Author

Michel Dominique Ferrari

Leiden University Medical CenterORCID 0000-0001-9691-9449Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aaron Kleinman· 1 shared Adam AutoniD· 1 shared Adele A. Mitchell· 1 shared Alfons MacayaiD· 1 shared Andrea Carmine BeliniD· 1 shared Andrés IngasoniD· 1 shared Ann-Louise EsserlindiD· 1 shared Anne Francke Christensen· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Aaron Kleinman

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2 papers

Recent·Most cited

NeuroscienceeLifePeer-reviewedMar 3, 2022

Mutated neuronal voltage-gated CaV2.1 channels causing familial hemiplegic migraine 1 increase the susceptibility for cortical spreading depolarization and seizures and worsen outcome after experimental traumatic brain injury

Nicole A. Terpolilli, R. Dolp, K. Waehner…·Nikolaus Plesnila

This study shows that FHM1 mutations in CaV2.1 channels worsen outcomes after TBI by increasing CSDs, seizures, and brain edema in mice.

16 citations

mouseexperimental assay

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GeneticsNeuronPeer-reviewedMay 1, 2018

Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families

Padhraig Gormley, Mitja Kurki, Marjo Eveliina Hiekkala…·George McMahon

This study shows common genetic variants significantly contribute to migraine family clustering, with higher burden in familial cases compared to population-based cases.

101 citationstop 1%

humanwhole-exome sequencing

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