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International Journal of Molecular Sciences|February 26, 2022
Cerebellar and Striatal Implications in Autism Spectrum Disorders: From Clinical Observations to Animal ModelsMathieu Thabault, Valentine Turpin, Alexandre Maisterrena, et al.
Cytogenetic and Genome Research|December 8, 2022
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal DeletionsCaroline Foucart, Gwenaël Le Guyader, Valérie Vequeau-Goua, et al.
Scientific Reports|June 13, 2026
Lifestyle factors impact sperm microbiota and are associated with biological and clinical issues in infertile patients undergoing assisted reproductive technologies, a proof-of-concept studyValentine Renouf, Clémence Gachet, Manon Prat, et al.
American Journal of Medical Genetics. Part A|July 8, 2020
12q21 deletion syndrome: Narrowing the critical region down to 1.6 Mb including SYT1 and PPP1R12ATanguy Niclass, Gwenael Le Guyader, Claire Beneteau, et al.
Clinical Genetics|July 22, 2025
French Guidelines of the AchroPuce Network for the Interpretation and Reporting of Constitutional Copy Number VariantsCéline Pebrel-Richard, Paul Kuentz, Anne-Claude Tabet, et al.
Tissue Engineering. Part B, Reviews|April 24, 2014
Translating cell-based regenerative medicines from research to successful products: challenges and solutionsYves Bayon, Alain A Vertès, Vincent Ronfard, et al.
European Journal of Human Genetics : EJHG|February 28, 2018
Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetranceMatthieu Egloff, Lam-Son Nguyen, Karine Siquier-Pernet, et al.
Cytogenetic and Genome Research|November 18, 2014
17q21.31 microdeletion: brain anomalies leading to prenatal diagnosisMatthieu Egloff, Ferechte Encha-Razavi, Catherine Garel, et al.
Reproductive Biomedicine Online|July 17, 2017
Potential selection of genetically balanced spermatozoa based on the hypo-osmotic swelling test in chromosomal rearrangement carriersAlexandre Rouen, Léa Carlier, Solveig Heide, et al.
Prenatal Diagnosis|July 13, 2019
SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defectsMarguerite Hureaux, Selima Ben Miled, Nicolas Chatron, et al.
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