358 related articles for article (PubMed ID: 26736064)
21. Heritability of lung function in severe alpha-1 antitrypsin deficiency.
DeMeo DL; Campbell EJ; Brantly ML; Barker AF; Eden E; McElvaney NG; Rennard SI; Stocks JM; Stoller JK; Strange C; Turino G; Sandhaus RA; Silverman EK
Hum Hered; 2009; 67(1):38-45. PubMed ID: 18931508
[TBL] [Abstract][Full Text] [Related]
22. IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease.
Lee JH; Cho MH; Hersh CP; McDonald ML; Wells JM; Dransfield MT; Bowler RP; Lynch DA; Lomas DA; Crapo JD; Silverman EK;
Am J Respir Cell Mol Biol; 2015 Mar; 52(3):365-76. PubMed ID: 25101718
[TBL] [Abstract][Full Text] [Related]
23. A genome-wide association study of chronic obstructive pulmonary disease in Hispanics.
Chen W; Brehm JM; Manichaikul A; Cho MH; Boutaoui N; Yan Q; Burkart KM; Enright PL; Rotter JI; Petersen H; Leng S; Obeidat M; Bossé Y; Brandsma CA; Hao K; Rich SS; Powell R; Avila L; Soto-Quiros M; Silverman EK; Tesfaigzi Y; Barr RG; Celedón JC
Ann Am Thorac Soc; 2015 Mar; 12(3):340-8. PubMed ID: 25584925
[TBL] [Abstract][Full Text] [Related]
24. Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.
Kim DK; Cho MH; Hersh CP; Lomas DA; Miller BE; Kong X; Bakke P; Gulsvik A; Agustí A; Wouters E; Celli B; Coxson H; Vestbo J; MacNee W; Yates JC; Rennard S; Litonjua A; Qiu W; Beaty TH; Crapo JD; Riley JH; Tal-Singer R; Silverman EK;
Am J Respir Crit Care Med; 2012 Dec; 186(12):1238-47. PubMed ID: 23144326
[TBL] [Abstract][Full Text] [Related]
25. Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene.
Saferali A; Yun JH; Parker MM; Sakornsakolpat P; Chase RP; Lamb A; Hobbs BD; Boezen MH; Dai X; de Jong K; Beaty TH; Wei W; Zhou X; Silverman EK; Cho MH; Castaldi PJ; Hersh CP; ;
PLoS Genet; 2019 Jul; 15(7):e1008229. PubMed ID: 31269066
[TBL] [Abstract][Full Text] [Related]
26. Genetic Association and Risk Scores in a Chronic Obstructive Pulmonary Disease Meta-analysis of 16,707 Subjects.
Busch R; Hobbs BD; Zhou J; Castaldi PJ; McGeachie MJ; Hardin ME; Hawrylkiewicz I; Sliwinski P; Yim JJ; Kim WJ; Kim DK; Agusti A; Make BJ; Crapo JD; Calverley PM; Donner CF; Lomas DA; Wouters EF; Vestbo J; Tal-Singer R; Bakke P; Gulsvik A; Litonjua AA; Sparrow D; Paré PD; Levy RD; Rennard SI; Beaty TH; Hokanson J; Silverman EK; Cho MH; ; ; ;
Am J Respir Cell Mol Biol; 2017 Jul; 57(1):35-46. PubMed ID: 28170284
[TBL] [Abstract][Full Text] [Related]
27. IL10 polymorphisms are associated with airflow obstruction in severe alpha1-antitrypsin deficiency.
Demeo DL; Campbell EJ; Barker AF; Brantly ML; Eden E; McElvaney NG; Rennard SI; Sandhaus RA; Stocks JM; Stoller JK; Strange C; Turino G; Silverman EK
Am J Respir Cell Mol Biol; 2008 Jan; 38(1):114-20. PubMed ID: 17690329
[TBL] [Abstract][Full Text] [Related]
28. Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution.
Boueiz A; Lutz SM; Cho MH; Hersh CP; Bowler RP; Washko GR; Halper-Stromberg E; Bakke P; Gulsvik A; Laird NM; Beaty TH; Coxson HO; Crapo JD; Silverman EK; Castaldi PJ; DeMeo DL;
Am J Respir Crit Care Med; 2017 Mar; 195(6):757-771. PubMed ID: 27669027
[TBL] [Abstract][Full Text] [Related]
29. Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease.
