• 2926 Citations
  • 27 h-Index
1988 …2019
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Fingerprint Dive into the research topics where Valeria Capra is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Neural Tube Defects Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Cell Polarity Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Folic Acid Medicine & Life Sciences
Central Nervous System Cavernous Hemangioma Medicine & Life Sciences
Pediatrics Medicine & Life Sciences

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Research Output 1988 2019

  • 2926 Citations
  • 27 h-Index
  • 126 Article
  • 1 Chapter
  • 1 Letter
  • 1 Review article

Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy

Scala, M., Amadori, E., Fusco, L., Marchese, F., Capra, V., Minetti, C., Vari, M. S. & Striano, P., May 24 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Brain Diseases
Circadian Rhythm
Sleep
Crying
Inborn Genetic Diseases

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., Aug 14 2019, In : Brain : a journal of neurology.

Research output: Contribution to journalArticle

Globus Pallidus
Homeobox Genes
Putamen
Basal Ganglia
Mutation

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2

De Mori, R., Severino, M., Mancardi, M. M., Anello, D., Tardivo, S., Biagini, T., Capra, V., Casella, A., Cereda, C., Copeland, B. R., Gagliardi, S., Gamucci, A., Ginevrino, M., Illi, B., Lorefice, E., Musaev, D., Stanley, V., Micalizzi, A., Gleeson, J. G., Mazza, T. & 2 others, Rossi, A. & Valente, E. M., 2019, In : Brain : a journal of neurology. 142, 10, p. 2965-2978 14 p.

Research output: Contribution to journalArticle

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

SYNAPS Study Group, Dec 1 2019, In : Nature Communications. 10, 1, 3094.

Research output: Contribution to journalArticle

Open Access
AMPA Receptors
mutations
disabilities
Brain Diseases
disorders