ScholarIQanswers from OpenAlex & ORCID
Samuel F. Berkovic
ResearcherPublications, citations & collaboration network
Samuel F. Berkovic is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Samuel F. Berkovic have?
ScholarIQindexed works
Samuel F. Berkovic has 1,136 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Samuel F. Berkovic have?
ScholarIQcitation count
Samuel F. Berkovic has 80,691 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Samuel F. Berkovic?
ScholarIQh-index
Samuel F. Berkovic has an h-index of 147 in OpenAlex.
What is the i10-index of Samuel F. Berkovic?
ScholarIQi10-index
Samuel F. Berkovic has an i10-index of 648 in OpenAlex.
What is the ORCID of Samuel F. Berkovic?
ScholarIQorcid
The ORCID for Samuel F. Berkovic is on the source record.
What is the OpenAlex record for Samuel F. Berkovic?
ScholarIQopenalex
The OpenAlex for Samuel F. Berkovic is on the source record.
What are the most-cited papers on Samuel F. Berkovic?
ScholarIQmost cited works
<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology
Ingrid E. Scheffer, Samuel F. Berkovic, Giuseppe Capovilla, Mary Connolly, Jacqueline A. French, Laura Maria de Figueiredo Ferreira Guilhoto, Édouard Hirsch, Satish Jain, Gary W. Mathern, Solomon L. Moshé, Douglas R. Nordli, Emilio Perucca, Torbjörn Tomson, Samuel Wiebe, Yue‐Hua Zhang, Sameer M. Zuberi
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
Anne T. Berg, Samuel F. Berkovic, Martin J. Brodie, Jeffrey Buchhalter, J. Helen Cross, W. van Emde Boas, Jerome Engel, Jacqueline A. French, Tracy A. Glauser, Gary W. Mathern, Solomon L. Moshé, Douglas R. Nordli, Perrine Plouin, Ingrid E. Scheffer
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
Ortrud K. Steinlein, John C. Mulley, Peter Propping, Robyn H. Wallace, Hilary A. Phillips, Grant R. Sutherland, Ingrid E. Scheffer, Samuel F. Berkovic
doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox, Edward D. Lamperti, Samuel F. Berkovic, Ingrid E. Scheffer, Edward C. Cooper, William B. Dobyns, Sharon Minnerath, M. Elizabeth Ross, Christopher A. Walsh
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B
Robyn H. Wallace, Dao Wen Wang, Rita Singh, Ingrid E. Scheffer, Alfred L. George, Hilary A. Phillips, Kathrin Saar, André Reis, Eric W. Johnson, Grant R. Sutherland, Samuel F. Berkovic, John C. Mulley