PanelDesign: Integrating Epidemiological Information into the Design of Diagnostic NGS Gene Panels
Schmidtke, Jörg, Philipp, Peter, Rommel, Kathrin, Glaubitz, Ralf, Epplen, Jörg T, Krawczak, Michael
Published in Genes (13.04.2022)
Published in Genes (13.04.2022)
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Myelin Genes and the Corpus Callosum: Proteolipid Protein 1 (PLP1) and Contactin 1 (CNTN1) Gene Variation Modulates Interhemispheric Integration
Ocklenburg, Sebastian, Gerding, Wanda M., Arning, Larissa, Genç, Erhan, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Published in Molecular neurobiology (01.12.2017)
Published in Molecular neurobiology (01.12.2017)
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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification
Rutsch, Frank, Suk, Anita, Ferre, Merry, Höhne, Wolfgang, Knisely, Alex, Hinrichs, Bernd, Lehmann, Mandy, Epplen, Jörg T, Ruf, Nico, Vallance, Hillary, Terkeltaub, Robert, Schnabel, Dirk, Schauer, Galen, Smith, Wendy, Sinaiko, Alan R, Roscioli, Tony, Filippone, Marco, Vaingankar, Sucheta, McGill, James, Toliat, Mohammad R, Superti-Furga, Andrea, Nürnberg, Peter
Published in Nature genetics (01.08.2003)
Published in Nature genetics (01.08.2003)
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Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability
Akkad, Denis A., Bellenberg, Barbara, Esser, Sarika, Weiler, Florian, Epplen, Jörg T., Gold, Ralf, Lukas, Carsten, Haghikia, Aiden
Published in Neurogenetics (01.07.2015)
Published in Neurogenetics (01.07.2015)
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Multiple sclerosis in families: risk factors beyond known genetic polymorphisms
Akkad, Denis A., Lee, De-Hyung, Bruch, Kathrin, Haghikia, Aiden, Epplen, Jörg T., Hoffjan, Sabine, Linker, Ralf A.
Published in Neurogenetics (01.04.2016)
Published in Neurogenetics (01.04.2016)
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Journal Article
EVIDENCE FOR A MONOPHYLETIC ORIGIN OF TRIPLOID CLONES OF THE AMAZON MOLLY, POECILIA FORMOSA
Lampert, Kathrin P, Lamatsch, Dunja K, Epplen, Jörg T, Schartl, Manfred
Published in Evolution (01.04.2005)
Published in Evolution (01.04.2005)
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Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes
Temudo, Teresa, Santos, Mónica, Ramos, Elisabete, Dias, Karin, Vieira, José Pedro, Moreira, Ana, Calado, Eulália, Carrilho, Inês, Oliveira, Guiomar, Levy, António, Barbot, Clara, Fonseca, Maria, Cabral, Alexandra, Cabral, Pedro, Monteiro, José, Borges, Luís, Gomes, Roseli, Mira, Graça, Aires Pereira, Susana, Santos, Manuela, Fernandes, Anabela, Epplen, Jorg T, Sequeiros, Jorge, Maciel, Patrícia
Published in Brain & development (Tokyo. 1979) (01.01.2011)
Published in Brain & development (Tokyo. 1979) (01.01.2011)
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Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/ initiating cell properties
Fahlbusch, Sera Selina, Keil, Silvia, Epplen, Jörg T, Zänker, Kurt S, Dittmar, Thomas
Published in BMC cancer (19.05.2020)
Published in BMC cancer (19.05.2020)
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Activation of NPY-Y2 receptors ameliorates disease pathology in the R6/2 mouse and PC12 cell models of Huntington's disease
Fatoba, Oluwaseun, Kloster, Eugen, Reick, Christiane, Saft, Carsten, Gold, Ralf, Epplen, Jörg T., Arning, Larissa, Ellrichmann, Gisa
Published in Experimental neurology (01.04.2018)
Published in Experimental neurology (01.04.2018)
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Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries
Ocklenburg, Sebastian, Schmitz, Judith, Moinfar, Zahra, Moser, Dirk, Klose, Rena, Lor, Stephanie, Kunz, Georg, Tegenthoff, Martin, Faustmann, Pedro, Francks, Clyde, Epplen, Jörg T, Kumsta, Robert, Güntürkün, Onur
Published in eLife (01.02.2017)
Published in eLife (01.02.2017)
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PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness
Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M, Hengstler, Jan G, Falkenstein, Michael, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian
Published in PloS one (27.06.2013)
Published in PloS one (27.06.2013)
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