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Journal Abstract Search
584 related items for PubMed ID: 11067779
21. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, Owen MJ, Craddock N. Arch Gen Psychiatry; 2005 Oct; 62(10):1081-8. PubMed ID: 16203953 [Abstract] [Full Text] [Related]
22. A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, Ghosh S, Magnuson VL, Colby K, Erdos MR, Hill JE, Hollstein P, Humphreys KM, Kasad RA, Lambert J, Lazaridis KN, Lin G, Morales-Mena A, Patzkowski K, Pfahl C, Porter R, Rha D, Segal L, Suh YD, Tovar J, Unni A, Welch C, Douglas JA, Epstein MP, Hauser ER, Hagopian W, Buchanan TA, Watanabe RM, Bergman RN, Tuomilehto J, Collins FS, Boehnke M. Diabetes; 2004 Mar; 53(3):821-9. PubMed ID: 14988269 [Abstract] [Full Text] [Related]
23. Examination of candidate chromosomal regions for type 2 diabetes reveals a susceptibility locus on human chromosome 8p23.1. Pezzolesi MG, Nam M, Nagase T, Klupa T, Dunn JS, Mlynarski WM, Rich SS, Warram JH, Krolewski AS. Diabetes; 2004 Feb; 53(2):486-91. PubMed ID: 14747302 [Abstract] [Full Text] [Related]
29. Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans. Duggirala R, Blangero J, Almasy L, Dyer TD, Williams KL, Leach RJ, O'Connell P, Stern MP. Am J Hum Genet; 1999 Apr; 64(4):1127-40. PubMed ID: 10090898 [Abstract] [Full Text] [Related]
30. Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers. Levinson DF, Evgrafov OV, Knowles JA, Potash JB, Weissman MM, Scheftner WA, Depaulo JR, Crowe RR, Murphy-Eberenz K, Marta DH, McInnis MG, Adams P, Gladis M, Miller EB, Thomas J, Holmans P. Am J Psychiatry; 2007 Feb; 164(2):259-64. PubMed ID: 17267788 [Abstract] [Full Text] [Related]
31. Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1. Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H. Genet Med; 2005 Feb; 7(6):397-405. PubMed ID: 16024971 [Abstract] [Full Text] [Related]
32. Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Ng MC, So WY, Lam VK, Cockram CS, Bell GI, Cox NJ, Chan JC. Diabetes; 2004 Oct; 53(10):2676-83. PubMed ID: 15448100 [Abstract] [Full Text] [Related]
33. Genome-wide scan for type 1 diabetic nephropathy in the Finnish population reveals suggestive linkage to a single locus on chromosome 3q. Osterholm AM, He B, Pitkaniemi J, Albinsson L, Berg T, Sarti C, Tuomilehto J, Tryggvason K. Kidney Int; 2007 Jan; 71(2):140-5. PubMed ID: 17021601 [Abstract] [Full Text] [Related]
34. A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study. Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA. Diabetes; 2002 Mar; 51(3):833-40. PubMed ID: 11872688 [Abstract] [Full Text] [Related]
37. Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration. Iyengar SK, Song D, Klein BE, Klein R, Schick JH, Humphrey J, Millard C, Liptak R, Russo K, Jun G, Lee KE, Fijal B, Elston RC. Am J Hum Genet; 2004 Jan; 74(1):20-39. PubMed ID: 14691731 [Abstract] [Full Text] [Related]
38. A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians. Busfield F, Duffy DL, Kesting JB, Walker SM, Lovelock PK, Good D, Tate H, Watego D, Marczak M, Hayman N, Shaw JT. Am J Hum Genet; 2002 Feb; 70(2):349-57. PubMed ID: 11742441 [Abstract] [Full Text] [Related]