-
1
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
1 Hindorff, L.A., Sethupathy, P., Junkins, H.A., et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci U S A 106 (2009), 9362–9367.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
-
2
-
-
79959344460
-
Expert Panel Report 3 (EPR-3)—Guidelines for the Diagnosis and Management of Asthma, Summary Report 2007
-
2 National Asthma Education and Prevention Program. Expert Panel Report 3 (EPR-3)—Guidelines for the Diagnosis and Management of Asthma, Summary Report 2007. J Allergy Clin Immunol 120:5 suppl 1 (2007), S94–S138.
-
(2007)
J Allergy Clin Immunol
, vol.120
, Issue.5
, pp. S94-S138
-
-
-
3
-
-
35348931194
-
National surveillance for asthma—United States 1980-2004
-
3 Moorman, J.E., Rudd, R.A., Johnson, C.A., et al. National surveillance for asthma—United States 1980-2004. Morbidity and Mortality Weekly Report 56 (2007), 1–54.
-
(2007)
Morbidity and Mortality Weekly Report
, vol.56
, pp. 1-54
-
-
Moorman, J.E.1
Rudd, R.A.2
Johnson, C.A.3
-
4
-
-
0035078622
-
Increasing U.S. asthma mortality rates: who is really dying?
-
4 Moorman, J.E., Mannino, D.M., Increasing U.S. asthma mortality rates: who is really dying?. J Asthma 38 (2001), 65–71.
-
(2001)
J Asthma
, vol.38
, pp. 65-71
-
-
Moorman, J.E.1
Mannino, D.M.2
-
5
-
-
84944166696
-
National surveillance of asthma: United States 2001-2010. National Center for Health Statistics
-
5 Moorman, J.E., Akinbami, L.J., Bailey, C.M., et al. National surveillance of asthma: United States 2001-2010. National Center for Health Statistics. Vital Health Stat 3:35 (2012), 1–67.
-
(2012)
Vital Health Stat
, vol.3
, Issue.35
, pp. 1-67
-
-
Moorman, J.E.1
Akinbami, L.J.2
Bailey, C.M.3
-
6
-
-
33751213587
-
The asthma epidemic
-
6 Eder, W., Ege, M.J., von Mutius, E., The asthma epidemic. N Engl J Med 355 (2006), 2226–2235.
-
(2006)
N Engl J Med
, vol.355
, pp. 2226-2235
-
-
Eder, W.1
Ege, M.J.2
von Mutius, E.3
-
7
-
-
0025598333
-
Genetics of asthma and hay fever in Australian twins
-
7 Duffy, D.L., Martin, N.G., Battistutta, D., Hopper, J.L., Mathews, J.D., Genetics of asthma and hay fever in Australian twins. Am Rev Respir Dis 142:6 Pt 1 (1990), 1351–1358.
-
(1990)
Am Rev Respir Dis
, vol.142
, Issue.6
, pp. 1351-1358
-
-
Duffy, D.L.1
Martin, N.G.2
Battistutta, D.3
Hopper, J.L.4
Mathews, J.D.5
-
8
-
-
34547216747
-
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
-
8 Moffatt, M.F., Kabesch, M., Liang, L., et al. Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature 448 (2007), 470–473.
-
(2007)
Nature
, vol.448
, pp. 470-473
-
-
Moffatt, M.F.1
Kabesch, M.2
Liang, L.3
-
9
-
-
84905595372
-
Genome-wide association study and admixture mapping identify different asthma-associated loci in Latinos: the Genes-environments & Admixture in Latino Americans study
-
9 Galanter, J.M., Gignoux, C.R., Torgerson, D.G., et al. Genome-wide association study and admixture mapping identify different asthma-associated loci in Latinos: the Genes-environments & Admixture in Latino Americans study. J Allergy Clin Immunol 134 (2014), 295–305.
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 295-305
-
-
Galanter, J.M.1
Gignoux, C.R.2
Torgerson, D.G.3
-
10
-
-
84901754015
-
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
-
10 Ferreira, M.A., Matheson, M.C., Tang, C.S., et al. Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. J Allergy Clin Immunol 133 (2014), 1564–1571.
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1564-1571
-
-
Ferreira, M.A.1
Matheson, M.C.2
Tang, C.S.3
-
11
-
-
84891372721
-
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
-
11 Bønnelykke, K., Sleiman, P., Nielsen, K., et al. A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations. Nat Genet 46 (2014), 51–55.
-
(2014)
Nat Genet
, vol.46
, pp. 51-55
-
-
Bønnelykke, K.1
Sleiman, P.2
Nielsen, K.3
-
12
-
-
84870167525
-
HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults
-
12 Lasky-Su, J., Himes, B., Raby, B., et al. HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults. Clin Exp Allergy 42 (2012), 1724–1733.
