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Gene expression of circadian genes and CIART in bipolar disorder: A preliminary case-control study
Cindie Courtin
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Cynthia Marie-Claire
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Gregory Gross
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Vincent Hennion
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Emeline Mundwiller
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et al.
Journal articles
inserm-03914243v1
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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations
Stephan Klebe
,
Alexander Lossos
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Hamid Azzedine
,
Emeline Mundwiller
,
Ruth Sheffer
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et al.
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
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Mirko Theis
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Dragomir B. Krastev
,
Sergey Samsonov
,
Emeline Mundwiller
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et al.
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
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et al.
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
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Iulia Blesneac
,
Arnaud Monteil
,
Marie-Lorraine Monin
,
Kunie Ando
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et al.
Journal articles
hal-01223815v1
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