Analysis of shared heritability in common disorders of the brain
2018 · Science · 1,991 citations
https://doi.org/10.1126/science.aap8757
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Christel Depienne
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Christel Depienne is an academic researcher from University of Duisburg-Essen. The author has contributed to research in topics: Genetics and Neurodevelopmental Disorders & Genomics and Rare Diseases & Epilepsy research and treatment. The author has an h-index of 71, co-authored 269 publications.
ORCID: 0000-0002-7212-9554Papers by this author
worksGenomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
2019 · Cell · 1,446 citations
https://doi.org/10.1016/j.cell.2019.11.020
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
2017 · Journal of Medical Genetics · 249 citations
https://doi.org/10.1136/jmedgenet-2016-104509
Delineating the <i>GRIN1</i> phenotypic spectrum
2016 · Neurology · 202 citations
https://doi.org/10.1212/wnl.0000000000002740
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
2019 · Nature Communications · 164 citations
https://doi.org/10.1038/s41467-019-12671-y
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
2017 · Human Genetics · 117 citations
https://doi.org/10.1007/s00439-017-1772-0
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