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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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Book chapter / Article in edited volumes
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Authored book
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Translation
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Thesis
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Conference contribution
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AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability (2017)
Brechet A, Buchert R, Schwenk J, Boudkkazi S, Zolles G, Siquier-Pernet K, Schaber I, et al.
Journal article
Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly (2017)
Tawamie H, Martianov I, Wohlfahrt N, Buchert R, Mengus G, Uebe S, Janiri L, et al.
Journal article
Crystal Structure of the Extracellular Domain of the Human Dendritic Cell Surface Marker CD83 (2017)
Heilingloh C, Klingl S, Egerer-Sieber C, Schmid B, Weiler S, Mühl-Zürbes P, Hofmann J, et al.
Journal article, Original article
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders (2017)
Reuter M, Tawamie H, Buchert R, Gebril OH, Froukh T, Thiel C, Uebe S, et al.
Journal article
Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes (2017)
Sighart R, Rech J, Hueber A, Blank N, Löhr S, Reis A, Sticht H, Hüffmeier U
Journal article
The genetic basis for most patients with pustular skin disease remains elusive (2017)
Mössner R, Wilsmann-Theis D, Oji V, Gkogkolou P, Löhr S, Schulz P, Körber A, et al.
Journal article
The human cytomegalovirus nuclear egress complex unites multiple functions: Recruitment of effectors, nuclear envelope rearrangement, and docking to nuclear capsids (2017)
Marschall M, Muller Y, Diewald B, Sticht H, Milbradt J
Journal article, Review article
A Homozygous Mutation in GPT2 Associated with Nonsyndromic Intellectual Disability in a Consanguineous Family from Costa Rica (2017)
Lobo-Prada T, Sticht H, Bogantes-Ledezma S, Ekici AB, Uebe S, Reis A, Leal A
Journal article
Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature (2017)
Hauer N, Sticht H, Boppudi S, Büttner C, Kraus C, Trautmann U, Zenker M, et al.
Journal article
Systematic analysis of phosphotyrosine antibodies recognizing single phosphorylated EPIYA-motifs in CagA of East Asian-type Helicobacter pylori strains (2016)
Lind J, Backert S, Hoffmann R, Eichler J, Yamaoka Y, Perez-Perez GI, Torres J, et al.
Journal article
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