Publications by authors named "A Superti-Furga"

Volume-regulated anion channels (VRACs) are multimeric proteins composed of different paralogs of the LRRC8 family. They are activated in response to hypotonic swelling, but little is known about their specific functions. We studied two human individuals with the same congenital syndrome affecting blood vessels, brain, eyes, and bones.

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Article Synopsis
  • * Diagnostic protocols for increased nuchal translucency include rapid tests for aneuploidy, cytogenetic analysis, and in some cases, whole exome sequencing (WES), though its role in isolated cases is still debated.
  • * In a study involving two euploid fetuses with isolated increased nuchal translucency, whole genome sequencing revealed variants in the NUP107 gene linked to severe nephrotic syndrome, highlighting the importance of advanced genetic testing
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A paper published in Orphanet Journal of Rare Diseases proposes a new classification of osteogenesis imperfecta (OI) based upon underlying pathological mechanisms. The proposed numbering of OI types conflicts with the currently used numbering and is likely to lead to confusion. In addition, classification of OI according to underlying pathogenic mechanisms is not novel.

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Large-scale next-generation sequencing (NGS) germline testing is technically feasible today, but variant interpretation represents a major bottleneck in analysis workflows. This includes extensive variant prioritization, annotation, and time-consuming evidence curation. The scale of the interpretation problem is massive, and variants of uncertain significance (VUSs) are a challenge to personalized medicine.

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