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Items: 1 to 20 of 129

1.

Impact of non-linear smoking effects on the identification of gene-by-smoking interactions in COPD genetics studies.

Castaldi PJ, Demeo DL, Hersh CP, Lomas DA, Soerheim IC, Gulsvik A, Bakke P, Rennard S, Pare P, Vestbo J; AATGM Investigators.; ICGN Investigators., Silverman EK.

Thorax. 2011 Oct;66(10):903-9. doi: 10.1136/thx.2010.146118. Epub 2010 Dec 16.

2.

Relationship of vitamin D binding protein polymorphisms and lung function in Korean chronic obstructive pulmonary disease.

Jung JY, Choi DP, Won S, Lee Y, Shin JH, Kim YS, Kim SK, Oh YM, Suh I, Lee SD.

Yonsei Med J. 2014 Sep;55(5):1318-25. doi: 10.3349/ymj.2014.55.5.1318.

3.

Lower FEV1 in non-COPD, nonasthmatic subjects: association with smoking, annual decline in FEV1, total IgE levels, and TSLP genotypes.

Masuko H, Sakamoto T, Kaneko Y, Iijima H, Naito T, Noguchi E, Hirota T, Tamari M, Hizawa N.

Int J Chron Obstruct Pulmon Dis. 2011;6:181-9. doi: 10.2147/COPD.S16383. Epub 2011 Mar 2.

4.

α₁-Antitrypsin protease inhibitor MZ heterozygosity is associated with airflow obstruction in two large cohorts.

Sørheim IC, Bakke P, Gulsvik A, Pillai SG, Johannessen A, Gaarder PI, Campbell EJ, Agustí A, Calverley PM, Donner CF, Make BJ, Rennard SI, Vestbo J, Wouters EF, Paré PD, Levy RD, Coxson HO, Lomas DA, Hersh CP, Silverman EK.

Chest. 2010 Nov;138(5):1125-32. doi: 10.1378/chest.10-0746. Epub 2010 Jul 1.

5.

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. Epub 2007 Aug 9.

6.

Gender differences in COPD: are women more susceptible to smoking effects than men?

Sørheim IC, Johannessen A, Gulsvik A, Bakke PS, Silverman EK, DeMeo DL.

Thorax. 2010 Jun;65(6):480-5. doi: 10.1136/thx.2009.122002.

PMID:
20522842
7.

Genetic variation in antioxidant enzymes, cigarette smoking, and longitudinal change in lung function.

Tang W, Bentley AR, Kritchevsky SB, Harris TB, Newman AB, Bauer DC, Meibohm B, Cassano PA; Health ABC study..

Free Radic Biol Med. 2013 Oct;63:304-12. doi: 10.1016/j.freeradbiomed.2013.05.016. Epub 2013 May 17.

8.

Genome-wide association study of smoking behaviours in patients with COPD.

Siedlinski M, Cho MH, Bakke P, Gulsvik A, Lomas DA, Anderson W, Kong X, Rennard SI, Beaty TH, Hokanson JE, Crapo JD, Silverman EK; COPDGene Investigators.; ECLIPSE Investigators..

Thorax. 2011 Oct;66(10):894-902. doi: 10.1136/thoraxjnl-2011-200154. Epub 2011 Jun 16.

9.

Association of IREB2 and CHRNA3/5 polymorphisms with COPD and COPD-related phenotypes in a Chinese Han population.

Zhou H, Yang J, Li D, Xiao J, Wang B, Wang L, Ma C, Xu S, Ou X, Feng Y.

J Hum Genet. 2012 Nov 26;57(11):738-46. doi: 10.1038/jhg.2012.104. Epub 2012 Aug 23.

PMID:
22914670
10.

Loci identified by genome-wide association studies influence different disease-related phenotypes in chronic obstructive pulmonary disease.

Pillai SG, Kong X, Edwards LD, Cho MH, Anderson WH, Coxson HO, Lomas DA, Silverman EK; ECLIPSE and ICGN Investigators..

Am J Respir Crit Care Med. 2010 Dec 15;182(12):1498-505. doi: 10.1164/rccm.201002-0151OC. Epub 2010 Jul 23.

11.

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;52(4):223-32.

PMID:
11713419
12.

PLAUR polymorphisms and lung function in UK smokers.

Stewart CE, Hall IP, Parker SG, Moffat MF, Wardlaw AJ, Connolly MJ, Ruse C, Sayers I.

BMC Med Genet. 2009 Oct 31;10:112. doi: 10.1186/1471-2350-10-112.

13.

Effect of gene environment interactions on lung function and cardiovascular disease in COPD.

Hackett TL, Stefanowicz D, Aminuddin F, Sin DD, Connett JE, Anthonisen NR, Paré PD, Sandford AJ.

Int J Chron Obstruct Pulmon Dis. 2011;6:277-87. doi: 10.2147/COPD.S18279. Epub 2011 May 10.

14.

Genetic variants in HHIP are associated with FEV1 in subjects with chronic obstructive pulmonary disease.

Kim WJ, Oh YM, Lee JH, Park CS, Park SW, Park JS, Lee SD.

Respirology. 2013 Nov;18(8):1202-9. doi: 10.1111/resp.12139.

PMID:
23731023
15.
16.

Variable DNA methylation is associated with chronic obstructive pulmonary disease and lung function.

Qiu W, Baccarelli A, Carey VJ, Boutaoui N, Bacherman H, Klanderman B, Rennard S, Agusti A, Anderson W, Lomas DA, DeMeo DL.

Am J Respir Crit Care Med. 2012 Feb 15;185(4):373-81. doi: 10.1164/rccm.201108-1382OC. Epub 2011 Dec 8.

17.

Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis.

Hersh CP, Dahl M, Ly NP, Berkey CS, Nordestgaard BG, Silverman EK.

Thorax. 2004 Oct;59(10):843-9. Review.

18.

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.

Hancock DB, Soler Artigas M, Gharib SA, Henry A, Manichaikul A, Ramasamy A, Loth DW, Imboden M, Koch B, McArdle WL, Smith AV, Smolonska J, Sood A, Tang W, Wilk JB, Zhai G, Zhao JH, Aschard H, Burkart KM, Curjuric I, Eijgelsheim M, Elliott P, Gu X, Harris TB, Janson C, Homuth G, Hysi PG, Liu JZ, Loehr LR, Lohman K, Loos RJ, Manning AK, Marciante KD, Obeidat M, Postma DS, Aldrich MC, Brusselle GG, Chen TH, Eiriksdottir G, Franceschini N, Heinrich J, Rotter JI, Wijmenga C, Williams OD, Bentley AR, Hofman A, Laurie CC, Lumley T, Morrison AC, Joubert BR, Rivadeneira F, Couper DJ, Kritchevsky SB, Liu Y, Wjst M, Wain LV, Vonk JM, Uitterlinden AG, Rochat T, Rich SS, Psaty BM, O'Connor GT, North KE, Mirel DB, Meibohm B, Launer LJ, Khaw KT, Hartikainen AL, Hammond CJ, Gläser S, Marchini J, Kraft P, Wareham NJ, Völzke H, Stricker BH, Spector TD, Probst-Hensch NM, Jarvis D, Jarvelin MR, Heckbert SR, Gudnason V, Boezen HM, Barr RG, Cassano PA, Strachan DP, Fornage M, Hall IP, Dupuis J, Tobin MD, London SJ.

PLoS Genet. 2012;8(12):e1003098. doi: 10.1371/journal.pgen.1003098. Epub 2012 Dec 20.

19.
20.

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. doi: 10.1159/000164397. Epub 2008 Oct 17.

PMID:
18931508

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