Author

Andrea Carmine Belin

Erasmus MCORCID 0000-0001-6668-3172Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Caroline RaniD· 2 shared Daniel I. ChasmaniD· 2 shared Dennis LaliD· 2 shared Dorret Irene BoomsmaiD· 2 shared Lannie LigthartiD· 2 shared M. Arfan IkramiD· 2 shared Marjo‐Riitta JärveliniD· 2 shared Markus Färkkilä· 2 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Caroline RanORCID

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3 papers

Recent·Most cited

Genetic & Genomic Medicinenpj Parkinson's DiseasePeer-reviewedApr 20, 2026

Genome-wide association study of copy number variations in Parkinson's disease

Z. Landoulsi, Ashwin Ashok Kumar Sreelatha, Kuznetsov N.…·Rachel J. Saunders-Pullman

This study conducts a genome-wide association study of copy number variations in Parkinson's disease, identifying a significant PRKN deletion but limited replication in an independent dataset.

DOI 10.1038/s41531-025-01245-z

humanGWAS summary statistics

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedFeb 1, 2022

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Heidi M Hautakangas, Bendik Slagsvold Winsvold, Sanni Ruotsalainen…·Matti Pirinen

This GWAS identifies 123 migraine risk loci, including subtype-specific variants and novel targets, supporting neurovascular mechanisms in migraine.

400 citationstop 1%

humanGWAS summary statistics

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GeneticsNeuronPeer-reviewedMay 1, 2018

Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families

Padhraig Gormley, Mitja Kurki, Marjo Eveliina Hiekkala…·George McMahon

This study shows common genetic variants significantly contribute to migraine family clustering, with higher burden in familial cases compared to population-based cases.

101 citationstop 1%

humanwhole-exome sequencing

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