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Epilepsia|April 6, 2023
Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansionsMark A Corbett, Christel Depienne, Liana Veneziano, et al.
Orphanet Journal of Rare Diseases|July 28, 2025
Lessons learned from a muscle study in nail-patella syndromeLuisa Paul, Anne Schänzer, Christel Depienne, et al.
Neurobiology of Disease|March 6, 2007
Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cellsAlexandre Chojnowski, Nicole Ravisé, Corinne Bachelin, et al.
Aging|November 29, 2023
Effects of paternal and chronological age on <i>BEGAIN</i> methylation and its possible role in autismRamya Potabattula, Andreas Prell, Marcus Dittrich, et al.
Archives of Neurology|January 13, 2010
Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutationsRabab Debs, Christel Depienne, Agnès Rastetter, et al.
Epilepsia Open|February 5, 2023
A novel FAME1 repeat configuration in a European family identified using a combined genomics approachTatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, et al.
Nature Reviews. Neurology|September 22, 2025
Progress and challenges in sporadic late-onset cerebellar ataxiasThomas Wirth, Jennifer Faber, Christel Depienne, et al.
Neurology|October 19, 2012
PRRT2 mutations cause hemiplegic migraineFlorence Riant, Emmanuel Roze, Cecile Barbance, et al.
Epilepsia|June 22, 2010
Familial form of typical childhood absence epilepsy in a consanguineous contextHanen Abouda, Yosr Hizem, Amina Gargouri, et al.
Experimental Neurology|May 19, 2005
Pleiotrophin mediates the neurotrophic effect of cyclic AMP on dopaminergic neurons: analysis of suppression-subtracted cDNA libraries and confirmation in vitroSophie Mourlevat, Thomas Debeir, Juan E Ferrario, et al.
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