Profil bibliographique

Katarína Štingl

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

289Publications signalées

5152Citations signalées

2Affiliations récentes

Institutions déclarées

Domaines associés

Retinal Development and DisordersNeuroscience and Neural EngineeringRetinal Diseases and TreatmentsPhotoreceptor and optogenetics researchOphthalmology and Visual Impairment Studies

Publications récentes

Accès ouvert 2026 preprintOpenAlex

A mutation-agnostic and allele-specific ASO strategy demonstrates potent functional rescue and retinal preservation in RHO-linked retinitis pigmentosa

Salome Spaag, Wen-Hsuan Wu, Justin Yun, Aykut Demirkol et autres

0 citationsbioRxiv (Cold Spring Harbor Laboratory)

Accès ouvert 2026 articleOpenAlex

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

Molly Marra, Benjamin Bakall, Samuel Koller, José Sahel et autres

0 citationsUNC Libraries

Accès ouvert 2026 articleOpenAlex

Three novel variants in the UBAP1L gene lead to a generalized retinal dystrophy

Milda Reith, Katarína Štingl, Lasse Wolfram, Tobias B. Haack et autres

0 citationsOphthalmic Genetics

Accès ouvert 2026 articleOpenAlex

Persistent diffuse photoreceptor disorganization: further evidence with potential associations, long-term clinical course and therapeutic responsiveness of a new clinical entity

Anton Sonntag, Theresia Zuleger, Susanne Kohl, Lasse Wolfram et autres

0 citationsGraefe s Archive for Clinical and Experimental Ophthalmology

Accès ouvert 2026 articleOpenAlex

Single-cell analysis reveals impaired Müller glia-mediated intercellular communication and photoreceptor pathology in USH1C retinal organoids

Nicole Wenck, Mark Zorin, Qiang Wang, Selina Kröll et autres

0 citationsCellular and Molecular Life Sciences

Accès ouvert 2026 preprintOpenAlex

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy

Carlo Rivolta, Karolina Kamińska, Abigail Moye, Mathieu Quinodoz et autres

0 citationsResearch Square

Accès ouvert 2026 articleOpenAlex

Clinical manifestations of dual‐gene variants in retinitis pigmentosa

Lasse Wolfram, Jan-Philipp Bodenbender, David A. Merle, Milda Reith et autres

0 citationsActa Ophthalmologica

Accès ouvert 2026 articleOpenAlex

Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa

Peggy Reuter, Jennifer Schroeder, Marc Sturm, Mathieu Quinodoz et autres

0 citationsMolecular Medicine

Accès ouvert 2026 datasetOpenAlex

Additional file 2 of Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa

Peggy Reuter, Jennifer Schroeder, Marc Sturm, Mathieu Quinodoz et autres

0 citationsFigshare

Accès ouvert 2026 otherOpenAlex

Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa

Peggy Reuter, Jennifer Schroeder, Marc Sturm, Mathieu Quinodoz et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 1 of Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa

Peggy Reuter, Jennifer Schroeder, Marc Sturm, Mathieu Quinodoz et autres

0 citationsFigshare

Accès ouvert 2026 datasetOpenAlex

Additional file 2 of Systematic functional evaluation of CNGA1 missense variants associated with retinitis pigmentosa

Peggy Reuter, Jennifer Schroeder, Marc Sturm, Mathieu Quinodoz et autres

0 citationsFigshare

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