Ellen Tsai

16PUBLICATIONS
177CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Toxicology (incl. clinical toxicology)
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Publications (16)

|Sep 07, 2026
Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

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

Paul J Hop, Maarten Kooyman, Brendan J Kenna

|Dec 15, 2025
High cell-type specificity of eQTLs revealed by single-nucleus analyses of brain and blood.

Martijn Vochteloo, Anoek Kooijmans, Joost Bakker

|Feb 26, 2024
Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression.

Ruoyu Tian, Tian Ge, Hyeokmoon Kweon

|Jan 23, 2024
PICALO: principal interaction component analysis for the identification of discrete technical, cell-type, and environmental factors that mediate eQTLs.

Martijn Vochteloo, Patrick Deelen, Britt Vink

|Jun 10, 2023
Rare genetic variants impact muscle strength.

Yunfeng Huang, Dora Bodnar, Chia-Yen Chen

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Frequent Collaborators

10 joint publications

Heiko Runz

5 joint publications

Wouter van Rheenen

5 joint publications

Lude Franke

5 joint publications

Jan Veldink