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Träfflista för sökning "WFRF:(Heikkinen T) "

Search: WFRF:(Heikkinen T)

  • Result 1-10 of 162
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1.
  • Sliz, E., et al. (author)
  • Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
  • 2023
  • In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 14:1
  • Journal article (peer-reviewed)abstract
    • Uterine leiomyomata (UL) are the most common tumours of the female genital tract and the primary cause of surgical removal of the uterus. Genetic factors contribute to UL susceptibility. To add understanding to the heritable genetic risk factors, we conduct a genome-wide association study (GWAS) of UL in up to 426,558 European women from FinnGen and a previous UL meta-GWAS. In addition to the 50 known UL loci, we identify 22 loci that have not been associated with UL in prior studies. UL-associated loci harbour genes enriched for development, growth, and cellular senescence. Of particular interest are the smooth muscle cell differentiation and proliferation-regulating genes functioning on the myocardin-cyclin dependent kinase inhibitor 1A pathway. Our results further suggest that genetic predisposition to increased fat-free mass may be causally related to higher UL risk, underscoring the involvement of altered muscle tissue biology in UL pathophysiology. Overall, our findings add to the understanding of the genetic pathways underlying UL, which may aid in developing novel therapeutics.
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2.
  • Tabassum, R, et al. (author)
  • Genetic architecture of human plasma lipidome and its link to cardiovascular disease
  • 2019
  • In: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 10:1, s. 4329-
  • Journal article (peer-reviewed)abstract
    • Understanding genetic architecture of plasma lipidome could provide better insights into lipid metabolism and its link to cardiovascular diseases (CVDs). Here, we perform genome-wide association analyses of 141 lipid species (n = 2,181 individuals), followed by phenome-wide scans with 25 CVD related phenotypes (n = 511,700 individuals). We identify 35 lipid-species-associated loci (P <5 ×10−8), 10 of which associate with CVD risk including five new loci-COL5A1, GLTPD2, SPTLC3, MBOAT7 and GALNT16 (false discovery rate<0.05). We identify loci for lipid species that are shown to predict CVD e.g., SPTLC3 for CER(d18:1/24:1). We show that lipoprotein lipase (LPL) may more efficiently hydrolyze medium length triacylglycerides (TAGs) than others. Polyunsaturated lipids have highest heritability and genetic correlations, suggesting considerable genetic regulation at fatty acids levels. We find low genetic correlations between traditional lipids and lipid species. Our results show that lipidomic profiles capture information beyond traditional lipids and identify genetic variants modifying lipid levels and risk of CVD.
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4.
  • Osorio, A., et al. (author)
  • Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 (CIMBA)
  • 2009
  • In: British Journal of Cancer. - : Nature Publishing Group. - 0007-0920 .- 1532-1827. ; 101:12, s. 2048-2054
  • Journal article (peer-reviewed)abstract
    • Background: In this study we aimed to evaluate the role of a SNP in intron 1 of the ERCC4 gene (rs744154), previously reported to be associated with a reduced risk of breast cancer in the general population, as a breast cancer risk modifier in BRCA1 and BRCA2 mutation carriers. Methods: We have genotyped rs744154 in 9408 BRCA1 and 5632 BRCA2 mutation carriers from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) and assessed its association with breast cancer risk using a retrospective weighted cohort approach. Results: We found no evidence of association with breast cancer risk for BRCA1 (per-allele HR: 0.98, 95% CI: 0.93-1.04, P0.5) or BRCA2 (per-allele HR: 0.97, 95% CI: 0.89-1.06, P0.5) mutation carriers. Conclusion: This SNP is not a significant modifier of breast cancer risk for mutation carriers, though weak associations cannot be ruled out.
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  • Result 1-10 of 162
Type of publication
journal article (151)
conference paper (6)
reports (2)
research review (1)
book chapter (1)
review (1)
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Type of content
peer-reviewed (154)
other academic/artistic (8)
Author/Editor
Heikkinen, T (52)
Nevanlinna, H (28)
Sorsa, T (27)
Hall, P (23)
Tervahartiala, T (23)
Chenevix-Trench, G (22)
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Aittomaki, K (21)
Czene, K (20)
Benitez, J. (19)
Blomqvist, C (19)
Hamann, U (19)
Mannermaa, A (19)
Chang-Claude, J (19)
Easton, DF (19)
Pharoah, PDP (19)
Southey, MC (18)
Anton-Culver, H (17)
Fasching, PA (17)
Couch, FJ (17)
Kosma, VM (17)
Garcia-Closas, M (17)
Lindblom, A (16)
Milne, RL (16)
Margolin, S (16)
Hopper, JL (16)
Beckmann, MW (16)
Kataja, V (16)
Lissowska, J (16)
Giles, GG (15)
Dunning, AM (15)
Cox, A (15)
Reed, MWR (15)
Nordestgaard, BG (15)
Brauch, H (14)
Schmidt, MK (14)
Ekici, AB (14)
Devilee, P (14)
Tollenaar, RAEM (14)
Seynaeve, C (14)
Dork, T (14)
Flyger, H (14)
Broeks, A (13)
Radice, P (13)
Peto, J (13)
Burwinkel, B (13)
Bojesen, SE (13)
Flesch-Janys, D (13)
Olson, JE (13)
Severi, G (13)
Baglietto, L (13)
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University
Karolinska Institutet (117)
Lund University (26)
Uppsala University (20)
Umeå University (19)
University of Gothenburg (12)
Stockholm University (6)
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Chalmers University of Technology (6)
Linköping University (5)
Jönköping University (4)
Royal Institute of Technology (3)
Luleå University of Technology (2)
Linnaeus University (2)
Swedish University of Agricultural Sciences (2)
University of Gävle (1)
University of Borås (1)
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Language
English (162)
Research subject (UKÄ/SCB)
Medical and Health Sciences (36)
Natural sciences (20)
Engineering and Technology (8)
Agricultural Sciences (3)
Social Sciences (2)

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