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Suggestive linkage of the parathyroid receptor type 1 to osteoporosis.
Duncan EL, Brown MA, Sinsheimer J, Bell J, Carr AJ, Wordsworth BP, Wass JA. Duncan EL, et al. Among authors: brown ma. J Bone Miner Res. 1999 Dec;14(12):1993-9. doi: 10.1359/jbmr.1999.14.12.1993. J Bone Miner Res. 1999. PMID: 10620056 Free article.
Genetic studies of osteoporosis.
Brown MA, Duncan EL. Brown MA, et al. Expert Rev Mol Med. 1999 Oct 19;1999:1-18. doi: 10.1017/S1462399499000964. Expert Rev Mol Med. 1999. PMID: 14585121
Genetic susceptibility to ankylosing spondylitis.
Sims AM, Wordsworth BP, Brown MA. Sims AM, et al. Among authors: brown ma. Curr Mol Med. 2004 Feb;4(1):13-20. doi: 10.2174/1566524043479284. Curr Mol Med. 2004. PMID: 15011955 Review.
Influence of LRP5 polymorphisms on normal variation in BMD.
Koay MA, Woon PY, Zhang Y, Miles LJ, Duncan EL, Ralston SH, Compston JE, Cooper C, Keen R, Langdahl BL, MacLelland A, O'Riordan J, Pols HA, Reid DM, Uitterlinden AG, Wass JA, Brown MA. Koay MA, et al. Among authors: brown ma. J Bone Miner Res. 2004 Oct;19(10):1619-27. doi: 10.1359/JBMR.040704. Epub 2004 Jul 7. J Bone Miner Res. 2004. PMID: 15355556 Free article.
PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton.
Vilariño-Güell C, Miles LJ, Duncan EL, Ralston SH, Compston JE, Cooper C, Langdahl BL, Maclelland A, Pols HA, Reid DM, Uitterlinden AG, Steer CD, Tobias JH, Wass JA, Brown MA. Vilariño-Güell C, et al. Among authors: brown ma. Calcif Tissue Int. 2007 Oct;81(4):270-8. doi: 10.1007/s00223-007-9072-7. Epub 2007 Sep 21. Calcif Tissue Int. 2007. PMID: 17885720
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC); Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cu… See abstract for full author list ➔ Wellcome Trust Case Control Consortium, et al. Among authors: brown mj, brown ma, brown m. Nat Genet. 2007 Nov;39(11):1329-37. doi: 10.1038/ng.2007.17. Epub 2007 Oct 21. Nat Genet. 2007. PMID: 17952073 Free PMC article. Clinical Trial.
1,544 results