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PUBMED FOR HANDHELDS

Journal Abstract Search


311 related items for PubMed ID: 11912177

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  • 3. Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease.
    Palmer LJ, Celedón JC, Chapman HA, Speizer FE, Weiss ST, Silverman EK.
    Hum Mol Genet; 2003 May 15; 12(10):1199-210. PubMed ID: 12719384
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  • 6. Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases.
    Silverman EK, Mosley JD, Rao DC, Palmer LJ, Province MA, Elston RC, Weiss ST, Campbell EJ.
    Hum Hered; 2001 May 15; 52(4):223-32. PubMed ID: 11713419
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  • 7. A genome-wide association study of pulmonary function measures in the Framingham Heart Study.
    Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, Brandler BJ, Myers RH, Borecki IB, Silverman EK, Weiss ST, O'Connor GT.
    PLoS Genet; 2009 Mar 15; 5(3):e1000429. PubMed ID: 19300500
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  • 10. Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis.
    Silverman EK, Chapman HA, Drazen JM, Weiss ST, Rosner B, Campbell EJ, O'DONNELL WJ, Reilly JJ, Ginns L, Mentzer S, Wain J, Speizer FE.
    Am J Respir Crit Care Med; 1998 Jun 15; 157(6 Pt 1):1770-8. PubMed ID: 9620904
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  • 12. [Study of the clinical phenotype of symptomatic chronic airways disease by hierarchical cluster analysis and two-step cluster analyses].
    Ning P, Guo YF, Sun TY, Zhang HS, Chai D, Li XM.
    Zhonghua Nei Ke Za Zhi; 2016 Sep 01; 55(9):679-83. PubMed ID: 27586974
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  • 13. A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.
    Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E.
    Am J Hum Genet; 2001 Jul 01; 69(1):96-105. PubMed ID: 11389481
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  • 14. 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
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  • 15. Transforming growth factor-beta receptor-3 is associated with pulmonary emphysema.
    Hersh CP, Hansel NN, Barnes KC, Lomas DA, Pillai SG, Coxson HO, Mathias RA, Rafaels NM, Wise RA, Connett JE, Klanderman BJ, Jacobson FL, Gill R, Litonjua AA, Sparrow D, Reilly JJ, Silverman EK, ICGN Investigators.
    Am J Respir Cell Mol Biol; 2009 Sep 08; 41(3):324-31. PubMed ID: 19131638
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  • 16. 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 08; 23(5):363-70. PubMed ID: 21112484
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  • 17. 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 Oct 08; 7(6):397-405. PubMed ID: 16024971
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  • 18. 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
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  • 19. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics.
    Lee JH, Mayeux R, Mayo D, Mo J, Santana V, Williamson J, Flaquer A, Ciappa A, Rondon H, Estevez P, Lantigua R, Kawarai T, Toulina A, Medrano M, Torres M, Stern Y, Tycko B, Rogaeva E, St George-Hyslop P, Knowles JA.
    Mol Psychiatry; 2004 Nov 15; 9(11):1042-51. PubMed ID: 15241431
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  • 20. Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.
    Celedón JC, Soto-Quiros ME, Avila L, Lake SL, Liang C, Fournier E, Spesny M, Hersh CP, Sylvia JS, Hudson TJ, Verner A, Klanderman BJ, Freimer NB, Silverman EK, Weiss ST.
    Hum Genet; 2007 Jan 15; 120(5):691-9. PubMed ID: 17024367
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