Author

Caroline Ran

Karolinska InstitutetORCID 0000-0003-0239-9871Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 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

Lannie LigthartiD· 3 shared Mikko KallelaiD· 3 shared Padhraig GormleyiD· 3 shared Tobias KurthiD· 3 shared Andrea Carmine BeliniD· 2 shared Daniel I. ChasmaniD· 2 shared Dorret Irene BoomsmaiD· 2 shared George McMahon· 2 shared

Activity by Year

2016-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Lannie LigthartORCID

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3 papers

Recent·Most cited

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, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman, Laurent F. Thomas, Raymond Noordam, Christian Benner, Padhraig Gormley, Ville Artto, Karina Banasik, Anna Bjornsdottir, Dorret Irene Boomsma, Ben Michael Brumpton, , Matti Pirinen

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

Nature Genetics · Feb 1, 2022Peer-reviewedGenetic & Genomic Medicine

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

Padhraig Gormley, Mitja Kurki, Marjo Eveliina Hiekkala, Kumar Veerapen, Paavo Häppölä, Adele A. Mitchell, Dennis Lal, Priit Palta, Ida L. Surakka, Mari Anneli Kaunisto, Eija Hämäläinen, Salli Vepsäläinen, Hannele Havanka, Hanna Harno, Matti Ilmavirta, , 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.

Neuron · May 1, 2018Peer-reviewedGenetics

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Padhraig Gormley, Verneri Anttila, Bendik S Winsvold, Priit Palta, Tonu Esko, Tune H Pers, Kai-How Farh, Ester Cuenca-Leon, Mikko Muona, Nicholas A Furlotte, Tobias Kurth, Andres Ingason, George McMahon, Lannie Ligthart, Gisela M Terwindt, , Ville Art

This study identifies 38 new migraine susceptibility loci through a meta-analysis of 375,000 individuals, including the first locus on chromosome X.

Nature Genetics · Jun 20, 2016Peer-reviewedGenetics