Jenny van der Wijst

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

Wouter M. Tiel Groenestege, Stéphanie Thebault, Jenny van der Wijst et al. · Journal of Clinical Investigation · 2007 · 359 citations · Full text

A missense mutation in the Kv1.1 voltage-gated potassium channel–encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

Bob Glaudemans, Jenny van der Wijst, Rosana Hermínia Scola et al. · Journal of Clinical Investigation · 2009 · 156 citations · Full text

Electrolyte Disorder, Genetics, Blood Mg2+ Levels +22

Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia

Sascha Vermeer, Alexander Hoischen, Rowdy Meijer et al. · The American Journal of Human Genetics · 2010 · 147 citations · Full text

Autosomal-recessive Cerebellar Ataxia, Mendelian Disorder, Neurogenomics +7

Structural insight into TRPV5 channel function and modulation

Shangyu Dang, Mark K. van Goor, Daniel Asarnow et al. · Proceedings of the National Academy of Sciences · 2019 · 102 citations · Full text

Proteinlipid Interaction, Molecular Biology, Structural Insight +17

New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

Sergio Laínez, Karl P. Schlingmann, Jenny van der Wijst et al. · European Journal of Human Genetics · 2013 · 89 citations · Full text

Genetic Disorder, Genetics, Molecular Biology +4