Thierry Hennet

-Acetylglucosaminyltransferase N 1,3 β Protein Is a Glycolipid-specific Drosophila melanogaster brainiac The ACCELERATED PUBLICATION:

Thierry Hennet, Reto Müller, Friedrich Altmann, 2014 .

CDG nomenclature: time for a change!

Gert Matthijs, Thierry Hennet, T. Hennet, 2009, Biochimica et biophysica acta.

Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.

Matthias Baumgartner, Thierry Hennet, M. Baumgartner, 2009, Human molecular genetics.

Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol‐linked oligosaccharides

Thierry Hennet, T. Hennet, Micha A Haeuptle, 2009, Human mutation.

Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic

Gert Matthijs, Ron A. Wevers, Thierry Hennet, 2000, Human Genetics.

Mechanisms and consequences of intestinal dysbiosis

Thierry Hennet, T. Hennet, G. A. Weiss, 2017, Cellular and Molecular Life Sciences.

NANS-mediated synthesis of sialic acid is required for brain and skeletal development

Dian Donnai, Sheila Unger, Andrea Superti-Furga, 2016, Nature Genetics.

Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction.

Thierry Hennet, T. Hennet, Jürg Cabalzar, 2015, Trends in biochemical sciences.