-
1
-
-
31844435204
-
Chronic obstructive pulmonary disease: current burden and future projections
-
Lopez AD, Shibuya K, Rao C, Mathers CD, Hansell AL, et al. (2006) Chronic obstructive pulmonary disease: current burden and future projections. Eur Respir J 27: 397-412.
-
(2006)
Eur Respir J
, vol.27
, pp. 397-412
-
-
Lopez, A.D.1
Shibuya, K.2
Rao, C.3
Mathers, C.D.4
Hansell, A.L.5
-
2
-
-
0031807729
-
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, et al. (1998) Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis. Am J Respir Crit Care Med 157: 1770-1778.
-
(1998)
Am J Respir Crit Care Med
, vol.157
, pp. 1770-1778
-
-
Silverman, E.K.1
Chapman, H.A.2
Drazen, J.M.3
Weiss, S.T.4
Rosner, B.5
-
3
-
-
73349111257
-
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function
-
Hancock DB, Eijgelsheim M, Wilk JB, Gharib SA, Loehr LR, et al. (2010) Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. Nat Genet 42: 45-52.
-
(2010)
Nat Genet
, vol.42
, pp. 45-52
-
-
Hancock, D.B.1
Eijgelsheim, M.2
Wilk, J.B.3
Gharib, S.A.4
Loehr, L.R.5
-
4
-
-
73349143302
-
Genome-wide association study identifies five loci associated with lung function
-
Repapi E, Sayers I, Wain LV, Burton PR, Johnson T, et al. (2010) Genome-wide association study identifies five loci associated with lung function. Nat Genet 42: 36-44.
-
(2010)
Nat Genet
, vol.42
, pp. 36-44
-
-
Repapi, E.1
Sayers, I.2
Wain, L.V.3
Burton, P.R.4
Johnson, T.5
-
5
-
-
80055008094
-
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
-
Soler Artigas M, Loth DW, Wain LV, Gharib SA, Obeidat M, et al. (2011) Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet 43: 1082-1090.
-
(2011)
Nat Genet
, vol.43
, pp. 1082-1090
-
-
Soler Artigas, M.1
Loth, D.W.2
Wain, L.V.3
Gharib, S.A.4
Obeidat, M.5
-
6
-
-
63449099623
-
A genome-wide association study of pulmonary function measures in the Framingham Heart Study
-
Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, et al. (2009) A genome-wide association study of pulmonary function measures in the Framingham Heart Study. PLoS Genet 5: e1000429.
-
(2009)
PLoS Genet
, vol.5
-
-
Wilk, J.B.1
Chen, T.H.2
Gottlieb, D.J.3
Walter, R.E.4
Nagle, M.W.5
-
7
-
-
82755165236
-
The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility
-
Castaldi PJ, Cho MH, Litonjua AA, Bakke P, Gulsvik A, et al. (2011) The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility. Am J Respir Cell Mol Biol 45: 1147-1153.
-
(2011)
Am J Respir Cell Mol Biol
, vol.45
, pp. 1147-1153
-
-
Castaldi, P.J.1
Cho, M.H.2
Litonjua, A.A.3
Bakke, P.4
Gulsvik, A.5
-
8
-
-
80053414310
-
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function
-
Soler Artigas M, Wain LV, Repapi E, Obeidat M, Sayers I, et al. (2011) Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. Am J Respir Crit Care Med 184: 786-795.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 786-795
-
-
Soler Artigas, M.1
Wain, L.V.2
Repapi, E.3
Obeidat, M.4
Sayers, I.5
-
9
-
-
84867130207
-
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
-
Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, et al. (2012) Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. Am J Respir Crit Care Med 186: 622-632.
-
(2012)
Am J Respir Crit Care Med
, vol.186
, pp. 622-632
-
-
Wilk, J.B.1
Shrine, N.R.2
Loehr, L.R.3
Zhao, J.H.4
Manichaikul, A.5
-
10
-
-
33751236493
-
Developing COPD: a 25 year follow up study of the general population
-
Lokke A, Lange P, Scharling H, Fabricius P, Vestbo J, (2006) Developing COPD: a 25 year follow up study of the general population. Thorax 61: 935-939.
