Author

Helena Garrido

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Carol A. MathewsiD· 1 shared Cathy L. BarriD· 1 shared Cathy L. BudmaniD· 1 shared Daniëlle C. CathiD· 1 shared David L. PaulsiD· 1 shared Dongmei YuiD· 1 shared Fortu BenarrochiD· 1 shared Franjo IvankoviciD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Carol A. MathewsORCID

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Author profile →

1 paper

Recent·Most cited

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

Lingyu Zhan, Dongmei Yu, Franjo Ivankovic, Maria Niarchou, Laura Domènech, Cathy L. Barr, Fortu Benarroch, Cathy L. Budman, Daniëlle C. Cath, Nelson B. Freimer, Helena Garrido, Marco A. Grados, Varda Gross‐Tsur, Luis Diego Herrera-Amighetti, Robert A. King, , 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.

bioRxiv · Nov 4, 2025 · PreprintNeuroscience