Boris Rogelj

15PUBLICATIONS
135CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsLiquid biopsiesEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (15)

|Mar 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Paul J Hop, Maarten Kooyman, Brendan J Kenna

|Sep 16, 2023
Phenylalanine-tRNA aminoacylation is compromised by ALS/FTD-associated C9orf72 C4G2 repeat RNA.

Mirjana Malnar Črnigoj, Urša Čerček, Xiaoke Yin

|Apr 18, 2023
Abl kinase-mediated FUS Tyr526 phosphorylation alters nucleocytoplasmic FUS localization in FTLD-FUS.

Helena Motaln, Urša Čerček, Alfred Yamoah

|Feb 01, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker

|Dec 07, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker

|Sep 17, 2021
Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA.

Janja Božič, Helena Motaln, Anja Pucer Janež

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Frequent Collaborators

4 joint publications

R Jeroen Pasterkamp

4 joint publications

Blaž Koritnik

4 joint publications

Simon Topp

4 joint publications

Guy Rouleau