Tally Lerman‐Sagie
Researcher Next ID · RN-042456
Researcher · Biochemistry, Genetics and Molecular Biology
Holon, Israel
- Works count
- 360
- Citation count
- 12,356
- H-index
- 59
- i10-index
- 188
Research interests
Publications
Mortality in Dravet syndrome
Epilepsy Research · 2016 · https://doi.org/10.1016/j.eplepsyres.2016.10.006
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Nature Genetics · 2013 · https://doi.org/10.1038/ng.2646
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
Nature Genetics · 2012 · https://doi.org/10.1038/ng.2331
Rare copy number variants are an important cause of epileptic encephalopathies
Annals of Neurology · 2011 · https://doi.org/10.1002/ana.22645
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Nature Genetics · 2008 · https://doi.org/10.1038/ng.149
Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus
The American Journal of Human Genetics · 2001 · https://doi.org/10.1086/319516
Current projects
No projects listed.