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Journal Abstract Search

156 related items for PubMed ID: 10441337

  • 21. 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]

  • 22. Full genome screen for Alzheimer disease: stage II analysis.
    Myers A, Wavrant De-Vrieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstall N, Jones L, Lovestone S, Williams J, Owen MJ, Hardy J, Goate A.
    Am J Med Genet; 2002 Mar 08; 114(2):235-44. PubMed ID: 11857588
    [Abstract] [Full Text] [Related]

  • 23. Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
    Martinez M, Goldin LR, Cao Q, Zhang J, Sanders AR, Nancarrow DJ, Taylor JM, Levinson DF, Kirby A, Crowe RR, Andreasen NC, Black DW, Silverman JM, Lennon DP, Nertney DA, Brown DM, Mowry BJ, Gershon ES, Gejman PV.
    Am J Med Genet; 1999 Aug 20; 88(4):337-43. PubMed ID: 10402499
    [Abstract] [Full Text] [Related]

  • 24. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
    Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H.
    Am J Hum Genet; 2000 Nov 20; 67(5):1201-7. PubMed ID: 11001582
    [Abstract] [Full Text] [Related]

  • 25. A genomewide screen for autism susceptibility loci.
    Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC, Autism Genetic Resource Exchange Consortium.
    Am J Hum Genet; 2001 Aug 20; 69(2):327-40. PubMed ID: 11452361
    [Abstract] [Full Text] [Related]

  • 26. Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India.
    Field LL, Ray AK, Cooper ME, Goldstein T, Shaw DF, Marazita ML.
    Am J Med Genet A; 2004 Oct 15; 130A(3):265-71. PubMed ID: 15378549
    [Abstract] [Full Text] [Related]

  • 27. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
    Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, Sanders AR, Antonarakis SE, Blouin JL, DeLeuze JF, Mallet J.
    Am J Hum Genet; 2000 Sep 15; 67(3):652-63. PubMed ID: 10924404
    [Abstract] [Full Text] [Related]

  • 28. Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p.
    Mori Y, Otabe S, Dina C, Yasuda K, Populaire C, Lecoeur C, Vatin V, Durand E, Hara K, Okada T, Tobe K, Boutin P, Kadowaki T, Froguel P.
    Diabetes; 2002 Apr 15; 51(4):1247-55. PubMed ID: 11916952
    [Abstract] [Full Text] [Related]

  • 29. Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
    Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, Concannon P.
    Am J Hum Genet; 2001 Oct 15; 69(4):820-30. PubMed ID: 11507694
    [Abstract] [Full Text] [Related]

  • 30. Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.
    Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin ML, Lönnqvist J, Peltonen L.
    Hum Mol Genet; 2000 Apr 12; 9(7):1049-57. PubMed ID: 10767329
    [Abstract] [Full Text] [Related]

  • 31. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
    Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Mar 05; 147B(2):209-15. PubMed ID: 17823922
    [Abstract] [Full Text] [Related]

  • 32. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.
    Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, Cardno AG.
    Am J Med Genet B Neuropsychiatr Genet; 2011 Dec 05; 156B(8):929-40. PubMed ID: 21960518
    [Abstract] [Full Text] [Related]

  • 33. Genetic susceptibility to tuberculosis in Africans: a genome-wide scan.
    Bellamy R, Beyers N, McAdam KP, Ruwende C, Gie R, Samaai P, Bester D, Meyer M, Corrah T, Collin M, Camidge DR, Wilkinson D, Hoal-Van Helden E, Whittle HC, Amos W, van Helden P, Hill AV.
    Proc Natl Acad Sci U S A; 2000 Jul 05; 97(14):8005-9. PubMed ID: 10859364
    [Abstract] [Full Text] [Related]

  • 34. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes.
    Hamshere ML, Williams NM, Norton N, Williams H, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, Holmans P, O'Donovan MC, Owen MJ, Craddock N.
    J Med Genet; 2006 Jul 05; 43(7):563-7. PubMed ID: 16227524
    [Abstract] [Full Text] [Related]

  • 35. A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
    Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.
    Hum Mol Genet; 2001 Nov 15; 10(24):2751-65. PubMed ID: 11734540
    [Abstract] [Full Text] [Related]

  • 36. Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
    Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV.
    Am J Hum Genet; 2006 Feb 15; 78(2):315-33. PubMed ID: 16400611
    [Abstract] [Full Text] [Related]

  • 37. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
    Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.
    Am J Med Genet; 2001 Aug 08; 105(6):548-57. PubMed ID: 11496373
    [Abstract] [Full Text] [Related]

  • 38. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
    Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B.
    Eur J Hum Genet; 2005 Jun 08; 13(6):763-71. PubMed ID: 15812564
    [Abstract] [Full Text] [Related]

  • 39. Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica.
    DeLisi LE, Mesen A, Rodriguez C, Bertheau A, LaPrade B, Llach M, Riondet S, Razi K, Relja M, Byerley W, Sherrington R.
    Am J Med Genet; 2002 Jul 08; 114(5):497-508. PubMed ID: 12116183
    [Abstract] [Full Text] [Related]

  • 40. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG, McLean DE, Nyholt DR, Mowry BJ.
    Arch Gen Psychiatry; 2009 Oct 08; 66(10):1058-67. PubMed ID: 19805696
    [Abstract] [Full Text] [Related]

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