-
(2012)
Clin Exp Allergy
, vol.42
, pp. 1724-1733
-
-
Lasky-Su, J.1
Himes, B.2
Raby, B.3
-
13
-
-
84869116213
-
Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases
-
13 Li, X., Ampleford, E.J., Howard, T.D., et al. Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. J Allergy Clin Immunol 130 (2012), 861–868.
-
(2012)
J Allergy Clin Immunol
, vol.130
, pp. 861-868
-
-
Li, X.1
Ampleford, E.J.2
Howard, T.D.3
-
14
-
-
84865291081
-
Genome-wide association study to identify genetic determinants of severe asthma
-
14 Wan, Y., Shrine, N., Artigas, M.S., et al. Genome-wide association study to identify genetic determinants of severe asthma. Thorax 67 (2012), 762–768.
-
(2012)
Thorax
, vol.67
, pp. 762-768
-
-
Wan, Y.1
Shrine, N.2
Artigas, M.S.3
-
15
-
-
83755174039
-
Genome-wide association study identifies PERLD1 as asthma candidate gene
-
15 Anantharaman, R., Andiappan, A.K., Nilkanth, P.P., Suri, B.K., Wang, D.Y., Chew, F.T., Genome-wide association study identifies PERLD1 as asthma candidate gene. BMC Med Genet, 12, 2011, 170.
-
(2011)
BMC Med Genet
, vol.12
, pp. 170
-
-
Anantharaman, R.1
Andiappan, A.K.2
Nilkanth, P.P.3
Suri, B.K.4
Wang, D.Y.5
Chew, F.T.6
-
16
-
-
80052721297
-
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
-
16 Ferreira, M.A., Matheson, M.C., Duffy, D.L., et al. Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet 378 (2011), 1006–1014.
-
(2011)
Lancet
, vol.378
, pp. 1006-1014
-
-
Ferreira, M.A.1
Matheson, M.C.2
Duffy, D.L.3
-
17
-
-
80052273202
-
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population
-
17 Hirota, T., Takahashi, A., Kubo, M., et al. Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population. Nat Genet 43 (2011), 893–896.
-
(2011)
Nat Genet
, vol.43
, pp. 893-896
-
-
Hirota, T.1
Takahashi, A.2
Kubo, M.3
-
18
-
-
80052259316
-
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations
-
18 Torgerson, D.G., Ampleford, E.J., Chiu, G.Y., et al. Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet 43 (2011), 887–892.
-
(2011)
Nat Genet
, vol.43
, pp. 887-892
-
-
Torgerson, D.G.1
Ampleford, E.J.2
Chiu, G.Y.3
-
19
-
-
79960942399
-
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations
-
19 Noguchi, E., Sakamoto, H., Hirota, T., et al. Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations. PLoS Genet, 7, 2011, e1002170.
-
(2011)
PLoS Genet
, vol.7
, pp. e1002170
-
-
Noguchi, E.1
Sakamoto, H.2
Hirota, T.3
-
20
-
-
79952745551
-
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia
-
20 Ferreira, M.A., McRae, A.F., Medland, S.E., et al. Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. Eur J Hum Genet 19 (2010), 458–464.
-
(2010)
Eur J Hum Genet
, vol.19
, pp. 458-464
-
-
Ferreira, M.A.1
McRae, A.F.2
Medland, S.E.3
-
21
-
-
77957113600
-
A large-scale, consortium-based genomewide association study of asthma
-
21 Moffatt, M.F., Gut, I.G., Demenais, F., et al. A large-scale, consortium-based genomewide association study of asthma. N Engl J Med 363 (2010), 1211–1221.
-
(2010)
N Engl J Med
, vol.363
, pp. 1211-1221
-
-
Moffatt, M.F.1
Gut, I.G.2
Demenais, F.3
-
22
-
-
74049129976
-
Variants of DENND1B associated with asthma in children
-
22 Sleiman, P.M., Flory, J., Imielinski, M., et al. Variants of DENND1B associated with asthma in children. N Engl J Med 362 (2010), 36–44.
-
(2010)
N Engl J Med
, vol.362
, pp. 36-44
-
-
Sleiman, P.M.1
Flory, J.2
Imielinski, M.3
-
23
-
-
73249127836
-
A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS)
-
23 Castro-Giner, F., Bustamante, M., González, J.R., et al. A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS). BMC Med Genet, 10, 2009, 128.
