GenomEast
Ariane Kröll-Hermi et al.
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability
The American Journal of Human Genetics 2025, vol. 112, issue 12
doi: 10.1016/j.ajhg.2025.10.014
Alice Billie Libri et al.
Senataxin promotes recombination fidelity during antigen receptor gene diversification
Science Signaling 2025, vol. 18, issue 908
doi: 10.1126/scisignal.adv8801
Ouzna Dali et al.
Prenatal nicotine exposure induces epigenetic alterations in the Notch signaling genes in the proximal colon in rats
BMC Genomics 2025, vol. 26, issue 1
doi: 10.1186/s12864-025-11960-9
Marianne Victoria Lemée et al.
Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant
Nucleic Acids Research 2025, vol. 53, issue 18
doi: 10.1093/nar/gkaf934
Ambre Bender et al.
UHRF2 mediates resistance to DNA methylation reprogramming in primordial germ cells
Nature Communications 2025, vol. 16, issue 1
doi: 10.1038/s41467-025-61954-0
Jan-Inge Bjune et al.
IRX3 controls a SUMOylation-dependent differentiation switch in adipocyte precursor cells
Nature Communications 2025, vol. 16, issue 1
doi: 10.1038/s41467-025-62361-1
Maulik K. Nariya et al.
Single-cell multiomics reveals the oscillatory dynamics of mRNA metabolism and chromatin accessibility during the cell cycle
Cell Reports 2025, vol. 44, issue 8
doi: 10.1016/j.celrep.2025.116089
Agathe Launay et al.
Upregulation of adenosine A2A receptor in astrocytes is sufficient to trigger hippocampal multicellular dysfunctions and memory deficits
Molecular Psychiatry 2025, vol. 30, issue 11
doi: 10.1038/s41380-025-03115-9
Maria Victoria Hinckelmann et al.
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis
Molecular Psychiatry 2025, vol. 30, issue 11
doi: 10.1038/s41380-025-03109-7
Adella Karam et al.
PIK3C2A ‐Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia Defect
Clinical Genetics 2025, vol. 108, issue 6
doi: 10.1111/cge.70005