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Analysis of shared heritability in common disorders of the brainScience, 2018, 360 (6395), eaap8757. ⟨10.1126/science.aap8757⟩
Journal articles
cea-01870483v1
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Deficiency for the Ubiquitin Ligase UBE3B in a Blepharophimosis-Ptosis-Intellectual-Disability SyndromeAmerican Journal of Human Genetics, 2012, 91 (6), pp.998-1010. ⟨10.1016/j.ajhg.2012.10.011⟩
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pasteur-01375146v1
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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical HeterogeneityStroke, 2023, 54 (3), pp.810-818. ⟨10.1161/STROKEAHA.122.040715⟩
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hal-04177403v1
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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.American Journal of Human Genetics, 2012, 91 (5), pp.919-27. ⟨10.1016/j.ajhg.2012.09.002⟩
Journal articles
pasteur-00796959v1
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