-
(2006)
Thorax
, vol.61
, pp. 935-939
-
-
Lokke, A.1
Lange, P.2
Scharling, H.3
Fabricius, P.4
Vestbo, J.5
-
11
-
-
0029057210
-
Dietary antioxidant vitamin intake and lung function in the general population
-
Britton JR, Pavord ID, Richards KA, Knox AJ, Wisniewski AF, et al. (1995) Dietary antioxidant vitamin intake and lung function in the general population. Am J Respir Crit Care Med 151: 1383-1387.
-
(1995)
Am J Respir Crit Care Med
, vol.151
, pp. 1383-1387
-
-
Britton, J.R.1
Pavord, I.D.2
Richards, K.A.3
Knox, A.J.4
Wisniewski, A.F.5
-
12
-
-
0036569616
-
Prospective study of diet and decline in lung function in a general population
-
McKeever TM, Scrivener S, Broadfield E, Jones Z, Britton J, et al. (2002) Prospective study of diet and decline in lung function in a general population. Am J Respir Crit Care Med 165: 1299-1303.
-
(2002)
Am J Respir Crit Care Med
, vol.165
, pp. 1299-1303
-
-
McKeever, T.M.1
Scrivener, S.2
Broadfield, E.3
Jones, Z.4
Britton, J.5
-
13
-
-
77951751034
-
Meta-analysis and imputation refines the association of 15q25 with smoking quantity
-
Liu JZ, Tozzi F, Waterworth DM, Pillai SG, Muglia P, et al. (2010) Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet 42: 436-440.
-
(2010)
Nat Genet
, vol.42
, pp. 436-440
-
-
Liu, J.Z.1
Tozzi, F.2
Waterworth, D.M.3
Pillai, S.G.4
Muglia, P.5
-
14
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
Huang da W, Sherman BT, Lempicki RA, (2009) Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 4: 44-57.
-
(2009)
Nat Protoc
, vol.4
, pp. 44-57
-
-
da Huang, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
15
-
-
84860608281
-
Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence
-
Zuo L, Zhang F, Zhang H, Zhang XY, Wang F, et al. (2012) Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. Am J Med Genet B Neuropsychiatr Genet 159B: 437-444.
-
(2012)
Am J Med Genet B Neuropsychiatr Genet
, vol.159 B
, pp. 437-444
-
-
Zuo, L.1
Zhang, F.2
Zhang, H.3
Zhang, X.Y.4
Wang, F.5
-
16
-
-
78651383514
-
Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia
-
McClay JL, Adkins DE, Aberg K, Bukszar J, Khachane AN, et al. (2011) Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. Neuropsychopharmacology 36: 616-626.
-
(2011)
Neuropsychopharmacology
, vol.36
, pp. 616-626
-
-
McClay, J.L.1
Adkins, D.E.2
Aberg, K.3
Bukszar, J.4
Khachane, A.N.5
-
17
-
-
84890314252
-
The relation of circulating YKL-40 to levels and decline of lung function in adult life
-
Guerra S, Halonen M, Sherrill DL, Venker C, Spangenberg A, et al. (2013) The relation of circulating YKL-40 to levels and decline of lung function in adult life. Respir Med 107: 1923-30.
-
(2013)
Respir Med
, vol.107
, pp. 1923-1930
-
-
Guerra, S.1
Halonen, M.2
Sherrill, D.L.3
Venker, C.4
Spangenberg, A.5
-
18
-
-
84862753452
-
Genetic association between human chitinases and lung function in COPD
-
Aminuddin F, Akhabir L, Stefanowicz D, Pare PD, Connett JE, et al. (2012) Genetic association between human chitinases and lung function in COPD. Hum Genet 131: 1105-1114.
-
(2012)
Hum Genet
, vol.131
, pp. 1105-1114
-
-
Aminuddin, F.1
Akhabir, L.2
Stefanowicz, D.3
Pare, P.D.4
Connett, J.E.5
-
19
-
-
84865411180
-
Chitinase 1 is a biomarker for and therapeutic target in scleroderma-associated interstitial lung disease that augments TGF-beta1 signaling
-
Lee CG, Herzog EL, Ahangari F, Zhou Y, Gulati M, et al. (2012) Chitinase 1 is a biomarker for and therapeutic target in scleroderma-associated interstitial lung disease that augments TGF-beta1 signaling. J Immunol 189: 2635-2644.
-
(2012)
J Immunol
, vol.189
, pp. 2635-2644
-
-
Lee, C.G.1
Herzog, E.L.2
Ahangari, F.3
Zhou, Y.4
Gulati, M.5
-
20
-
-
77951748276
-
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
-
Thorgeirsson TE, Gudbjartsson DF, Surakka I, Vink JM, Amin N, et al. (2010) Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet 42: 448-453.
