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Lehrstuhl für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Overview
Publications
(506)
Research Grants
(9)
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Journal article
Journal article
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A NEW DIAGNOSTIC APPROACH TO HLA TESTING IN KIDNEY TRANSPLANT RECIPIENTS USING CULTURED URINE DERIVED TUBULAR CELLS (2020)
Spriewald BM, Herrmann M, Bach C, Knaup K, Krumbiegel M, Reis A, Schiffer M, Wiesener M
Conference contribution
Role of Endogenous Regulators of Hem- And Lymphangiogenesis in Corneal Transplantation (2020)
Clahsen T, Büttner C, Hatami N, Reis A, Cursiefen C
Journal article, Review article
Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster (2020)
Straub J, Gregor A, Sauerer T, Fliedner A, Distel L, Suchy C, Ekici AB, et al.
Journal article
Molecular diagnosis of kidney transplant failure based on urine (2020)
Wiesener A, Knaup K, Büttner-Herold M, Dieterle A, Stoeckert J, Riedl B, Morath C, et al.
Journal article
Modeling Cell-Cell Interactions in Parkinson’s Disease Using Human Stem Cell-Based Models (2020)
Simmnacher K, Lanfer J, Rizo T, Kaindl J, Winner B
Journal article, Review article
De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females (2020)
Polla DL, Bhoj EJ, Verheij JB, Wassink-Ruiter JS, Reis A, Deshpande C, Gregor A, et al.
Journal article
Regulatory eosinophils induce the resolution of experimental arthritis and appear in remission state of human rheumatoid arthritis (2020)
Andreev D, Liu M, Kachler K, Llerins Perez M, Kirchner P, Kölle J, Gießl A, et al.
Journal article
New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics (2020)
Begemann A, Sticht H, Begtrup A, Vitobello A, Faivre L, Banka S, Alhaddad B, et al.
Journal article
A novel splice variant expands the LAMC3-associated cortical phenotype to frontal only polymicrogyria and adult-onset epilepsy (2020)
Kasper B, Kraus C, Schwarz M, Rösch J, Thiel C, Reis A, Zweier C
Journal article
7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder (2020)
Rieger M, Krumbiegel M, Reuter M, Schützenberger A, Reis A, Zweier C
Journal article
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