Author

Anders Franco‐Cereceda

Karolinska University HospitalORCID 0000-0002-3427-9455Unclaimed 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:gene regulatory network inference· 2 Assay:GWAS summary statistics· 2 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Per Olof ErikssoniD· 3 shared Hanna M. BjörckiD· 2 shared Amanda RantaiD· 1 shared Anders HamsteniD· 1 shared Andreas MartinssoniD· 1 shared Andrey BuyaniD· 1 shared Anna HelgadóttiriD· 1 shared Arnar GeirssoniD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Per Olof ErikssonORCID

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3 papers

Recent·Most cited

Rare gain-of-function regulatory mutations explain the missing heritability of bicuspid aortic valve

Artemy Zhigulev, Andrey Buyan, Enikő Lázár, Nikita Gryzunov, Karin Lång, Raphaël Mauron, Vladimir Nozdrin, Rapolas Spalinskas, Sailendra Pradhananga, Madeleine Petersson Sjögren, Doreen Schwochow, Anders Franco‐Cereceda, Joakim Lundeberg, Ivan V. Kulakovskiy, Per Eriksson, , Pelin Sahlén

The paper identifies rare gain-of-function regulatory mutations as significant contributors to the missing heritability of bicuspid aortic valve.

Nature Communications · Apr 18, 2026Peer-reviewedGenetic & Genomic Medicine

A functional genomic framework to elucidate novel causal non-alcoholic fatty liver disease genes

Peter Saliba‐Gustafsson, Johanne Marie Justesen, Amanda Ranta, Disha Sharma, Ewa Bielczyk-Maczyńska, Jiehan Li, Laeya Abdoli Najmi, Maider Apodaka‐Biguri, Patricia Aspichueta, Hanna M. Björck, Per Olof Eriksson, Theresia Maria Schnurr, Anders Franco‐Cereceda, Michael J. Gloudemans, Endrina Mújica, , Joshua W. Knowles

This study identifies novel causal genes for NAFLD using a combination of GWAS, genetic colocalization, and CRISPRi functional screens.

Hepatology · Aug 27, 2024Peer-reviewedGenetic & Genomic Medicine

Genome-wide analysis yields new loci associating with aortic valve stenosis

Anna Helgadóttir, Guðmar Þorleifsson, Sólveig Grétarsdóttir, Ólafur Andri Stefánsson, Vinicius Tragante, Rósa B. Þórólfsdóttir, Ingileif Jónsdóttir, Þorsteinn Björnsson, Valgerður Steinthórsdóttir, Niek Verweij, Jonas Bille Nielsen, Wei Zhou, Lasse Folkersen, Andreas Martinsson, Mahyar Heydarpour, , Kāri Stefánsson

This study identifies two new genetic loci associated with aortic valve stenosis through a large genome-wide association study.

Nature Communications · Mar 1, 2018Peer-reviewedGenetics