Prof. Dr. Heinrich Sticht

2022

• Aillaud, I., Kaniyappan, S., Chandupatla, R.R., Ramirez, L.M., Alkhashrom, S., Eichler, J.,... Funke, S.A. (2022). A novel D-amino acid peptide with therapeutic potential (ISAD1) inhibits aggregation of neurotoxic disease-relevant mutant Tau and prevents Tau toxicity in vitro. Alzheimer's Research and Therapy, 14(1). https://dx.doi.org/10.1186/s13195-022-00959-z
• Beudert, M., Hahn, L., Horn, A., Hauptstein, N., Sticht, H., Meinel, L.,... Luehmann, T. (2022). Merging bioresponsive release of insulin-like growth factor I with 3D printable thermogelling hydrogels. Journal of Controlled Release, 347, 115-126. https://dx.doi.org/10.1016/j.jconrel.2022.04.028
• Boonsawat, P., Horn, A.H.C., Steindl, K., Baumer, A., Joset, P., Kraemer, D.,... Rauch, A. (2022). Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders. npj Genomic Medicine, 7(1). https://dx.doi.org/10.1038/s41525-022-00316-x
• Brand, L., Garkisch, M., Lotter, S., Schäfer, M., Burkovski, A., Sticht, H.,... Schober, R. (2022). Media Modulation based Molecular Communication. IEEE Transactions on Communications, 1-1. https://dx.doi.org/10.1109/TCOMM.2022.3205949
• Breitinger, U., Farag, N.S., Sticht, H., & Breitinger, H.G. (2022). Viroporins: Structure, function, and their role in the life cycle of SARS-CoV-2. International Journal of Biochemistry and Cell Biology, 145. https://dx.doi.org/10.1016/j.biocel.2022.106185
• Conrad, M., Söldner, C., & Sticht, H. (2022). Effect of Ions and Sequence Variants on the Antagonist Binding Properties of the Histamine H1 Receptor. International Journal of Molecular Sciences, 23(3). https://dx.doi.org/10.3390/ijms23031420
• Gerber, C.B., Fliedner, A., Bartsch, O., Berland, S., Dewenter, M., Haug, M.,... Zweier, C. (2022). Further characterization of Borjeson-Forssman-Lehmann syndrome in females due to de novo variants in PHF6. Clinical Genetics. https://dx.doi.org/10.1111/cge.14173
• Gregor, A., Meerbrei, T., Gerstner, T., Toutain, A., Lynch, S.A., Stals, K.,... Zweier, C. (2022). De novo missense variants in FBXO11 alter its protein expression and subcellular localization. Human Molecular Genetics, 31(3), 440-454. https://dx.doi.org/10.1093/hmg/ddab265
• Kerker, I., Löhr, S., Uebe, S., Popp, B., Vasileiou, G., Bowes, J.,... Hüffmeier, U. (2022). Common RUNX3 missense variant contributes to psoriatic arthritis by modifying differentiation of CD8(+) T-cells. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 554-555). LONDON: SPRINGERNATURE.
• Kicuntod, J., Häge, S., Hahn, F., Sticht, H., & Marschall, M. (2022). The Oligomeric Assemblies of Cytomegalovirus Core Nuclear Egress Proteins Are Associated with Host Kinases and Show Sensitivity to Antiviral Kinase Inhibitors. Viruses, 14(5). https://dx.doi.org/10.3390/v14051021
• Kloeckner, C., Murray, J.P.F., Tavasoli, M., Sticht, H., Stoltenburg-Didinger, G., Scholle, L.M.,... Platzer, K. (2022). Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly. Brain. https://dx.doi.org/10.1093/brain/awac074
• Linck-Paulus, L., Horn, A., Matthies, A.O., Fischer, S., Meister, G., Sticht, H.,... Boßerhoff, A.K. (2022). A novel splice variant of Argonaut 2 affects microRNA target genes and cell viability of melanoma cells. In JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT (pp. 36-36). HOBOKEN: WILEY.
