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Nature Genetics|March 2, 2010
Multiple common variants for celiac disease influencing immune gene expressionPatrick C A Dubois, Gosia Trynka, Lude Franke, et al.Human Molecular Genetics|July 14, 2011
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility geneThorunn Rafnar, Sita H Vermeulen, Patrick Sulem, et al.Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.Genome Biology|March 27, 2021
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disordersMarta F Nabais, Simon M Laws, Tian Lin, et al.Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.Nature Genetics|November 17, 2020
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factorsMark K Bakker, Rick A A van der Spek, Wouter van Rheenen, et al.Circulation Research|December 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great ArteriesDoris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada, et al.Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.Nature Genetics|July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosisKevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.Pageof 28