Louise Wain
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British genetic epidemiologist
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Louise Wain's Degrees
- Masters Epidemiology Imperial College London
Why Is Louise Wain Influential?
(Suggest an Edit or Addition)According to Wikipedia, Louise V. Wain is a British genetic epidemiologist currently serving as the British Lung Foundation Chair in Respiratory Research at the University of Leicester. Her research considers idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease. During the COVID-19 pandemic, Wain studied the long-term impacts of COVID-19.
Louise Wain's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
- The UK10K project identifies rare variants in health and disease (2015) (926)
- Chimpanzee Reservoirs of Pandemic and Nonpandemic HIV-1 (2006) (912)
- Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (600)
- Genome-wide association study identifies five loci associated with lung function (2010) (560)
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) (465)
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function (2011) (401)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes (2017) (353)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
- Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) (326)
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) (296)
- A Comprehensive Evaluation of Potential Lung Function Associated Genes in the SpiroMeta General Population Sample (2011) (281)
- Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis (2017) (275)
- New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. (2018) (257)
- Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (249)
- Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
- Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets (2017) (217)
- Genomic copy number variation, human health, and disease (2009) (203)
- Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study (2021) (201)
- Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study (2021) (201)
- Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell type and phenotype associations (2019) (200)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- Haplotype estimation for biobank scale datasets (2016) (178)
- Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function (2012) (167)
- Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study (2017) (162)
- Copy number variation. (2011) (156)
- 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) (144)
- Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study (2019) (141)
- Genome-wide association analysis identifies six new loci associated with forced vital capacity (2014) (141)
- Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis (2019) (133)
- Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport (2016) (131)
- Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney (2017) (121)
- Adaptation of HIV-1 to its human host. (2007) (118)
- Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness (2017) (113)
- Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa (2019) (112)
- Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation (2015) (110)
- Translational genomics and precision medicine: Moving from the lab to the clinic (2019) (95)
- Common Genetic Variation in the 3′-BCL11B Gene Desert Is Associated With Carotid-Femoral Pulse Wave Velocity and Excess Cardiovascular Disease Risk: The AortaGen Consortium (2012) (91)
- Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study (2021) (90)
- Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
- Molecular mechanisms underlying variations in lung function: a systems genetics analysis. (2015) (71)
- A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans (2014) (69)
- Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies (2009) (67)
- Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (61)
- Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. (2019) (61)
- Adjustment for index event bias in genome-wide association studies of subsequent events (2018) (60)
- Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function (2014) (59)
- Physical, cognitive and mental health impacts of COVID-19 following hospitalisation: a multi-centre prospective cohort study (2021) (56)
- Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study (2013) (54)
- A large genome scan for rare CNVs in amyotrophic lateral sclerosis. (2010) (53)
- The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci (2009) (52)
- Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia (2017) (52)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (52)
- Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (51)
- New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
- Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (49)
- Shared genetic etiology between idiopathic pulmonary fibrosis and COVID-19 severity (2020) (48)
- Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts (2020) (47)
- Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
- GSTCD and INTS12 Regulation and Expression in the Human Lung (2013) (44)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
- Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) (2013) (41)
- Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study. (2020) (39)
- Evidence for large-scale gene-by-smoking interaction effects on pulmonary function (2017) (38)
- Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts (2020) (35)
- Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction (2014) (34)
- A Genome‐Wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos (2018) (34)
- Common Variation in the WNK1 Gene and Blood Pressure in Childhood: The Avon Longitudinal Study of Parents and Children (2008) (33)
- Meta-analysis of exome array data identifies six novel genetic loci for lung function (2017) (31)
- Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis (2019) (31)
- Age at menarche and lung function: a Mendelian randomization study (2017) (31)
- Phenotypic and functional translation of IL1RL1 locus polymorphisms in lung tissue and asthmatic airway epithelium (2020) (28)
- Integrative pathway genomics of lung function and airflow obstruction. (2015) (28)
- A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
- Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline (2017) (26)
- Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12 (2016) (26)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2018) (22)
- Genome-wide association studies in lung disease (2011) (22)
- The United Kingdom Research study into Ethnicity And COVID-19 outcomes in Healthcare workers (UK-REACH): protocol for a prospective longitudinal cohort study of healthcare and ancillary workers in UK healthcare settings (2021) (20)
- The United Kingdom Research study into Ethnicity And COVID-19 outcomes in Healthcare workers (UK-REACH): protocol for a prospective longitudinal cohort study of healthcare and ancillary workers in UK healthcare settings (2021) (20)
- Understanding the burden of interstitial lung disease post-COVID-19: the UK Interstitial Lung Disease-Long COVID Study (UKILD-Long COVID) (2021) (19)
- Phenotypic and functional translation of IL33 genetics in asthma. (2020) (19)
- Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants (2020) (19)
- Common Variation in the WNK 1 Gene and Blood Pressure in Childhood The Avon Longitudinal Study of Parents and Children (2008) (18)
- Correction: Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (18)
- Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
- Novel idiopathic pulmonary fibrosis susceptibility variants revealed by deep sequencing (2019) (17)
- Reversal of Aging‐Induced Increases in Aortic Stiffness by Targeting Cytoskeletal Protein‐Protein Interfaces (2018) (16)
- Copy Number Variation of the Beta-Defensin Genes in Europeans: No Supporting Evidence for Association with Lung Function, Chronic Obstructive Pulmonary Disease or Asthma (2014) (16)
- Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. (2020) (14)
- Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
- Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2017) (14)
- Genetic overlap between idiopathic pulmonary fibrosis and COVID−19 (2021) (13)
- Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis (2021) (12)
- New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries (2018) (12)
- The vitamin D binding protein axis modifies disease severity in lymphangioleiomyomatosis (2018) (12)
- Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED) (2018) (12)
- Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis (2021) (11)
- Rare variants and cardiovascular disease. (2014) (11)
- Defining genetic risk factors for scleroderma-associated interstitial lung disease (2020) (11)
- What can genetics tell us about the cause of fixed airflow obstruction? (2012) (10)
- Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function (2021) (9)
- Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics (2021) (9)
- Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) (2018) (8)
- Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function (2018) (8)
- Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations (2020) (7)
- Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls (2017) (7)
- Krebs von den Lungen‐6 (KL‐6) is a pathophysiological biomarker of early‐stage acute hypersensitivity pneumonitis among pigeon fanciers (2020) (7)
- Genetic Associations and Architecture of Asthma-COPD Overlap (2022) (7)
