1. Olivier, Guillaume, Corton, Marta, Intartaglia, Daniela, Meunier, Isabelle, Manes, Gaël. 2020. Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa. In Journal of medical genetics, 58, 570-578. doi:10.1136/jmedgenet-2020-107150. https://pubmed.ncbi.nlm.nih.gov/32817297/
2. Olivier, Guillaume, Brabet, Philippe, Pirot, Nelly, Kalatzis, Vasiliki, Manes, Gaël. 2022. SPACR Encoded by IMPG1 Is Essential for Photoreceptor Survival by Interplaying between the Interphotoreceptor Matrix and the Retinal Pigment Epithelium. In Genes, 13, . doi:10.3390/genes13091508. https://pubmed.ncbi.nlm.nih.gov/36140676/
3. Gehrig, A, Felbor, U, Kelsell, R E, Maumenee, I H, Weber, B H. . Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1). In Journal of medical genetics, 35, 641-5. doi:. https://pubmed.ncbi.nlm.nih.gov/9719369/
4. Felbor, U, Gehrig, A, Sauer, C G, Schmid, M, Weber, B H. . Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies. In Cytogenetics and cell genetics, 81, 12-7. doi:. https://pubmed.ncbi.nlm.nih.gov/9691169/
5. Kuehn, M H, Hageman, G S. . Expression and characterization of the IPM 150 gene (IMPG1) product, a novel human photoreceptor cell-associated chondroitin-sulfate proteoglycan. In Matrix biology : journal of the International Society for Matrix Biology, 18, 509-18. doi:. https://pubmed.ncbi.nlm.nih.gov/10601738/
6. Manes, Gaël, Meunier, Isabelle, Avila-Fernández, Almudena, Ayuso García, Carmen, Hamel, Christian P. 2013. Mutations in IMPG1 cause vitelliform macular dystrophies. In American journal of human genetics, 93, 571-8. doi:10.1016/j.ajhg.2013.07.018. https://pubmed.ncbi.nlm.nih.gov/23993198/
7. Meunier, Isabelle, Manes, Gaël, Bocquet, Béatrice, Dhaenens, Claire-Marie, Hamel, Christian P. 2014. Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes. In Ophthalmology, 121, 2406-14. doi:10.1016/j.ophtha.2014.06.028. https://pubmed.ncbi.nlm.nih.gov/25085631/
8. Yuan, Ming, Chatterjee, Souradip, Leys, Monique, Odom, J Vernon, Salido, Ezequiel M. 2025. Prevalence of IMPG1 and IMPG2 Mutations Leading to Retinitis Pigmentosa or Vitelliform Macular Dystrophy in a Cohort of Patients with Inherited Retinal Dystrophies. In Genes, 16, . doi:10.3390/genes16010043. https://pubmed.ncbi.nlm.nih.gov/39858590/