Renata Collard

Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5

Peter R. Baker, Marisa W. Friederich, Michael A. Swanson et al. · Brain · 2013 · 219 citations · Full text

Genetics, Pathology, Molecular Genetics +18

A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment

Kenneth N. Maclean, Jakub Sikora, Viktor Kožich et al. · Molecular Genetics and Metabolism · 2010 · 70 citations · Full text

Pathology, Fatty Liver Disease, Classical Homocystinuria +18

Cystathionine γ-lyase: Clinical, metabolic, genetic, and structural studies

Jan P. Kraus, Jindřich Hašek, Viktor Kožich et al. · Molecular Genetics and Metabolism · 2009 · 65 citations · Full text

Cystathionine γ-Lyase, Biosynthesis, Biochemical Genetics +1

Long-Term Sex-Biased Correction of Circulating Propionic Acidemia Disease Markers by Adeno-Associated Virus Vectors

Adam J. Guenzel, Renata Collard, Jan P. Kraus et al. · Human Gene Therapy · 2015 · 37 citations · Full text

Stabilization of antibody structure upon association to a human carbonic anhydrase IX epitope studied by X‐ray crystallography, microcalorimetry, and molecular dynamics simulations

Vlastimil Král, P. Mäder, Renata Collard et al. · Proteins Structure Function and Bioinformatics · 2007 · 29 citations