-
(2009)
BMC Med Genet
, vol.10
, pp. 128
-
-
Castro-Giner, F.1
Bustamante, M.2
González, J.R.3
-
24
-
-
65549123032
-
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene
-
24 Himes, B.E., Hunninghake, G.M., Baurley, J.W., et al. Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Am J Hum Genet 84 (2009), 581–593.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 581-593
-
-
Himes, B.E.1
Hunninghake, G.M.2
Baurley, J.W.3
-
25
-
-
77957786819
-
PDE11A associations with asthma: results of a genome-wide association scan
-
25 DeWan, A.T., Triche, E.W., Xu, X., et al. PDE11A associations with asthma: results of a genome-wide association scan. J Allergy Clin Immunol 126 (2010), 871–873.
-
(2010)
J Allergy Clin Immunol
, vol.126
, pp. 871-873
-
-
DeWan, A.T.1
Triche, E.W.2
Xu, X.3
-
26
-
-
61349089164
-
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
-
26 Gudbjartsson, D.F., Bjornsdottir, U.S., Halapi, E., et al. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat Genet 41 (2009), 342–347.
-
(2009)
Nat Genet
, vol.41
, pp. 342-347
-
-
Gudbjartsson, D.F.1
Bjornsdottir, U.S.2
Halapi, E.3
-
27
-
-
84862817980
-
Genome-wide association study of lung function decline in adults with and without asthma
-
27 Imboden, M., Bouzigon, E., Curjuric, I., et al. Genome-wide association study of lung function decline in adults with and without asthma. J Allergy Clin Immunol 129 (2012), 1218–1228.
-
(2012)
J Allergy Clin Immunol
, vol.129
, pp. 1218-1228
-
-
Imboden, M.1
Bouzigon, E.2
Curjuric, I.3
-
28
-
-
42249103640
-
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function
-
28 Ober, C., Tan, Z., Sun, Y., et al. Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. N Engl J Med 358 (2008), 1682–1691.
-
(2008)
N Engl J Med
, vol.358
, pp. 1682-1691
-
-
Ober, C.1
Tan, Z.2
Sun, Y.3
-
29
-
-
84875632468
-
Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population
-
29 Park, B.L., Kim, T.-H., Kim, J.-H., et al. Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population. Hum Genet 132 (2013), 313–321.
-
(2013)
Hum Genet
, vol.132
, pp. 313-321
-
-
Park, B.L.1
Kim, T.-H.2
Kim, J.-H.3
-
30
-
-
84896732436
-
Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics
-
30 Wu, A.C., Himes, B.E., Lasky-Su, J., et al. Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics. J Allergy Clin Immunol 133 (2014), 723–728.
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 723-728
-
-
Wu, A.C.1
Himes, B.E.2
Lasky-Su, J.3
-
31
-
-
84862585029
-
Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus
-
31 Tantisira, K.G., Damask, A., Szefler, S.J., et al. Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus. Am J Respir Crit Care Med 185 (2012), 1286–1291.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 1286-1291
-
-
Tantisira, K.G.1
Damask, A.2
Szefler, S.J.3
-
32
-
-
80053370268
-
Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma
-
32 Tantisira, K.G., Lasky-Su, J., Harada, M., et al. Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma. N Engl J Med 365 (2011), 1173–1183.
-
(2011)
N Engl J Med
, vol.365
, pp. 1173-1183
-
-
Tantisira, K.G.1
Lasky-Su, J.2
Harada, M.3
-
33
-
-
0034443957
-
Heterogeneity of therapeutic responses in asthma
-
33 Drazen, J.M., Silverman, E.K., Lee, T.H., Heterogeneity of therapeutic responses in asthma. Br Med Bull 56 (2000), 1054–1070.
-
(2000)
Br Med Bull
, vol.56
, pp. 1054-1070
-
-
Drazen, J.M.1
Silverman, E.K.2
Lee, T.H.3
-
34
-
-
66749141807
-
Systemic manifestations and comorbidities of COPD
-
34 Barnes, P., Celli, B., Systemic manifestations and comorbidities of COPD. Eur Respir J 33 (2009), 1165–1185.
-
(2009)