-
(2010)
Nat Genet
, vol.42
, pp. 448-453
-
-
Thorgeirsson, T.E.1
Gudbjartsson, D.F.2
Surakka, I.3
Vink, J.M.4
Amin, N.5
-
21
-
-
77951711343
-
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
-
Tobacco, Genetics C, (2010) Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Nat Genet 42: 441-447.
-
(2010)
Nat Genet
, vol.42
, pp. 441-447
-
-
-
22
-
-
77957942910
-
Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits
-
Segre AV, Consortium D, investigators M, Groop L, Mootha VK, et al. (2010) Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits. PLoS Genet 6: e1001058.
-
(2010)
PLoS Genet
, vol.6
-
-
Segre, A.V.1
Consortium, D.2
Groop, L.3
Mootha, V.K.4
-
23
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, et al. (2011) Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 89: 82-93.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
-
24
-
-
84858729755
-
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data
-
Asimit JL, Day-Williams AG, Morris AP, Zeggini E, (2012) ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data. Hum Hered 73: 84-94.
-
(2012)
Hum Hered
, vol.73
, pp. 84-94
-
-
Asimit, J.L.1
Day-Williams, A.G.2
Morris, A.P.3
Zeggini, E.4
-
25
-
-
0018128288
-
Natural history and life expectancy in severe alpha1-antitrypsin deficiency, Pi Z
-
Larsson C, (1978) Natural history and life expectancy in severe alpha1-antitrypsin deficiency, Pi Z. Acta Med Scand 204: 345-351.
-
(1978)
Acta Med Scand
, vol.204
, pp. 345-351
-
-
Larsson, C.1
-
27
-
-
78651254549
-
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation
-
Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, et al. (2011) The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet 43: 79-84.
-
(2011)
Nat Genet
, vol.43
, pp. 79-84
-
-
Becker-Heck, A.1
Zohn, I.E.2
Okabe, N.3
Pollock, A.4
Lenhart, K.B.5
-
28
-
-
78651260210
-
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs
-
Merveille AC, Davis EE, Becker-Heck A, Legendre M, Amirav I, et al. (2011) CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet 43: 72-78.
-
(2011)
Nat Genet
, vol.43
, pp. 72-78
-
-
Merveille, A.C.1
Davis, E.E.2
Becker-Heck, A.3
Legendre, M.4
Amirav, I.5
-
29
-
-
78650034777
-
Towards a knowledge-based Human Protein Atlas
-
Uhlen M, Oksvold P, Fagerberg L, Lundberg E, Jonasson K, et al. (2010) Towards a knowledge-based Human Protein Atlas. Nat Biotechnol 28: 1248-1250.
-
(2010)
Nat Biotechnol
, vol.28
, pp. 1248-1250
-
-
Uhlen, M.1
Oksvold, P.2
Fagerberg, L.3
Lundberg, E.4
Jonasson, K.5
-
30
-
-
3042693023
-
Novel role for Netrins in regulating epithelial behavior during lung branching morphogenesis
-
Liu Y, Stein E, Oliver T, Li Y, Brunken WJ, et al. (2004) Novel role for Netrins in regulating epithelial behavior during lung branching morphogenesis. Curr Biol 14: 897-905.
-
(2004)
Curr Biol
, vol.14
, pp. 897-905
-
-
Liu, Y.1
Stein, E.2
Oliver, T.3
Li, Y.4
Brunken, W.J.5
-
31
-
-
20944436797
-
The ciliary rootlet maintains long-term stability of sensory cilia
-
Yang J, Gao J, Adamian M, Wen XH, Pawlyk B, et al. (2005) The ciliary rootlet maintains long-term stability of sensory cilia. Mol Cell Biol 25: 4129-4137.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 4129-4137
-
-
Yang, J.1
Gao, J.2
Adamian, M.3
Wen, X.H.4
Pawlyk, B.5
-
32
-
-
77954063235
-
Smoking is associated with shortened airway cilia
-
Leopold PL, O'Mahony MJ, Lian XJ, Tilley AE, Harvey BG, et al. (2009) Smoking is associated with shortened airway cilia. PLoS One 4: e8157.
