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Jacques Motté
ResearcherPublications, citations & collaboration network
Jacques Motté is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 59 works, 4,284 citations, an h-index of 33 and an i10-index of 46.
59
Works
4,284
Citations
33
h-index
46
i10-index
IDs:OpenAlex
How has Jacques Motté's publication output changed over time?
ScholarIQpublication output · 1998–2013
Output declined50% over the shown period — from 2 works in 1998 to 1 in 2013.
2
1
1
1
1
1
3
1
19982000200120082009201120122013
What are the most-cited papers on Jacques Motté?
ScholarIQmost cited works
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
Vincent des Portes, Jean Marc Pinard, Pierre Billuart, Marie Claude Vinet, Annette Koulakoff, Alain Carrié, A. Gélot, Elisabeth Dupuis, Jacques Motté, Yoheved Berwald‐Netter, Martin Catala, Axel Kahn, Chérif Beldjord, Jamel Chelly
S110447773. 1998738 CitationsOPEN ACCESS
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
Gaëtan Lesca, Gabrielle Rudolf, Nadine Bruneau, Natalia Lozovaya, Audrey Labalme, Nadia Boutry‐Kryza, Manal Salmi, Timur Tsintsadze, Laura Addis, Jacques Motté, Sukhvir Wright, Vera Tsintsadze, Anne Michel, Diane Doummar, Karine Lascelles, Lisa J. Strug, Patrick Waters, Julitta de Bellescize, Pascal Vrielynck, Anne de Saint Martin, Dorothée Ville, Philippe Ryvlin, Alexis Arzimanoglou, Édouard Hirsch, Angela Vincent, Deb K. Pal, Nail Burnashev, Damien Sanlaville, Pierre Szepetowski
S137905309. 2013442 Citations
Levodopa-responsive dystonia
Johann Tassin, Alexandra Dürr, Muriel Bonnet, Roger Gil, Marie Vidailhet, Christoph B. Lücking, Jean-Yves Goas, Franck Durif, Myriem Abada, Bernard Échenne, Jacques Motté, A Lagueny, Lucette Lacomblez, Pierre Jedynak, Barbara Bartholomé, Yves Agid, Alexis Brice
Brain. 2000192 CitationsOPEN ACCESS
The three stages of epilepsy in patients with <i>CDKL5</i> mutations
Nadia Bahi‐Buisson, Anna Kamińska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar, Marion Gérard, Fabienne Giuliano, Jacques Motté, Delphine Héron, Marie Ange N'Guyen Morel, Perrine Plouin, Christian Richelme, Vincent des Portes, Olivier Dulac, Christophe Philippe, Catherine Chiron, Rima Nabbout, Thierry Bienvenu
Epilepsia. 2008190 Citations
Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism
Gaëtan Lesca, Gabrielle Rudolf, Audrey Labalme, Édouard Hirsch, Alexis Arzimanoglou, Pierre Genton, Jacques Motté, Anne de Saint Martin, Maria‐Paola Valenti, Clotilde Boulay, Julitta de Bellescize, Pascale Kéo‐Kosal, Nadia Boutry‐Kryza, Patrick Edery, Damien Sanlaville, Pierre Szepetowski
Epilepsia. 2012189 CitationsOPEN ACCESS
Related on ScholarIQ
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
Paper
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
Paper
Levodopa-responsive dystonia
Paper
The three stages of epilepsy in patients with <i>CDKL5</i> mutations
Paper
Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism
Paper
Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome
Paper