Eur Respir J
, vol.33
, pp. 1165-1185
-
-
Barnes, P.1
Celli, B.2
-
35
-
-
84868328280
-
Emerging genetics of COPD
-
35 Berndt, A., Leme, A.S., Shapiro, S.D., Emerging genetics of COPD. EMBO Mol Med 4 (2012), 1144–1155.
-
(2012)
EMBO Mol Med
, vol.4
, pp. 1144-1155
-
-
Berndt, A.1
Leme, A.S.2
Shapiro, S.D.3
-
36
-
-
69149102202
-
Chronic obstructive pulmonary disease in non-smokers
-
36 Salvi, S.S., Barnes, P.J., Chronic obstructive pulmonary disease in non-smokers. Lancet 374 (2009), 733–743.
-
(2009)
Lancet
, vol.374
, pp. 733-743
-
-
Salvi, S.S.1
Barnes, P.J.2
-
37
-
-
84919676397
-
Early events in the pathogenesis of chronic obstructive pulmonary disease. smoking-induced reprogramming of airway epithelial basal progenitor cells
-
37 Shaykhiev, R., Crystal, R.G., Early events in the pathogenesis of chronic obstructive pulmonary disease. smoking-induced reprogramming of airway epithelial basal progenitor cells. Ann Am Thorac Soc 11:suppl 5 (2014), S252–S258.
-
(2014)
Ann Am Thorac Soc
, vol.11
, pp. S252-S258
-
-
Shaykhiev, R.1
Crystal, R.G.2
-
38
-
-
80054693306
-
The state of genome-wide association studies in pulmonary disease: a new perspective
-
38 Todd, J.L., Goldstein, D.B., Ge, D., Christie, J., Palmer, S.M., The state of genome-wide association studies in pulmonary disease: a new perspective. Am J Respir Crit Care Med 184 (2011), 873–880.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 873-880
-
-
Todd, J.L.1
Goldstein, D.B.2
Ge, D.3
Christie, J.4
Palmer, S.M.5
-
39
-
-
84895799527
-
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis
-
39 Cho, M.H., McDonald, M.L., Zhou, X., et al. Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. Lancet Respir Med 2 (2014), 214–225.
-
(2014)
Lancet Respir Med
, vol.2
, pp. 214-225
-
-
Cho, M.H.1
McDonald, M.L.2
Zhou, X.3
-
40
-
-
84894259001
-
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study
-
40 Manichaikul, A., Hoffman, E.A., Smolonska, J., et al. Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. Am J Respir Crit Care Med 189 (2014), 408–418.
-
(2014)
Am J Respir Crit Care Med
, vol.189
, pp. 408-418
-
-
Manichaikul, A.1
Hoffman, E.A.2
Smolonska, J.3
-
41
-
-
84856337050
-
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13
-
41 Cho, M.H., Castaldi, P.J., Wan, E.S., et al. A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. Hum Mol Genet 21 (2012), 947–957.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 947-957
-
-
Cho, M.H.1
Castaldi, P.J.2
Wan, E.S.3
-
42
-
-
80051640577
-
Genome-wide association analysis of body mass in chronic obstructive pulmonary disease
-
42 Wan, E.S., Cho, M.H., Boutaoui, N., et al. Genome-wide association analysis of body mass in chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol 45 (2011), 304–310.
-
(2011)
Am J Respir Cell Mol Biol
, vol.45
, pp. 304-310
-
-
Wan, E.S.1
Cho, M.H.2
Boutaoui, N.3
-
43
-
-
77649189442
-
Variants in FAM13A are associated with chronic obstructive pulmonary disease
-
43 Cho, M.H., Boutaoui, N., Klanderman, B.J., et al. Variants in FAM13A are associated with chronic obstructive pulmonary disease. Nat Genet 42 (2010), 200–202.
-
(2010)
Nat Genet
, vol.42
, pp. 200-202
-
-
Cho, M.H.1
Boutaoui, N.2
Klanderman, B.J.3
-
44
-
-
63449101907
-
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci
-
44 Pillai, S.G., Ge, D., Zhu, G., et al. A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. PLoS Genet, 5, 2009, e1000421.
-
(2009)
PLoS Genet
, vol.5
, pp. e1000421
-
-
Pillai, S.G.1
Ge, D.2
Zhu, G.3
-
45
-
-
80053272831
-
Genome-wide association study of smoking behaviours in patients with COPD
-
45 Siedlinski, M., Cho, M.H., Bakke, P., et al. Genome-wide association study of smoking behaviours in patients with COPD. Thorax 66 (2011), 894–902.
-
(2011)
Thorax
, vol.66
, pp. 894-902
-
-
Siedlinski, M.1
Cho, M.H.2
Bakke, P.3
-
46
-
-
84870713668
-
Lung eQTLs to help reveal the molecular underpinnings of asthma
-
46 Hao, K., Bossé, Y., Nickle, D.C., et al. Lung eQTLs to help reveal the molecular underpinnings of asthma. PLoS Genet, 8, 2012, e1003029.