-
(2009)
PLoS One
, vol.4
-
-
Leopold, P.L.1
O'Mahony, M.J.2
Lian, X.J.3
Tilley, A.E.4
Harvey, B.G.5
-
33
-
-
0028920130
-
Ciliary abnormalities in bronchial epithelium of smokers, ex-smokers, and nonsmokers
-
Verra F, Escudier E, Lebargy F, Bernaudin JF, De Cremoux H, et al. (1995) Ciliary abnormalities in bronchial epithelium of smokers, ex-smokers, and nonsmokers. Am J Respir Crit Care Med 151: 630-634.
-
(1995)
Am J Respir Crit Care Med
, vol.151
, pp. 630-634
-
-
Verra, F.1
Escudier, E.2
Lebargy, F.3
Bernaudin, J.F.4
De Cremoux, H.5
-
34
-
-
77957769295
-
Ciliary dysfunction and ultrastructural abnormalities are features of severe asthma
-
Thomas B, Rutman A, Hirst RA, Haldar P, Wardlaw AJ, et al. (2010) Ciliary dysfunction and ultrastructural abnormalities are features of severe asthma. J Allergy Clin Immunol 126: 722-e722, 722-729, e722.
-
(2010)
J Allergy Clin Immunol
, vol.126
-
-
Thomas, B.1
Rutman, A.2
Hirst, R.A.3
Haldar, P.4
Wardlaw, A.J.5
-
35
-
-
2942720573
-
The nature of small-airway obstruction in chronic obstructive pulmonary disease
-
Hogg JC, Chu F, Utokaparch S, Woods R, Elliott WM, et al. (2004) The nature of small-airway obstruction in chronic obstructive pulmonary disease. N Engl J Med 350: 2645-2653.
-
(2004)
N Engl J Med
, vol.350
, pp. 2645-2653
-
-
Hogg, J.C.1
Chu, F.2
Utokaparch, S.3
Woods, R.4
Elliott, W.M.5
-
36
-
-
84873353231
-
Chronic bronchitis and chronic obstructive pulmonary disease
-
Kim V, Criner GJ, (2013) Chronic bronchitis and chronic obstructive pulmonary disease. Am J Respir Crit Care Med 187: 228-237.
-
(2013)
Am J Respir Crit Care Med
, vol.187
, pp. 228-237
-
-
Kim, V.1
Criner, G.J.2
-
37
-
-
80053004806
-
Spectrum of clinical diseases caused by disorders of primary cilia
-
Ware SM, Aygun MG, Hildebrandt F, (2011) Spectrum of clinical diseases caused by disorders of primary cilia. Proc Am Thorac Soc 8: 444-450.
-
(2011)
Proc Am Thorac Soc
, vol.8
, pp. 444-450
-
-
Ware, S.M.1
Aygun, M.G.2
Hildebrandt, F.3
-
38
-
-
84857054679
-
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD
-
Lucas JS, Adam EC, Goggin PM, Jackson CL, Powles-Glover N, et al. (2012) Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD. Hum Mutat 33: 495-503.
-
(2012)
Hum Mutat
, vol.33
, pp. 495-503
-
-
Lucas, J.S.1
Adam, E.C.2
Goggin, P.M.3
Jackson, C.L.4
Powles-Glover, N.5
-
39
-
-
0036678117
-
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia
-
Bartoloni L, Blouin JL, Pan Y, Gehrig C, Maiti AK, et al. (2002) Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia. Proc Natl Acad Sci U S A 99: 10282-10286.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 10282-10286
-
-
Bartoloni, L.1
Blouin, J.L.2
Pan, Y.3
Gehrig, C.4
Maiti, A.K.5
-
40
-
-
0036479029
-
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
-
Olbrich H, Haffner K, Kispert A, Volkel A, Volz A, et al. (2002) Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Nat Genet 30: 143-144.
-
(2002)
Nat Genet
, vol.30
, pp. 143-144
-
-
Olbrich, H.1
Haffner, K.2
Kispert, A.3
Volkel, A.4
Volz, A.5
-
41
-
-
84886402463
-
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease
-
Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW, (2013) Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. Am J Respir Crit Care Med 188: 913-922.
-
(2013)
Am J Respir Crit Care Med
, vol.188
, pp. 913-922
-
-
Knowles, M.R.1
Daniels, L.A.2
Davis, S.D.3
Zariwala, M.A.4
Leigh, M.W.5
-
42
-
-
77955581331
-
Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa
-
Bandah-Rozenfeld D, Collin RW, Banin E, van den Born LI, Coene KL, et al. (2010) Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. Am J Hum Genet 87: 199-208.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 199-208
-
-
Bandah-Rozenfeld, D.1
Collin, R.W.2
Banin, E.3
van den Born, L.I.4
Coene, K.L.5
-
43
-
-
3242749615
-
The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein
-
Liu Q, Zuo J, Pierce EA, (2004) The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein. J Neurosci 24: 6427-6436.
