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hal-00775889v1 Article dans une revue
Mariem Ben Khelifa, Charles Coutton, Michael G B Blum, Farid Abada, Radu Harbuz et al. Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia.
Human Reproduction, Oxford University Press (OUP), 2012, 27 (11), pp.3337-46. 〈10.1093/humrep/des296〉

inserm-00763211v1 Article dans une revue
Nathalie Roux-Buisson, Marine Cacheux, Anne Fourest-Lieuvin, Jérémy Fauconnier, Julie Brocard et al. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (12), pp.2759-67. 〈10.1093/hmg/dds104〉

inserm-00880088v1 Article dans une revue
Thomas Karaouzène, Michèle El Atifi, Jean-Paul Issartel, Marianne Grepillat, Charles Coutton et al. Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out mice
Basic and Clinical Andrology, 2013, 23 (1), pp.7

inserm-00520132v1 Article dans une revue
Régis Barattin, Bastien Gerby, Kevin Bourges, Gaëlle Hardy, Jose Olivares et al. Iodination increases the activity of verapamil derivatives in reversing PGP multidrug resistance.
Anticancer Research, International Institute of Anticancer Research, 2010, 30 (7), pp.2553-9

inserm-00410501v1 Article dans une revue
Anne Sophie Gauchez, Emilie Pez, Jean Boutonnat, Jean Cyril Bourre, Laurent Pelletier et al. [Early detection of leptomeningeal metastasis in patients with metastatic breast carcinoma: validation of CA 15-3 measurement in cerebrospinal fluid]
Annales de Biologie Clinique, John Libbey Eurotext, 2007, 65 (6), pp.653-8

hal-00809646v1 Article dans une revue
Charles Coutton, Farid Abada, Thomas Karaouzene, Damien Sanlaville, Véronique Satre et al. Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population.
PLoS Genetics, Public Library of Science, 2013, 9 (3), pp.e1003363. 〈10.1371/journal.pgen.1003363〉

inserm-01077407v1 Article dans une revue
Audrey Bouchet, Marie Bidart, Imen Miladi, Céline Le Clec'H, Raphaël Serduc et al. Characterization of the 9L gliosarcoma implanted in the Fischer rat: an orthotopic model for a grade IV brain tumor.
Tumor Biology, Springer Verlag, 2014, pp.6221-33

pasteur-01061012v1 Article dans une revue
Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, Thomas Karaouzène, John Rendu et al. Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (1), pp.95-104. 〈10.1016/j.ajhg.2013.11.017〉

inserm-00588067v1 Article dans une revue
Radu Harbuz, Raoudha Zouari, Virginie Pierre, Mariem Ben Khelifa, Mahmoud Kharouf et al. A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.
American Journal of Human Genetics, Elsevier (Cell Press), 2011, 88 (3), pp.351-61. 〈10.1016/j.ajhg.2011.02.007〉

hal-01618630v1 Article dans une revue
Guillaume Martinez, Jean-Pascal Hograindleur, Sébastien Voisin, Roland Abi Nahed, Tarek M. Abd El Aziz et al. Spermaurin, an La1-like peptide from the venom of the scorpion Scorpio maurus palmatus , improves sperm motility and fertilization in different mammalian species
Molecular Human Reproduction, Oxford University Press (OUP), 2017, 〈10.1093/molehr/gaw075〉

inserm-00639414v1 Article dans une revue
Mariem Ben Khelifa, Raoudha Zouari, Radu Harbuz, Lazhar Halouani, Christophe Arnoult et al. A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis.
Molecular Human Reproduction, Oxford University Press (OUP), 2011, 17 (12), pp.762-8. 〈10.1093/molehr/gar050〉

hal-00271980v1 Article dans une revue
J.-M. Beis, C. Keller, N. Morin, P. Bartolomeo, T. Bernati et al. Right spatial neglect after left hemisphere stroke: qualitative and quantitative study.
Neurology, American Academy of Neurology, 2004, 63 (9), pp.1600-5

hal-01579009v1 Article dans une revue
Jean-François Emile, Catherine Julié, Karine Le Malicot, Come Lepage, Josep Tabernero et al. Prospective validation of a lymphocyte infiltration prognostic test in stage III colon cancer patients treated with adjuvant FOLFOX.
European journal of cancer (Oxford, England : 1990), 2017, 82, pp.16-24. 〈http://www.sciencedirect.com/science/article/pii/S0959804917309528?via%3Dihub#!〉. 〈10.1016/j.ejca.2017.04.025〉

hal-00731431v1 Article dans une revue
Jessica Escoffier, Virginie J Pierre, Ikram Jemel, Léa Munch, Zied Boudhraa et al. Group X secreted phospholipase A₂ specifically decreases sperm motility in mice.
Journal of Cellular Physiology, Wiley, 2011, 226 (10), pp.2601-9. 〈10.1002/jcp.22606〉

hal-01469066v1 Article dans une revue
Alice Goldenberg, Florence Riccardi, Aude Tessier, Rolph Pfundt, Tiffany Busa et al. Clinical and Molecular Findings in 39 Patients with KBG Syndrome Caused by Deletion or Mutation of ANKRD11
American Journal of Medical Genetics Part A, Wiley, 2016, 170 (11), pp.2847-2859. 〈10.1002/ajmg.a.37878〉

inserm-00567441v1 Article dans une revue
Anette Bygum, Christina Fagerberg, D. Ponard, Nicole Monnier, Joel Lunardi et al. Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.
Allergy, Wiley, 2011, 66 (1), pp.76-84. 〈10.1111/j.1398-9995.2010.02456.x〉

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