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Lehrstuhl für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Overview
Publications
(506)
Research Grants
(9)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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Common RUNX3 missense variant contributes to psoriatic arthritis by modifying differentiation of CD8(+) T-cells (2022)
Kerker I, Löhr S, Uebe S, Popp B, Vasileiou G, Bowes J, Kirchner P, et al.
Conference contribution
Investigating consanguineous families from Turkey to identify autosomal recessive neurodevelopmental disorders (2022)
Gumuslu E, Guemues E, Oz O, Ozkan M, Karaer K, Ekici AB, Yildiz EP, et al.
Conference contribution
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
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
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
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, Vancoil R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, et al.
Journal article
Midkine Promotes Metastasis and Therapeutic Resistance via mTOR/RPS6 in Uveal Melanoma. (2022)
Karg M, John L, Refaian N, Büttner C, Rottmar T, Sommer J, Bock B, et al.
Journal article
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