-
(2012)
PLoS Genet
, vol.8
, pp. e1003029
-
-
Hao, K.1
Bossé, Y.2
Nickle, D.C.3
-
47
-
-
84880043679
-
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
-
47 Noth, I., Zhang, Y., Ma, S.-F., et al. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. Lancet Respir Med 1 (2013), 309–317.
-
(2013)
Lancet Respir Med
, vol.1
, pp. 309-317
-
-
Noth, I.1
Zhang, Y.2
Ma, S.-F.3
-
48
-
-
84878686854
-
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
-
48 Fingerlin, T.E., Murphy, E., Zhang, W., et al. Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. Nat Genet 45 (2013), 613–620.
-
(2013)
Nat Genet
, vol.45
, pp. 613-620
-
-
Fingerlin, T.E.1
Murphy, E.2
Zhang, W.3
-
49
-
-
54049136464
-
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis
-
49 Mushiroda, T., Wattanapokayakit, S., Takahashi, A., et al. A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. J Med Genet 45 (2008), 654–656.
-
(2008)
J Med Genet
, vol.45
, pp. 654-656
-
-
Mushiroda, T.1
Wattanapokayakit, S.2
Takahashi, A.3
-
50
-
-
84875847895
-
Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis
-
50 Hofmann, S., Fischer, A., Nothnagel, M., et al. Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis. Eur Respir J 41 (2013), 888–900.
-
(2013)
Eur Respir J
, vol.41
, pp. 888-900
-
-
Hofmann, S.1
Fischer, A.2
Nothnagel, M.3
-
51
-
-
84868031310
-
A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1
-
51 Fischer, A., Schmid, B., Ellinghaus, D., et al. A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1. Am J Respir Crit Care Med 186 (2012), 877–885.
-
(2012)
Am J Respir Crit Care Med
, vol.186
, pp. 877-885
-
-
Fischer, A.1
Schmid, B.2
Ellinghaus, D.3
-
52
-
-
80355127123
-
A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1
-
52 Hofmann, S., Fischer, A., Till, A., et al. A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1. Eur Respir J 38 (2011), 1127–1135.
-
(2011)
Eur Respir J
, vol.38
, pp. 1127-1135
-
-
Hofmann, S.1
Fischer, A.2
Till, A.3
-
53
-
-
50449095436
-
Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis
-
53 Hofmann, S., Franke, A., Fischer, A., et al. Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. Nat Genet 40 (2008), 1103–1106.
-
(2008)
Nat Genet
, vol.40
, pp. 1103-1106
-
-
Hofmann, S.1
Franke, A.2
Fischer, A.3
-
54
-
-
53049097281
-
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2
-
54 Franke, A., Fischer, A., Nothnagel, M., et al. Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. Gastroenterology 135 (2008), 1207–1215.
-
(2008)
Gastroenterology
, vol.135
, pp. 1207-1215
-
-
Franke, A.1
Fischer, A.2
Nothnagel, M.3
-
55
-
-
80055008094
-
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
-
55 Artigas, M.S., Loth, D.W., Wain, L.V., et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet 43 (2011), 1082–1090.
-
(2011)
Nat Genet
, vol.43
, pp. 1082-1090
-
-
Artigas, M.S.1
Loth, D.W.2
Wain, L.V.3
-
56
-
-
84881669432
-
An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias
-
56 Travis, W.D., Costabel, U., Hansell, D.M., et al. An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 188 (2013), 733–748.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, pp. 733-748
-
-
Travis, W.D.1
Costabel, U.2
Hansell, D.M.3
-
57
-
-
84937066042
-
Interstitial lung disease: raising the index of suspicion in primary care
-
57 Zibrak, J.D., Price, D., Interstitial lung disease: raising the index of suspicion in primary care. NPJ Prim Care Respir Med, 24, 2014, 14054.
-
(2014)
NPJ Prim Care Respir Med
, vol.24
, pp. 14054
-
-
Zibrak, J.D.1
Price, D.2
-
58
-
-
84878576691
-
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension
-
58 Germain, M., Eyries, M., Montani, D., et al. Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension. Nat Genet 45 (2013), 518–521.
-
(2013)
Nat Genet
, vol.45
, pp. 518-521
-
-
Germain, M.1
Eyries, M.2
Montani, D.3
-
59
-
-
81455155717
-
Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia
-
59 Hadchouel, A., Durrmeyer, X., Bouzigon, E., et al. Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia. Am J Respir Crit Care Med 184 (2011), 1164–1170.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 1164-1170
-
-
Hadchouel, A.1
Durrmeyer, X.2
Bouzigon, E.3
-
60
-
-
79955144623
-
A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis
-
60 Zhang, Y., Noth, I., Garcia, J.G., Kaminski, N., A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis. N Engl J Med 364 (2011), 1576–1577.
