony T. Moore, Peter N. Robinson, Julius O.B. Jacobsen, Damian Smedley	2020	33
12	Comparison of Fundus Autofluorescence with Photopic and Scotopic Fine Matrix Mapping in Patients with Retinitis Pigmentosa: 4- to 8-Year Follow-up Investigative Ophthalmology & Visual Science ·Anthony G. Robson, Eva Lenassi, Zubin Saihan, Vy Luong, Fred W. Fitzke, Graham E. Holder, Andrew R. Webster	2012	31
13	Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation Ophthalmology ·Eva Lenassi, Zubin Saihan, Valentina Cipriani, Polona Le Quesne Stabej, Anthony T. Moore, Linda Luxon, Maria Bitner‐Glindzicz, Andrew R. Webster	2013	27
14	The effect of the common c.2299delG mutation in USH2A on RNA splicing Experimental Eye Research ·Eva Lenassi, Zubin Saihan, Maria Bitner‐Glindzicz, Andrew R. Webster	2014	23
15	Efficacy of 12-month treatment of neovascular age-related macular degeneration with intravitreal bevacizumab based on individually determined injection strategies after three consecutive monthly injections Acta Ophthalmologica ·Polona Jaki Mekjavič, Aleksandra Kraut, Mojca Urbančič, Eva Lenassi, Marko Hawlina	2009	22
16	Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease European Journal of Human Genetics ·Omamah A. Jiman, Rachel L. Taylor, Eva Lenassi, Jill Smith, Sofia Douzgou, Jamie M. Ellingford, Stephanie Barton, Claire Hardcastle, Tracy Fletcher, Christopher Campbell, Jane Ashworth, Susmito Biswas, Simon Ramsden, Forbes Manson, Graeme C. Black	2019	20
17	THE VALUE OF TWO-FIELD PATTERN ELECTRORETINOGRAM IN ROUTINE CLINICAL ELECTROPHYSIOLOGIC PRACTICE Retina ·Eva Lenassi, Anthony G. Robson, Marko Hawlina, Graham E. Holder	2011	18
18	Pattern electroretinography of larger stimulus field size and spectral-domain optical coherence tomography in patients with Stargardt disease British Journal of Ophthalmology ·Eva Lenassi, Martina Jarc-Vidmar, Damjan Glavač, Marko Hawlina	2009	16
19	Establishing Genotype–phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and Rehabilitation Otology & Neurotology ·Leslie P. Molina‐Ramírez, Eva Lenassi, Jamie M. Ellingford, Panagiotis I. Sergouniotis, Simon Ramsden, Iain Bruce, Graeme C. Black	2020	12
20	Clinical and Genetic Findings in CTNNA1-Associated Macular Pattern Dystrophy Ophthalmology ·Alexander Tanner, Hwei Wuen Chan, José S. Pulido, Gavin Arno, Rola Ba‐Abbad, Neringa Jurkutė, Anthony G. Robson, Catherine Egan, Hannah Knight, Antonio Calcagni, Rachel L. Taylor, Eva Lenassi, Graeme C. Black, Anthony T. Moore, Michel Michaelides, Andrew R. Webster, Omar A. Mahroo	2020	10

About Eva Lenassi

Eva Lenassi is a scholar working on Ophthalmology, Sensory Systems, Genetics, Molecular Biology and Radiology, Nuclear Medicine and Imaging, having authored 29 papers that have together received 859 indexed citations. Recurring topics across this work include Retinal Development and Disorders (14 papers), Retinal Diseases and Treatments (12 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers), Retinal and Optic Conditions (4 papers), Genetic and Kidney Cyst Diseases (3 papers), Retinal Imaging and Analysis (3 papers), Genomics and Rare Diseases (3 papers) and Biomedical Research and Pathophysiology (2 papers). The work is most often cited by research in Ophthalmology (436 citations), Sensory Systems (77 citations), Molecular Biology (595 citations), Neurology (70 citations) and Radiology, Nuclear Medicine and Imaging (168 citations). Eva Lenassi has collaborated with scholars based in United Kingdom, Slovenia and United States. Frequent co-authors include Glen Jeffery, Jaimie Hoh Kam, Andrew R. Webster, Anthony T. Moore, Panagiotis I. Sergouniotis, Marko Hawlina, Maria Bitner‐Glindzicz, Zubin Saihan, Anthony G. Robson and Linda Luxon. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Ophthalmology, European Journal of Human Genetics, Acta Ophthalmologica and The American Journal of Human Genetics.

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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