Single-cell RNA sequencing of adult mouse testes

Tekijä Lukassen, Soeren, Bosch, Elisabeth, Ekici, Arif B., Winterpacht, Andreas
Julkaisussa Sci Data (2018)

GPFrontend and GPGraphics: graphical analysis tools for genetic association studies

Tekijä Uebe, Steffen, Pasutto, Francesca, Krumbiegel, Mandy, Schanze, Denny, Ekici, Arif B, Reis, André
Julkaistu 2010

Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases

Tekijä Moosmann, Julia, Uebe, Steffen, Dittrich, Sven, Rüffer, André, Ekici, Arif B., Toka, Okan
Julkaisussa PLoS One (2015)

Loss of PHF6 leads to aberrant development of human neuron-like cells

Tekijä Fliedner, Anna, Gregor, Anne, Ferrazzi, Fulvia, Ekici, Arif B., Sticht, Heinrich, Zweier, Christiane
Julkaisussa Sci Rep (2020)

Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability

Tekijä Scheller, Ute, Pfisterer, Kathrin, Uebe, Steffen, Ekici, Arif B., Reis, André, Jamra, Rami, Ferrazzi, Fulvia
Julkaisussa BMC Med Genomics (2018)

CRISPR/Cas9-Mediated Knock-Out of Kras(G12D) Mutated Pancreatic Cancer Cell Lines

Tekijä Lentsch, Eva, Li, Lifei, Pfeffer, Susanne, Ekici, Arif B., Taher, Leila, Pilarsky, Christian, Grützmann, Robert
Julkaisussa Int J Mol Sci (2019)

Lymphocyte Immune Response and T Cell Differentiation in Fontan Patients with protein-losing enteropathy

Tekijä Moosmann, Julia, Toka, Okan, Lukassen, Sören, Ekici, Arif B., Mackensen, Andreas, Völkl, Simon, Dittrich, Sven
Julkaisussa Thorac Cardiovasc Surg (2021)

Tracing Myelin Protein Zero (P0) in vivo by construction of P0-GFP fusion proteins

Tekijä Ekici, Arif B, Oezbey, Sevinc, Fuchs, Christina, Nelis, Eva, Van Broeckhoven, Christine, Schachner, Melitta, Rautenstrauss, Bernd
Julkaistu 2002

Exome Pool-Seq in neurodevelopmental disorders

Tekijä Popp, Bernt, Ekici, Arif B., Thiel, Christian T., Hoyer, Juliane, Wiesener, Antje, Kraus, Cornelia, Reis, André, Zweier, Christiane
Julkaisussa Eur J Hum Genet (2017)

The Transient Chondrocyte Phenotype in Human Osteophytic Cartilage: A Role of Pigment Epithelium-Derived Factor?

Tekijä Klinger, Patricia, Beyer, Christian, Ekici, Arif B., Carl, Hans-Dieter, Schett, Georg, Swoboda, Bernd, Hennig, Friedrich F., Gelse, Kolja
Julkaisussa Cartilage (2013)

High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder

Tekijä Grünblatt, Edna, Oneda, Beatrice, Ekici, Arif B., Ball, Juliane, Geissler, Julia, Uebe, Steffen, Romanos, Marcel, Rauch, Anita, Walitza, Susanne
Julkaisussa BMC Med Genomics (2017)

Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster

Tekijä Straub, Jonas, Gregor, Anne, Sauerer, Tatjana, Fliedner, Anna, Distel, Laila, Suchy, Christine, Ekici, Arif B., Ferrazzi, Fulvia, Zweier, Christiane
Julkaisussa Sci Rep (2020)

Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling

Tekijä Vasileiou, Georgia, Ekici, Arif B., Uebe, Steffen, Zweier, Christiane, Hoyer, Juliane, Engels, Hartmut, Behrens, Jürgen, Reis, André, Hadjihannas, Michel V.
Julkaisussa Am J Hum Genet (2015)

Associations between genetic risk variants for kidney diseases and kidney disease etiology

Tekijä Wunnenburger, Sebastian, Schultheiss, Ulla T., Walz, Gerd, Hausknecht, Birgit, Ekici, Arif B., Kronenberg, Florian, Eckardt, Kai-Uwe, Köttgen, Anna, Wuttke, Matthias
Julkaisussa Sci Rep (2017)

Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease

Tekijä Jing, Jiaojiao, Ekici, Arif B., Sitter, Thomas, Eckardt, Kai-Uwe, Schaeffner, Elke, Li, Yong, Kronenberg, Florian, Köttgen, Anna, Schultheiss, Ulla T.
Julkaisussa Sci Rep (2018)

Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability

Tekijä Popp, Bernt, Agaimy, Abbas, Kraus, Cornelia, Knaup, Karl X., Ekici, Arif B., Uebe, Steffen, Reis, André, Wiesener, Michael, Zweier, Christiane
Julkaisussa BMC Cancer (2019)

scRNA sequencing uncovers a TCF4-dependent transcription factor network regulating commissure development in mouse

Tekijä Wittmann, Marie-Theres, Katada, Sayako, Sock, Elisabeth, Kirchner, Philipp, Ekici, Arif B., Wegner, Michael, Nakashima, Kinichi, Lie, Dieter Chichung, Reis, André
Julkaisussa Development (2021)

Reactivation of codogenic endogenous retroviral (ERV) envelope genes in human endometrial carcinoma and prestages: Emergence of new molecular targets

Tekijä Strissel, Pamela L., Ruebner, Matthias, Thiel, Falk, Wachter, David, Ekici, Arif B., Wolf, Friedericke, Thieme, Franziska, Ruprecht, Klemens, Beckmann, Matthias W., Strick, Reiner
Julkaistu 2012

The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

Tekijä Hebebrand, Moritz, Hüffmeier, Ulrike, Trollmann, Regina, Hehr, Ute, Uebe, Steffen, Ekici, Arif B., Kraus, Cornelia, Krumbiegel, Mandy, Reis, André, Thiel, Christian T., Popp, Bernt
Julkaisussa Orphanet J Rare Dis (2019)

Rare Copy Number Variants Are a Common Cause of Short Stature

Tekijä Zahnleiter, Diana, Uebe, Steffen, Ekici, Arif B., Hoyer, Juliane, Wiesener, Antje, Wieczorek, Dagmar, Kunstmann, Erdmute, Reis, André, Doerr, Helmuth-Guenther, Rauch, Anita, Thiel, Christian T.
Julkaistu 2013