Author

Caterina Galandra

University of PaviaORCID 0000-0002-7048-814XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:database / resource· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ai Huey TaniD· 2 shared Anastasia IllarionovaiD· 2 shared Andrew SingletoniD· 2 shared Christine KleiniD· 2 shared Cornelis BlauwendraatiD· 2 shared Enza Maria ValenteiD· 2 shared Harutyun MadoeviD· 2 shared Ignacio Juan Keller SarmientoiD· 2 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ai Huey TanORCID

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2 papers

Recent·Most cited

Understanding monogenic Parkinson's disease at a global scale

Johanna Junker, Lara Mariah Lange, Eva‐Juliane Vollstedt, Karisha Roopnarain, Maria Leila M. Doquenia, Azlina Ahmad‐Annuar, Micol Avenali, Soraya Bardien, Natascha Bahr, Melina Ellis, Caterina Galandra, Thomas Gasser, Peter Heutink, Anastasia Illarionova, Yuliia Kanana, , the Global Parkinson's Genetics Program (GP2)

This paper combines two global monogenic Parkinson's disease initiatives to create a comprehensive cohort and infrastructure for studying multi-ancestry genetic factors and disease expression.

Movement Disorders · Jul 30, 2024Peer-reviewedGenetic & Genomic Medicine

Global Parkinson's Genetics Program (GP2) Monogenic Network Protocol: Elucidating causative gene variants in hereditary Parkinson's disease

Lara Mariah Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio Juan Keller Sarmiento, Ai Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Cook Solle, Claire Wegel, Zih‐Hua Fang, Peter Heutink, Kishore Raj Kumar, , the Global Parkinson’s Genetic Program (GP2)

The paper establishes a protocol for whole-genome sequencing to identify genetic causes of Parkinson's disease, focusing on monogenic variants and their clinical implications.

medRxiv · Dec 1, 2022 · PreprintGenetic & Genomic Medicine