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authFullName_s : Emeline Mundwiller
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Gene expression of circadian genes and CIART in bipolar disorder: A preliminary case-control study

Cindie Courtin , Cynthia Marie-Claire , Gregory Gross , Vincent Hennion , Emeline Mundwiller , et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2022, 122, pp.110691. ⟨10.1016/j.pnpbp.2022.110691⟩
Journal articles inserm-03914243v1

KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

Stephan Klebe , Alexander Lossos , Hamid Azzedine , Emeline Mundwiller , Ruth Sheffer , et al.
European Journal of Human Genetics, 2012, 20 (6), pp.645-649. ⟨10.1038/ejhg.2011.261⟩
Journal articles hal-02565698v1
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A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia.

Mikołaj Słabicki , Mirko Theis , Dragomir B. Krastev , Sergey Samsonov , Emeline Mundwiller , et al.
PLoS Biology, 2010, 8 (6), pp.e1000408. ⟨10.1371/journal.pbio.1000408⟩
Journal articles inserm-00707271v1
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A DNA methylation signature discriminates between excellent and non-response to lithium in patients with bipolar disorder type 1

Cynthia Marie-Claire , François-Xavier Lejeune , Emeline Mundwiller , Damien Ulveling , Ivan Moszer , et al.
Scientific Reports, 2020, 10 (1), pp.12239. ⟨10.1038/s41598-020-69073-0⟩
Journal articles inserm-02937821v1
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A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia

Marie Coutelier , Iulia Blesneac , Arnaud Monteil , Marie-Lorraine Monin , Kunie Ando , et al.
American Journal of Human Genetics, 2015, 97 (5), pp.726-737. ⟨10.1016/j.ajhg.2015.09.007⟩
Journal articles hal-01223815v1