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603 results

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Page 1
Association of Obesity With Cognitive Decline in Black and White Americans.
Quaye E, Galecki AT, Tilton N, Whitney R, Briceño EM, Elkind MSV, Fitzpatrick AL, Gottesman RF, Griswold M, Gross AL, Heckbert SR, Hughes TM, Longstreth WT Jr, Sacco RL, Sidney S, Windham BG, Yaffe K, Levine DA. Quaye E, et al. Among authors: sidney s. Neurology. 2023 Jan 10;100(2):e220-e231. doi: 10.1212/WNL.0000000000201367. Epub 2022 Oct 18. Neurology. 2023. PMID: 36257719 Free PMC article.
Norplant implants and cardiovascular disease.
Petitti DB, Siscovick DS, Sidney S, Schwartz SM, Quesenberry CP, Psaty BM, Raghunathan TE, Koepsell TD, Longstreth WT Jr. Petitti DB, et al. Among authors: sidney s. Contraception. 1998 May;57(5):361-2. doi: 10.1016/s0010-7824(98)00036-5. Contraception. 1998. PMID: 9673845
Midlife obesity and long-term risk of nursing home admission.
Elkins JS, Whitmer RA, Sidney S, Sorel M, Yaffe K, Johnston SC. Elkins JS, et al. Among authors: sidney s. Obesity (Silver Spring). 2006 Aug;14(8):1472-8. doi: 10.1038/oby.2006.167. Obesity (Silver Spring). 2006. PMID: 16988091 Free article.
Acute seizures predict epilepsy after childhood stroke.
Fox CK, Glass HC, Sidney S, Lowenstein DH, Fullerton HJ. Fox CK, et al. Among authors: sidney s. Ann Neurol. 2013 Aug;74(2):249-56. doi: 10.1002/ana.23916. Ann Neurol. 2013. PMID: 23613472 Free PMC article.
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
Johnsen JM, Auer PL, Morrison AC, Jiao S, Wei P, Haessler J, Fox K, McGee SR, Smith JD, Carlson CS, Smith N, Boerwinkle E, Kooperberg C, Nickerson DA, Rich SS, Green D, Peters U, Cushman M, Reiner AP; NHLBI Exome Sequencing Project. Johnsen JM, et al. Blood. 2013 Jul 25;122(4):590-7. doi: 10.1182/blood-2013-02-485094. Epub 2013 May 20. Blood. 2013. PMID: 23690449 Free PMC article.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, Flannick J, Zhang J, Fuchsberger C, Gaulton K, Lindgren C, Locke A, Manning A, Sim X, Rivas MA, Holmen OL, Gottesman O, Lu Y, Ruderfer D, Stahl EA, Duan Q, Li Y, Durda P, Jiao S, Isaacs A, Hofman A, Bis JC, Correa A, Griswold ME, Jakobsdottir J, Smith AV, Schreiner PJ, Feitosa MF, Zhang Q, Huffman JE, Crosby J, Wassel CL, Do R, Franceschini N, Martin LW, Robinson JG, Assimes TL, Crosslin DR, Rosenthal EA, Tsai M, Rieder MJ, Farlow DN, Folsom AR, Lumley T, Fox ER, Carlson CS, Peters U, Jackson RD, van Duijn CM, Uitterlinden AG, Levy D, Rotter JI, Taylor HA, Gudnason V Jr, Siscovick DS, Fornage M, Borecki IB, Hayward C, Rudan I, Chen YE, Bottinger EP, Loos RJ, Sætrom P, Hveem K, Boehnke M, Groop L, McCarthy M, Meitinger T, Ballantyne CM, Gabriel SB, O'Donnell CJ, Post WS, North KE, Reiner AP, Boerwinkle E, Psaty BM, Altshuler D, Kathiresan S, Lin DY, Jarvik GP, Cupples LA, Kooperberg C, Wilson JG, Nickerson DA, Abecasis GR, Rich SS, Tracy RP, Willer CJ; NHLBI Grand Opportunity Exome Sequencing Project. Lange LA, et al. Am J Hum Genet. 2014 Feb 6;94(2):233-45. doi: 10.1016/j.ajhg.2014.01.010. Am J Hum Genet. 2014. PMID: 24507775 Free PMC article.
603 results