• Linck-Paulus, L., Meißgeier, T., Pieger, K., Horn, A., Matthies, A.O., Fischer, S.,... Boßerhoff, A.K. (2022). A previously unknown Argonaute 2 variant positively modulates the viability of melanoma cells. Cellular and Molecular Life Sciences, 79(9). https://dx.doi.org/10.1007/s00018-022-04496-8
• Luppe, J., Sticht, H., Lecoquierre, F., Goldenberg, A., Gorman, K.M., Molloy, B.,... Platzer, K. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. https://dx.doi.org/10.1038/s41431-022-01269-6
• Lösing, J., Haege, S., Schütz, M., Wagner, S., Wardin, J., Sticht, H., & Marschall, M. (2022). 'Shared-Hook' and 'Changed-Hook' Binding Activities of Herpesviral Core Nuclear Egress Complexes Identified by Random Mutagenesis. Cells, 11(24). https://dx.doi.org/10.3390/cells11244030
• Peter, A.S., Grüner, E., Socher, E., Fraedrich, K., Richel, E., Müller-Schmucker, S.,... Überla, K. (2022). Characterization of SARS-CoV-2 Escape Mutants to a Pair of Neutralizing Antibodies Targeting the RBD and the NTD. International Journal of Molecular Sciences, 23(15). https://dx.doi.org/10.3390/ijms23158177
• Platzer, K., Sticht, H., Bupp, C., Ganapathi, M., Pereira, E.M., Le Guyader, G.,... Wojcik, S.M. (2022). De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission. Annals of Neurology. https://dx.doi.org/10.1002/ana.26485
• Popp, B., Bienvenu, T., Giurgea, I., Metreau, J., Kraus, C., Reis, A.,... Zweier, C. (2022). The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt-Hopkins syndrome. Clinical Genetics. https://dx.doi.org/10.1111/cge.14206
• Rahimi, M.J., Urban, N., Wegler, M., Sticht, H., Schaefer, M., Popp, B.,... Oppermann, H. (2022). De novo variants in ATP2B1 lead to neurodevelopmental delay. American Journal of Human Genetics, 109(5), 944-952. https://dx.doi.org/10.1016/j.ajhg.2022.03.009
• Rosenhahn, E., O'Brien, T.J., Zaki, M.S., Sorge, I., Wieczorek, D., Rostasy, K.,... Platzer, K. (2022). Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications. American Journal of Human Genetics, 109(8), 1421-1435. https://dx.doi.org/10.1016/j.ajhg.2022.06.008
• Schweininger, J., Kriegel, M., Häge, S., Conrad, M., Alkhashrom, S., Lösing, J.,... Muller, Y. (2022). The crystal structure of the varicella-zoster Orf24-Orf27 nuclear egress complex spotlights multiple determinants of herpesvirus subfamily specificity. Journal of Biological Chemistry, 298(3). https://dx.doi.org/10.1016/j.jbc.2022.101625
• Schütz, M., Müller, R., Socher, E., Wangen, C., Full, F., Wyler, E.,... Marschall, M. (2022). Highly Conserved Interaction Profiles between Clinically Relevant Mutants of the Cytomegalovirus CDK-like Kinase pUL97 and Human Cyclins: Functional Significance of Cyclin H. International Journal of Molecular Sciences, 23, 11814. https://dx.doi.org/10.3390/ijms231911814
• Thuma, N., Döhler, D., Mielenz, D., Sticht, H., Radtke, D., Reimann, L.,... Vöhringer, D. (2022). A newly identified secreted larval antigen elicits basophil-dependent protective immunity against N. brasiliensis infection. Frontiers in Immunology, 13. https://dx.doi.org/10.3389/fimmu.2022.979491
