Florence Riant

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Venues

European journal of human genetics : EJHG

Journal of medical genetics

Neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Terry Granchon-Riolzir, Pierre Labauge, Elisabeth Tournier-Lasserve, Florence Riant
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European journal of human genetics : EJHG (2024)
Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Terry Granchon-Riolzir, Pierre Labauge, Elisabeth Tournier-Lasserve, Florence Riant
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European journal of human genetics : EJHG 32 (7) (2024)
Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Terry Granchon-Riolzir, Pierre Labauge, Elisabeth Tournier-Lasserve, Florence Riant
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European journal of human genetics : EJHG 32 (7) (2024)
Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Terry Granchon-Riolzir, Pierre Labauge, Elisabeth Tournier-Lasserve, Florence Riant
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European journal of human genetics : EJHG 32 (7) (2024)
Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Terry Granchon-Riolzir, Pierre Labauge, Elisabeth Tournier-Lasserve, Florence Riant
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European journal of human genetics : EJHG 32 (7) (2024)
Florence Riant, Caroline Roos, Agathe Roubertie, Cécile Barbance, Jessica Hadjadj, Stéphane Auvin, Guillaume Baille, Marion Beltramone, Cécile Boulanger, Alice Cahn, Florina Cata, Emmanuel Cheuret, Jean-Christophe Cuvellier, Antoine Defo, Genevieve Demarquay, Anne Donnet, Nicolas Gaillard, Evelyne Massardier, Nathalie Guy, Sylvie Lamoureux, Laurence Le Moigno, Christian Lucas, Diana Ratiu, Sylvain Redon, Caroline Rey, Christel Thauvin, François Viallet, Elisabeth Tournier-Lasserve, Anne Ducros
Hemiplegic Migraine Associated With PRRT2 Mutations: A Clinical and Genetic Study. Neurology (2021)
Chaker Aloui, Stéphanie Guey, Eva Pipiras, Manoelle Kossorotoff, Sophie Guéden, Michaelle Corpechot, Pierre Bessou, Jean-Michel Pedespan, Marie Husson, Dominique Hervé, Florence Riant, Markus Kraemer, Julie Steffann, Olivier Quenez, Elisabeth Tournier-Lasserve
Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome. Journal of medical genetics 57 (5) (2020)
Françoise Bergametti, Geraldine Viot, Christophe Verny, Marie Pierre Brechard, Christian Denier, Pierre Labauge, Paul Petit, Aurélien Nouet, François Viallet, Annabelle Chaussenot, Dominique Hervé, Elisabeth Tournier-Lasserve, Florence Riant
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations. Journal of medical genetics 57 (6) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Florence Riant