Results 151 to 160 of about 182,322 (225)
Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort. [PDF]
Fam CancerSipilä LJ, Aavikko M, Ravantti J, Martin S, Kuopio T, Lahtinen L, FinnGen, Peltomäki P, Mecklin JP, Aaltonen LA, Seppälä TT. +10 moreeuropepmc +1 more sourceNovel Genetic Risk Variants Associated with Oral Tongue Squamous Cell Carcinoma. [PDF]
Head Neck PatholNikkilä R, Mäkitie A, Joensuu H, Markkanen S, Elenius K, Monni O, Palotie A, Saarentaus E, FinnGen, Salo T, Bizaki-Vallaskangas A. +10 moreeuropepmc +1 more sourceGenome-wide association analyses identify distinct genetic architectures for early-onset and late-onset depression. [PDF]
Nat GenetShorter JR, Pasman JA, Kurvits S, Jangmo A, Naamanka J, Harder A, Hagen E, Kowalec K, Frilander N, Zetterberg R, Meijsen JJ, Gådin JR, Bergstedt J, Xiong Y, Hägg S, Landén M, Rück C, Wallert J, Skalkidou A, Koch E, Akdeniz BC, Frei O, FinnGen, Hovatta I, Reichborn-Kjennerud T, Werge TM, Sullivan PF, Andreassen OA, Tesli M, Lehto K, Buil A, Lu Y. +31 moreeuropepmc +1 more sourceQuantifying the contribution of genetic variation to healthcare expenditure across diverse healthcare systems
May-Wilson S, Lee J, Nakanishi T, van der Laan C, Louloudis I, Lin K, Kanoni S, Fahr P, Richmond A, Saad C, Lind PA, Al-Kanaani Z, Artomov M, Banasik K, Byrne EM, Chen Z, Erikstrup C, Sørensen E, German J, Brunelli G, Guðbjartsson DF, Þorsteinsdóttir U, Hickie IB, Kolosov N, Koyama S, Kukkonen A, Li L, McCartney DL, Mortensen LH, Ostrowski SR, Pedersen OB, Bundgaard H, Siskind DJ, Speed D, Sulem P, Võrk A, Wordsworth S, Yang Z, Zguro K, Genes & Health Research Team, FinnGen, Medland SE, Martin NG, Mbarek H, Boomsma DI, Marioni RE, Buchanan J, Natarajan P, Finer S, van Heel DA, Walters R, Abner E, Brunak S, Davies NM, Pons TC, Dixon P, Ganna A. +56 moreeuropepmc +1 more source