• Vintschger, E., Kraemer, D., Joset, P., Horn, A., Rauch, A., Sticht, H., & Bachmann-Gagescu, R. (2022). Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies. European Journal of Human Genetics. https://dx.doi.org/10.1038/s41431-022-01267-8
• Wegler, M., Jia, X., Alders, M., Bouman, A., Chen, J., Duan, X.,... Abou Jamra, R. (2022). De novo variants in the PABP domain of PABPC1 lead to developmental delay. Genetics in Medicine. https://dx.doi.org/10.1016/j.gim.2022.04.013
• Weißenborn, L., Richel, E., Hueseman, H., Welzer, J., Beck, S., Schäfer, S.,... Eichler, J. (2022). Smaller, Stronger, More Stable: Peptide Variants of a SARS-CoV-2 Neutralizing Miniprotein. International Journal of Molecular Sciences, 23(11). https://dx.doi.org/10.3390/ijms23116309

2021

• Appelhof, B., Wagner, M., Hoefele, J., Heinze, A., Roser, T., Koch-Hogrebe, M.,... Abou Jamra, R. (2021). Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1. European Journal of Human Genetics, 29(3), 411-421. https://dx.doi.org/10.1038/s41431-020-00749-x
• Averdunk, L., Sticht, H., Surowy, H., Luedecke, H.-J., Koch-Hogrebe, M., Alsaif, H.S.,... Wieczorek, D. (2021). Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype (Journal of Molecular Medicine, (2021), 10.1007/s00109-021-02124-9). Journal of Molecular Medicine. https://dx.doi.org/10.1007/s00109-021-02153-4
• Averdunk, L., Sticht, H., Surowy, H., Luedecke, H.-J., Koch-Hogrebe, M., Alsaif, H.S.,... Wieczorek, D. (2021). The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. Journal of Molecular Medicine. https://dx.doi.org/10.1007/s00109-021-02124-9
• Bachert, W., Klotz, L., Sticht, H., & Enz, R. (2021). Homodimerization of a proximal region within the C-terminus of the orphan G-protein coupled receptor GPR179. Neurochemistry International, 149. https://dx.doi.org/10.1016/j.neuint.2021.105150
• Breitinger, U., Ali, N.K., Sticht, H., & Breitinger, H.G. (2021). Inhibition of SARS CoV Envelope Protein by Flavonoids and Classical Viroporin Inhibitors. Frontiers in Microbiology, 12. https://dx.doi.org/10.3389/fmicb.2021.692423
• Breitinger, U., Sticht, H., & Breitinger, H.G. (2021). Modulation of recombinant human alpha 1 glycine receptor by flavonoids and gingerols. Biological Chemistry. https://dx.doi.org/10.1515/hsz-2020-0360
• Durmus, H., Mertoğlu, E., Sticht, H., Ceylaner, S., Kulaksızoğlu, I.B., Hashemolhosseini, S.,... Parman, Y. (2021). Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3). Neurological Sciences. https://dx.doi.org/10.1007/s10072-021-05100-w
• Höring, C., Conrad, M., Söldner, C., Wang, J., Sticht, H., Strasser, A., & Miao, Y. (2021). Specific engineered G protein coupling to histamine receptors revealed from cellular assay experiments and accelerated molecular dynamics simulations. International Journal of Molecular Sciences, 22(18). https://dx.doi.org/10.3390/ijms221810047
• Kicuntod, J., Alkhashrom, S., Häge, S., Diewald, B., Müller, R., Hahn, F.,... Marschall, M. (2021). Properties of Oligomeric Interaction of the Cytomegalovirus Core Nuclear Egress Complex (NEC) and Its Sensitivity to an NEC Inhibitory Small Molecule. Viruses, 13(3). https://dx.doi.org/10.3390/v13030462
• Klöckner, C., Sticht, H., Zacher, P., Popp, B., Babcock, H.E., Bakker, D.P.,... Platzer, K. (2021). 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). Genetics in Medicine. https://dx.doi.org/10.1038/s41436-020-01090-w
