Prof. Dr. Heinrich Sticht

Professur für Bioinformatik

De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission (2022) Platzer K, Sticht H, Bupp C, Ganapathi M, Pereira EM, Le Guyader G, Bilan F, et al. Journal article A novel splice variant of Argonaut 2 affects microRNA target genes and cell viability of melanoma cells (2022) Linck-Paulus L, Horn A, Matthies AO, Fischer S, Meister G, Sticht H, Kappelmann-Fenzl M, Boßerhoff AK Conference contribution A previously unknown Argonaute 2 variant positively modulates the viability of melanoma cells (2022) Linck-Paulus L, Meißgeier T, Pieger K, Horn A, Matthies AO, Fischer S, Meister G, et al. Journal article A newly identified secreted larval antigen elicits basophil-dependent protective immunity against N. brasiliensis infection (2022) Thuma N, Döhler D, Mielenz D, Sticht H, Radtke D, Reimann L, Warscheid B, Vöhringer D 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 Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications (2022) Rosenhahn E, O'Brien TJ, Zaki MS, Sorge I, Wieczorek D, Rostasy K, Vitobello A, et al. Journal article Characterization of SARS-CoV-2 Escape Mutants to a Pair of Neutralizing Antibodies Targeting the RBD and the NTD (2022) Peter AS, Grüner E, Socher E, Fraedrich K, Richel E, Müller-Schmucker S, Cordsmeier A, et al. Journal article Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6 (2022) Gerber CB, Fliedner A, Bartsch O, Berland S, Dewenter M, Haug M, Hayes I, et al. Journal article Smaller, Stronger, More Stable: Peptide Variants of a SARS-CoV-2 Neutralizing Miniprotein (2022) Weißenborn L, Richel E, Hueseman H, Welzer J, Beck S, Schäfer S, Sticht H, et al. Journal article De novo variants in the PABP domain of PABPC1 lead to developmental delay (2022) Wegler M, Jia X, Alders M, Bouman A, Chen J, Duan X, Lauzon JL, et al. Journal article