Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisDavid R. Booth, Mark B. Pepys, Sheena E. Radford et al.|Nature|1997Cited by 1k
Misdiagnosis of Hereditary Amyloidosis as AL (Primary) AmyloidosisHelen J. Lachmann, Philip N. Hawkins, David R. Booth et al.|New England Journal of Medicine|2002Cited by 686
Human lysozyme gene mutations cause hereditary systemic amyloidosisMark B. Pepys, J. Justin Hsuan, Philip N. Hawkins et al.|Nature|1993Cited by 660
A High-Density Screen for Linkage in Multiple SclerosisStephen Sawcer, Jonathan L. Haines, Maria Ban et al.|The American Journal of Human Genetics|2005Cited by 295