-
(2011)
N Engl J Med
, vol.364
, pp. 1576-1577
-
-
Zhang, Y.1
Noth, I.2
Garcia, J.G.3
Kaminski, N.4
-
61
-
-
84878883513
-
Recent advances in the genetics of sarcoidosis
-
61 Spagnolo, P., Grunewald, J., Recent advances in the genetics of sarcoidosis. J Med Genet 50 (2013), 290–297.
-
(2013)
J Med Genet
, vol.50
, pp. 290-297
-
-
Spagnolo, P.1
Grunewald, J.2
-
62
-
-
35848952935
-
Chronic lung disease after premature birth
-
62 Baraldi, E., Filippone, M., Chronic lung disease after premature birth. N Engl J Med 357 (2007), 1946–1955.
-
(2007)
N Engl J Med
, vol.357
, pp. 1946-1955
-
-
Baraldi, E.1
Filippone, M.2
-
63
-
-
33745553210
-
Summary proceedings from the bronchopulmonary dysplasia group
-
63 Walsh, M.C., Szefler, S., Davis, J., et al. Summary proceedings from the bronchopulmonary dysplasia group. Pediatrics 117:suppl 1 (2006), S52–S56.
-
(2006)
Pediatrics
, vol.117
, pp. S52-S56
-
-
Walsh, M.C.1
Szefler, S.2
Davis, J.3
-
64
-
-
51649115601
-
Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health
-
64 Lavoie, P.M., Pham, C., Jang, K.L., Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health. Pediatrics 122 (2008), 479–485.
-
(2008)
Pediatrics
, vol.122
, pp. 479-485
-
-
Lavoie, P.M.1
Pham, C.2
Jang, K.L.3
-
65
-
-
84882257642
-
A genome-wide association study (GWAS) for bronchopulmonary dysplasia
-
65 Wang, H., Julien, K.R.S., Stevenson, D.K., et al. A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Pediatrics 132 (2013), 290–297.
-
(2013)
Pediatrics
, vol.132
, pp. 290-297
-
-
Wang, H.1
Julien, K.R.S.2
Stevenson, D.K.3
-
66
-
-
84890049738
-
Genetics and the molecular pathogenesis of pulmonary arterial hypertension
-
66 Liu, D., Morrell, N.W., Genetics and the molecular pathogenesis of pulmonary arterial hypertension. Curr Hypertens Rep 15 (2013), 632–637.
-
(2013)
Curr Hypertens Rep
, vol.15
, pp. 632-637
-
-
Liu, D.1
Morrell, N.W.2
-
67
-
-
33748998458
-
Pulmonary arterial hypertension
-
67 McLaughlin, V.V., McGoon, M.D., Pulmonary arterial hypertension. Circulation 114 (2006), 1417–1431.
-
(2006)
Circulation
, vol.114
, pp. 1417-1431
-
-
McLaughlin, V.V.1
McGoon, M.D.2
-
68
-
-
84890738424
-
Updated clinical classification of pulmonary hypertension
-
68 Simonneau, G., Gatzoulis, M.A., Adatia, I., et al. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 62:25 suppl (2013), D34–D41.
-
(2013)
J Am Coll Cardiol
, vol.62
, Issue.25
, pp. D34-D41
-
-
Simonneau, G.1
Gatzoulis, M.A.2
Adatia, I.3
-
69
-
-
68649101805
-
Common vs. rare allele hypotheses for complex diseases
-
69 Schork, N.J., Murray, S.S., Frazer, K.A., Topol, E.J., Common vs. rare allele hypotheses for complex diseases. Curr Opin Genet Dev 19 (2009), 212–219.
-
(2009)
Curr Opin Genet Dev
, vol.19
, pp. 212-219
-
-
Schork, N.J.1
Murray, S.S.2
Frazer, K.A.3
Topol, E.J.4
-
70
-
-
84867114056
-
Whole-exome sequencing of a pedigree segregating asthma
-
70 DeWan, A.T., Egan, K.B., Hellenbrand, K., et al. Whole-exome sequencing of a pedigree segregating asthma. BMC Med Genet, 13, 2012, 95.
-
(2012)
BMC Med Genet
, vol.13
, pp. 95
-
-
DeWan, A.T.1
Egan, K.B.2
Hellenbrand, K.3
-
71
-
-
84905913420
-
Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma
-
71 Campbell, C.D., Mohajeri, K., Malig, M., et al. Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. PLoS One, 9, 2014, e104396.
