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Prof. Dr. André Wiesmann da Silva Reis
List of publications:
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Lehrstuhl für Humangenetik
Award(s)
(2)
Project Leads
(4)
Project Memberships
(2)
Publications
(219)
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Journal article
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Book chapter / Article in edited volumes
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Thesis
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Conference contribution
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Dentate gyrus astrocytes exhibit layer-specific molecular, morphological and physiological features (2022)
Karpf J, Unichenko P, Chalmers N, Beyer F, Wittmann MT, Schneider J, Fidan E, et al.
Journal article
Cystathionine β-synthase as novel endogenous regulator of lymphangiogenesis via modulating VEGF receptor 2 and 3 (2022)
Hatami N, Büttner C, Bock F, Simfors S, Musial G, Reis A, Cursiefen C, Clahsen T
Journal article
Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study (2022)
Popp B, Ekici AB, Knaup K, Schneider K, Uebe S, Park J, Bafna V, et al.
Journal article
The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt-Hopkins syndrome (2022)
Popp B, Bienvenu T, Giurgea I, Metreau J, Kraus C, Reis A, Fischer J, et al.
Journal article
Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer (2022)
Fasching P, Liu D, Scully S, Ingle JN, Lyra PC, Rack B, Hein A, et al.
Journal article
Familial acute aortic dissection associated with a novel ACTA2 germline variant (2022)
Strecker T, Wiesmueller F, Rudnik-Schoeneborn S, Hoyer J, Wiesmann da Silva Reis A, Weyand M, Agaimy A
Journal article
Tyrosinase reduces expression of vascular endothelial growth factors and improves corneal graft survival (2022)
Clahsen T, Hatami N, Büttner C, Reis A, Cursiefen C
Conference contribution
SRD5A3-CDG: Twins with an intragenic tandem duplication (2022)
Rieger M, Türk M, Kraus C, Uebe S, Ekici AB, Krumbiegel M, Huchzermeyer C, et al.
Journal article
Astrogenesis in the murine dentate gyrus is a life-long and dynamic process (2022)
Schneider J, Weigel J, Wittmann MT, Svehla P, Ehrt S, Zheng F, Elmzzahi T, et al.
Journal article
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum (2022)
Hüffmeier U, Kraus C, Reuter M, Uebe S, Abbott MA, Ahmed SA, Rawson KL, et al.
Conference contribution
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