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Ophthalmic Genetics Volume 37, 2016 - Issue 4
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Review

OR2W3 sequence variants are unlikely to cause inherited retinal diseases

Dror SharonDepartment of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, IsraelCorrespondence[email protected]
,
Adva KimchiDepartment of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
&
Carlo RivoltaDepartment of Computational Biology, Unit of Medical Genetics, University of Lausanne, Lausanne, SwitzerlandCorrespondence[email protected]
Pages 366-368 | Received 03 Jun 2015, Accepted 30 Jul 2015, Published online: 18 Feb 2016

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Rifat Nowshin Raka, Hua Wu, Junsong Xiao, Imam Hossen, Yanping Cao, Mingquan Huang & Jianming Jin. (2022) Human ectopic olfactory receptors and their food originated ligands: a review. Critical Reviews in Food Science and Nutrition 62:20, pages 5424-5443.
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Junxing Yang, Xueshan Xiao, Wenmin Sun, Shiqiang Li, Xiaoyun Jia & Qingjiong Zhang. (2021) Variants in RCBTB1 are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVR. Current Eye Research 46:6, pages 839-844.
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Articles from other publishers (8)

Junwen Wang, Xueshan Xiao, Shiqiang Li, Hongmei Jiang, Wenmin Sun, Panfeng Wang & Qingjiong Zhang. (2022) Landscape of pathogenic variants in six pre‐mRNA processing factor genes for retinitis pigmentosa based on large in‐house data sets and database comparisons. Acta Ophthalmologica 100:7.
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Nina Schneider, Yogapriya Sundaresan, Prakadeeswari Gopalakrishnan, Avigail Beryozkin, Mor Hanany, Erez Y. Levanon, Eyal Banin, Shay Ben-Aroya & Dror Sharon. (2022) Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities. Progress in Retinal and Eye Research 89, pages 101029.
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Yujie Xia, Xiaojie Li, Xinlin Chen, Changjin Lu & Xiaoyi Yu. (2022) Inferring Retinal Degeneration-Related Genes Based on Xgboost. Frontiers in Molecular Biosciences 9.
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Marta Del Pozo-Valero, Inmaculada Martin-Merida, Belen Jimenez-Rolando, Ana Arteche, Almudena Avila-Fernandez, Fiona Blanco-Kelly, Rosa Riveiro-Alvarez, Caroline Van Cauwenbergh, Elfride De Baere, Carlo Rivolta, Blanca Garcia-Sandoval, Marta Corton & Carmen Ayuso. (2019) Expanded Phenotypic Spectrum of Retinopathies Associated with Autosomal Recessive and Dominant Mutations in PROM1. American Journal of Ophthalmology 207, pages 204-214.
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Mor Hanany & Dror Sharon. (2019) Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variants. Journal of Medical Genetics 56:8, pages 536-542.
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Désirée Maßberg & Hanns Hatt. (2018) Human Olfactory Receptors: Novel Cellular Functions Outside of the Nose. Physiological Reviews 98:3, pages 1739-1763.
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Dimitra Athanasiou, Monica Aguila, James Bellingham, Wenwen Li, Caroline McCulley, Philip J. Reeves & Michael E. Cheetham. (2018) The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy. Progress in Retinal and Eye Research 62, pages 1-23.
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Nikolina Jovancevic, Soumaya Khalfaoui, Markus Weinrich, Daniel Weidinger, Annika Simon, Benjamin Kalbe, Marcus Kernt, Anselm Kampik, Günter Gisselmann, Lian Gelis & Hanns Hatt. (2017) Odorant Receptor 51E2 Agonist β-ionone Regulates RPE Cell Migration and Proliferation. Frontiers in Physiology 8.
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