-
(2014)
PLoS One
, vol.9
, pp. e104396
-
-
Campbell, C.D.1
Mohajeri, K.2
Malig, M.3
-
72
-
-
84901625706
-
Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction
-
72 Wain, L.V., Sayers, I., Artigas, M.S., et al. Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction. PLoS Genet, 10, 2014, e1004314.
-
(2014)
PLoS Genet
, vol.10
, pp. e1004314
-
-
Wain, L.V.1
Sayers, I.2
Artigas, M.S.3
-
73
-
-
84864330965
-
Whole exome sequencing to identify a novel gene (caveolin-1) associated with human pulmonary arterial hypertension
-
73 Austin, E.D., Ma, L., LeDuc, C., et al. Whole exome sequencing to identify a novel gene (caveolin-1) associated with human pulmonary arterial hypertension. Circ Cardiovasc Genet 5 (2012), 336–343.
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 336-343
-
-
Austin, E.D.1
Ma, L.2
LeDuc, C.3
-
74
-
-
84880704857
-
A novel channelopathy in pulmonary arterial hypertension
-
74 Ma, L., Roman-Campos, D., Austin, E.D., et al. A novel channelopathy in pulmonary arterial hypertension. N Engl J Med 369 (2013), 351–361.
-
(2013)
N Engl J Med
, vol.369
, pp. 351-361
-
-
Ma, L.1
Roman-Campos, D.2
Austin, E.D.3
-
75
-
-
84901047991
-
Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension
-
75 De Jesus Perez, V.A., Yuan, K., Lyuksyutova, M.A., et al. Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension. Am J Respir Crit Care Med 189 (2014), 1260–1272.
-
(2014)
Am J Respir Crit Care Med
, vol.189
, pp. 1260-1272
-
-
De Jesus Perez, V.A.1
Yuan, K.2
Lyuksyutova, M.A.3
-
76
-
-
84910664406
-
Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq
-
76 Shortt, K., Chaudhary, S., Grigoryev, D., et al. Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq. PLoS One, 9, 2014, e111953.
-
(2014)
PLoS One
, vol.9
, pp. e111953
-
-
Shortt, K.1
Chaudhary, S.2
Grigoryev, D.3
-
77
-
-
84899660153
-
Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma development
-
77 Dannemiller, K.C., Mendell, M.J., Macher, J.M., et al. Next-generation DNA sequencing reveals that low fungal diversity in house dust is associated with childhood asthma development. Indoor Air 24 (2014), 236–247.
-
(2014)
Indoor Air
, vol.24
, pp. 236-247
-
-
Dannemiller, K.C.1
Mendell, M.J.2
Macher, J.M.3
-
78
-
-
84908045907
-
Microbial communities in the upper respiratory tract of patients with asthma and chronic obstructive pulmonary disease
-
78 Park, H., Shin, J.W., Park, S.-G., Kim, W., Microbial communities in the upper respiratory tract of patients with asthma and chronic obstructive pulmonary disease. PLoS One, 9, 2014, e109710.
-
(2014)
PLoS One
, vol.9
, pp. e109710
-
-
Park, H.1
Shin, J.W.2
Park, S.-G.3
Kim, W.4
-
79
-
-
84887435078
-
Microbial communities in the respiratory tract of patients with interstitial lung disease
-
79 Garzoni, C., Brugger, S.D., Qi, W., et al. Microbial communities in the respiratory tract of patients with interstitial lung disease. Thorax 68 (2013), 1150–1156.
-
(2013)
Thorax
, vol.68
, pp. 1150-1156
-
-
Garzoni, C.1
Brugger, S.D.2
Qi, W.3
-
80
-
-
84903993583
-
Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study
-
80 Han, M.K., Zhou, Y., Murray, S., et al. Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study. Lancet Respir Med 2 (2014), 548–556.
-
(2014)
Lancet Respir Med
, vol.2
, pp. 548-556
-
-
Han, M.K.1
Zhou, Y.2
Murray, S.3
-
81
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
81 Manolio, T.A., Collins, F.S., Cox, N.J., et al. Finding the missing heritability of complex diseases. Nature 461 (2009), 747–753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
82
-
-
55549147191
-
The case of the missing heritability
-
82 Maher, B., The case of the missing heritability. Nature 456 (2008), 18–21.
-
(2008)
Nature
, vol.456
, pp. 18-21
-
-
Maher, B.1
-
83
-
-
7444260846
-
The ENCODE (ENCyclopedia of DNA elements) Project
-
83 ENCODE Project Consortium. The ENCODE (ENCyclopedia of DNA elements) Project. Science 306 (2004), 636–640.
-
(2004)
Science
, vol.306
, pp. 636-640
-
-
-
84
-
-
84865800494
-
The long-range interaction landscape of gene promoters
-
84 Sanyal, A., Lajoie, B.R., Jain, G., Dekker, J., The long-range interaction landscape of gene promoters. Nature 489 (2012), 109–113.