- Pleiotropic associations of heterozygosity for the SERPINA1 Z allele in the UK Biobank (2021) (6)
- Expanded genetic landscape of chronic obstructive pulmonary disease reveals heterogeneous cell type and phenotype associations (2018) (6)
- Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank (2021) (6)
- GENETIC ANALYSIS OF OVER ONE MILLION PEOPLE IDENTIFIES 535 NOVEL LOCI ASSOCIATED WITH BLOOD PRESSURE AND RISK OF CARDIOVASCULAR DISEASE (2018) (5)
- A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease. (2021) (5)
- Joint patient and clinician priority setting to identify 10 key research questions regarding the long-term sequelae of COVID-19 (2022) (4)
- Genome-wide gene-air pollution interaction analysis of lung function in 300,000 individuals (2021) (4)
- Recurrent mutation at the classical haptoglobin structural polymorphism (2016) (4)
- Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study. (2022) (4)
- Smoking Interaction with a Polygenic Risk Score for Reduced Lung Function (2021) (4)
- Cluster analysis of transcriptomic datasets to identify endotypes of idiopathic pulmonary fibrosis (2021) (4)
- Hesitancy for receiving regular SARS-CoV-2 vaccination in UK healthcare workers: a cross-sectional analysis from the UK-REACH study (2022) (4)
- Blood Pressure Genetics and Hypertension: Genome-Wide Analysis and Role of Ancestry (2014) (4)
- A weighted genetic risk score based on 279 signals of association with lung function predicts Chronic Obstructive Pulmonary Disease (2018) (3)
- Faculty Opinions recommendation of A Genetic Risk Score Associated with Chronic Obstructive Pulmonary Disease Susceptibility and Lung Structure on Computed Tomography. (2019) (3)
- Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment (2020) (3)
- Causal analyses, statistical efficiency and phenotypic precision through Recall-by-Genotype study design (2017) (3)
- Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study (2021) (3)
- Evidence that Telomere Length is Causal for Idiopathic Pulmonary Fibrosis but not Chronic Obstructive Pulmonary Disease: A Mendelian Randomisation Study (2020) (3)
- Variants associated with HHIP expression have sex-differential effects on lung function. (2020) (3)
- Identification of a novel missense variant in SPDL1 associated with idiopathic pulmonary fibrosis (2020) (3)
- Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study (2022) (3)
- Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (3)
- Prevalence, risk factors and treatments for post-COVID-19 breathlessness: a systematic review and meta-analysis (2022) (2)
- Genome-Wide Association Study To Identify Genetic Determinants Of Severe Asthma (AUGOSA) (2011) (2)
- Edinburgh Research Explorer Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry (2017) (2)
- Integrative analyses for the identification of idiopathic pulmonary fibrosis-associated genes and shared loci with other diseases (2022) (2)
- Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney (2017) (2)
- A Statistical Framework to Identify Cell Types Whose Genetically Regulated Proportions are Associated with Complex Diseases (2021) (2)
- A Genome Wide Association Study of Moderate-Severe Asthma in subjects from the United Kingdom (2017) (2)
- Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
- Faculty Opinions recommendation of Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. (2019) (2)
- Cohort Profile: The United Kingdom Research study into Ethnicity and COVID-19 outcomes in Healthcare workers (UK-REACH) (2022) (2)
- Bronchial epithelial gene expression of NOX isoforms are related to important clinical characteristics in COPD (2016) (2)
- Corrigendum to: Cohort profile: Extended Cohort for E-health, Environment and DNA (EXCEED) (2019) (2)
- Pleiotropic effects of heterozygosity for the SERPINA1 Z allele in the UK Biobank (2020) (2)
- Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (2023) (2)
- Identi fi cation of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (1)
- Device-assessed sleep and physical activity in individuals recovering from a hospital admission for COVID-19: a multicentre study (2022) (1)
- Hostility in a mad, mad world. (1969) (1)
- Effects of sleep disturbance on dyspnoea and impaired lung function following hospital admission due to COVID-19 in the UK: a prospective multicentre cohort study (2023) (1)
- The effect of COVID rehabilitation for ongoing symptoms Post HOSPitalisation with COVID-19 (PHOSP-R): protocol for a randomised parallel group controlled trial on behalf of the PHOSP consortium (2023) (1)
- New Loci Associated with Lung Function and Chronic Obstructive Pulmonary Disease (2010) (1)
- A genome-wide association study of survival in patients with sepsis (2022) (1)
