Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction
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T. Spector | L. Wain | N. Shrine | J. Cook | M. Obeidat | Y. Bossé | I. Sayers | E. Zeggini | M. Tobin | I. Hall | D. Nickle | D. Sin | M. Soler Artigas | T. McKeever | C. Vangjeli | C. Brandsma | E. Hollox | S. Jelinsky | S. John | I. Kilty | A. Malarstig | M. Portelli | Shrina Patel | Sally John | Ciara Vangjeli | María Soler Artigas
[1] J. Sunyer,et al. The relation of circulating YKL-40 to levels and decline of lung function in adult life. , 2013, Respiratory medicine.
[2] L. A. Daniels,et al. Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. , 2013, American journal of respiratory and critical care medicine.
[3] L. Wain,et al. GSTCD and INTS12 Regulation and Expression in the Human Lung , 2013, PloS one.
[4] Michael Boehnke,et al. Recommended Joint and Meta‐Analysis Strategies for Case‐Control Association Testing of Single Low‐Count Variants , 2013, Genetic epidemiology.
[5] Don D. Sin,et al. Refining Susceptibility Loci of Chronic Obstructive Pulmonary Disease with Lung eqtls , 2013, PloS one.
[6] D. MacArthur,et al. Negligible impact of rare autoimmune-locus coding-region variants on missing heritability , 2013, Nature.
[7] V. Kim,et al. Chronic bronchitis and chronic obstructive pulmonary disease. , 2013, American journal of respiratory and critical care medicine.
[8] T. Spector,et al. Genes Contributing to Pain Sensitivity in the Normal Population: An Exome Sequencing Study , 2012, PLoS genetics.
[9] David C. Nickle,et al. Lung eQTLs to Help Reveal the Molecular Underpinnings of Asthma , 2012, PLoS genetics.
[10] Edwin K Silverman,et al. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. , 2012, American journal of respiratory and critical care medicine.
[11] S. Jimenez,et al. Chitinase 1 Is a Biomarker for and Therapeutic Target in Scleroderma-Associated Interstitial Lung Disease That Augments TGF-β1 Signaling , 2012, The Journal of Immunology.
[12] C. Li,et al. Genome‐wide search for replicable risk gene regions in alcohol and nicotine co‐dependence , 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[13] Eleftheria Zeggini,et al. ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data , 2012, Human Heredity.
[14] E. Falconnet,et al. Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD , 2012, Human mutation.
[15] T. Beaty,et al. Genetic association between human chitinases and lung function in COPD , 2012, Human Genetics.
[16] Blair H. Smith,et al. Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. , 2011, American journal of respiratory and critical care medicine.
[17] Christian Gieger,et al. Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function , 2011, Nature Genetics.
[18] S. Ware,et al. Spectrum of clinical diseases caused by disorders of primary cilia. , 2011, Proceedings of the American Thoracic Society.
[19] Xihong Lin,et al. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[20] N. Laird,et al. The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility. , 2011, American journal of respiratory cell and molecular biology.
[21] Jeffrey A Lieberman,et al. Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia , 2011, Neuropsychopharmacology.
[22] K. Anderson,et al. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation , 2011, Nature Genetics.
[23] J. Belmont,et al. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs , 2011, Nature Genetics.
[24] Inês Barroso,et al. Genome-wide association study identifies five loci associated with lung function , 2010, Nature Genetics.
[25] E. Lundberg,et al. Towards a knowledge-based Human Protein Atlas , 2010, Nature Biotechnology.
[26] C. Brightling,et al. Ciliary dysfunction and ultrastructural abnormalities are features of severe asthma. , 2010, The Journal of allergy and clinical immunology.
[27] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[28] C. Klaver,et al. Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. , 2010, American journal of human genetics.
[29] Ayellet V. Segrè,et al. Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits , 2010, PLoS genetics.
[30] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[31] Tariq Ahmad,et al. Meta-analysis and imputation refines the association of 15q25 with smoking quantity , 2010, Nature Genetics.
[32] Ming D. Li,et al. Genome-wide meta-analyses identify multiple loci associated with smoking behavior , 2010, Nature Genetics.
[33] C. Gieger,et al. Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior , 2010, Nature Genetics.
[34] T. Ideker,et al. Functional genomic screen for modulators of ciliogenesis and cilium length , 2010, Nature.
[35] A. Hofman,et al. Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function , 2010, Nature Genetics.
[36] C. Gieger,et al. Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior , 2010 .
[37] R. Crystal,et al. Smoking Is Associated with Shortened Airway Cilia , 2009, PloS one.
[38] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[39] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[40] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[41] Scott T. Weiss,et al. A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study , 2009, PLoS genetics.
[42] Brad T. Sherman,et al. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.
[43] Tim D Spector,et al. The UK Adult Twin Registry (TwinsUK) , 2006, Twin Research and Human Genetics.
[44] J Vestbo,et al. Developing COPD: a 25 year follow up study of the general population , 2006, Thorax.
[45] C. D. Mathers,et al. Chronic obstructive pulmonary disease: current burden and future projections , 2006, European Respiratory Journal.
[46] M. Sanderson,et al. The Ciliary Rootlet Maintains Long-Term Stability of Sensory Cilia , 2005, Molecular and Cellular Biology.
[47] E. Pierce,et al. The Retinitis Pigmentosa 1 Protein Is a Photoreceptor Microtubule-Associated Protein , 2004, The Journal of Neuroscience.
[48] P. Paré,et al. The nature of small-airway obstruction in chronic obstructive pulmonary disease. , 2004, The New England journal of medicine.
[49] B. Hogan,et al. Novel Role for Netrins in Regulating Epithelial Behavior during Lung Branching Morphogenesis , 2004, Current Biology.
[50] Rafael A Irizarry,et al. Exploration, normalization, and summaries of high density oligonucleotide array probe level data. , 2003, Biostatistics.
[51] Miguel Armengot,et al. Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[52] E. Broadfield,et al. Prospective study of diet and decline in lung function in a general population. , 2002, American journal of respiratory and critical care medicine.
[53] H. Lehrach,et al. Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry , 2002, Nature Genetics.
[54] P. Burkhard,et al. Coiled coils: a highly versatile protein folding motif. , 2001, Trends in cell biology.
[55] B Rosner,et al. Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis. , 1998, American journal of respiratory and critical care medicine.
[56] I. Pavord,et al. Dietary antioxidant vitamin intake and lung function in the general population. , 1995, American journal of respiratory and critical care medicine.
[57] J. Bernaudin,et al. Ciliary abnormalities in bronchial epithelium of smokers, ex-smokers, and nonsmokers. , 1995, American journal of respiratory and critical care medicine.
[58] C. Larsson. Natural history and life expectancy in severe alpha1-antitrypsin deficiency, Pi Z. , 2009, Acta medica Scandinavica.