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Publications by Jean Muller

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

American Journal of Human Genetics
Genetics
2019English

Orthology Prediction Methods: A Quality Assessment Using Curated Protein Families

BioEssays
BiochemistryGeneticsMolecular Biology
2011English

Exome Sequencing of Bardet–Biedl Syndrome Patient Identifies a Null Mutation in the BBSome subunitBBIP1(BBS18)

Journal of Medical Genetics
Genetics
2013English

Mutations in KARS Cause a Severe Neurological and Neurosensory Disease With Optic Neuropathy

Human Mutation
Genetics
2019English

A Nitrile Hydratase in the Eukaryote Monosiga Brevicollis

PLoS ONE
Multidisciplinary
2008English

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Multidimensional Proteomics for Cell Biology

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