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Page 1
Microcephaly genes and risk of late-onset Alzheimer disease.
Erten-Lyons D, Wilmot B, Anur P, McWeeney S, Westaway SK, Silbert L, Kramer P, Kaye J. Erten-Lyons D, et al. Among authors: kramer p. Alzheimer Dis Assoc Disord. 2011 Jul-Sep;25(3):276-82. doi: 10.1097/WAD.0b013e31820a1d32. Alzheimer Dis Assoc Disord. 2011. PMID: 21297427 Free PMC article.
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.
Kramer PL, Xu H, Woltjer RL, Westaway SK, Clark D, Erten-Lyons D, Kaye JA, Welsh-Bohmer KA, Troncoso JC, Markesbery WR, Petersen RC, Turner RS, Kukull WA, Bennett DA, Galasko D, Morris JC, Ott J. Kramer PL, et al. Neurobiol Aging. 2011 Dec;32(12):2113-22. doi: 10.1016/j.neurobiolaging.2010.01.010. Epub 2010 May 7. Neurobiol Aging. 2011. PMID: 20452100 Free PMC article.
Neuropathologic basis of age-associated brain atrophy.
Erten-Lyons D, Dodge HH, Woltjer R, Silbert LC, Howieson DB, Kramer P, Kaye JA. Erten-Lyons D, et al. Among authors: kramer p. JAMA Neurol. 2013 May;70(5):616-22. doi: 10.1001/jamaneurol.2013.1957. JAMA Neurol. 2013. PMID: 23552688 Free PMC article.
Translational gene mapping of cognitive decline.
Wilmot B, McWeeney SK, Nixon RR, Montine TJ, Laut J, Harrington CA, Kaye JA, Kramer PL. Wilmot B, et al. Neurobiol Aging. 2008 Apr;29(4):524-41. doi: 10.1016/j.neurobiolaging.2006.11.008. Epub 2006 Dec 14. Neurobiol Aging. 2008. PMID: 17174450 Free PMC article.
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, Baldwin CT, Jarvik GP, Crane PK, Rogaeva E, Barmada MM, Demirci FY, Cruchaga C, Kramer PL, Ertekin-Taner N, Hardy J, Graff-Radford NR, Green RC, Larson EB, St George-Hyslop PH, Buxbaum JD, Evans DA, Schneider JA, Lunetta KL, Kamboh MI, Saykin AJ, Reiman EM, De Jager PL, Bennett DA, Morris JC, Montine TJ, Goate AM, Blacker D, Tsuang DW, Hakonarson H, Kukull WA, Foroud TM, Martin ER, Haines JL, Mayeux RP, Farrer LA, Schellenberg GD, Pericak-Vance MA; Alzheimer Disease Genetics Consortium; Albert MS, Albin RL, Apostolova LG, Arnold SE, Barber R, Barnes LL, Beach TG, Becker JT, Beekly D, Bigio EH, Bowen JD, Boxer A, Burke JR, Cairns NJ, Cantwell LB, Cao C, Carlson CS, Carney RM, Carrasquillo MM, Carroll SL, Chui HC, Clark DG, Corneveaux J, Cribbs DH, Crocco EA, DeCarli C, DeKosky ST, Dick M, Dickson DW, Duara R, Faber KM, Fallon KB, Farlow MR, Ferris S, Frosch MP, Galasko DR, Ganguli M, Gearing M, Geschwind DH, Ghetti B, Gilbert JR, Glass JD, Growdon JH, Hamilton RL, Harrell LE, Head E, Honig LS, Hulette CM, Hyman BT… See abstract for full author list ➔ Naj AC, et al. Among authors: kramer pl, kramer jh. JAMA Neurol. 2014 Nov;71(11):1394-404. doi: 10.1001/jamaneurol.2014.1491. JAMA Neurol. 2014. PMID: 25199842 Free PMC article.
Review of selected databases of longitudinal aging studies.
Erten-Lyons D, Sherbakov LO, Piccinin AM, Hofer SM, Dodge HH, Quinn JF, Woltjer RL, Kramer PL, Kaye JA. Erten-Lyons D, et al. Alzheimers Dement. 2012 Nov;8(6):584-9. doi: 10.1016/j.jalz.2011.09.232. Alzheimers Dement. 2012. PMID: 23102128 Free PMC article. Review.
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Trojanowski JQ, Schellenberg GD, Yearout D, Huston H, Fritts-Penniman A, Mata IF, Wan JY, Edwards KL, Montine TJ, Zabetian CP. Tsuang D, et al. Among authors: kramer p. Neurology. 2012 Nov 6;79(19):1944-50. doi: 10.1212/WNL.0b013e3182735e9a. Epub 2012 Oct 3. Neurology. 2012. PMID: 23035075 Free PMC article.
Exceptional brain aging in a rural population-based cohort.
Kaye J, Michael Y, Calvert J, Leahy M, Crawford D, Kramer P. Kaye J, et al. Among authors: kramer p. J Rural Health. 2009 Summer;25(3):320-5. doi: 10.1111/j.1748-0361.2009.00237.x. J Rural Health. 2009. PMID: 19566620 Free PMC article.
A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia.
Tian W, Fu Y, Garcia-Elias A, Fernández-Fernández JM, Vicente R, Kramer PL, Klein RF, Hitzemann R, Orwoll ES, Wilmot B, McWeeney S, Valverde MA, Cohen DM. Tian W, et al. Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):14034-9. doi: 10.1073/pnas.0904084106. Epub 2009 Aug 4. Proc Natl Acad Sci U S A. 2009. PMID: 19666518 Free PMC article.
1,185 results