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Translational Vision Science & Technology|May 18, 2021
Correlation of Morphology and Function of Flecks Using Short-Wave Fundus Autofluorescence and Microperimetry in Patients With Stargardt DiseasePatty P A Dhooge, Esmee H Runhart, Stanley Lambertus, et al.
Ophthalmology|September 17, 2019
Highly Variable Disease Courses in Siblings with Stargardt DiseaseDyon Valkenburg, Esmee H Runhart, Nathalie M Bax, et al.
Plos One|June 25, 2021
Systemic complement activation levels in Stargardt diseasePatty P A Dhooge, Esmee H Runhart, Catherina H Z Li, et al.
American Journal of Human Genetics|February 5, 2022
Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severityStéphanie S Cornelis, Esmee H Runhart, Miriam Bauwens, et al.
Ophthalmology|August 20, 2023
Study of Late-Onset Stargardt Type 1 Disease: Characteristics, Genetics, and ProgressionCatherina H Z Li, Jeroen A A H Pas, Zelia Corradi, et al.
JAMA Ophthalmology|August 21, 2020
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt DiseaseEsmee H Runhart, Mubeen Khan, Stéphanie S Cornelis, et al.
Investigative Ophthalmology & Visual Science|October 17, 2019
Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 AllelesEsmee H Runhart, Dyon Valkenburg, Stéphanie S Cornelis, et al.
Acta Ophthalmologica|August 25, 2021
Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registryEsmee H Runhart, Patty Dhooge, Magda Meester-Smoor, et al.
JAMA Ophthalmology|April 11, 2024
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-AnalysisStéphanie S Cornelis, Joanna IntHout, Esmee H Runhart, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe VariantsEsmee H Runhart, Riccardo Sangermano, Stéphanie S Cornelis, et al.
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