Prof. Dr. André Wiesmann da Silva Reis



close-button

Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

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