Author

Tommaso Schirinzi

University of Rome Tor VergataORCID 0000-0002-2517-6278Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Andrew SingletoniD· 2 shared Christine KleiniD· 2 shared Cornelis BlauwendraatiD· 2 shared Katja LohmanniD· 2 shared Lara Mariah LangeiD· 2 shared Rejko KrügeriD· 2 shared Zih‐Hua FangiD· 2 shared Ai Huey TaniD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew SingletonORCID

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2 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Parkinson s DiseasePeer-reviewedDec 2, 2025

TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations.

Wenhua Sun, Claudia Schulte, Thomas Gasser…·Rejko Krüger

This study identifies genetic associations between lysosomal genes and Parkinson's disease risk across diverse populations using GWAS and whole genome sequencing data.

5 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineMovement DisordersPeer-reviewedOct 11, 2025

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease

Lara Mariah Lange, Zih‐Hua Fang, Laurel A. Screven…·the Global Parkinson's Genetics Program (GP2)

The paper assesses the frequency of dystonia-linked pathogenic variants in Parkinson's disease patients and finds they are present in 0.57% of cases, with GCH1 being the most common gene affected.

5 citations

humanwhole-exome sequencing

𝕏 PostBluesky