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Prof. Dr. Heinrich Sticht
List of publications:
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Professur für Bioinformatik
Award(s)
(1)
Project Leads
(1)
Project Memberships
(3)
Publications
(259)
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Journal article
Journal article
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Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2020), 10.1038/s41436-020-01020-w) (2021)
Klöckner C, Sticht H, Zacher P, Popp B, Babcock HE, Bakker DP, Barwick K, et al.
Journal article, Erratum
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3) (2021)
Durmus H, Mertoğlu E, Sticht H, Ceylaner S, Kulaksızoğlu IB, Hashemolhosseini S, Uçar EÖ, Parman Y
Journal article
Campylobacter jejuni Serine Protease HtrA Cleaves the Tight Junction Component Claudin-8 (2020)
Sharafutdinov I, Soltan Esmaeili D, Harrer A, Tegtmeyer N, Sticht H, Backert S
Journal article
Expanding the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and functional proof of aberrant WRC-mediated actin dynamics (2020)
Begemann A, Sticht H, Mcwalter K, Vitobello A, Faivre L, Alhaddad B, Banka S, et al.
Conference contribution
Common RUNX3 missense variant contributes to psoriatic arthritis by affecting splicing and modifying signaling, activation and differentiation of T-cells (2020)
Hüffmeier U, Löhr S, Uebe S, Popp B, Bowes J, Kirchner P, Giardina E, et al.
Conference contribution
Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype (2020)
Zanoni P, Steindl K, Sengupta D, Sticht H, Joset P, Baar A, Van Ravenswaaij-Arts CMA, et al.
Conference contribution
Further clinical and molecular delineation of spondylocostal dysostosis type 3 (2020)
Schuhmann S, Koller H, Sticht H, Kraus C, Krumbiegel M, Uebe S, Ekici AB, et al.
Conference contribution
Mono-allelic deleterious variants in autosomal recessive skeletal dysplasia genes are strongly associated with idiopathic short stature (2020)
Thiel CT, Hauer N, Vogl C, Uebe S, Sticht H, Ekici AB, Kraus C, et al.
Conference contribution
Loss of PHF6 leads to aberrant development of human neuron-like cells (2020)
Fliedner A, Gregor A, Ferrazzi F, Ekici AB, Sticht H, Zweier C
Journal article
A Survey of Biological Building Blocks for Synthetic Molecular Communication Systems (2020)
Söldner C, Socher E, Jamali V, Wicke W, Ahmadzadeh A, Breitinger HG, Burkovski A, et al.
Journal article
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