Manfred Gessler

Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor

Advancing sarcoma diagnostics with expanded DNA methylation-based classification

Genomic characterization of DICER1-associated neoplasms uncovers molecular classes

Hallmark discoveries in the biology of Wilms tumour

The genomic landscape of pediatric renal cell carcinomas

Sarcoma classification by DNA methylation profiling

Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (<scp>SIOP</scp>) 93‐01, 2001 and <scp>UK‐IMPORT</scp> database: A report of the <scp>SIOP‐Renal</scp> Tumor Study Group

Fifty years of clinical and research studies for childhood renal tumors within the International Society of Pediatric Oncology (SIOP)

Identification and Analyses of Extra-Cranial and Cranial Rhabdoid Tumor Molecular Subgroups Reveal Tumors with Cytotoxic T Cell Infiltration

The landscape of genomic alterations across childhood cancers

Primary intracranial spindle cell sarcoma with rhabdomyosarcoma-like features share a highly distinct methylation profile and DICER1 mutations

Array-based DNA-methylation profiling in sarcomas with small blue round cell histology provides valuable diagnostic information

Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants

Author Correction: The landscape of genomic alterations across childhood cancers

REGGAE: a novel approach for the identification of key transcriptional regulators

Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP–RTSG 2016 protocol

Gene expression profiles of brain endothelial cells during embryonic development at bulk and single-cell levels

The transcriptional repressor Hes1 attenuates inflammation by regulating transcription elongation

Mutations in the SIX1/2 Pathway and the DROSHA/DGCR8 miRNA Microprocessor Complex Underlie High-Risk Blastemal Type Wilms Tumors

Multiple mechanisms of MYCN dysregulation in Wilms tumour

Abstract A1-59: Multiple mechanisms of MYCN dysregulation in Wilms tumor

Abstract A1-67: Prognostic significance of copy number aberrations in Wilms tumor

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

COUP-TFII orchestrates venous and lymphatic endothelial identity by homo- or hetero-dimerisation with PROX1

Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney