Lena Kjellén

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 4

Top Topics

Subarachnoid Hemorrhage

Intellectual Disability

Hydrogen Peroxide

Top Venues

Human molecular genetics

The Journal of experimental medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Elham Khosrowabadi, Cécile Mignon-Ravix, Florence Riccardi, Pierre Cacciagli, Béatrice Desnous, Sabine Sigaudy, Mathieu Milh, Laurent Villard, Lena Kjellén, Florence Molinari
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability. Human molecular genetics 33 (6) (2024)
Marie Tauber, Lilian Basso, Jeremy Martin, Luciana E Bostan, Marlene Magalhaes Pinto, Guilhem R Thierry, Raïssa Houmadi, Nadine Serhan, Alexia Loste, Camille Blériot, Jasper B J Kamphuis, Mirjana Grujic, Lena Kjellén, Gunnar Pejler, Carle F Paul, Xinzhong Dong, Stephen J Galli, Laurent Lionel Reber, Florent Ginhoux, Marc Bajenoff, Rebecca Gentek, Nicolas Gaudenzio
Landscape of mast cell populations across organs in mice and humans. The Journal of experimental medicine 220 (10) (2023)
Elham Khosrowabadi, Cécile Mignon-Ravix, Florence Riccardi, Pierre Cacciagli, Béatrice Desnous, Sabine Sigaudy, Mathieu Milh, Laurent Villard, Lena Kjellén, Florence Molinari
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability. Human molecular genetics (2023)
Parisa Missaghian, Tabea Dierker, Elham Khosrowabadi, Fredrik Axling, Inger Eriksson, Abdurrahman Ghanem, Marion Kusche-Gullberg, Sakari Kellokumpu, Lena Kjellén
A dominant negative splice variant of the heparan sulfate biosynthesis enzyme NDST1 reduces heparan sulfate sulfation. Glycobiology 32 (6) (2022)