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Stem Cell Reports|June 18, 2014
3D In vitro model of a functional epidermal permeability barrier from human embryonic stem cells and induced pluripotent stem cellsAnastasia Petrova, Anna Celli, Laureen Jacquet, et al.
Stem Cells and Development|July 28, 2016
Induced Pluripotent Stem Cell Differentiation and Three-Dimensional Tissue Formation Attenuate Clonal Epigenetic Differences in TrichohyalinAnastasia Petrova, Antonio Capalbo, Laureen Jacquet, et al.
Human Molecular Genetics|March 10, 2009
Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survivalLydia Quaye, Dimitra Dafou, Susan J Ramus, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2019
RNA editing alterations define manifestation of prion diseasesEirini Kanata, Franc Llorens, Dimitra Dafou, et al.
Cell Death & Disease|April 8, 2026
The deubiquitinase activity of CYLD is required for B cell differentiationAthanasios Pseftogas, Jessica Bordini, George Gavriilidis, et al.
American Journal of Human Genetics|August 26, 2014
Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndromeGabriela Petrof, Arti Nanda, Jake Howden, et al.
Neoplasia (New York, N.Y.)|July 24, 2010
Microcell-mediated chromosome transfer identifies EPB41L3 as a functional suppressor of epithelial ovarian cancersDimitra Dafou, Barbara Grun, John Sinclair, et al.
Plos Pathogens|January 23, 2018
Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesisFranc Llorens, Katrin Thüne, Eulàlia Martí, et al.
Nature Genetics|September 6, 2011
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)Pia Ostergaard, Michael A Simpson, Fiona C Connell, et al.
American Journal of Human Genetics|January 24, 2012
De novo mutations of the gene encoding the histone acetyltransferase KAT6B cause Genitopatellar syndromeMichael A Simpson, Charu Deshpande, Dimitra Dafou, et al.
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