ScholarIQanswers from OpenAlex & ORCID
Lucette Lacomblez
ResearcherPublications, citations & collaboration network
Lucette Lacomblez is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Lucette Lacomblez have?
ScholarIQindexed works
Lucette Lacomblez has 253 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Lucette Lacomblez have?
ScholarIQcitation count
Lucette Lacomblez has 17,036 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Lucette Lacomblez?
ScholarIQh-index
Lucette Lacomblez has an h-index of 62 in OpenAlex.
What is the i10-index of Lucette Lacomblez?
ScholarIQi10-index
Lucette Lacomblez has an i10-index of 142 in OpenAlex.
What is the OpenAlex record for Lucette Lacomblez?
ScholarIQopenalex
The OpenAlex for Lucette Lacomblez is on the source record.
What are the most-cited papers on Lucette Lacomblez?
ScholarIQmost cited works
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion, Dan Spiegelman, Brendan J. McConkey, Christine Vande Velde, Jean‐Pierre Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, François Salachas, Pierre‐François Pradat, William Camu, Vincent Meininger, Nicolas Dupré, Guy A. Rouleau
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
Isabelle Le Ber, Agnès Camuzat, Didier Hannequin, Florence Pasquier, Éric Guedj, Anne Rovelet‐Lecrux, Valérie Hahn‐Barma, Julie van der Zee, Fabienne Clot, Serge Bakchine, Michèle Puel, Mustapha Ghanim, Lucette Lacomblez, Jacqueline Mikol, Vincent Deramecourt, Pascal Lejeune, Vincent de La Sayette, Serge Belliard, Martine Vercelletto, C Meyrignac, Christine Van Broeckhoven, Jean‐Charles Lambert, Patrice Verpillat, Dominique Campion, Marie‐Odile Habert, Bruno Dubois, Alexis Brice
<i>TARDBP</i> mutations in motoneuron disease with frontotemporal lobar degeneration
Lina Benajiba, Isabelle Le Ber, Agnès Camuzat, Mathieu Lacoste, Catherine Thomas-Antérion, Philippe Couratier, Solenn Legallic, François Salachas, Didier Hannequin, M. Décousus, Lucette Lacomblez, Eric Guedj, Véronique Golfier, William Camu, Bruno Dubois, Dominique Campion, Vincent Meininger, Alexis Brice
<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
Stéphanie Millecamps, François Salachas, C. Cazeneuve, Paul Gordon, Bernard Bricka, A. Camuzat, Léna Guillot‐Noël, Odile Russaouen, Gaëlle Bruneteau, Pierre‐François Pradat, Nadine Le Forestier, N. Vandenberghe, Véronique Danel-Brunaud, Nathalie Guy, Christel Thauvin-Robinet, Lucette Lacomblez, P. Couratier, Didier Hannequin, Danielle Seilhean, Isabelle Le Ber, Philippe Corcia, William Camu, Alexis Brice, Guy A. Rouleau, Eric Leguern, Vincent Meininger
Glutamate levels in cerebrospinal fluid in amyotrophic lateral sclerosis: a reappraisal using a new HPLC method with coulometric detection in a large cohort of patients
Odile Spreux‐Varoquaux, Gilbert Bensimon, Lucette Lacomblez, François Salachas, Pierre Pradat, Nadine Le Forestier, Abdellatif Marouan, Michel Dib, Vincent Meininger