ScholarIQanswers from OpenAlex & ORCID
John C. Mulley
ResearcherPublications, citations & collaboration network
John C. Mulley is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does John C. Mulley have?
ScholarIQindexed works
John C. Mulley has 266 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does John C. Mulley have?
ScholarIQcitation count
John C. Mulley has 24,937 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of John C. Mulley?
ScholarIQh-index
John C. Mulley has an h-index of 81 in OpenAlex.
What is the i10-index of John C. Mulley?
ScholarIQi10-index
John C. Mulley has an i10-index of 189 in OpenAlex.
What is the ORCID of John C. Mulley?
ScholarIQorcid
The ORCID for John C. Mulley is on the source record.
What is the OpenAlex record for John C. Mulley?
ScholarIQopenalex
The OpenAlex for John C. Mulley is on the source record.
What are the most-cited papers on John C. Mulley?
ScholarIQmost cited works
Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes
Michael McDermott, Ivona Aksentijevich, Jérôme Galon, Elizabeth McDermott, B Ogunkolade, Michael Centola, Elizabeth Mansfield, Massimo Gadina, Leena Karenko, Tom Pettersson, John McCarthy, David M. Frucht, Martin Aringer, Yelizaveta Torosyan, Anna‐Maija Teppo, Meredith Wilson, H.Mehmet Karaarslan, Ying Wan, Ian Todd, Geryl Wood, Ryan Schlimgen, Thisum R. Kumarajeewa, Sheldon M. Cooper, John P. Vella, Christopher I. Amos, John C. Mulley, Kathleen A. Quane, Michael G. Molloy, Annamari Ranki, Richard J. Powell, G. A. Hitman, John J. O’Shea, Daniel L. Kastner
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
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
The spectrum of SCN1A-related infantile epileptic encephalopathies
Louise A. Harkin, Jacinta M. McMahon, Xenia Iona, Leanne M. Dibbens, James T. Pelekanos, Sameer M. Zuberi, Lynette G. Sadleir, Eva Andermann, Deepak Gill, K Farrell, Mary Connolly, Thorsten Stanley, Michael Harbord, Frédérick Andermann, Jing Wang, Sat Dev Batish, Jeffrey G. Jones, William Seltzer, Alison Gardner, Grant Sutherland, Samuel F. Berkovic, John C. Mulley, Ingrid E. Scheffer
<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova, Albena Jordanova, Berten Ceulemans, Anna Jansen, Danièle Hasaerts, Filip Roelens, Lieven Lagae, Simone C. Yendle, Thorsten Stanley, Sarah E. Heron, John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Peter De Jonghe