- Variants associated with HHIP expression have sex-differential effects on lung function (2021) (1)
- The Use of Genetic Information to Define Idiopathic Pulmonary Fibrosis in UK Biobank (2022) (1)
- The Uk Bileve Study: The First Genetic Study In Uk Biobank Identifies Novel Regions Associated With Airway Obstruction And Smoking Behaviour (2015) (1)
- Characteristics and risk factors for post-COVID-19 breathlessness after hospitalisation for COVID-19 (2022) (1)
- Trans-ethnic association study of blood pressure determinants in over 750,000 individuals (2018) (1)
- A genome-wide association study of asthma-COPD overlap syndrome (ACOS) (2020) (1)
- Interdisciplinary Research and Pandemics (2020) (1)
- Evolutionary origins of diversity in human viruses (2007) (1)
- Genome-wide association study of susceptibility to hospitalised respiratory infections [version 1; peer review: awaiting peer review] (2021) (1)
- Use of FEV1 as a measure of lung health in the UK BiLEVE study - Authors' reply. (2015) (1)
- Low-frequency variation in TP53 has large effects on head circumference and intracranial volume (2019) (1)
- Mendelian randomisation of eosinophils and other cell types in relation to lung function and disease (2022) (1)
- PCSK6 and Survival in Idiopathic Pulmonary Fibrosis (2022) (1)
- Extended Cohort for E-health, Environment and DNA (EXCEED) COVID-19 focus (2021) (1)
- Genetic Analysis Identifies a Novel Missense Variant in SPDL1 Associated with Idiopathic Pulmonary Fibrosis (2020) (1)
- Mendelian randomisation analyses of eosinophils and other blood cell types in relation to lung function and disease. (2020) (1)
- in MOCS 3 , IFIT 3 and SERPINA 12 (2016) (1)
- Genetics of forced vital capacity: genome-wide association study meta-analysis and follow-up identifies six new loci (2014) (1)
- Implementable Deep Learning for Multi-sequence Proton MRI Lung Segmentation: A Multi-center, Multi-vendor, and Multi-disease Study. (2023) (1)
- DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies (2023) (1)
- Sweetness coyed love into its smile (1996) (1)
- Call for Papers: "Morphology is the link between genetics and function": A tribute to Ewald R. Weibel. (2020) (1)
- Genome-wide association study of susceptibility to hospitalised respiratory infections (2021) (1)
- Forced vital capacity trajectories in patients with idiopathic pulmonary fibrosis: a secondary analysis of a multicentre, prospective, observational cohort. (2022) (1)
- Genome-wide association and large scale follow-up identifies 16 novel loci for lung function (2011) (1)
- Genome-Wide Analyses of Survival Time in the Rare Disease, Idiopathic Pulmonary Fibrosis (2016) (0)
- Decision letter: Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts (2019) (0)
- New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (0)
- Re-sequencing of IL33 and IL1RL1 in severe asthma patients identifies novel variation (2014) (0)
- Joint Effect of Single-Nucleotide Polymorphisms and Smoking Exposure in Chronic Obstructive Pulmonary Disease Risk (2012) (0)
- Adjustment for index event bias in genome-wide association studies of subsequent events (2019) (0)
- Shared polygenic effects of FEV1 in the first genetic study in UK Biobank (2015) (0)
- Human exome-chip meta-analysis identifies novel genetic loci associated with smoking behaviour (2016) (0)
- Correction: The effect of COVID rehabilitation for ongoing symptoms Post HOSPitalisation with COVID-19 (PHOSP-R): protocol for a randomised parallel group controlled trial on behalf of the PHOSP consortium (2023) (0)
- Polygenic Risk Scores in Chronic Obstructive Pulmonary Disease and Related Phenotypes (2020) (0)
- Krebs Von Den Lungen-6 Is a Molecular Biomarker of Early-Stage Acute Hypersensitivity Pneumonitis Among Pigeon Fanciers (2020) (0)
- A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples (2022) (0)
- Ninety seven independent genomic signals for lung function predict susceptibility to moderate to severe COPD (2016) (0)
- Phenotypic and functional translation of IL1RL1 locus polymorphisms in lung tissue and airway epithelium in asthma (2018) (0)
- Whole genome sequence analysis of pulmonary function and COPD in 19,996 multiethnic participants. (2020) (0)
- Faculty of 1000 evaluation for Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. (2018) (0)
- UK 10 K Consortium (2019) (0)
- University of Groningen Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation (2018) (0)
- Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for Forced Vital Capacity. BMC Genetics (2016) (0)
- Long-term follow up of adults hospitalised with COVID19 (2020) (0)
- CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (0)
- Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
- Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis (2021) (0)
- Obeidat et al. 2013 PLoS ONE (2015) (0)
- Macmillan's French readings for Children (2009) (0)
- Faculty Opinions recommendation of Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice. (2019) (0)
- Haplotype estimation for biobank scale datasets 1 2 (2016) (0)
- ERS International Congress 2018: highlights from best-abstract awardees (2018) (0)
- Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk (2018) (0)
- on in the Human Lung (2013) (0)
- Integrative Analyses Reveal Novel Disease-associated Loci and Genes for Idiopathic Pulmonary Fibrosis (2021) (0)
- Louis Wain's Cats (1983) (0)
- Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
- Classifying the unclassifiable - A Delphi study to reach consensus on the fibrotic nature of diseases. (2023) (0)
- Translational genomics: from genetic discovery to translational impact (0)
- The Role of Common Copy Number Variation in Amyotrophic Lateral Sclerosis (ALS) (2010) (0)
- Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations (2019) (0)
- Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference (2018) (0)
- Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease susceptibility and age-of-onset (2022) (0)
- Genome-wide association analysis identifies six new loci associated with forced vital capacity | NOVA. The University of Newcastle's Digital Repository (2014) (0)
- The causal relationship between gastro-esophageal reflux disease and idiopathic pulmonary fibrosis: A bidirectional two-sample Mendelian randomization study (2022) (0)
- A Genome-Wide Association Study of > 250,000 Subjects Identifies Novel Risk Loci for COPD (2018) (0)
- T76FEASIBILITY OF DEFINING TREATMENT RESISTANT DEPRESSION IN PRIMARY CARE RECORDS FOR PHARMACOGENETIC STUDIES (2019) (0)
- Interaction with air pollution exposure for genetic loci associated with lung function (2019) (0)
- Towards genetic reclassification of idiopathic pulmonary fibrosis. (2018) (0)
- Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease (2023) (0)
- Re-Sequencing To Identify Rare Variants Within IL1RL1 And IL33 Genes In Severe Asthma And Control Subjects (2012) (0)
- Title : Identification and functional characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease (2021) (0)
- Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity (2016) (0)
- Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
- Faculty Opinions recommendation of A cellular census of human lungs identifies novel cell states in health and in asthma. (2019) (0)
- Re-sequencing of PLAUR in severe asthma patients identifies novel variation (2014) (0)
- Investigating the Association of Rare Genetic Variants with Blood Pressure traits (2015) (0)
- Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank (2022) (0)
- Integrative -Omics Identify Potential Biomarkers and Therapeutic Targets for Idiopathic Pulmonary Fibrosis (2020) (0)
- Proportion of idiopathic pulmonary fibrosis risk explained by known genetic loci (2020) (0)
- Reply to: PCSK6: The endogenous PAR-1 agonist driving pulmonary fibrosis? (2023) (0)
- Determinants of recovery from post-COVID-19 dyspnoea: analysis of UK prospective cohorts of hospitalised COVID-19 patients and community-based controls (2023) (0)
- Differential bronchial epithelial gene expression in COPD versus controls (2016) (0)
- Plasma steroid concentrations reflect disease severity during acute illness but not recovery after hospitalisation with COVID-19 (2022) (0)
- Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data (2019) (0)
- Discovery and validation of 107 blood pressure loci from UK Biobank offers novel biological insights into cardiovascular risk (2016) (0)
- P040 Identification and functional characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease (2021) (0)
- Functional Translation of IL33 Locus Polymorphisms Into Altered Epithelial Cell Function Underlying Asthma (2019) (0)
- Prevalence of Klhl3 and Cul3 Mutations in Familial Hyperkalemic Hypertension (2014) (0)
- OP-IJEJ190076_cohort 678..689 (2019) (0)
- Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment (2021) (0)
- Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (2019) (0)
- Prevalence of physical frailty, including risk factors, up to 1 year after hospitalisation for COVID-19 in the UK: a multicentre, longitudinal cohort study (2023) (0)
- Comprehensive Evaluation Of Mild-To-Moderate Asthma Genes In Severe Asthma (augosa) (2011) (0)
- Determining the contribution of IL33 and IL1RL1 polymorphisms to clinical and immunological features of asthma (2016) (0)
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What Schools Are Affiliated With Louise Wain?
Louise Wain is affiliated with the following schools:
