Hereditary Systemic Amyloidosis Due to Asp76Asn Variant β<sub>2</sub>-MicroglobulinSophie Valleix, Vittorio Bellotti, Mathieu Boimard et al.|New England Journal of Medicine|2012Cited by 188
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profileSophie Valleix, Vittorio Bellotti, Guglielmo Verona et al.|Nature Communications|2016Cited by 66
VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variantsCyrille Garnier, Sophie Valleix, Fatma Briki et al.|Blood|2017Cited by 18