Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.

by Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Aftab Iqbal, Muhammad Imran Khan, Anneke I den Hollander
Published 2016-01-01

Genetics of Unilateral and Bilateral Age-Related Macular Degeneration Severity Stages.

by Tina Schick, Lebriz Altay, Eva Viehweger, Carel B Hoyng, Anneke I den Hollander, Moritz Felsch, Sascha Fauser
Published 2016-01-01

Nutritional Risk Factors for Age-Related Macular Degeneration

by Lebriz Ersoy, Tina Ristau, Yara T. Lechanteur, Moritz Hahn, Carel B. Hoyng, Bernd Kirchhof, Anneke I. den Hollander, Sascha Fauser
Published 2014-01-01

Corrigendum to “Nutritional Risk Factors for Age-Related Macular Degeneration”

by Lebriz Ersoy, Tina Ristau, Yara T. Lechanteur, Moritz Hahn, Carel B. Hoyng, Bernd Kirchhof, Anneke I. den Hollander, Sascha Fauser
Published 2016-01-01

Metabolomics and Age-Related Macular Degeneration

by Connor N. Brown, Brian D. Green, Richard B. Thompson, Anneke I. den Hollander, Imre Lengyel, on behalf of the EYE-RISK consortium
Published 2018-12-01

Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290

by Rob WJ Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, Jeannette Bennicelli, Jean Bennett, Frans PM Cremers
Published 2012-01-01

A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium

by Eszter Emri, Elod Kortvely, Sascha Dammeier, Franziska Klose, David Simpson, EYE-RISK Consortium, Anneke I. Den Hollander, Marius Ueffing, Imre Lengyel
Published 2020-10-01

A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

by Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Cristina Villanueva-Mendoza, Vianney Cortés-González, Muhammad Imran Khan, Anneke I den Hollander
Published 2016-01-01

The Molecular Basis of Retinal Dystrophies in Pakistan

by Muhammad Imran Khan, Maleeha Azam, Muhammad Ajmal, Rob W. J. Collin, Anneke I. den Hollander, Frans P. M. Cremers, Raheel Qamar
Published 2014-03-01

Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotype.

by Qin Liu, Rob W J Collin, Frans P M Cremers, Anneke I den Hollander, L Ingeborgh van den Born, Eric A Pierce
Published 2012-01-01

Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma.

by Shazia Micheal, Humaira Ayub, Farrah Islam, Sorath Noorani Siddiqui, Wajid Ali Khan, Farah Akhtar, Raheel Qamar, Muhammad Imran Khan, Anneke I den Hollander
Published 2015-01-01

ERAP2 Increases the Abundance of a Peptide Submotif Highly Selective for the Birdshot Uveitis-Associated HLA-A29

by Wouter J. Venema, Wouter J. Venema, Sanne Hiddingh, Sanne Hiddingh, Joke H. de Boer, Frans H. J. Claas, Arend Mulder, Anneke I. den Hollander, Anneke I. den Hollander, Efstratios Stratikos, Siranush Sarkizova, Siranush Sarkizova, Lars T. van der Veken, George M. C. Janssen, Peter A. van Veelen, Jonas J. W. Kuiper, Jonas J. W. Kuiper
Published 2021-02-01

Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels.

by Tina Ristau, Constantin Paun, Lebriz Ersoy, Moritz Hahn, Yara Lechanteur, Carel Hoyng, Eiko K de Jong, Mohamed R Daha, Bernd Kirchhof, Anneke I den Hollander, Sascha Fauser
Published 2014-01-01

Systemic complement activation levels in Stargardt disease.

by Patty P A Dhooge, Esmee H Runhart, Catherina H Z Li, Corrie M de Kat Angelino, Carel B Hoyng, Renate G van der Molen, Anneke I den Hollander
Published 2021-01-01

Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma.

by Humaira Ayub, Shazia Micheal, Farah Akhtar, Muhammad Imran Khan, Shaheena Bashir, Nadia K Waheed, Mahmood Ali, Frederieke E Schoenmaker-Koller, Sobia Shafique, Raheel Qamar, Anneke I den Hollander
Published 2014-01-01

Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular Degeneration.

by Nicole T M Saksens, Yara T E Lechanteur, Sanne K Verbakel, Joannes M M Groenewoud, Mohamed R Daha, Tina Schick, Sascha Fauser, Camiel J F Boon, Carel B Hoyng, Anneke I den Hollander
Published 2016-01-01

A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290

by Susanne Roosing, Frans P. M. Cremers, Frans C. C. Riemslag, Marijke N. Zonneveld-Vrieling, Herman E. Talsma, Francoise J. M. Klessens-Godfroy, Anneke I. den Hollander, L. Ingeborgh van den Born
Published 2017-08-01

Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and T...

by Louise F. Porter, Neil Saptarshi, Yongxiang Fang, Sonika Rathi, Anneke I. den Hollander, Eiko K. de Jong, Simon J. Clark, Paul N. Bishop, Timothy W. Olsen, Triantafillos Liloglou, Venkata R. M. Chavali, Luminita Paraoan
Published 2019-01-01

Aberrant leukocyte telomere length in Birdshot Uveitis.

by Nadia Vazirpanah, Fleurieke H Verhagen, Anna Rothova, Tom O A R Missotten, Mirjam van Velthoven, Anneke I Den Hollander, Carel B Hoyng, Timothy R D J Radstake, Jasper C A Broen, Jonas J W Kuiper
Published 2017-01-01

Metabolomics in serum of patients with non-advanced age-related macular degeneration reveals aberrations in the glutamine pathway.

by Eveline Kersten, Sascha Dammeier, Soufiane Ajana, Joannes M M Groenewoud, Marius Codrea, Franziska Klose, Yara T Lechanteur, Sascha Fauser, Marius Ueffing, Cécile Delcourt, Carel B Hoyng, Eiko K de Jong, Anneke I den Hollander, EYE-RISK Consortium
Published 2019-01-01