Christine Lonjou

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

EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension

Mélanie Eyries, David Montani, Barbara Girerd et al. · Nature Genetics · 2013 · 445 citations

Pulmonary Arterial Hypertension, Pulmonary Circulation, Genetics +12

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

Genetic epidemiology of single-nucleotide polymorphisms

Andrew Collins, Christine Lonjou, Newton E. Morton · Proceedings of the National Academy of Sciences · 1999 · 279 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +16

Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome

Kinga M. Bujakowska, Qi Zhang, Anna M. Siemiatkowska et al. · Human Molecular Genetics · 2014 · 155 citations · Full text

Ocular Disease, Developmental Biology, Retina +15