Claudia de Toma

A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs

Christine Lonjou, Nicolas Borot, Peggy Sekula et al. · Pharmacogenetics and Genomics · 2008 · 614 citations

A marker for Stevens-Johnson syndrome …: ethnicity matters

Christine Lonjou, Laure Thomas, Nicolas Borot et al. · The Pharmacogenomics Journal · 2006 · 393 citations

Ethnicity, Genetic Disorder, Histopathology +7

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Pervin Dinçer, France Leturcq, Isabelle Richard et al. · Annals of Neurology · 1997 · 120 citations

A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set

Tara C. Matise, Ravi Sachidanandam, Andrew G. Clark et al. · The American Journal of Human Genetics · 2003 · 115 citations · Full text

Genetics, Human Polymorphism, Linkage Analysis +6

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).

Alain Carrié, Fédérica Piccolo, France Leturcq et al. · Journal of Medical Genetics · 1997 · 115 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +13