ScholarIQanswers from OpenAlex & ORCID
Alain Verloès
ResearcherPublications, citations & collaboration network
Alain Verloès is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Alain Verloès have?
ScholarIQindexed works
Alain Verloès has 628 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Alain Verloès have?
ScholarIQcitation count
Alain Verloès has 24,978 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Alain Verloès?
ScholarIQh-index
Alain Verloès has an h-index of 85 in OpenAlex.
What is the i10-index of Alain Verloès?
ScholarIQi10-index
Alain Verloès has an i10-index of 354 in OpenAlex.
What is the ORCID of Alain Verloès?
ScholarIQorcid
The ORCID for Alain Verloès is on the source record.
What is the OpenAlex record for Alain Verloès?
ScholarIQopenalex
The OpenAlex for Alain Verloès is on the source record.
What are the most-cited papers on Alain Verloès?
ScholarIQmost cited works
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, Philippe Lemay, Dan Spiegelman, Alexandre D. Laporte, Christina Nassif, Ousmane Diallo, Jean Monlong, Maxime Cadieux‐Dion, Sylvia Dobrzeniecka, Caroline Meloche, Kyle Retterer, Megan T. Cho, Jill A. Rosenfeld, Weimin Bi, Christine Massicotte, Marguerite Miguet, Ledia Brunga, Brigid M. Regan, Kelly Mo, Cory Tam, Amy Schneider, Georgie Hollingsworth, David Fitzpatrick, Alan Donaldson, Natalie Canham, Edward Blair, Bronwyn Kerr, Andrew E. Fry, Rhys H. Thomas, Joss Shelagh, Jane A. Hurst, Helen Brittain, Moira Blyth, Robert Roger Lebel, Erica H. Gerkes, Laura Davis‐Keppen, Quinn Stein, Wendy K. Chung, Sara J. Dorison, Paul J. Benke, Emily Fassi, Nicole Corsten‐Janssen, Erik‐Jan Kamsteeg, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Alain Verloès, Katrin Õunap, Monica H. Wojcik, Dara V.F. Albert, Sunita Venkateswaran, Tyson L. Ware, Dean Jones, Yu‐Chi Liu, Shekeeb S. Mohammad, Peyman Bizargity, Carlos A. Bacino, Vincenzo Leuzzi, Simone Martinelli, Bruno Dallapiccola, Marco Tartaglia, Lubov Blumkin, Klaas J. Wierenga, Gabriela Purcarin, James J. O’Byrne, Sylvia Stöckler, Anna Lehman, Boris Keren, Marie‐Christine Nouguès, Cyril Mignot, Stéphane Auvin, Caroline Nava, Susan M. Hiatt, Martina Bebin, Yunru Shao, Fernando Scaglia, Seema R. Lalani, Richard E. Frye, Imad T. Jarjour, Stéphanie Jacques, Renee-Myriam Boucher, Émilie Riou, Myriam Srour, Lionel Carmant, Anne Lortie, Philippe Major, Paola Diadori, François Dubeau, Guy D’Anjou, Guillaume Bourque, Samuel F. Berkovic, Lynette G. Sadleir, Philippe M. Campeau, Zoha Kibar, Ronald G. Lafrenière, Simon Girard, Saadet Mercimek‐Mahmutoglu, Cyrus Boelman, Guy A. Rouleau
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
Ichizo Nishino, Antonella Spinazzola, Alexandros Papadimitriou, Simon Hammans, Israel Steiner, Cecil D. Hahn, Anne M. Connolly, Alain Verloès, Jo�o Guimar�es, Ivan Maillard, H Hamano, Maria Alice Donati, Carol E. Semrad, James A. Russell, Antoni L. Andreu, Giorgos M. Hadjigeorgiou, Tuan Vu, S. Tadesse, Torbjoern G. Nygaard, Ikuya Nonaka, Ikuo Hirano, E. Bonilla, Lewis P. Rowland, S. DiMauro, Michio Hirano
Mutation screening of the <i>PTEN</i> gene in patients with autism spectrum disorders and macrocephaly
Joseph D. Buxbaum, Guiqing Cai, Pauline Chaste, Gudrun Nygren, Juliet Goldsmith, Jennifer Reichert, Henrik Anckarsäter, Maria Råstam, Christopher J. Smith, Jeremy M. Silverman, Eric Hollander, Marion Leboyer, Christopher Gillberg, Alain Verloès, Catalina Betancur