Aberrant DNA methylation is co-regulated across the genome in leukemia and other types of cancer
Monica Varona Baranda, Sven Liesenfelder, Florian Kraft, Chao‐Chung Kuo et autres
0 citationsbioRxiv (Cold Spring Harbor Laboratory)
Florian Kraft
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97Publications signalées
1848Citations signalées
1Affiliations récentes
Institutions déclarées
Domaines associés
Genetic Syndromes and ImprintingSpeech Recognition and SynthesisRNA modifications and cancerGenomics and Rare DiseasesSpeech and dialogue systems
Publications récentes
Genolator: A Multimodal Large Language Model Fusing Natural Language, Genomic, and Structural Tokens for Protein Function Interpretation
Martin Danner, Tanhim Islam, Matthias Begemann, Florian Kraft et autres
0 citationsbioRxiv (Cold Spring Harbor Laboratory)
Direct RNA sequencing enables improved transcriptome assessment and tracking of RNA modifications for medical applications
Charlotte Hewel, Anna Wierczeiko, Johannes Miedema, Johannes Friedrich et autres
20 citationsNucleic Acids Research
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
Elsa Leitão, Benjamin Cogné, Miriam Essid, Maria Athanasiadou et autres
8 citationsmedRxiv
04PNovel mouse model for inclusion body myositis: transgenic upregulation of lymphotoxin together with impaired autophagy induces inflammation and protein accumulation in skeletal muscle
Jeroen Bremer, J. Nagel, Jana Zschüntzsch, Kamil K. Zajt et autres
0 citationsNeuromuscular Disorders
Mutual reinforcement of lymphotoxin-driven myositis and impaired autophagy in murine muscle
Juliane Bremer, Judith Nagel, Jana Zschüntzsch, Kamil K. Zajt et autres
0 citationsBrain
Allogeneic stem cell transplantation from variant-carrying family donors leads to long-term engraftment in Telomere Biology Disorders
Nergis Güzel, Yannic Schumacher, Kim Kricheldorf, Margherita Vieri et autres
0 citationsBlood Cancer Journal
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet et autres
0 citationsNature Genetics
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption
Caroline Nava, Benjamin Cogné, Elsa Leitão, François Lecoquierre et autres
49 citationsNature Genetics
Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver–Russell phenotype
Matthias Begemann, Anna Lengyel, Éva Pinti, Árpád Ferenc Kovács et autres
4 citationsClinical Epigenetics
Direct RNA sequencing enables improved transcriptome assessment and tracking of RNA modifications for medical applications
Susanne Gerber, Charlotte Hewel, Anna Wierczeiko, Johannes Miedema et autres
1 citationResearch Square
Mutational constraint analysis workflow for overlapping short open reading frames and genomic neighbors
Martin Danner, Matthias Begemann, Florian Kraft, Miriam Elbracht et autres
0 citationsBMC Genomics
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