Carel B. Hoyng

Also affiliated with Radboud University Medical Center

Medicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Family-based exome sequencing identifies rare coding variants in age-related macular degeneration”.

Family-based exome sequencing identifies rare coding variants in age-related macular degeneration

Human Molecular Genetics(2020)10.1093/hmg/ddaa057

N/A

0DataRank · unranked

36 citations

İlhan E. Acar, Maartje J. Geerlings, Kari Branham, Alan Kwong, Nicole T.M. Saksens +14 more

Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.002

N/A

0DataRank · unranked

65 citations

Anna E. van Beek, Esther Willems, Judith Zandstra, Gerard van Mierlo, Alfred Einhaus +13 more

Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium

Translational Vision Science & Technology(2021)10.1167/tvst.10.4.23

N/A

0DataRank · unranked

13 citations

Jacque L. Duncan, Allison R. Ayala, David G. Birch, Janet K. Cheetham, Frederick L. Ferris +4 more

Tissue‐specific genotype–phenotype correlations among USH2A‐related disorders in the RUSH2A study

Human Mutation(2022)10.1002/humu.24365

N/A

0DataRank · unranked

23 citations

Wendi Liang, Jacque L. Duncan, Carmen C. Brewer, Isabelle Audo, Allison R. Ayala +14 more

Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100237

N/A

0DataRank · unranked

13 citations

Mubeen Khan, Rebekkah J. Hitti‐Malin, Ketan Mishra, Laura Whelan, Stéphanie S. Cornelis +14 more

Endpoints and Design for Clinical Trials in USH2A-Related Retinal Degeneration: Results and Recommendations From the RUSH2A Natural History Study

Translational Vision Science & Technology(2024)10.1167/tvst.13.10.15

N/A

0DataRank · unranked

16 citations

David G. Birch, Jacque L. Duncan, Allison R. Ayala, Lauren N. Ayton, Janet K. Cheetham +17 more

Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathy

Scientific Reports(2025)10.1038/s41598-025-92210-6

N/A

0DataRank · unranked

4 citations

Elon H. C. van Dijk, Masahiro Miyake, Yoshikatsu Hosoda, Anneke I. den Hollander, Suzanne Yzer +29 more

Natural History of Microperimetry and Optical Coherence Tomography in USH2A-Retinopathy: A Structure-Function Association Study

American Journal of Ophthalmology(2025)10.1016/j.ajo.2025.04.034

N/A

0DataRank · unranked

1 citations

Wendi Liang, Maureen G. Maguire, Jacque L. Duncan, Allison R. Ayala, Paul S. Bernstein +15 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169

N/A

0DataRank · unranked

15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement

Nature Communications(2025)10.1038/s41467-025-65903-9

N/A

0DataRank · unranked

0 citations

Carla J. Abbott, Brendan R. E. Ansell, Zhichao Wu, Lebriz Altay, Ella Arnon +48 more