Large-scale studies of the functional K variant of the butyrylcholinesterase gene in relation to Type 2 diabetes and insulin secretion

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

Nathalie Vionnet, El Habib Hani, S. Dupont et al. · The American Journal of Human Genetics · 2000 · 680 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 660 citations

Life Sciences, Genetics, Molecular Biology +12

Measurement of the β-sheet-forming propensities of amino acids

Daniel L. Minor, Peter S. Kim · Nature · 1994 · 601 citations

Life Sciences, Biochemistry, Molecular Biology +14

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

Kenneth H. Buetow, Michael N. Edmonson, Richard MacDonald et al. · Proceedings of the National Academy of Sciences · 2001 · 460 citations

Life Sciences, Genetics, Molecular Genetics +17

Mutation analysis of peroxisome proliferator-activated receptor-γ coactivator-1 (PGC-1) and relationships of identified amino acid polymorphisms to Type II diabetes mellitus

Jakob Ek, Gary L. Andersen, Søren A. Urhammer et al. · Diabetologia · 2001 · 296 citations · Full text

Medicine, Genetics, Molecular Genetics +17