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Journal Abstract Search

233 related items for PubMed ID: 24035701

  • 21. 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; 66(10):1058-67. PubMed ID: 19805696
    [Abstract] [Full Text] [Related]

  • 22. A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.
    Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM.
    BMC Med Genomics; 2010 Jun 07; 3():22. PubMed ID: 20529293
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  • 25. A genome-wide quantitative trait locus (QTL) linkage scan of NEO personality factors in Latino families segregating bipolar disorder.
    Lee BD, Gonzalez S, Villa E, Camarillo C, Rodriguez M, Yao Y, Guo W, Flores D, Jerez A, Raventos H, Ontiveros A, Nicolini H, Escamilla M.
    Am J Med Genet B Neuropsychiatr Genet; 2017 Oct 07; 174(7):683-690. PubMed ID: 28556497
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  • 26. Genome-wide linkage and regional association study of obesity-related phenotypes: the GenSalt study.
    Liu AY, Gu D, Hixson JE, Rao DC, Shimmin LC, Jaquish CE, Liu DP, He J, Kelly TN.
    Obesity (Silver Spring); 2014 Feb 07; 22(2):545-56. PubMed ID: 23526746
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  • 27. Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
    Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, Mowry BJ, Brzustowicz LM, Maziade M, Sklar P, Garver DL, Abecasis GR, Lerer B, Fallin MD, Gurling HM, Gejman PV, Lindholm E, Moises HW, Byerley W, Wijsman EM, Forabosco P, Tsuang MT, Hwu HG, Okazaki Y, Kendler KS, Wormley B, Fanous A, Walsh D, O'Neill FA, Peltonen L, Nestadt G, Lasseter VK, Liang KY, Papadimitriou GM, Dikeos DG, Schwab SG, Owen MJ, O'Donovan MC, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Bassett AS, Roy MA, Mérette C, Pato CN, Pato MT, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis CM.
    Mol Psychiatry; 2009 Aug 07; 14(8):774-85. PubMed ID: 19349958
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  • 28. Linkage of schizophrenia with chromosome 1q32 in Korean multiplex families.
    Jang YL, Kim JW, Lee YS, Park DY, Cho EY, Jeun HO, Lee D, Hong KS.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Apr 05; 144B(3):279-84. PubMed ID: 17171664
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  • 29. Genome-wide and interaction linkage scan for nonsyndromic cleft lip with or without cleft palate in two multiplex families in Shenyang, China.
    Wang Y, Li X, Zhu WL, Guo JZ, Song XM, Li SQ, Li Y.
    Biomed Environ Sci; 2010 Oct 05; 23(5):363-70. PubMed ID: 21112484
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  • 30. Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample.
    Alkelai A, Lupoli S, Greenbaum L, Giegling I, Kohn Y, Sarner-Kanyas K, Ben-Asher E, Lancet D, Rujescu D, Macciardi F, Lerer B.
    FASEB J; 2011 Nov 05; 25(11):4011-23. PubMed ID: 21795503
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  • 31. Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.
    Fallin MD, Lasseter VK, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Liang KY, Pulver AE.
    Am J Hum Genet; 2003 Sep 05; 73(3):601-11. PubMed ID: 12929083
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  • 32. An autosomal genome-wide scan for loci linked to pre-diabetic phenotypes in nondiabetic Chinese subjects from the Stanford Asia-Pacific Program of Hypertension and Insulin Resistance Family Study.
    Chiu YF, Chuang LM, Hsiao CF, Hung YJ, Lin MW, Chen YT, Grove J, Jorgenson E, Quertermous T, Risch N, Hsiung CA.
    Diabetes; 2005 Apr 05; 54(4):1200-6. PubMed ID: 15793262
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  • 34. Genome-wide linkage and association scans for pulse pressure in Chinese twins.
    Zhang D, Pang Z, Li S, Jiang W, Wang S, Thomassen M, Hjelmborg JV, Kruse TA, Ohm Kyvik K, Christensen K, Zhu G, Tan Q.
    Hypertens Res; 2012 Nov 05; 35(11):1051-7. PubMed ID: 22763476
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  • 35. Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.
    Francks C, Tozzi F, Farmer A, Vincent JB, Rujescu D, St Clair D, Muglia P.
    Mol Psychiatry; 2010 Mar 05; 15(3):319-25. PubMed ID: 18794890
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  • 37. Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective.
    Chen WJ.
    Am J Med Genet B Neuropsychiatr Genet; 2013 Oct 05; 162B(7):636-47. PubMed ID: 24132895
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  • 38. Linkage analysis of high myopia susceptibility locus in 26 families.
    Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.
    Mol Vis; 2008 Oct 05; 14():2566-74. PubMed ID: 19122830
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  • 39. Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.
    IrmansyahDepartment of Psychiatry, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia., Schwab SG, Heriani, Handoko HY, Kusumawardhani A, Widyawati I, Amir N, Nasrun MW, Holmans P, Knapp M, Wildenauer DB.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Oct 05; 147B(7):1245-52. PubMed ID: 18449910
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  • 40. Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.
    Faraone SV, Hwu HG, Liu CM, Chen WJ, Tsuang MM, Liu SK, Shieh MH, Hwang TJ, Ou-Yang WC, Chen CY, Chen CC, Lin JJ, Chou FH, Chueh CM, Liu WM, Hall MH, Su J, Van Eerdewegh P, Tsuang MT.
    Am J Psychiatry; 2006 Oct 05; 163(10):1760-6. PubMed ID: 17012687
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