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Stem Cell Research|December 25, 2013
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsAntonietta Coppola, Antonio Romito, Christelle Borel, et al.
Plos One|May 9, 2015
HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES CellsAudrey Letourneau, Gilda Cobellis, Alexandre Fort, et al.
Nature Communications|October 5, 2019
Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalanceGeorgios Stamoulis, Marco Garieri, Periklis Makrythanasis, et al.
Nature|July 31, 2010
New class of gene-termini-associated human RNAs suggests a novel RNA copying mechanismPhilipp Kapranov, Fatih Ozsolak, Sang Woo Kim, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2015
A Case of Wiedemann-Steiner Syndrome Associated with a 46,XY Disorder of Sexual Development and Gonadal DysgenesisPierre Calvel, Kamila Kusz-Zamelczyk, Periklis Makrythanasis, et al.
Human Molecular Genetics|March 11, 2021
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2Stylianos E Antonarakis, Aleš Holoubek, Melivoia Rapti, et al.
Genome Biology|June 24, 2010
A mouse embryonic stem cell bank for inducible overexpression of human chromosome 21 genesRossella De Cegli, Antonio Romito, Simona Iacobacci, et al.
American Journal of Human Genetics|January 6, 2015
Biased allelic expression in human primary fibroblast single cellsChristelle Borel, Pedro G Ferreira, Federico Santoni, et al.
Plos Genetics|March 25, 2015
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App regionVéronique Brault, Arnaud Duchon, Caroline Romestaing, et al.
Genome Research|December 15, 2010
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblastsChristelle Borel, Samuel Deutsch, Audrey Letourneau, et al.
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