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Proceedings of the National Academy of Sciences of the United States of America|December 5, 2018
Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblastsMarco Garieri, Georgios Stamoulis, Xavier Blanc, et al.
Plos One|September 23, 2014
Germ cell-specific targeting of DICER or DGCR8 reveals a novel role for endo-siRNAs in the progression of mammalian spermatogenesis and male fertilityCéline Zimmermann, Yannick Romero, Maria Warnefors, et al.
Cell Reports|February 10, 2018
Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA SequencingIsabelle Stévant, Yasmine Neirijnck, Christelle Borel, et al.
American Journal of Human Genetics|August 2, 2007
Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypesPraveen Sethupathy, Christelle Borel, Maryline Gagnebin, et al.
Human Molecular Genetics|November 5, 2013
DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivationNeeta Bala Tannan, Manisha Brahmachary, Paras Garg, et al.
Molecular Endocrinology (Baltimore, Md.)|February 25, 2015
Research resource: the dynamic transcriptional profile of sertoli cells during the progression of spermatogenesisCéline Zimmermann, Isabelle Stévant, Christelle Borel, et al.
Human Mutation|April 24, 2009
Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generationKaren Bedard, Homa Attar, Jérôme Bonnefont, et al.
Human Mutation|May 11, 2012
Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTBChristelle Borel, Eugenia Migliavacca, Audrey Letourneau, et al.
Human Genetics|May 31, 2012
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunctionChristelle Borel, Fanny Cheung, Helen Stewart, et al.
Human Mutation|May 10, 2005
Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitroMarie Wattenhofer, Alexandre Reymond, Véronique Falciola, et al.
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