Ellen Tsai

15PUBLICATIONS
164CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsToxicology (incl. clinical toxicology)
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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

|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

|May 25, 2023
The impact of rare protein coding genetic variation on adult cognitive function.

Chia-Yen Chen, Ruoyu Tian, Tian Ge

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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