Results 21 to 28 of about 32 (28)
Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET). [PDF]
Genome Med, 2013 Bookman EB, Din-Lovinescu C, Worrall BB, Manolio TA, Bennett SN, Laurie C, Mirel DB, Doheny KF, Anderson GL, Wehr K, Weinshilboum R, Chen DT. +11 moreeuropepmc +1 more sourceCharacterizing genetic variants for clinical action. [PDF]
Am J Med Genet C Semin Med Genet, 2014 Ramos EM, Din-Lovinescu C, Berg JS, Berg JS, Brooks LD, Duncanson A, Dunn M, Good P, Hubbard TJ, Jarvik GP, O'Donnell C, Sherry ST, Aronson N, Biesecker LG, Blumberg B, Calonge N, Colhoun HM, Epstein RS, Flicek P, Gordon ES, Green ED, Green RC, Hurles M, Kawamoto K, Knaus W, Ledbetter DH, Levy HP, Lyon E, Maglott D, McLeod HL, Rahman N, Randhawa G, Wicklund C, Manolio TA, Chisholm RL, Williams MS. +35 moreeuropepmc +1 more sourceA mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee. [PDF]
Am J Hum Genet, 2013 Ramos EM, Din-Lovinescu C, Bookman EB, McNeil LJ, Baker CC, Godynskiy G, Harris EL, Lehner T, McKeon C, Moss J, Starks VL, Sherry ST, Manolio TA, Rodriguez LL. +13 moreeuropepmc +1 more sourceRhinosinusitis: Evidence and experience - 2024. [PDF]
Braz J OtorhinolaryngolRomano FR, Anselmo-Lima WT, Kosugi EM, Sakano E, Valera FCP, Lessa M, Roithmann R, Pignatari S, Felippu AWD, Meotti CD, Barreto CC, Solé D, Goudouris ES, Kuschnir FC, Pinna FR, Serpa FS, Matsumoto GRLL, Freire GSM, Mello JF, Boechat JL, Balsalobre Filho LL, Miyake MM, Nakanishi M, Fornazieri MA, Toro MDC, Tepedino MS, Rubini NPM, Mion OG, Dolci RLL, Voegels RL, Guimarães RE, Dortas SD, Bezerra TFP, Dinarte VRP, Tamashiro E, Piltcher OB. +35 moreeuropepmc +1 more source