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Prof. Dr. André Wiesmann da Silva Reis
List of publications:
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Lehrstuhl für Humangenetik
Award(s)
(2)
Project Leads
(4)
Project Memberships
(2)
Publications
(219)
Types of publications
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Journal article
Journal article
Book chapter / Article in edited volumes
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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CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome (2020)
Börstler T, Wend H, Krumbiegel M, Kavyanifar A, Reis A, Lie DC, Winner B, Turan S
Journal article
Breast MRI texture analysis for prediction of BRCA-associated genetic risk (2020)
Vasileiou G, Costa MJ, Long C, Wetzler I, Hoyer J, Kraus C, Popp B, et al.
Journal article
CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome. (2020)
Turan S, Winner B, Winner B, Krumbiegel M, Wiesmann da Silva Reis A, Lie DC, Börstler T, et al.
Journal article
Analysis of genetically determined gene expression suggest role of inflammatory processes in etiology of exfoliation syndrome (2020)
Hirbo J, Pasutto F, Sealock J, Evans P, Pawar P, Tao R, Straub P, et al.
Conference contribution
Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation (2020)
Wedel M, Fröb F, Elsesser O, Wittmann MT, Lie DC, Reis A, Wegner M
Journal article
Sox11 is an Activity-Regulated Gene with Dentate-Gyrus-Specific Expression Upon General Neural Activation (2020)
von Wittgenstein J, Zheng F, Wittmann MT, Balta EA, Ferrazzi F, Schäffner I, Häberle B, et al.
Journal article
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
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
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
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