-
(2012)
Nature
, vol.489
, pp. 109-113
-
-
Sanyal, A.1
Lajoie, B.R.2
Jain, G.3
Dekker, J.4
-
85
-
-
84882796945
-
Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases
-
85 Lee, Y., Li, H., Li, J., et al. Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases. J Am Med Inform Assoc 20 (2013), 619–629.
-
(2013)
J Am Med Inform Assoc
, vol.20
, pp. 619-629
-
-
Lee, Y.1
Li, H.2
Li, J.3
-
86
-
-
77951439152
-
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS
-
86 Nicolae, D.L., Gamazon, E., Zhang, W., Duan, S., Dolan, M.E., Cox, N.J., Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. PLoS Genet, 6, 2010, e1000888.
-
(2010)
PLoS Genet
, vol.6
, pp. e1000888
-
-
Nicolae, D.L.1
Gamazon, E.2
Zhang, W.3
Duan, S.4
Dolan, M.E.5
Cox, N.J.6
-
87
-
-
84891671739
-
Pharmacogenetics: implications of race and ethnicity on defining genetic profiles for personalized medicine
-
87 Ortega, V.E., Meyers, D.A., Pharmacogenetics: implications of race and ethnicity on defining genetic profiles for personalized medicine. J Allergy Clin Immunol 133 (2014), 16–26.
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 16-26
-
-
Ortega, V.E.1
Meyers, D.A.2
-
88
-
-
84870302327
-
Genetic ancestry and its association with asthma exacerbations among African American subjects with asthma
-
88 Rumpel, J.A., Ahmedani, B.K., Peterson, E.L., et al. Genetic ancestry and its association with asthma exacerbations among African American subjects with asthma. J Allergy Clin Immunol 130 (2012), 1302–1306.
-
(2012)
J Allergy Clin Immunol
, vol.130
, pp. 1302-1306
-
-
Rumpel, J.A.1
Ahmedani, B.K.2
Peterson, E.L.3
-
89
-
-
33646259468
-
Asthma prevalence among US adults, 1998–2000: role of Puerto Rican ethnicity and behavioral and geographic factors
-
89 Rose, D., Mannino, D.M., Leaderer, B.P., Asthma prevalence among US adults, 1998–2000: role of Puerto Rican ethnicity and behavioral and geographic factors. Am J Public Health 96 (2006), 880–888.
-
(2006)
Am J Public Health
, vol.96
, pp. 880-888
-
-
Rose, D.1
Mannino, D.M.2
Leaderer, B.P.3
-
90
-
-
35248864320
-
Latino populations: a unique opportunity for epidemiological research of asthma
-
90 Salari, K., Burchard, E.G., Latino populations: a unique opportunity for epidemiological research of asthma. Paediatr Perinat Epidemiol 21:suppl 3 (2007), 15–22.
-
(2007)
Paediatr Perinat Epidemiol
, vol.21
, pp. 15-22
-
-
Salari, K.1
Burchard, E.G.2
-
91
-
-
33750435382
-
Ancestry–environment interactions and asthma risk among Puerto Ricans
-
91 Choudhry, S., Burchard, E.G., Borrell, L.N., et al. Ancestry–environment interactions and asthma risk among Puerto Ricans. Am J Respir Crit Care Med 174 (2006), 1088–1093.
-
(2006)
Am J Respir Crit Care Med
, vol.174
, pp. 1088-1093
-
-
Choudhry, S.1
Burchard, E.G.2
Borrell, L.N.3
-
92
-
-
84892387037
-
Asthma attacks among persons with current asthma—United States
-
92 Moorman, J.E., Person, C.J., Zahran, H.S., Centers for Disease Control and Prevention (CDC). Asthma attacks among persons with current asthma—United States. MMWR Surveill Summ 62:suppl 3 (2013), 93–98.
-
(2013)
MMWR Surveill Summ
, vol.62
, pp. 93-98
-
-
Moorman, J.E.1
Person, C.J.2
Zahran, H.S.3
-
93
-
-
84901817527
-
Staging of idiopathic pulmonary fibrosis: past, present and future
-
93 Kolb, M., Collard, H.R., Staging of idiopathic pulmonary fibrosis: past, present and future. Eur Respir Rev 23 (2014), 220–224.
-
(2014)
Eur Respir Rev
, vol.23
, pp. 220-224
-
-
Kolb, M.1
Collard, H.R.2
|