Francesca Capon

Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

Giuseppe Novelli, Antoine Muchir, Federica Sangiuolo et al. · The American Journal of Human Genetics · 2002 · 532 citations · Full text

Lmna-encoding Lamin A/c, Mendelian Disorder, Genetic Disorder +3

Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis

Alexandros Onoufriadis, Michael A. Simpson, Andrew Pink et al. · The American Journal of Human Genetics · 2011 · 521 citations · Full text

Inflammation, Rheumatology, Autoimmune Disease +8

Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis

Francesca Capon, Paola Di Meglio, Joanna Szaub et al. · Human Genetics · 2007 · 411 citations

Inflammation, Cytokine, Sequence Variants +9

A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups

Francesca Capon, Michael H. Allen, Mahreen Ameen et al. · Human Molecular Genetics · 2004 · 267 citations · Full text

Synonymous Snp, Neutral Haplotype, Medicine +15

Clinical and genetic differences between pustular psoriasis subtypes

Sophie Twelves, Alshimaa Mostafa, Nick Dand et al. · Journal of Allergy and Clinical Immunology · 2018 · 259 citations · Full text