Ingileif Jonsdottir
0000-0001-8339-150X
3 papers found
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A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
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