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Page 1
Multigene panels in prostate cancer risk assessment: a systematic review.
Little J, Wilson B, Carter R, Walker K, Santaguida P, Tomiak E, Beyene J, Usman Ali M, Raina P. Little J, et al. Among authors: beyene j. Genet Med. 2016 Jun;18(6):535-44. doi: 10.1038/gim.2015.125. Epub 2015 Oct 1. Genet Med. 2016. PMID: 26426883 Free article. Review.
Treatment for Depression After Unsatisfactory Response to SSRIs [Internet].
Santaguida PL, MacQueen G, Keshavarz H, Levine M, Beyene J, Raina P. Santaguida PL, et al. Among authors: beyene j. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Apr. Report No.: 12-EHC050-EF. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Apr. Report No.: 12-EHC050-EF. PMID: 22696777 Free Books & Documents. Review.
Multigene panels in prostate cancer risk assessment.
Little J, Wilson B, Carter R, Walker K, Santaguida P, Tomiak E, Beyene J, Raina P. Little J, et al. Among authors: beyene j. Evid Rep Technol Assess (Full Rep). 2012 Jul;(209):1-166. Evid Rep Technol Assess (Full Rep). 2012. PMID: 24423032 Free PMC article. Review.
Total fructose intake and risk of hypertension: a systematic review and meta-analysis of prospective cohorts.
Jayalath VH, Sievenpiper JL, de Souza RJ, Ha V, Mirrahimi A, Santaren ID, Blanco Mejia S, Di Buono M, Jenkins AL, Leiter LA, Wolever TM, Beyene J, Kendall CW, Jenkins DJ. Jayalath VH, et al. Among authors: beyene j. J Am Coll Nutr. 2014;33(4):328-39. doi: 10.1080/07315724.2014.916237. Epub 2014 Aug 21. J Am Coll Nutr. 2014. PMID: 25144126 Free PMC article. Review.
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
Nead KT, Li A, Wehner MR, Neupane B, Gustafsson S, Butterworth A, Engert JC, Davis AD, Hegele RA, Miller R, den Hoed M, Khaw KT, Kilpeläinen TO, Wareham N, Edwards TL, Hallmans G, Varga TV, Kardia SL, Smith JA, Zhao W, Faul JD, Weir D, Mi J, Xi B, Quinteros SC, Cooper C, Sayer AA, Jameson K, Grøntved A, Fornage M, Sidney S, Hanis CL, Highland HM, Häring HU, Heni M, Lasky-Su J, Weiss ST, Gerhard GS, Still C, Melka MM, Pausova Z, Paus T, Grant SF, Hakonarson H, Price RA, Wang K, Scherag A, Hebebrand J, Hinney A; BioBank Japan, AGEN-BMI, GIANT Consortium; Franks PW, Frayling TM, McCarthy MI, Hirschhorn JN, Loos RJ, Ingelsson E, Gerstein HC, Yusuf S, Beyene J, Anand SS, Meyre D. Nead KT, et al. Among authors: beyene j. Hum Mol Genet. 2015 Jun 15;24(12):3582-94. doi: 10.1093/hmg/ddv097. Epub 2015 Mar 17. Hum Mol Genet. 2015. PMID: 25784503 Free PMC article. Review.
Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes.
Ghemlas I, Li H, Zlateska B, Klaassen R, Fernandez CV, Yanofsky RA, Wu J, Pastore Y, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Sinha R, Belletrutti M, Breakey VR, Jardine L, Goodyear L, Sung L, Dhanraj S, Reble E, Wagner A, Beyene J, Ray P, Meyn S, Cada M, Dror Y. Ghemlas I, et al. Among authors: beyene j. J Med Genet. 2015 Sep;52(9):575-84. doi: 10.1136/jmedgenet-2015-103270. Epub 2015 Jul 1. J Med Genet. 2015. PMID: 26136524
369 results