Concepedia

Author

Eva Lenassi

University College London

Also Known As

David Budd, E LENASSI, E Lenassi, Eva Lenassi

53

Publications

1.2K

Citations

19

H-Index

37

Concepts

All Affiliations

University College LondonLjubljana University Medical CentreMoorfields Eye HospitalUniversity of ManchesterManchester Royal Eye Hospital
EL

About

Eva Lenassi is an author at University College London specializing in medicine, ophthalmology, and molecular biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

8

8

402

2

Cell Biology

2

2

128

3

Natural Sciences

1

1

30

4

Social Sciences

1

1

62

5

Child Development

1

1

62

Eva Lenassi

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26

Publications

1.2K

Citations

19

H-Index

YearCitations

Viewing Ageing Eyes: Diverse Sites of Amyloid Beta Accumulation in the Ageing Mouse Retina and the Up-Regulation of Macrophages

Jaimie Hoh Kam, Eva Lenassi, Glen Jeffery

PLoS ONE

2010

128

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants

Eva Lenassi, Ajoy Vincent, Zheng Li,

European Journal of Human Genetics

2015

119

Retinal Structure, Function, and Molecular Pathologic Features in Gyrate Atrophy

Panagiotis I. Sergouniotis, Alice E. Davidson, Eva Lenassi,

Ophthalmology

2011

116

Biallelic Variants in TTLL5, Encoding a Tubulin Glutamylase, Cause Retinal Dystrophy

Panagiotis I. Sergouniotis, Christina Chakarova, Cian Murphy,

The American Journal of Human Genetics

2014

84

Complement Component C3 Plays a Critical Role in Protecting the Aging Retina in a Murine Model of Age-Related Macular Degeneration

Jaimie Hoh Kam, Eva Lenassi, Talat H. Malik,

American Journal Of Pathology

2013

81

An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data

Valentina Cipriani, Nikolas Pontikos, Gavin Arno,

Genes

2020

65

VEP maturation and visual acuity in infants and preschool children

Eva Lenassi, Katarina Likar, Branka Stirn-Kranjc,

Documenta Ophthalmologica

2008

62

Clinical utility of genetic testing in 201 preschool children with inherited eye disorders

Eva Lenassi, Jill Clayton‐Smith, Sofia Douzgou,

Genetics in Medicine

2019

62

Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing

Heather B. Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi,

Orphanet Journal of Rare Diseases

2013

48

Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina

Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay,

The American Journal of Human Genetics

2011

47

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