Broad genomic workup including optical genome mapping uncovers a DDX3X: MLLT10 gene fusion in acute myeloid leukemia von Nilius-Eliliwi, Verena, Tembrink, Marco, Gerding, Wanda Maria, Lubieniecki, Krzystof P., Lubieniecka, Joanna M., Kankel, Stefanie, Liehr, Thomas, Mika, Thomas, Dimopoulos, Fotios, Döhner, Konstanze, Schroers, Roland, Nguyen, Hoa Huu Phuc, Vangala, Deepak Ben

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Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes von Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T, Arning, Larissa

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bHLH Transcription Factor Math6 Antagonizes TGF-β Signalling in Reprogramming, Pluripotency and Early Cell Fate Decisions von Divvela, Satya Srirama Karthik, Nell, Patrick, Napirei, Markus, Zaehres, Holm, Chen, Jiayu, Gerding, Wanda Maria, Nguyen, Huu Phuc, Gao, Shaorong, Brand-Saberi, Beate

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Novel NUP98::ASH1L Gene Fusion in Acute Myeloid Leukemia Detected by Optical Genome Mapping von Tembrink, Marco, Gerding, Wanda Maria, Wieczorek, Stefan, Mika, Thomas, Schroers, Roland, Nguyen, Huu Phuc, Vangala, Deepak Ben, Nilius-Eliliwi, Verena

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Novel INUP98::ASH1L/I Gene Fusion in Acute Myeloid Leukemia Detected by Optical Genome Mapping von Tembrink, Marco, Gerding, Wanda Maria, Wieczorek, Stefan, Mika, Thomas, Schroers, Roland, Nguyen, Huu Phuc, Vangala, Deepak Ben, Nilius-Eliliwi, Verena

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Optical Genome Mapping Reveals Disruption of the RASGRF2 Gene in a Patient with Developmental Delay Carrying a De Novo Balanced Reciprocal Translocation von Lederbogen, Rosa Catalina, Hoffjan, Sabine, Thiels, Charlotte, Mau-Holzmann, Ulrike Angelika, Singer, Sylke, Yusenko, Maria Viktorovna, Nguyen, Hoa Huu Phuc, Gerding, Wanda Maria

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Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL von Vieler, Lisa-Marie, Nilius-Eliliwi, Verena, Schroers, Roland, Vangala, Deepak Ben, Nguyen, Huu Phuc, Gerding, Wanda Maria

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Excessive brain iron accumulation in spinocerebellar ataxia type 17 von Claassen, Jens, Gerding, Wanda Maria, Kastrup, Oliver, Uslar, Ellen, Goericke, Sophia, Timmann, Dagmar

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Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF von Gerding, Wanda Maria, Koetting, Judith, Epplen, Jörg Thomas, Neusch, Clemens

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Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position von Gerding, Wanda Maria, Koetting, Judith, Rey, Lucía Paola, Bibas Bonet, Hilda, Abdala, Mirta Esther, Mazzeo, Anna, Mostacciuolo, Maria Luisa, Arning, Larissa, Carrero-Valenzuela, Roque

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Optical genome mapping reveals and characterizes recurrent aberrations and new fusion genes in adult ALL von Vieler, Lisa-Marie, Nilius-Eliliwi, Verena, Schroers, Roland, Vangala, Deepak Ben, Nguyen, Huu Phuc, Gerding, Wanda Maria

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