Author

Luis Diego Herrera-Amighetti

Hospital MetropolitanoORCID 0000-0003-0376-9774Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Cathy L. BarriD· 2 shared Cathy L. BudmaniD· 2 shared Daniëlle C. CathiD· 2 shared Dongmei YuiD· 2 shared Fortu BenarrochiD· 2 shared Franjo IvankoviciD· 2 shared James Frederick LeckmaniD· 2 shared Laura DomènechiD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Cathy L. BarrORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 13, 2026

Genome-Wide Association Analysis of Tic Disorders Reveals 6 Independent Risk Loci and Highlights Tic-Associated Cell Types and Brain Circuitry

Dongmei Yu, Nora I. Strom, Zachary F. Gerring…·Pablo Mir

This study identifies six genome-wide significant risk loci for tic disorders and links genetic risk to specific brain cell types and circuits.

2 citations

humanGWAS summary statistics

𝕏 PostBluesky

NeurosciencebioRxivPreprintNov 4, 2025

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology

Lingyu Zhan, Dongmei Yu, Franjo Ivankovic…·Roel A. Ophoff

This study identifies distinct rare de novo coding variants associated with Tourette Syndrome, highlighting loss-of-function mutations and novel candidate genes.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky