Virginie Verhoeven

About Virginie Verhoeven

Virginie Verhoeven, With an exceptional h-index of 34 and a recent h-index of 31 (since 2020), a distinguished researcher at Erasmus Universiteit Rotterdam, specializes in the field of myopia, ophthalmology, GWAS.

His recent articles reflect a diverse array of research interests and contributions to the field:

Gender issues in myopia: a changing paradigm in generations

Parafoveal cone loss in inherited retinal dystrophy patients using the rtx1 adaptive optics retinal camera

IMI—management and investigation of high myopia in infants and young children

A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

Myopia control in mendelian forms of myopia

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis

Web-accessible application for identifying pathogenic transcripts with RNA-Seq: increased sensitivity in diagnosis of neurodevelopmental disorders

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Virginie Verhoeven Information

University

Position

Erasmus Medical Center

Citations(all)

6581

Citations(since 2020)

4631

Cited By

3859

hIndex(all)

34

hIndex(since 2020)

31

i10Index(all)

51

i10Index(since 2020)

48

Email

University Profile Page

Google Scholar

Virginie Verhoeven Skills & Research Interests

myopia

ophthalmology

GWAS

Top articles of Virginie Verhoeven

Gender issues in myopia: a changing paradigm in generations

2024/1/24

Hein Raat
Hein Raat

H-Index: 57

Virginie Verhoeven
Virginie Verhoeven

H-Index: 29

Parafoveal cone loss in inherited retinal dystrophy patients using the rtx1 adaptive optics retinal camera

Investigative Ophthalmology & Visual Science

2023/6/1

IMI—management and investigation of high myopia in infants and young children

Investigative ophthalmology & visual science

2023/5/1

Myopia control in mendelian forms of myopia

Ophthalmic and Physiological Optics

2023/5

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis

Frontiers in cell and developmental biology

2023/2/3

Web-accessible application for identifying pathogenic transcripts with RNA-Seq: increased sensitivity in diagnosis of neurodevelopmental disorders

The American Journal of Human Genetics

2023/2/2

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Communications biology

2023/1/3

The 18th International Myopia Conference 2022 in Rotterdam, The Netherlands

2023

De myopie-epidemie: voorkomen is beter dan genezen

Huisarts en wetenschap

2023/1

Virginie Verhoeven
Virginie Verhoeven

H-Index: 29

Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing

Ophthalmology Science

2023/12/1

Diagnostic gene panel testing in (non)-syndromic patients with cleft lip, alveolus and/or palate in the Netherlands

Molecular syndromology

2023/8/9

Diagnostic whole exome sequencing in presumably autosomal recessively inherited retinal dystrophies in an Iranian population

Investigative Ophthalmology & Visual Science

2023/6/1

Early onset X‐linked female limited high myopia in three multigenerational families caused by novel mutations in the ARR3 gene

Human mutation

2022/3

Genetics of myopia: Gene finding and beyond

Acta Ophthalmologica

2022/12

Whole exome sequencing of known eye genes reveals genetic causes for high myopia

Human Molecular Genetics

2022/10/1

Association analyses of rare variants identify two genes associated with refractive error

PloS one

2022/9/22

RNA-sequencing improves diagnosis for neurodevelopmental disorders by identifying pathogenic non-coding variants and reinterpretation of coding variants

medRxiv

2022/6/7

Diagnosis and identification of the genetic defect in a large Dutch cohort of children with retinal dystrophy: the RD5000 consortium

Investigative Ophthalmology & Visual Science

2022/6/1

Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia

Human molecular genetics

2022/6/1

See List of Professors in Virginie Verhoeven University(Erasmus Universiteit Rotterdam)

Co-Authors

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