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125 related items for PubMed ID: 19552595

  • 1. A genome-wide scan for the Sasang constitution in a Korean family suggests significant linkage at chromosomes 8q11.22-23 and 11q22.1-3.
    Won HH, Lee S, Jang E, Kim KK, Park YK, Kim YJ, Kim YS, Kim BY, Kim JY, Kim JW.
    J Altern Complement Med; 2009 Jul; 15(7):765-9. PubMed ID: 19552595
    [Abstract] [Full Text] [Related]

  • 2. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.
    Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M.
    Am J Hum Genet; 2004 Dec; 75(6):998-1014. PubMed ID: 15497111
    [Abstract] [Full Text] [Related]

  • 3. Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.
    Hong KS, Won HH, Cho EY, Jeun HO, Cho SS, Lee YS, Park DY, Jang YL, Choi KS, Lee D, Kim MJ, Kim S, Han WS, Kim JW.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Jul 05; 150B(5):647-52. PubMed ID: 18980222
    [Abstract] [Full Text] [Related]

  • 4. Genome-wide association analysis of Sasang constitution in the Korean population.
    Kim BY, Jin HJ, Kim JY.
    J Altern Complement Med; 2012 Mar 05; 18(3):262-9. PubMed ID: 22394158
    [Abstract] [Full Text] [Related]

  • 5. Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea.
    Suh YJ, Kim S, Kim SH, Park J, Lim HA, Park HJ, Choi H, Ng D, Lee MK, Nam M.
    J Korean Med Sci; 2013 Mar 05; 28(3):415-23. PubMed ID: 23487342
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.
    Ryu S, Won HH, Oh S, Kim JW, Park T, Cho EY, Cho Y, Park DY, Lee YS, Kwon JS, Hong KS.
    Psychiatry Res; 2013 Dec 30; 210(3):756-60. PubMed ID: 24035701
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22.
    Wang X, Li X, Zhang YB, Zhang F, Sun L, Lin J, Wang DM, Wang LY.
    PLoS One; 2011 Dec 30; 6(10):e24838. PubMed ID: 22022364
    [Abstract] [Full Text] [Related]

  • 8. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.
    Ammar M, Bouchlaka-Souissi C, Helms CA, Zaraa I, Jordan CT, Anbunathan H, Bouhaha R, Kouidhi S, Doss N, Dhaoui R, Ben Osman A, Ben Ammar El Gaied A, Marrakchi R, Mokni M, Bowcock AM.
    Br J Dermatol; 2013 Mar 30; 168(3):583-7. PubMed ID: 23013406
    [Abstract] [Full Text] [Related]

  • 9. High-resolution genome-wide linkage mapping identifies susceptibility loci for BMI in the Chinese population.
    Zhang DF, Pang Z, Li S, Thomassen M, Wang S, Jiang W, Hjelmborg Jv, Kruse TA, Kyvik KO, Christensen K, Tan Q.
    Obesity (Silver Spring); 2012 Apr 30; 20(4):830-3. PubMed ID: 21273998
    [Abstract] [Full Text] [Related]

  • 10. An international collaborative family-based whole-genome linkage scan for high-grade myopia.
    Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, Young TL.
    Invest Ophthalmol Vis Sci; 2009 Jul 30; 50(7):3116-27. PubMed ID: 19324860
    [Abstract] [Full Text] [Related]

  • 11. Pathways involved in sasang constitution from genome-wide analysis in a Korean population.
    Kim BY, Yu SG, Kim JY, Song KH.
    J Altern Complement Med; 2012 Nov 30; 18(11):1070-80. PubMed ID: 22889377
    [Abstract] [Full Text] [Related]

  • 12. Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.
    Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T, Japanese Genetic Research Group for Eating Disorders (JGRED), Shirasawa S.
    J Hum Genet; 2009 Sep 30; 54(9):531-7. PubMed ID: 19680270
    [Abstract] [Full Text] [Related]

  • 13. [Genome-wide linkage scan for an ethnic Han Chinese pedigree affected with schizophrenia].
    Zhao LS, Wang YC, Wei JX, Liu X, Yang ZX, Li T, Chen XG, Ma XH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 30; 30(1):5-8. PubMed ID: 23450469
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.
    Ichihara S, Yamamoto K, Asano H, Nakatochi M, Sukegawa M, Ichihara G, Izawa H, Hirashiki A, Takatsu F, Umeda H, Iwase M, Inagaki H, Hirayama H, Sone T, Nishigaki K, Minatoguchi S, Cho MC, Jang Y, Kim HS, Park JE, Tada-Oikawa S, Kitajima H, Matsubara T, Sunagawa K, Shimokawa H, Kimura A, Lee JY, Murohara T, Inoue I, Yokota M.
    Circ Cardiovasc Genet; 2013 Dec 15; 6(6):569-78. PubMed ID: 24122612
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 35(11):1051-7. PubMed ID: 22763476
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population.
    Kim JW, Lee YS, Cho EY, Jang YL, Park DY, Choi KS, Jeun HO, Cho SH, Jang SY, Hong KS.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):281-6. PubMed ID: 16526041
    [Abstract] [Full Text] [Related]

  • 19. [A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].
    Yu ZQ, Li YB, Huang CX, Chu RY, Hu DN, Shen ZH, Huang W.
    Zhonghua Yan Ke Za Zhi; 2007 Mar 05; 43(3):233-8. PubMed ID: 17605906
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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