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Plos One|September 15, 2009
A comprehensive microarray-based DNA methylation study of 367 hematological neoplasmsJose I Martin-Subero, Ole Ammerpohl, Marina Bibikova, et al.
Cancer Cell|November 16, 2016
Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell LineageAna C Queirós, Renée Beekman, Roser Vilarrasa-Blasi, et al.
Sports Medicine (Auckland, N.Z.)|July 3, 2025
Sports Preparticipation Evaluation for Healthy Adults: A Consensus-Based German GuidelineChristine Joisten, Anja Hirschmüller, Pascal Bauer, et al.
Journal of Medicinal Chemistry|September 15, 2023
Identification and Optimization of RNA-Splicing Modulators as Huntingtin Protein-Lowering Agents for the Treatment of Huntington's DiseaseLongbin Liu, Karine Malagu, Alan F Haughan, et al.
Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Plos Genetics|July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Nature Genetics|October 6, 2015
DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional controlHelene Kretzmer, Stephan H Bernhart, Wei Wang, et al.
Genome Medicine|September 17, 2025
Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosisDaniel Kaschta, Christina Post, Franziska Gaass, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
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