• Kohrt, S., Strobel, S., Mann, M., Sticht, H., Fleckenstein, B., & Thoma-Kreß, A. (2021). Characterizing the interaction between the htlv-1 transactivator tax-1 with transcription elongation factor ell2 and its impact on viral transactivation. International Journal of Molecular Sciences, 22(24). https://dx.doi.org/10.3390/ijms222413597
• Konieczny, A., Conrad, M., Ertl, F.J., Gleixner, J., Gattor, A.O., Grätz, L.,... Keller, M. (2021). N-Terminus to Arginine Side-Chain Cyclization of Linear Peptidic Neuropeptide y Y4Receptor Ligands Results in Picomolar Binding Constants. Journal of Medicinal Chemistry, 64(22), 16746-16769. https://dx.doi.org/10.1021/acs.jmedchem.1c01574
• Malhis, M., Kaniyappan, S., Aillaud, I., Chandupatla, R.R., Ramirez, L.M., Zweckstetter, M.,... Funke, S.A. (2021). Potent Tau Aggregation Inhibitor D-Peptides Selected against Tau-Repeat 2 Using Mirror Image Phage Display. ChemBioChem. https://dx.doi.org/10.1002/cbic.202100287
• Peter, A.S., Roth, E., Schulz, S., Fraedrich, K., Steinmetz, T., Damm, D.,... Jäck, H.-M. (2021). A pair of non‐competing neutralizing human monoclonal antibodies protecting from disease in a SARS‐CoV‐2 infection model. European Journal of Immunology. https://dx.doi.org/10.1002/eji.202149374
• Regensburger, D., Tenkerian, C., Pürzer, V., Schmid, B., Wohlfahrt, T., Stolzer, I.,... Naschberger, E. (2021). Matricellular Protein SPARCL1 Regulates Blood Vessel Integrity and Antagonizes Inflammatory Bowel Disease. Inflammatory Bowel Diseases. https://dx.doi.org/10.1093/ibd/izaa346
• Richard, E.M., Bakhtiari, S., Marsh, A.P., Kaiyrzhanov, R., Wagner, M., Shetty, S.,... Kruer, M.C. (2021). Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss. American Journal of Human Genetics, 108(10), 2006-2016. https://dx.doi.org/10.1016/j.ajhg.2021.08.003
• Schuhmann, S., Koller, H., Sticht, H., Kraus, C., Krumbiegel, M., Uebe, S.,... Thiel, C. (2021). Clinical and molecular delineation of spondylocostal dysostosis type 3. Clinical Genetics. https://dx.doi.org/10.1111/cge.13952
• Schütz, M., Steingruber, M., Socher, E., Müller, R., Wagner, S., Kögel, M.,... Marschall, M. (2021). Functional Relevance of the Interaction between Human Cyclins and the Cytomegalovirus-Encoded CDK-Like Protein Kinase pUL97. Viruses, 13, 1248. https://dx.doi.org/10.3390/v13071248
• Socher, E., Conrad, M., Heger, L., Paulsen, F., Sticht, H., Zunke, F., & Arnold, P. (2021). Computational decomposition reveals reshaping of the SARS‐CoV‐2–ACE2 interface among viral variants expressing the N501Y mutation. Journal of Cellular Biochemistry. https://dx.doi.org/10.1002/jcb.30142
• Socher, E., Conrad, M., Heger, L., Paulsen, F., Sticht, H., Zunke, F., & Arnold, P. (2021). Mutations in the B.1.1.7 SARS-CoV-2 Spike Protein Reduce Receptor-Binding Affinity and Induce a Flexible Link to the Fusion Peptide. Biomedicines, 9(5). https://dx.doi.org/10.3390/biomedicines9050525
• Söldner, C., Sticht, H., & Horn, A. (2021). Molecular Simulations and Alzheimer׳s Disease. In Olaf Wolkenhauer (Eds.), Systems Medicine: Integrative, qualitative, and computational approaches. (pp. 54-70). Amsterdam: Elsevier.
