Aaron Wilson

A Common Variant in Methionine Synthase Reductase Combined with Low Cobalamin (Vitamin B12) Increases Risk for Spina Bifida

Aaron Wilson, Robert W. Platt, Qing Wu et al. · Molecular Genetics and Metabolism · 1999 · 436 citations

Vitamin Nutrition, Biosynthesis, Systems Biology +7

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

Daniel Leclerc, Aaron Wilson, Renaud Dumas et al. · Proceedings of the National Academy of Sciences · 1998 · 391 citations

Identification of the gene responsible for the <i>cblA</i> complementation group of vitamin B ₁₂ -responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

Chris Dobson, Timothy Wai, Daniel Leclerc et al. · Proceedings of the National Academy of Sciences · 2002 · 136 citations · Full text

Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L

David Watkins, Ming Ru, Hye‐Yeon Hwang et al. · The American Journal of Human Genetics · 2002 · 116 citations · Full text

Mendelian Disorder, Biochemistry, Common Mutation +11

Crystal structure of type I ryanodine receptor amino-terminal β-trefoil domain reveals a disease-associated mutation “hot spot” loop

Fernando Amador, Shuang Liu, Noboru Ishiyama et al. · Proceedings of the National Academy of Sciences · 2009 · 94 citations · Full text

Crystal Structure, Muscle Function, Molecular Biology +19