Histone methyltransferase DOT1L differentially affects the development of dendritic cell subsets

Source
Life Science Alliance - ISSN 2575-1077-9:6 (2026) p. 1-20
Author(s)
    Rianne G. Bouma, Willem-Jan De Leeuw, Aru Z. Wang, Muddassir Malik, Joeke G.C. Stolwijk, Veronique A.L. Konijn, Anne Mensink, Natalie Proost, Maarten K. Nijen Twilhaar, Tibor Van Welsem, Negisa Seyed Toutounchi, Alsya J. Affandi, Jip T. Van Dinter, Fred Van Leeuwen, Joke M.M. Den Haan

RNA sequencing offers new diagnostic opportunities in neurodevelopmental disorders : a systematic review

Source
Genetics in medicine - ISSN 1098-3600-28:4 (2026) p. 1-12
Author(s)

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions

Source
Nature genetics - ISSN 1061-4036- (2026) p.
Author(s)

Dominant and recessive ATOH1 variants cause distinct neurodevelopmental disorders with hearing loss

Source
The American journal of human genetics - ISSN 1537-6605-113:2 (2026) p. 1-21
Author(s)
    Nicole Bertola, Eléonore Blondiaux, Madeleine Harion, Imen Dorboz, Sandrine Passemard, Sandra Mercier, Solène Conrad, Benjamin Cogné, Julie Boyer, Sophie Uyttebroeck, Kristof Van Schil, Wim Wuyts, Nanna Dahl Rendtorff, Mette Bertelsen, Kristianna Mey, Pierre Blanc, Jerome Champ, Odile Boespflug-Tanguy, Vincent Cantagrel, Lydie Burglen, Marion Coolen