• Thomas, M., Kropff, B., Schneider, A., Winkler, T., Görzer, I., Sticht, H.,... Reuter, N. (2021). A novel strain-specific neutralizing epitope on glycoprotein H of human cytomegalovirus. Journal of Virology, 95(18). https://dx.doi.org/10.1128/JVI.00657-21
• Zanoni, P., Steindl, K., Sengupta, D., Joset, P., Bahr, A., Sticht, H.,... Rauch, A. (2021). Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-021-01158-1

2020

• Abdelfattah, F., Kariminejad, A., Kahlert, A.K., Morrison, P.J., Gumus, E., Mathews, K.D.,... Schanze, D. (2020). Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders. Human Mutation. https://dx.doi.org/10.1002/humu.24067
• Begemann, A., Sticht, H., Begtrup, A., Vitobello, A., Faivre, L., Banka, S.,... Rauch, A. (2020). New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-020-01011-x
• Begemann, A., Sticht, H., Mcwalter, K., Vitobello, A., Faivre, L., Alhaddad, B.,... Rauch, A. (2020). Expanding the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and functional proof of aberrant WRC-mediated actin dynamics. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 329-331). LONDON: SPRINGERNATURE.
• Breitinger, U., Weinländer, K., Pechmann, Y., Langlhofer, G., Enz, R., Becker, C.-M.,... Breitinger, H.G. (2020). A proline-rich motif in the large intracellular loop of the glycine receptor α1 subunit interacts with the Pleckstrin homology domain of collybistin. Journal of Advanced Research. https://dx.doi.org/10.1016/j.jare.2020.09.009
• Conrad, M., Söldner, C., Miao, Y., & Sticht, H. (2020). Agonist binding and g protein coupling in histamine h2 receptor: A molecular dynamics study. International Journal of Molecular Sciences, 21(18), 1-18. https://dx.doi.org/10.3390/ijms21186693
• Donhauser, N., Socher, E., Millen, S., Heym, S., Sticht, H., & Thoma-Kreß, A. (2020). Transfer of htlv-1 p8 and gag to target t-cells depends on vasp, a novel interaction partner of p8. PLoS Pathogens, 16(9). https://dx.doi.org/10.1371/journal.ppat.1008879
• Durmus, H., Sticht, H., Ceylaner, S., Hashemolhosseini, S., & Deymeer, F. (2020). Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine. Acta Neurologica Belgica. https://dx.doi.org/10.1007/s13760-020-01505-0
• Durmus, H., Sticht, H., Ceylaner, S., Hashemolhosseini, S., & Parmn, Y. (2020). EPISODIC PSYCHOSIS, ATAXIA, MOTOR NEUROPATHY CAUSED BY A NOVEL MUTATION IN ADPRHL2. In NEUROLOGY. Toronto, CANADA: PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS.
• Fliedner, A., Gregor, A., Ferrazzi, F., Ekici, A.B., Sticht, H., & Zweier, C. (2020). Loss of PHF6 leads to aberrant development of human neuron-like cells. Scientific Reports, 10(1). https://dx.doi.org/10.1038/s41598-020-75999-2
• Frey, S., Sticht, H., Wilsmann-Theis, D., Gerschütz, A., Wolf, K., Löhr, S.,... Hüffmeier, U. (2020). Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis. Journal of Investigative Dermatology. https://dx.doi.org/10.1016/j.jid.2019.11.024
• Grosche, L., Knippertz, I., König, C., Royzman, D., Wild, A., Zinser, E.,... Lechmann, M. (2020). The CD83 Molecule – An Important Immune Checkpoint. Frontiers in Immunology, 11. https://dx.doi.org/10.3389/fimmu.2020.00721
• Haskamp, S., Bruns, H., Hahn, M., Hoffmann, M., Gregor, A., Löhr, S.,... Schauer, C. (2020). Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases. American Journal of Human Genetics, 107(3), 527-538. https://dx.doi.org/10.1016/j.ajhg.2020.07.001
• Hussein, R.A., Ahmed, M., Sticht, H., Breitinger, H.G., & Breitinger, U. (2020). Fine-Tuning of Neuronal Ion Channels-Mapping of Residues Involved in Glucose Sensitivity of Recombinant Human Glycine Receptors. ACS Chemical Neuroscience. https://dx.doi.org/10.1021/acschemneuro.0c00566
• Hüffmeier, U., Löhr, S., Uebe, S., Popp, B., Bowes, J., Kirchner, P.,... Reis, A. (2020). Common RUNX3 missense variant contributes to psoriatic arthritis by affecting splicing and modifying signaling, activation and differentiation of T-cells. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 314-315). LONDON: SPRINGERNATURE.
