Virginie Laugel

Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects

Agnès Bloch‐Zupan, Xavier Jamet, Christelle Etard et al. · The American Journal of Human Genetics · 2011 · 104 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

Graciana Jaureguiberry, Muriel de La Dure‐Molla, David Parry et al. · Nephron Physiology · 2013 · 103 citations · Full text

Medicine, Genetics, Nephrology +16

Genetic Inactivation of Prokineticin Receptor-1 Leads to Heart and Kidney Disorders

Mounia Boulberdaa, Gülen Türkeri, Kyoji Urayama et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2011 · 30 citations

Medicine, Cardiology, Pharmacology +16

A possible cranio-oro-facial phenotype in Cockayne syndrome

Agnès Bloch‐Zupan, Morgan Rousseaux, Virginie Laugel et al. · Orphanet Journal of Rare Diseases · 2013 · 26 citations · Full text

Dentistry, Craniofacial Biology, Craniofacial Genetics +16