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Year Number of Results
2019 4
2020 3
2021 6
2022 4
2023 2
2024 2

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20 results

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Page 1
Anisometropia and asymmetric ABCA4-related cone-rod dystrophy.
Santos C, Almeida A, Pinto R, Kaminska K, Peter VG, Sousa AB, Rivolta C, Coutinho-Santos L. Santos C, et al. Among authors: peter vg. Ophthalmic Genet. 2022 Aug;43(4):576-580. doi: 10.1080/13816810.2022.2103834. Epub 2022 Jul 28. Ophthalmic Genet. 2022. PMID: 35903041 No abstract available.
Investigating the Ocular Surface Microbiome: What Can It Tell Us?
Peter VG, Morandi SC, Herzog EL, Zinkernagel MS, Zysset-Burri DC. Peter VG, et al. Clin Ophthalmol. 2023 Jan 19;17:259-271. doi: 10.2147/OPTH.S359304. eCollection 2023. Clin Ophthalmol. 2023. PMID: 36698849 Free PMC article. Review.
Genomic and transcriptomic landscape of conjunctival melanoma.
Cisarova K, Folcher M, El Zaoui I, Pescini-Gobert R, Peter VG, Royer-Bertrand B, Zografos L, Schalenbourg A, Nicolas M, Rimoldi D, Leyvraz S, Riggi N, Moulin AP, Rivolta C. Cisarova K, et al. Among authors: peter vg. PLoS Genet. 2020 Dec 31;16(12):e1009201. doi: 10.1371/journal.pgen.1009201. eCollection 2020 Dec. PLoS Genet. 2020. PMID: 33383577 Free PMC article.
A novel phenotype associated with the R162W variant in the KCNJ13 gene.
Schroeder M, Peter VG, Gränse L, Andréasson S, Rivolta C, Kjellström U. Schroeder M, et al. Among authors: peter vg. Ophthalmic Genet. 2022 Aug;43(4):500-507. doi: 10.1080/13816810.2022.2068041. Epub 2022 Apr 27. Ophthalmic Genet. 2022. PMID: 35477418
Genetic profile of syndromic retinitis pigmentosa in Portugal.
Cortinhal T, Santos C, Vaz-Pereira S, Marta A, Duarte L, Miranda V, Costa J, Sousa AB, Peter VG, Kaminska K, Rivolta C, Carvalho AL, Saraiva J, Soares CA, Silva R, Murta J, Santos LC, Marques JP. Cortinhal T, et al. Among authors: peter vg. Graefes Arch Clin Exp Ophthalmol. 2024 Jan 8. doi: 10.1007/s00417-023-06360-2. Online ahead of print. Graefes Arch Clin Exp Ophthalmol. 2024. PMID: 38189974 Free article.
AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data.
Quinodoz M, Peter VG, Bedoni N, Royer Bertrand B, Cisarova K, Salmaninejad A, Sepahi N, Rodrigues R, Piran M, Mojarrad M, Pasdar A, Ghanbari Asad A, Sousa AB, Coutinho Santos L, Superti-Furga A, Rivolta C. Quinodoz M, et al. Among authors: peter vg. Nat Commun. 2021 Jan 22;12(1):518. doi: 10.1038/s41467-020-20584-4. Nat Commun. 2021. PMID: 33483490 Free PMC article.
Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
Rehman AU, Sepahi N, Bedoni N, Ravesh Z, Salmaninejad A, Cancellieri F, Peter VG, Quinodoz M, Mojarrad M, Pasdar A, Asad AG, Ghalamkari S, Piran M, Piran M, Superti-Furga A, Rivolta C. Rehman AU, et al. Among authors: peter vg. Sci Rep. 2021 Sep 29;11(1):19332. doi: 10.1038/s41598-021-98677-3. Sci Rep. 2021. PMID: 34588515 Free PMC article.
20 results