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2016
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.Jarvis, D., Mitchell JS, Law PJ, Palin K., Tuupanen S., Gylfe A., Hänninen UA, Cajuso T., Tanskanen T., Kondelin J., Kaasinen E., Sarin AP, Kaprio J., Eriksson JG, Rissanen H., Knekt P., Pukkala E., Jousilahti P., Salomaa V., Ripatti S., et al. British journal of cancer, 2016/06/23, (2016) Read More / View Supplemental Materials
Abstract
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.Gormley, P., Anttila V., Winsvold BS, Palta P., Esko T., Pers TH, Farh KH, Cuenca-Leon E., Muona M., Furlotte NA, Kurth T., Ingason A., McMahon G., Ligthart L., Terwindt GM, Kallela M., Freilinger TM, Ran C., Gordon SG, Stam AH, et al. Nature genetics, 2016/06/20, (2016) Read More / View Supplemental Materials
Abstract
Genome-wide association study identifies 74 loci associated with educational attainment.Okbay, A., Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P., Chen GB, Emilsson V., Meddens SF, Oskarsson S., Pickrell JK, Thom K., Timshel P., de Vlaming R., Abdellaoui A., Ahluwalia TS, Bacelis J., Baumbach C., Bjornsdottir G., et al. Nature, 2016/05/11, Volume 533, Issue 7604, p.539-42, (2016) Read More / View Supplemental Materials
Abstract
The Contribution of GWAS Loci in Familial Dyslipidemias.Ripatti, P., Rämö JT, Söderlund S., Surakka I., Matikainen N., Pirinen M., Pajukanta P., Sarin AP, Service SK, Laurila PP, Ehnholm C., Salomaa V., Wilson RK, Palotie A., Freimer NB, Taskinen MR, and Ripatti S. PLoS genetics, 2016/05/01, Volume 12, Issue 5, p.e1006078, (2016) Read More / View Supplemental Materials
Abstract
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.Orlando, G., Law PJ, Palin K., Tuupanen S., Gylfe A., Hänninen U., Cajuso T., Tanskanen T., Kondelin J., Kaasinen E., Sarin AP, Kaprio J., Eriksson JG, Rissanen H., Knekt P., Pukkala E., Jousilahti P., Salomaa V., Ripatti S., Palotie A., et al. Human molecular genetics, 2016/03/22, (2016) Read More / View Supplemental Materials
Abstract
2015
Directional dominance on stature and cognition in diverse human populations.Joshi, PK, Esko T., Mattsson H., Eklund N., Gandin I., Nutile T., Jackson AU, Schurmann C., Smith AV, Zhang W., Okada Y., Stančáková A., Faul JD, Zhao W., Bartz TM, Concas MP, Franceschini N., Enroth S., Vitart V., Trompet S., et al. Nature, 2015/07/01, (2015) Read More / View Supplemental Materials
Abstract
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.Horikoshi, M., Mӓgi R., van de Bunt M., Surakka I., Sarin AP, Mahajan A., Marullo L., Thorleifsson G., Hӓgg S., Hottenga JJ, Ladenvall C., Ried JS, Winkler TW, Willems SM, Pervjakova N., Esko T., Beekman M., Nelson CP, Willenborg C., Wiltshire S., et al. PLoS genetics, 2015/07/01, Volume 11, Issue 7, p.e1005230, (2015) Read More / View Supplemental Materials
Abstract
Adiposity as a cause of cardiovascular disease: a Mendelian randomization study.Hägg, S., Fall T., Ploner A., Mägi R., Fischer K., Draisma HH, Kals M., de Vries PS, Dehghan A., Willems SM, Sarin AP, Kristiansson K., Nuotio ML, Havulinna AS, de Bruijn RF, Ikram MA, Kuningas M., Stricker BH, Franco OH, Benyamin B., et al. International journal of epidemiology, 2015/05/27, (2015) Read More / View Supplemental Materials
Abstract
The impact of low-frequency and rare variants on lipid levels.Surakka, I., Horikoshi M., Mägi R., Sarin AP, Mahajan A., Lagou V., Marullo L., Ferreira T., Miraglio B., Timonen S., Kettunen J., Pirinen M., Karjalainen J., Thorleifsson G., Hägg S., Hottenga JJ, Isaacs A., Ladenvall C., Beekman M., Esko T., et al. Nature genetics, 2015/05/11, (2015) Read More / View Supplemental Materials
Abstract
Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors.Fall, T., Hägg S., Ploner A., Mägi R., Fischer K., Draisma HH, Sarin AP, Benyamin B., Ladenvall C., Åkerlund M., Kals M., Esko T., Nelson CP, Kaakinen M., Huikari V., Mangino M., Meirhaeghe A., Kristiansson K., Nuotio ML, Kobl M., et al. Diabetes, 2015/02/23, (2015) Read More / View Supplemental Materials
Abstract
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population.Salo, PP, Vaara S., Kettunen J., Pirinen M., Sarin AP, Huikuri H., Karhunen PJ, Eskola M., Nikus K., Lokki ML, Ripatti S., Havulinna AS, Salomaa V., Palotie A., Nieminen MS, Sinisalo J., and Perola M. PloS one, 2015/01/01, Volume 10, Issue 10, p.e0140576, (2015) Read More / View Supplemental Materials
Abstract
Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty.Cousminer, DL, Leinonen JT, Sarin AP, Chheda H., Surakka I., Wehkalampi K., Ellonen P., Ripatti S., Dunkel L., Palotie A., and Widén E. PloS one, 2015/01/01, Volume 10, Issue 6, p.e0128524, (2015) Read More / View Supplemental Materials
Abstract
2014
Chromosome x-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation.Tukiainen, T., Pirinen M., Sarin AP, Ladenvall C., Kettunen J., Lehtimäki T., Lokki ML, Perola M., Sinisalo J., Vlachopoulou E., Eriksson JG, Groop L., Jula A., Järvelin MR, Raitakari OT, Salomaa V., and Ripatti S. PLoS genetics, 2014/02/01, Volume 10, Issue 2, p.e1004127, (2014) Read More / View Supplemental Materials
Abstract
  • Showing 1-13 of 13 Results