ScholarIQanswers from OpenAlex & ORCID
Michel Vekemans
ResearcherPublications, citations & collaboration network
Michel Vekemans is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Michel Vekemans have?
ScholarIQindexed works
Michel Vekemans has 365 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Michel Vekemans have?
ScholarIQcitation count
Michel Vekemans has 17,251 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Michel Vekemans?
ScholarIQh-index
Michel Vekemans has an h-index of 65 in OpenAlex.
What is the i10-index of Michel Vekemans?
ScholarIQi10-index
Michel Vekemans has an i10-index of 211 in OpenAlex.
What is the ORCID of Michel Vekemans?
ScholarIQorcid
The ORCID for Michel Vekemans is on the source record.
What is the OpenAlex record for Michel Vekemans?
ScholarIQopenalex
The OpenAlex for Michel Vekemans is on the source record.
What are the most-cited papers on Michel Vekemans?
ScholarIQmost cited works
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kálmán Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou, Imane Moutkine, Nathan E. Hellman, Isabelle Anselme, Flora Silbermann, Christine Vesque, Christoph Gerhardt, Eleanor Rattenberry, Matthias T. F. Wolf, Marie-Claire Gübler, Jéléna Martinovic, Férechté Encha‐Razavi, Nathalie Boddaert, Marie Gonzalès, Marie Alice Macher, Hubert Nivet, Gérard Champion, Jean Pierre Berthélémé, Patrick Niaudet, Fiona McDonald, Friedhelm Hildebrandt, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Ulrich Rüther, Sylvie Schneider‐Maunoury, Tania Attié‐Bitach, Sophie Saunier
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
Valérie Belin, Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, Anne Moncla, Michel Vekemans, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire
Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome
Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlène Rio, Valérie Malan, Nathalie Boddaert, Christine Soufflet, Capucine Pïcard, Anne Durandy, Angus Dobbie, Delphine Héron, Bertrand Isidor, Jacques Motté, Ruth Newburry-Ecob, Laurent Pasquier, Marc Tardieu, G��raldine Viot, Francis Jaubert, Arnold Münnich, Laurence Colleaux, Michel Vekemans, Heather Etchevers, Stanislas Lyonnet, Jeanne Amiel