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Nature Genetics|February 28, 2012
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophyJaakko Sarparanta, Per Harald Jonson, Christelle Golzio, et al.European Journal of Human Genetics : EJHG|January 5, 2006
A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2pSreekumar G Pillai, Mathias N Chiano, Nicola J White, et al.Nature Genetics|June 29, 2023
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk lociXikun Han, Puya Gharahkhani, Andrew R Hamel, et al.Nature Communications|February 25, 2021
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestriesPuya Gharahkhani, Eric Jorgenson, Pirro Hysi, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|May 15, 2023
EAACI Molecular Allergology User's Guide 2.0Stephanie Dramburg, Christiane Hilger, Alexandra F Santos, et al.JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.Science (New York, N.Y.)|March 21, 2020
The genetic architecture of the human cerebral cortexKatrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.Pageof 8