-
(2004)
J Neurosci
, vol.24
, pp. 6427-6436
-
-
Liu, Q.1
Zuo, J.2
Pierce, E.A.3
-
44
-
-
77951128108
-
Functional genomic screen for modulators of ciliogenesis and cilium length
-
Kim J, Lee JE, Heynen-Genel S, Suyama E, Ono K, et al. (2010) Functional genomic screen for modulators of ciliogenesis and cilium length. Nature 464: 1048-1051.
-
(2010)
Nature
, vol.464
, pp. 1048-1051
-
-
Kim, J.1
Lee, J.E.2
Heynen-Genel, S.3
Suyama, E.4
Ono, K.5
-
45
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, et al. (2009) Finding the missing heritability of complex diseases. Nature 461: 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
-
46
-
-
84878994629
-
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
-
Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, et al. (2013) Negligible impact of rare autoimmune-locus coding-region variants on missing heritability. Nature 498: 232-235.
-
(2013)
Nature
, vol.498
, pp. 232-235
-
-
Hunt, K.A.1
Mistry, V.2
Bockett, N.A.3
Ahmad, T.4
Ban, M.5
-
47
-
-
84881614989
-
Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants
-
Ma C, Blackwell T, Boehnke M, Scott LJ, Go TDi, (2013) Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants. Genet Epidemiol 37: 539-550.
-
(2013)
Genet Epidemiol
, vol.37
, pp. 539-550
-
-
Ma, C.1
Blackwell, T.2
Boehnke, M.3
Scott, L.J.4
Go, T.D.5
-
49
-
-
84872021031
-
Genes contributing to pain sensitivity in the normal population: an exome sequencing study
-
Williams FM, Scollen S, Cao D, Memari Y, Hyde CL, et al. (2012) Genes contributing to pain sensitivity in the normal population: an exome sequencing study. PLoS Genet 8: e1003095.
-
(2012)
PLoS Genet
, vol.8
-
-
Williams, F.M.1
Scollen, S.2
Cao, D.3
Memari, Y.4
Hyde, C.L.5
-
50
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R, (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
51
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
-
52
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20: 1297-1303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
-
53
-
-
77956534324
-
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Hakonarson H, (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38: e164.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
54
-
-
84870713668
-
Lung eQTLs to help reveal the molecular underpinnings of asthma
-
Hao K, Bosse Y, Nickle DC, Pare PD, Postma DS, et al. (2012) Lung eQTLs to help reveal the molecular underpinnings of asthma. PLoS Genet 8: e1003029.
-
(2012)
PLoS Genet
, vol.8
-
-
Hao, K.1
Bosse, Y.2
Nickle, D.C.3
Pare, P.D.4
Postma, D.S.5
-
55
-
-
84880796513
-
Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls
-
Lamontagne M, Couture C, Postma DS, Timens W, Sin DD, et al. (2013) Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls. PLoS One 8: e70220.
-
(2013)
PLoS One
, vol.8
-
-
Lamontagne, M.1
Couture, C.2
Postma, D.S.3
Timens, W.4
Sin, D.D.5
-
56
-
-
84884233567
-
GSTCD and INTS12 regulation and expression in the human lung
-
Obeidat M, Miller S, Probert K, Billington CK, Henry AP, et al. (2013) GSTCD and INTS12 regulation and expression in the human lung. PLoS One 8: e74630.
-
(2013)
PLoS One
, vol.8
-
-
Obeidat, M.1
Miller, S.2
Probert, K.3
Billington, C.K.4
Henry, A.P.5
-
57
-
-
0142121516
-
Exploration, normalization, and summaries of high density oligonucleotide array probe level data
-
Irizarry RA, Hobbs B, Collin F, Beazer-Barclay YD, Antonellis KJ, et al. (2003) Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 4: 249-264.
-
(2003)
Biostatistics
, vol.4
, pp. 249-264
-
-
Irizarry, R.A.1
Hobbs, B.2
Collin, F.3
Beazer-Barclay, Y.D.4
Antonellis, K.J.5
|