PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness von Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M, Hengstler, Jan G, Falkenstein, Michael, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian

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Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD G... von Erbe, Leoni S., Hoffjan, Sabine, Janßen, Sören, Kneifel, Moritz, Krause, Karsten, Gerding, Wanda M., Döring, Kristina, Güttsches, Anne-Katrin, Roos, Andreas, Buena Atienza, Elena, Gross, Caspar, Lücke, Thomas, Nguyen, Hoa Huu Phuc, Vorgerd, Matthias, Köhler, Cornelia

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Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1 -Related Myopathy von Janßen, Sören, Erbe, Leoni S, Kneifel, Moritz, Vorgerd, Matthias, Döring, Kristina, Lubieniecki, Krzysztof P, Lubieniecka, Joanna M, Gerding, Wanda M, Casadei, Nicolas, Güttsches, Anne-Katrin, Heyer, Christoph, Lücke, Thomas, Nguyen, Hoa Huu Phuc, Köhler, Cornelia, Hoffjan, Sabine

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Handedness and the X chromosome: The role of androgen receptor CAG-repeat length von Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M., Hengstler, Jan G., Falkenstein, Michael, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Optical Genome Mapping Reveals Genomic Alterations upon Gene Editing in hiPSCs: Implications for Neural Tissue Differentiation and Brain Organoid Research von Gallego Villarejo, Lucia, Gerding, Wanda M, Bachmann, Lisa, Hardt, Luzie H I, Bormann, Stefan, Nguyen, Huu Phuc, Müller, Thorsten

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SOX9 duplication linked to intersex in deer von Kropatsch, Regina, Dekomien, Gabriele, Akkad, Denis A, Gerding, Wanda M, Petrasch-Parwez, Elisabeth, Young, Neil D, Altmüller, Janine, Nürnberg, Peter, Gasser, Robin B, Epplen, Jörg T

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Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patients von Gerding, Wanda M., Tembrink, Marco, Nilius‐Eliliwi, Verena, Mika, Thomas, Dimopoulos, Fotios, Ladigan‐Badura, Swetlana, Eckhardt, Matthias, Pohl, Michael, Wünnenberg, Max, Farshi, Pakhshan, Reimer, Peter, Schroers, Roland, Nguyen, Huu Phuc, Vangala, Deepak B.

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Optical Genome Mapping for Cytogenetic Diagnostics in AML von Nilius-Eliliwi, Verena, Gerding, Wanda M, Schroers, Roland, Nguyen, Huu Phuc, Vangala, Deepak B

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Ccdc66 null mutation causes retinal degeneration and dysfunction von GERDING, Wanda M, SCHREIBER, Sabrina, RÜLICKE, Thomas, IBRAHIM, Saleh, EPPLEN, Jörg T, PETRASCH-PARWEZ, Elisabeth, SCHULTE-MIDDELMANN, Tobias, DE CASTRO MARQUES, Andreia, ATORF, Jenny, AKKAD, Denis A, DEKOMIEN, Gabriele, KREMERS, Jan, DERMIETZEL, Rolf, GAL, Andreas

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Structural Asymmetry in the Frontal and Temporal Lobes Is Associated with PCSK6 VNTR Polymorphism von Berretz, Gesa, Arning, Larissa, Gerding, Wanda M., Friedrich, Patrick, Fraenz, Christoph, Schlüter, Caroline, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Genç, Erhan, Ocklenburg, Sebastian

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Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families von Kastner, Simone, Thiemann, Ina-Janine, Dekomien, Gabriele, Petrasch-Parwez, Elisabeth, Schreiber, Sabrina, Akkad, Denis A, Gerding, Wanda M, Hoffjan, Sabine, Günes, Sezgin, Günes, Selçuk, Bagci, Hasan, Epplen, Jörg T

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PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum von Anderson, Catrona, Gerding, Wanda M., Fraenz, Christoph, Schlüter, Caroline, Friedrich, Patrick, Raane, Maximilian, Arning, Larissa, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Genç, Erhan, Ocklenburg, Sebastian

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PLP1 Gene Variation Modulates Leftward and Rightward Functional Hemispheric Asymmetries von Ocklenburg, Sebastian, Gerding, Wanda M., Raane, Maximilian, Arning, Larissa, Genç, Erhan, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Myelin Genes and the Corpus Callosum: Proteolipid Protein 1 (PLP1) and Contactin 1 (CNTN1) Gene Variation Modulates Interhemispheric Integration von Ocklenburg, Sebastian, Gerding, Wanda M., Arning, Larissa, Genç, Erhan, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults von Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Hengstler, Jan G., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Akkad, Denis A.

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Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization von Ocklenburg, Sebastian, Arning, Larissa, Hahn, Constanze, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1 von Beste, Christian, Arning, Larissa, Gerding, Wanda M., Epplen, Jörg T., Mertins, Alexandra, Röder, Melanie C., Bless, Josef J., Hugdahl, Kenneth, Westerhausen, René, Güntürkün, Onur, Ocklenburg, Sebastian

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MS-like presentation of Alexander disease with multifocal lesions and oligoclonal bands von Tschampa, Henriette J., Greschus, Susanne, Vinahl, Michael, Urbach, Horst, Mueller, Marcus M., Gerding, Wanda M.

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Unusual Charcot–Marie–Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero von Schneider‐Gold, Christiane, Kötting, Judith, Epplen, Jörg T., Gold, Ralf, Gerding, Wanda M.

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Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero ( MPZ/P 0 ) von Zschüntzsch, Jana, Dibaj, Payam, Pilgram, Sara, Kötting, Judith, Gerding, Wanda M, Neusch, C

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