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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(729)
Research Grants
(48)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Microdeletions at 19p13.11 in four individuals with neurodevelopmental delay (2022)
Rieger M, Moutton S, Verheyen S, Speicher M, Leheup B, Bonnet C, Steindl K, et al.
Conference contribution
Nimodipine Exerts Beneficial Effects on the Rat Oligodendrocyte Cell Line OLN-93 (2022)
Boltz F, Enders M, Feigenspan A, Kirchner P, Ekici AB, Kürten S
Journal article
Acute care and secondary prevention of stroke with newly detected versus known atrial fibrillation (2022)
Wang R, Macha K, Haupenthal D, Gaßmann L, Siedler G, Stoll S, Fröhlich K, et al.
Journal article
Differential vulnerability of adult neurogenic niches to dosage of the neurodevelopmental-disorder linked gene Foxg1 (2022)
Schäffner I, Wittmann MT, Vogel T, Lie DC
Journal article
Adult alcohol drinking and emotional tone are mediated by neutral sphingomyelinase during development in males (2022)
Kalinichenko L, Mühle C, Jia T, Anderheiden F, Datz M, Eberle AL, Eulenburg V, et al.
Journal article
Interaction of Alpha Synuclein and Microtubule Organization Is Linked to Impaired Neuritic Integrity in Parkinson’s Patient-Derived Neuronal Cells (2022)
Schneider Y, Drobny A, Prots I, Zunke F, Xiang W, Seebauer L, Schneider Y, et al.
Journal article, Review article
De novo missense variants in FBXO11 alter its protein expression and subcellular localization (2022)
Gregor A, Meerbrei T, Gerstner T, Toutain A, Lynch SA, Stals K, Maxton C, et al.
Journal article, Original article
A saturated map of common genetic variants associated with human height (2022)
Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, et al.
Journal article
Anti-CD19 CAR T cell therapy for refractory systemic lupus erythematosus (2022)
Mackensen A, Müller F, Mougiakakos D, Böltz S, Wilhelm A, Aigner M, Völkl S, et al.
Journal article
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling (2022)
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, et al.
Journal article
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