Unnur Styrkarsdottir
educated at: University of Copenhagen
occupation: researcher
Articles 58
-
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
-
Disentangling the genetics of lean mass
-
Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry
-
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
-
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density
-
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
-
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
-
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
-
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.
-
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
-
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
-
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
-
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
-
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
-
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.
-
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
-
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
-
The rate of meiotic gene conversion varies by sex and age.
-
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
-
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
-
Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland
-
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
-
Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus
-
Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies
-
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
-
A common biological basis of obesity and nicotine addiction
-
The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males
-
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
-
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.
-
Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition
Human - wd:Q30430779