Hereditary Systemic Amyloidosis Due to Asp76Asn Variant β<sub>2</sub>-MicroglobulinSophie Valleix, Vittorio Bellotti, Pierre Lozeron 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
Mass spectrometry-based proteomics in clinical practice amyloid typing: state-of-the-art from a French nationwide cohortMagali Colombat, Odile Burlet‐Schiltz, Margot Gaspard et al.|Haematologica|2022Cited by 26
New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosisMagali Colombat, Sophie Valleix, Jean‐Claude Aldigier et al.|Kidney International|2020Cited by 23
VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variantsCyrille Garnier, Sophie Valleix, Gilles Grateau et al.|Blood|2017Cited by 18