Hafdís T. Helgadóttir
Karolinska University Hospital(SE)Karolinska Institutet(SE)Karolinska Development (Sweden)(SE)
Publications by Year
Research Areas
Genomics and Rare Diseases, Cancer Genomics and Diagnostics, Genetic Associations and Epidemiology, Cutaneous Melanoma Detection and Management, Genetic factors in colorectal cancer
Most-Cited Works
- → Large-scale whole-genome sequencing of the Icelandic population(2015)827 cited
- → Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction(2009)760 cited
- → Sequence variants at the TERT-CLPTM1L locus associate with many cancer types(2009)611 cited
- → Mutations in BRIP1 confer high risk of ovarian cancer(2011)427 cited
- → Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations(2009)392 cited
- → Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes(2014)328 cited
- → A germline variant in the TP53 polyadenylation signal confers cancer susceptibility(2011)303 cited