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Valérie Cormier‐Daire

ResearcherPublications, citations & collaboration network

Valérie Cormier‐Daire is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Valérie Cormier‐Daire have?

ScholarIQindexed works

Valérie Cormier‐Daire has 1,141 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Valérie Cormier‐Daire have?

ScholarIQcitation count

Valérie Cormier‐Daire has 35,021 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Valérie Cormier‐Daire?

ScholarIQh-index

Valérie Cormier‐Daire has an h-index of 99 in OpenAlex.

What is the i10-index of Valérie Cormier‐Daire?

ScholarIQi10-index

Valérie Cormier‐Daire has an i10-index of 425 in OpenAlex.

What is the ORCID of Valérie Cormier‐Daire?

ScholarIQorcid

The ORCID for Valérie Cormier‐Daire is on the source record.

What is the OpenAlex record for Valérie Cormier‐Daire?

ScholarIQopenalex

The OpenAlex for Valérie Cormier‐Daire is on the source record.

What are the most-cited papers on Valérie Cormier‐Daire?

ScholarIQmost cited works
Nosology and classification of genetic skeletal disorders: 2019 revision
Geert Mortier, Daniel H. Cohn, Valérie Cormier‐Daire, Christine M Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Andrea Superti‐Furga, Sheila Unger, Matthew L. Warman
American Journal of Medical Genetics Part A. 2019617 Citations
Nosology and classification of genetic skeletal disorders: 2015 revision
Luisa Bonafé, Valérie Cormier‐Daire, Christine M Hall, Ralph Lachman, Geert Mortier, Stefan Mundlos, Gen Nishimura, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Jürgen W. Spranger, Andrea Superti‐Furga, Matthew L. Warman, Sheila Unger
American Journal of Medical Genetics Part A. 2015567 Citations
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
Nature Genetics. 1998361 Citations
International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia
Ravi Savarirayan, Penny Ireland, Melita Irving, Dominic Thompson, Inês Alves, Wagner Antonio da Rosa Baratela, James A. Betts, Michael B. Bober, Silvio Boero, Jenna W. Briddell, Jeffrey W. Campbell, Philippe M. Campeau, Patricia Carl-Innig, Moira Cheung, Martyn T. Cobourne, Valérie Cormier‐Daire, Muriel de La Dure‐Molla, Mariana del Pino, Heather Elphick, Virginia Fano, Brigitte Fauroux, Jonathan Gibbins, Mari L. Groves, Lars Hagenäs, Therese Hannon, Julie Hoover‐Fong, Morrys C. Kaisermann, Antonio Leiva‐Gea, Juan Clinton Llerena, William G. Mackenzie, Kenneth W. Martin, Fabio Mazzoleni, Sharon Mcdonnell, Maria Costanza Meazzini, J Milerad, Klaus Mohnike, Geert Mortier, Amaka C Offiah, Keiichi Ozono, John A. Phillips, Steven Powell, Y Prasad, Cathleen Raggio, Pablo Rosselli, Judith Pratt Rossiter, Angelo Selicorni, Marco Sessa, Mary C. Theroux, Matthew Thomas, Laura Trespedi, David E. Tunkel, Colin Wallis, Michael Wright, Natsuo Yasui, Svein O. Fredwall
Nature Reviews Endocrinology. 2021191 CitationsOPEN ACCESS

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