Author

Antonio Julià

Vall d'Hebron Institut de RecercaORCID 0000-0001-6064-3620Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 3 Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 5 Approach:statistical model· 5 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Research Focus:benchmarking· 2 Research Focus:gene regulatory network inference· 2 Assay:scRNA-seq· 2 Approach:Bayesian inference· 1

Frequent Co-Authors

Anke HinneyiD· 3 shared Andreas J. ForstneriD· 2 shared Angela FavaroiD· 2 shared Beate Herpertz‐DahlmanniD· 2 shared Christian Dina CiD· 2 shared Christopher HübeliD· 2 shared Claudette Boni· 2 shared Daniela Degortes· 2 shared

Activity by Year

2020-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Anke HinneyORCID

Mutual co-authors in cluster

Author profile →

6 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 23, 2026

Resolving inflammatory bowel disease risk variants to genes and cell types

Laura Fachal, Rui Zhang, Kyle Gettler…·Judy H. Cho

This study identifies 619 IBD risk signals, resolves 81 high-confidence variants, and prioritizes 664 candidate effector genes using GWAS, eQTL, and exome sequencing.

DOI 10.64898/2026.05.13.26352926

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineHuman Molecular GeneticsPeer-reviewedJul 15, 2022

New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations

Frauke C. Degenhardt, David Ellinghaus, Simonas Juzėnas…·Elio Scarpini

This study identifies a new susceptibility locus for severe COVID-19 through a detailed GWAS analysis in European populations, focusing on genetic variants associated with disease severity.

108 citationstop 4%

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 26, 2021

Seven chain adaptive immune receptor repertoire analysis in rheumatoid arthritis: association to disease and clinically relevant phenotypes

Adrià Aterido, Maria Lopez Lasanta, Francisco Javier Blanco…·Antonio Julià

This study analyzes the seven-chain adaptive immune receptor repertoire in rheumatoid arthritis, identifying disease associations and treatment response markers through immunosequencing and HLA integration.

1 citation

humanCITE-seq

𝕏 PostBluesky

GenomicsNature GeneticsPeer-reviewedApr 27, 2020

Genetic Identification of Cell Types Underlying Brain Complex Traits Yields Novel Insights Into the Etiology of Parkinson's Disease

Julien Bryois, Nathan Skene, Thomas Folkmann Hansen…·Jaakko A. Kaprio

This study identifies cell types associated with brain complex traits using GWAS and single-cell transcriptomics, revealing novel roles for oligodendrocytes in Parkinson's disease.

368 citationstop 1%

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsAddiction BiologyPeer-reviewedFeb 16, 2020

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

Melissa A. Munn‐Chernoff, Emma C. Johnson, Yi‐Ling Chou…·Maria C. La Via

The paper estimates genetic correlations between eating disorder and substance-use-related phenotypes using GWAS data, finding both positive and negative associations.

76 citationstop 4%

humanGWAS summary statistics

𝕏 PostBluesky

GenomicsbioRxivPreprintJan 15, 2020

Sampling artifacts in single-cell genomics cohort studies

Ramon Massoni-Badosa, Giovanni Lo Iacono, Cátia Moutinho…·Holger Heyn

The paper identifies sampling artifacts in single-cell genomics and proposes solutions to mitigate them in cohort studies.

5 citations

scRNA-seqscATAC-seq

𝕏 PostBluesky