(Q36123192)

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Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

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scholarly article

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Europe PubMed Central

12 August 2017

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (English)

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Europe PubMed Central

12 August 2017

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chronic obstructive pulmonary disease

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based on heuristic

inferred from title

19

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31

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Eleftheria Zeggini

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Richard J Allen

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Richard Allen

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Victoria E Jackson

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Victoria E Jackson

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Nick Shrine

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object named as

Suzanne Miller

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María Soler Artigas

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María Soler Artigas

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Adaikalavan Ramasamy

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Adaikalavan Ramasamy

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Louise V Wain

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Ian P Hall

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Ian Pavord

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Ian Sayers

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Martin D Tobin

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Anna L Hansell

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Mark McCarthy

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22

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Erik Melén

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12 August 2017

Jonathan Marchini

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object named as

Jonathan Marchini

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15

object named as

Dirkje S Postma

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Evelin Mihailov

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object named as

Evelin Mihailov

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ORCID Public Data File 2021

Andrew P Morris

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object named as

Andrew P Morris

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13

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Yohan Bossé

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12 August 2017

author name string

Ioanna Ntalla

5

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12 August 2017

Charlotte K Billington

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Abdul Kader Kheirallah

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James P Cook

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Kelly Probert

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Ma'en Obeidat

12

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12 August 2017

Ke Hao

14

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Peter D Paré

16

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UK Brain Expression Consortium (UKBEC)

18

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Eva Reinmaa

21

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12 August 2017

Jared O'Connell

23

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Eleni Frangou

24

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Olivier Delaneau

25

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OxGSK Consortium

26

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12 August 2017

Colin Freeman

27

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Desislava Petkova

28

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Richard Hubbard

32

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Neil C Thomson

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David P Strachan

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publication date

25 September 2015

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The Lancet. Respiratory medicine

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12 August 2017

3

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10

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769-781

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12 August 2017

Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

The UK10K project identifies rare variants in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Genetic variability in the regulation of gene expression in ten regions of the human brain

1 reference

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2 October 2017

Genome-wide association analysis identifies six new loci associated with forced vital capacity

1 reference

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2 October 2017

Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis

1 reference

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2 October 2017

Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study

1 reference

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2 October 2017

GSTCD and INTS12 regulation and expression in the human lung

1 reference

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Systematic identification of trans eQTLs as putative drivers of known disease associations

1 reference

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2 October 2017

Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls

1 reference

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Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants

1 reference

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1 reference

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A dynamic bronchial airway gene expression signature of chronic obstructive pulmonary disease and lung function impairment

1 reference

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2 October 2017

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

1 reference

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Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

1 reference

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Lung eQTLs to help reveal the molecular underpinnings of asthma

1 reference

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Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

1 reference

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Structural diversity and African origin of the 17q21.31 inversion polymorphism

1 reference

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2 October 2017

Structural haplotypes and recent evolution of the human 17q21.31 region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

1 reference

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2 October 2017

Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Expression analysis of asthma candidate genes during human and murine lung development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

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A map of human genome variation from population-scale sequencing

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2 October 2017

Hundreds of variants clustered in genomic loci and biological pathways affect human height

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2 October 2017

A large-scale, consortium-based genomewide association study of asthma

1 reference

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2 October 2017

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

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Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

1 reference

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Variants in FAM13A are associated with chronic obstructive pulmonary disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

2 October 2017

Genome-wide association study identifies five loci associated with lung function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

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Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4593935

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A genome-wide association study of pulmonary function measures in the Framingham Heart Study

1 reference

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A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.

1 reference

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Chromosome 17: association of a large inversion polymorphism with corticosteroid response in asthma

1 reference

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Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila

1 reference

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Standardisation of spirometry

1 reference

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A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men.

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1 reference

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Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.

1 reference

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1 reference

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Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations.

1 reference

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Lesion to the nigrostriatal dopamine system disrupts stimulus-response habit formation.

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Mapping and verification of susceptibility loci for smoking quantity using permutation linkage analysis

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Familial aggregation and heritability of adult lung function: results from the Busselton Health Study

1 reference

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7 January 2021

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Identifiers

10.1016/S2213-2600(15)00283-0

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Europe PubMed Central

12 August 2017

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Europe PubMed Central

12 August 2017

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Europe PubMed Central

12 August 2017

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