Pierre Lebon

机构：Délégation Paris 5, Université Paris Cité

发表论文 361 篇 · 总被引 24134 次 · h-index 74

代表论文

• Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature (2012 · Nature Genetics · 被引 967)
• Characterization of human disease phenotypes associated with mutations in TREX1 , RNASEH2A , RNASEH2B , RNASEH2C , SAMHD1 , ADAR , and IFIH1 (2015 · American Journal of Medical Genetics Part A · 被引 617)
• Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling (2014 · Nature Genetics · 被引 601)
• Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation (2014 · Nature · 被引 587)
• Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study (2013 · The Lancet Neurology · 被引 449)
• Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency (2011 · Journal of Clinical Investigation · 被引 312)