Supplemental material for: "A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathways"
Published: 28 November 2024| Version 1 | DOI: 10.17632/jvpgmxs3n6.1
Contributors:
Rune Kjærsgaard Andersen, Lilja Stefansdottir, Peter Riis, Gisli Halldorsson, Egil Ferkingstad, Asmundur Oddsson, Bragi Walters, Thorunn Olafsdottir, Gudrun Rutsdottir, Claus Zachariae, Simon Thomsen, Thorsten Brodersen, Khoa Dinh, Kirk Knowlton, Stacey Knight, Lincoln Nadauld, Karina Banasik, Søren Brunak, Thomas Hansen, Henerik Hjalgrim, Erik Sørensen, Christina Mikkelsen, Henrik Ullum, Mette Nyegaard, Mie Brunn, Christian Erikstrup, Sisse Ostrowski, Liv Eidsmo, Ditte Saunte, Bardur Sigurgeirsson, Kjartar Ovar, Jona Saemundsdottir, Pall Melsted, Gudmundur Norddahl, Patrick Sulem, Hreinn Stefansson, Hilma Holm, Daniel Gudbjartsson, Gudmar Thorleifsson, Ingileif Jonsdottir, Ole Pedersen, Gregor Jemec, Kari StefanssonDescription
Supplemental material for the manuscript "A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathways"
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Institutions
Kobenhavns Universitet Sundhedsvidenskabelige Fakultet
Categories
Genetics, Dermatology, Genome Wide Association Study, Hidradenitis Suppurativa
Funding
LEO Fondet
LF 18002
Novo Nordisk Fonden
NNF20SA0064340
Aase og Ejnar Danielsens Fond