• Kloeckner, C., Sticht, H., Zacher, P., Popp, B., Babcock, H.E., Bakker, D.P.,... Platzer, K. (2020). De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-020-01020-w
• Marschall, M., Häge, S., Conrad, M., Alkhashrom, S., Kicuntod, J., Schweininger, J.,... Sticht, H. (2020). Nuclear Egress Complexes of HCMV and Other Herpesviruses: Solving the Puzzle of Sequence Coevolution, Conserved Structures and Subfamily-Spanning Binding Properties. Viruses, 12(6). https://dx.doi.org/10.3390/v12060683
• Muller, Y., Häge, S., Alkhashrom, S., Höllriegl, T., Weigert, S., Dolles, S.,... Marschall, M. (2020). High-resolution crystal structures of two prototypical β- And γ-herpesviral nuclear egress complexes unravel the determinants of subfamily specificity. Journal of Biological Chemistry, 295(10), 3189-3201. https://dx.doi.org/10.1074/jbc.RA119.011546
• Schuhmann, S., Koller, H., Sticht, H., Kraus, C., Krumbiegel, M., Uebe, S.,... Thiel, C.T. (2020). Further clinical and molecular delineation of spondylocostal dysostosis type 3. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 841-841). LONDON: SPRINGERNATURE.
• Schütz, M., Thomas, M., Wangen, C., Wagner, S., Rauschert, L., Errerd, T.,... Marschall, M. (2020). The peptidyl-prolyl cis/trans isomerase Pin1 interacts with three early regulatory proteins of human cytomegalovirus. Virus Research, 285. https://dx.doi.org/10.1016/j.virusres.2020.198023
• Sharafutdinov, I., Soltan Esmaeili, D., Harrer, A., Tegtmeyer, N., Sticht, H., & Backert, S. (2020). Campylobacter jejuni Serine Protease HtrA Cleaves the Tight Junction Component Claudin-8. Frontiers in Cellular and Infection Microbiology, 10. https://dx.doi.org/10.3389/fcimb.2020.590186
• Söldner, C., Socher, E., Jamali, V., Wicke, W., Ahmadzadeh, A., Breitinger, H.G.,... Sticht, H. (2020). A Survey of Biological Building Blocks for Synthetic Molecular Communication Systems. IEEE Communications Surveys & Tutorials, 22(4), 2765-2800. https://dx.doi.org/10.1109/COMST.2020.3008819
• Tegtmeyer, N., Neddermann, M., Lind, J., Suneesh Kumar, P., Sharafutdinov, I., Gutiérrez-Escobar, A.J.,... Vieth, M. (2020). Toll-like Receptor 5 Activation by the CagY Repeat Domains of Helicobacter pylori. Cell Reports, 32(11). https://dx.doi.org/10.1016/j.celrep.2020.108159
• Thiel, C.T., Hauer, N., Vogl, C., Uebe, S., Sticht, H., Ekici, A.B.,... Reis, A. (2020). Mono-allelic deleterious variants in autosomal recessive skeletal dysplasia genes are strongly associated with idiopathic short stature. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 240-240). LONDON: SPRINGERNATURE.
• Zanoni, P., Steindl, K., Sengupta, D., Sticht, H., Joset, P., Baar, A.,... Rauch, A. (2020). Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 355-356). LONDON: SPRINGERNATURE.