<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE307nnn/GSE307279/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome variation profiling by SNP array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE307279</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>High-resolution mapping of IRF4 translocations in children and adults large B-cell lymphomas [CytoScanHD_Array]</name><description>Large B-cell lymphoma with IRF4 rearrangement (LBCL-IRF4) predominantly affects children and young adults (CAYA) presenting as localized disease with excellent prognosis. Although IRF4::IGH translocations are demonstrable in most tumors, cryptic rearrangements have been suggested. Next-generation sequencing (NGS) studies have identified a distinct mutational landscape. Whether large B-cell lymphomas (LBCL) harboring IRF4 rearrangements in adults represent the same biological entity remains uncertain. A total of 35 pediatric and young adult (CAYA) patients diagnosed with LBCL-IRF4 (38/42 positive by fluorescence-in-situ-hybridization, FISH) and 7 adult LBCL with IRF4-R were analyzed with integrative molecular approach.</description><dates><publication>2026/09/01</publication></dates><accession>GSE307279</accession><cross_references><GSM>GSM9220356</GSM><GSM>GSM9220353</GSM><GSM>GSM9220352</GSM><GSM>GSM9220355</GSM><GSM>GSM9220354</GSM><GPL>16131</GPL><GSE>307279</GSE><taxon>Homo sapiens</taxon><PMID>[42466980]</PMID></cross_references></HashMap>