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Nature Aging|April 28, 2023
The burden of rare protein-truncating genetic variants on human lifespanJimmy Z Liu, Chia-Yen Chen, Ellen A Tsai, et al.Journal of Personalized Medicine|March 2, 2016
Bioinformatics Workflow for Clinical Whole Genome Sequencing at Partners HealthCare Personalized MedicineEllen A Tsai, Rimma Shakbatyan, Jason Evans, et al.Scientific Reports|February 19, 2020
Exome Sequencing in Individuals with Isolated Biliary AtresiaRamakrishnan Rajagopalan, Ellen A Tsai, Christopher M Grochowski, et al.Genome Biology|January 23, 2024
PICALO: principal interaction component analysis for the identification of discrete technical, cell-type, and environmental factors that mediate eQTLsMartijn Vochteloo, Patrick Deelen, Britt Vink, et al.Molecular Neurodegeneration Advances|December 26, 2025
Serum metabolomic-lipidomic signatures track long-term neurological performance in multiple sclerosisRose Noroozi, Hui-Hsin Tsai, Ketian Yu, et al.Human Mutation|March 14, 2015
Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresiaEllen A Tsai, Christopher M Grochowski, Alexandra M Falsey, et al.Bioinformatics (Oxford, England)|August 15, 2013
DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experimentsChiao-Feng Lin, Otto Valladares, D Micah Childress, et al.Human Genetics|October 10, 2013
Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresiaEllen A Tsai, Christopher M Grochowski, Kathleen M Loomes, et al.Gastroenterology|January 23, 2013
Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility geneShuang Cui, Melissa Leyva-Vega, Ellen A Tsai, et al.Nature Communications|June 10, 2023
Rare genetic variants impact muscle strengthYunfeng Huang, Dora Bodnar, Chia-Yen Chen, et al.Pageof 3