Publications by authors named "Christina Zeitz"

97Publications

Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations.

Invest Ophthalmol Vis Sci 2020 Dec;61(14):36

Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli," Naples, Italy.

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December 2020

The genetics of rod-cone dystrophy in Arab countries: a systematic review.

Eur J Hum Genet 2020 Nov 13. Epub 2020 Nov 13.

Department of Medical Laboratory Technology, Faculty of Health Sciences, Beirut Arab University, Beirut, 1107 2809, Lebanon.

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November 2020

Interplay between cell-adhesion molecules governs synaptic wiring of cone photoreceptors.

Proc Natl Acad Sci U S A 2020 09 2;117(38):23914-23924. Epub 2020 Sep 2.

Department of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458;

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September 2020

Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes.

Genes (Basel) 2019 12 16;10(12). Epub 2019 Dec 16.

Rammal Hassan Rammal Research Laboratory, Physiotoxicity (PhyTox), Faculty of Sciences, Lebanese University, Nabatieh 1700, Lebanon.

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December 2019

Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease.

Invest Ophthalmol Vis Sci 2019 12;60(15):4951-4957

Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientfique, Institut de la Vision, Paris, France.

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December 2019

Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother.

Stem Cell Res 2019 12 5;41:101625. Epub 2019 Nov 5.

INSERM, CNRS, Institut de la Vision, Sorbonne Université, 17 rue Moreau, Paris, F-75012, France; CHNO des Quinze-Vingts, INSERM-DGOS CIC 1423, 28 rue de Charenton, Paris, F-75012, France. Electronic address:

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December 2019

Outer Retinal Alterations Associated With Visual Outcomes in Best Vitelliform Macular Dystrophy.

Am J Ophthalmol 2019 12 26;208:429-437. Epub 2019 Aug 26.

Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts, Centre de Maladies Rares "dystrophies rétiniennes d'origine génétique," Département hospitalo-universitaire Sight Restore, Institut National de la Santé et de la Recherche Médicale, DHOS Centre d'Investigation Clinique 1423, Paris, France; Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Institut de la Vision, Paris, France.

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December 2019