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Journal Abstract Search
242 related items for PubMed ID: 9718052
1. Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity. Rogaeva E, Premkumar S, Song Y, Sorbi S, Brindle N, Paterson A, Duara R, Levesque G, Yu G, Nishimura M, Ikeda M, O'Toole C, Kawarai T, Jorge R, Vilarino D, Bruni AC, Farrer LA, St George-Hyslop PH. JAMA; 1998 Aug 19; 280(7):614-8. PubMed ID: 9718052 [Abstract] [Full Text] [Related]
2. Genetic studies on chromosome 12 in late-onset Alzheimer disease. Wu WS, Holmans P, Wavrant-DeVrièze F, Shears S, Kehoe P, Crook R, Booth J, Williams N, Pérez-Tur J, Roehl K, Fenton I, Chartier-Harlin MC, Lovestone S, Williams J, Hutton M, Hardy J, Owen MJ, Goate A. JAMA; 1998 Aug 19; 280(7):619-22. PubMed ID: 9718053 [Abstract] [Full Text] [Related]
3. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12. Pericak-Vance MA, Bass MP, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Vance JM, Saunders AM, Roses AD, Haines JL. JAMA; 1997 Oct 15; 278(15):1237-41. PubMed ID: 9333264 [Abstract] [Full Text] [Related]
4. Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity. Scott WK, Grubber JM, Conneally PM, Small GW, Hulette CM, Rosenberg CK, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. Am J Hum Genet; 2000 Mar 15; 66(3):922-32. PubMed ID: 10712207 [Abstract] [Full Text] [Related]
9. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease. Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R. Arch Neurol; 2006 Nov 15; 63(11):1591-8. PubMed ID: 17101828 [Abstract] [Full Text] [Related]
10. Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage. Pericak-Vance MA, Bebout JL, Gaskell PC, Yamaoka LH, Hung WY, Alberts MJ, Walker AP, Bartlett RJ, Haynes CA, Welsh KA. Am J Hum Genet; 1991 Jun 15; 48(6):1034-50. PubMed ID: 2035524 [Abstract] [Full Text] [Related]
13. Chromosome 14 and late-onset familial Alzheimer disease (FAD). Schellenberg GD, Payami H, Wijsman EM, Orr HT, Goddard KA, Anderson L, Nemens E, White JA, Alonso ME, Ball MJ. Am J Hum Genet; 1993 Sep 15; 53(3):619-28. PubMed ID: 8352272 [Abstract] [Full Text] [Related]
14. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Mol Psychiatry; 2006 Mar 15; 11(3):280-5. PubMed ID: 16222332 [Abstract] [Full Text] [Related]
15. Genome scan on Swedish Alzheimer's disease families. Sillén A, Forsell C, Lilius L, Axelman K, Björk BF, Onkamo P, Kere J, Winblad B, Graff C. Mol Psychiatry; 2006 Feb 15; 11(2):182-6. PubMed ID: 16288313 [Abstract] [Full Text] [Related]
16. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p. Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q. Am J Hum Genet; 2004 May 15; 74(5):876-85. PubMed ID: 15077200 [Abstract] [Full Text] [Related]
17. Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease. Martinez M, Campion D, Brice A, Hannequin D, Dubois B, Didierjean O, Michon A, Thomas-Anterion C, Puel M, Frebourg T, Agid Y, Clerget-Darpoux F. Arch Neurol; 1998 Jun 15; 55(6):810-6. PubMed ID: 9626772 [Abstract] [Full Text] [Related]
18. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families. Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S. Cleft Palate Craniofac J; 2000 Jul 15; 37(4):357-62. PubMed ID: 10912714 [Abstract] [Full Text] [Related]
19. Linkage studies of NIDDM with 23 chromosome 11 markers in a sample of whites of northern European descent. Elbein SC, Bragg KL, Hoffman MD, Mayorga RA, Leppert MF. Diabetes; 1996 Mar 15; 45(3):370-5. PubMed ID: 8593945 [Abstract] [Full Text] [Related]
20. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm. Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A. Stroke; 2007 Apr 15; 38(4):1174-8. PubMed ID: 17322081 [Abstract] [Full Text] [Related] Page: [Next] [New Search]