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FERREIRA DA SILVA Izabela

Main Referenced Co-authors
Epi25 Collaborative (1)
KRAUSE, Roland  (1)
MAY, Patrick  (1)
ZIZOVIC, Milena  (1)
Main Referenced Keywords
DNA Copy Number Variations/genetics (1); Epilepsy/genetics (1); Exome Sequencing (1); Exome/genetics (1); Female (1);
Main Referenced Unit & Research Centers
Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) (1)
Main Referenced Disciplines
Neurology (1)
Genetics & genetic processes (1)

Publications (total 1)

The most downloaded
74 downloads
Epi25 Collaborative, KRAUSE, R., FERREIRA DA SILVA, I., ZIZOVIC, M., & MAY, P. (October 2024). Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience, 27 (10), 1864 - 1879. doi:10.1038/s41593-024-01747-8 https://hdl.handle.net/10993/62172

The most cited

10 citations (OpenAlex)

Epi25 Collaborative, KRAUSE, R., FERREIRA DA SILVA, I., ZIZOVIC, M., & MAY, P. (October 2024). Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience, 27 (10), 1864 - 1879. doi:10.1038/s41593-024-01747-8 https://hdl.handle.net/10993/62172

Epi25 Collaborative, KRAUSE, R., FERREIRA DA SILVA, I., ZIZOVIC, M., & MAY, P. (October 2024). Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nature Neuroscience, 27 (10), 1864 - 1879. doi:10.1038/s41593-024-01747-8
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