Joost Haan
Researcher Next ID · RN-033823
Researcher · Biochemistry, Genetics and Molecular Biology
Leiden University Medical Center
Leiden, Netherlands
- Works count
- 734
- Citation count
- 10,335
- H-index
- 49
- i10-index
- 112
Research interests
Publications
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
Nature Genetics · 2012 · https://doi.org/10.1038/ng.2358
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
Nature Genetics · 2012 · https://doi.org/10.1038/ng.2358
C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Nature Genetics · 2007 · https://doi.org/10.1038/ng2082
Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
Annals of Neurology · 2001 · https://doi.org/10.1002/ana.1031
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
Cell · 1996 · https://doi.org/10.1016/s0092-8674(00)81373-2
Current projects
No projects listed.