McDonald ML; Cho MH; Sørheim IC; Lutz SM; Castaldi PJ; Lomas DA; Coxson HO; Edwards LD; MacNee W; Vestbo J; Yates JC; Agusti A; Calverley PM; Celli B; Crim C; Rennard SI; Wouters EF; Bakke P; Tal-Singer R; Miller BE; Gulsvik A; Casaburi R; Wells JM; Regan EA; Make BJ; Hokanson JE; Lange C; Crapo JD; Beaty TH; Silverman EK; Hersh CP;
Am J Respir Cell Mol Biol; 2014 Nov; 51(5):678-87. PubMed ID: 24825563
[TBL] [Abstract][Full Text] [Related]
30. Translating Lung Function Genome-Wide Association Study (GWAS) Findings: New Insights for Lung Biology.
Kheirallah AK; Miller S; Hall IP; Sayers I
Adv Genet; 2016; 93():57-145. PubMed ID: 26915270
[TBL] [Abstract][Full Text] [Related]
31. Relation of functional characteristics and serum alpha-1-antitrypsin (AAT) concentration in patients with PiMM phenotype and chronic obstructive pulmonary disease (COPD).
Zarić B; Stojčević J; Andrijević L; Andrijević I; Kuruc V; Veselinović I; Salatić I
Eur J Intern Med; 2011 Dec; 22(6):603-6. PubMed ID: 22075288
[TBL] [Abstract][Full Text] [Related]
32. [Genetics risk factors in chronic obstructive pulmonary disease].
Makowska M; Romanowicz H; Kulig A; Smolarz B
Pol Merkur Lekarski; 2010 Apr; 28(166):302-6. PubMed ID: 20491342
[TBL] [Abstract][Full Text] [Related]
33. The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility.
Castaldi PJ; Cho MH; Litonjua AA; Bakke P; Gulsvik A; Lomas DA; Anderson W; Beaty TH; Hokanson JE; Crapo JD; Laird N; Silverman EK;
Am J Respir Cell Mol Biol; 2011 Dec; 45(6):1147-53. PubMed ID: 21659657
[TBL] [Abstract][Full Text] [Related]
34. Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.
Jackson VE; Ntalla I; Sayers I; Morris R; Whincup P; Casas JP; Amuzu A; Choi M; Dale C; Kumari M; Engmann J; Kalsheker N; Chappell S; Guetta-Baranes T; McKeever TM; Palmer CN; Tavendale R; Holloway JW; Sayer AA; Dennison EM; Cooper C; Bafadhel M; Barker B; Brightling C; Bolton CE; John ME; Parker SG; Moffat MF; Wardlaw AJ; Connolly MJ; Porteous DJ; Smith BH; Padmanabhan S; Hocking L; Stirrups KE; Deloukas P; Strachan DP; Hall IP; Tobin MD; Wain LV
Thorax; 2016 Jun; 71(6):501-9. PubMed ID: 26917578
[TBL] [Abstract][Full Text] [Related]
35. Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays.
Castaldi PJ; Guo F; Qiao D; Du F; Naing ZZC; Li Y; Pham B; Mikkelsen TS; Cho MH; Silverman EK; Zhou X
Am J Respir Crit Care Med; 2019 Jan; 199(1):52-61. PubMed ID: 30079747
[TBL] [Abstract][Full Text] [Related]
36. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
Petrovski S; Todd JL; Durheim MT; Wang Q; Chien JW; Kelly FL; Frankel C; Mebane CM; Ren Z; Bridgers J; Urban TJ; Malone CD; Finlen Copeland A; Brinkley C; Allen AS; O'Riordan T; McHutchison JG; Palmer SM; Goldstein DB
Am J Respir Crit Care Med; 2017 Jul; 196(1):82-93. PubMed ID: 28099038
[TBL] [Abstract][Full Text] [Related]
37. Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.
Zhu Z; Wang X; Li X; Lin Y; Shen S; Liu CL; Hobbs BD; Hasegawa K; Liang L; ; Boezen HM; Camargo CA; Cho MH; Christiani DC
Respir Res; 2019 Apr; 20(1):64. PubMed ID: 30940143
[TBL] [Abstract][Full Text] [Related]
38. Genetic profiling for disease stratification in chronic obstructive pulmonary disease and asthma.
Rathnayake SNH; Van den Berge M; Faiz A
Curr Opin Pulm Med; 2019 May; 25(3):317-322. PubMed ID: 30762612
[TBL] [Abstract][Full Text] [Related]
39. Familial risks for chronic obstructive pulmonary disease among siblings based on hospitalisations in Sweden.
Hemminki K; Li X; Sundquist K; Sundquist J
J Epidemiol Community Health; 2008 May; 62(5):398-401. PubMed ID: 18413451
[TBL] [Abstract][Full Text] [Related]
40. Genetics of COPD and emphysema.
Wan ES; Silverman EK
Chest; 2009 Sep; 136(3):859-866. PubMed ID: 19736190
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]