Search Results - "Mendelian Randomization Analysis/methods"
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1
Authors: et al.
Contributors: et al.
Source: Nat Genet
Nature genetics, vol. 57, no. 7, pp. 1620-1627Subject Terms: Cardiovascular outcomes, Biomedicine, Propensity score, Genetics, developmental biology, physiology, Humans, Multifactorial Inheritance/genetics, Randomized Controlled Trials as Topic/methods, Mendelian Randomization Analysis/methods, Research Design, Computer Simulation, Empagliflozin, Warfarin, Mortality, Article, Causal inference
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2
Authors: et al.
Source: Eur J Epidemiol
European journal of epidemiology, vol. 40, no. 6, pp. 631-647Subject Terms: Mendelian Randomization, name=Bristol Population Health Science Institute, Mendelian Randomization Analysis/methods, Humans, Bias, Computer Simulation, Causality, Nonlinear Dynamics, Genotype, Biostatistics, Mendelian randomisation, Methods, NLMR
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3
Authors: et al.
Contributors: et al.
Source: Nat Commun
Nature communications, vol. 16, no. 1, pp. 6112Subject Terms: Mendelian Randomization Analysis/methods, Genetic Pleiotropy, Humans, Quantitative Trait Loci, Linkage Disequilibrium, Causality, Computer Simulation, Genome-Wide Association Study, Polymorphism, Single Nucleotide, Metabolic Networks and Pathways/genetics, Article, ddc
File Description: application/pdf
Access URL: https://pure.eur.nl/en/publications/a64df5d4-8d0d-4245-bd8e-273e9b05f2c2
https://doi.org/10.1038/s41467-025-60868-1
https://serval.unil.ch/notice/serval:BIB_B36431D3CE3B
https://serval.unil.ch/resource/serval:BIB_B36431D3CE3B.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B36431D3CE3B0
https://mediatum.ub.tum.de/1791958 -
4
Authors: et al.
Contributors: et al.
Source: Mol Psychiatry
Subject Terms: Male, Conduct Disorder, 0301 basic medicine, ddc:610, Substance-Related Disorders, Antisocial Personality Disorder/epidemiology [MeSH], Antisocial Personality Disorder/genetics [MeSH], Risk Factors [MeSH], 692/699/476, Attention Deficit Disorder with Hyperactivity/genetics [MeSH], Polymorphism, Single Nucleotide/genetics [MeSH], Genome-Wide Association Study/methods [MeSH], Male [MeSH], Conduct Disorder/epidemiology [MeSH], 45/43, Child Abuse/psychology [MeSH], Phenotype [MeSH], Child [MeSH], Genetic Predisposition to Disease/genetics [MeSH], Substance-Related Disorders/psychology [MeSH], Gene-Environment Interaction [MeSH], Female [MeSH], Conduct Disorder/genetics [MeSH], 631/208, Humans [MeSH], 631/477, Article, Substance-Related Disorders/genetics [MeSH], Mendelian Randomization Analysis/methods [MeSH], article, 610 Medizin, Antisocial Personality Disorder, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide, 3. Good health, 03 medical and health sciences, Phenotype, 0302 clinical medicine, Risk Factors, Attention Deficit Disorder with Hyperactivity, Humans, Female, Genetic Predisposition to Disease, Gene-Environment Interaction, Child Abuse, Child, Genome-Wide Association Study
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5
Authors: et al.
Source: Nutr J
Nutrition Journal, Vol 24, Iss 1, Pp 1-10 (2025)
Nutrition journal, vol. 24, no. 1, pp. 20Subject Terms: Male, Humans, Mendelian Randomization Analysis/methods, Cognition/physiology, Aged, Female, Dairy Products/statistics & numerical data, Middle Aged, Lactase/genetics, Cohort Studies, Netherlands, Diet/methods, Diet/statistics & numerical data, Longitudinal Studies, Canada, Genotype, CLSA, Cognitive function, Dairy, Lactase persistence, Mendelian randomization, RC620-627, Cognition, TX341-641, Nutritional diseases. Deficiency diseases, Lactase, Nutrition. Foods and food supply, Research, Mendelian Randomization Analysis, Diet, Dairy Products
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Access URL: https://pubmed.ncbi.nlm.nih.gov/39891239
https://doaj.org/article/aa11d18a26904ce58d02f86d10d105a4
https://serval.unil.ch/resource/serval:BIB_4822D2C59E2D.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_4822D2C59E2D
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4822D2C59E2D9
https://hdl.handle.net/11380/1373048
https://doi.org/10.1186/s12937-025-01083-y -
6
Authors: et al.
Contributors: et al.
Source: Int J Obes (Lond)
Subject Terms: Male, 2. Zero hunger, Cancer och onkologi, Waist-Hip Ratio, Female [MeSH], Waist-Hip Ratio [MeSH], Humans [MeSH], Waist Circumference [MeSH], Risk Factors [MeSH], Colorectal Neoplasms/epidemiology [MeSH], Body Mass Index [MeSH], Article, Male [MeSH], 692/499, Mendelian Randomization Analysis/methods [MeSH], 692/699/67, Colorectal Neoplasms/genetics [MeSH], article, Folkhälsovetenskap, global hälsa och socialmedicin, Mendelian Randomization Analysis, Public Health, Global Health and Social Medicine, Body Mass Index, 3. Good health, Risk Factors, Cancer and Oncology, Life Science, Humans, Female, Waist Circumference, Colorectal Neoplasms, 10. No inequality
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Access URL: https://pubmed.ncbi.nlm.nih.gov/38297030
https://repository.publisso.de/resource/frl:6500369
https://research.wur.nl/en/publications/allometric-versus-traditional-body-shape-indices-and-risk-of-colo
https://doi.org/10.1038/s41366-024-01479-6
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-220884 -
7
Authors: et al.
Source: Nicotine Tob Res
Subject Terms: Editorial, Research Design, Humans, Mendelian Randomization Analysis/methods, Mendelian Randomization Analysis
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8
Authors: et al.
Contributors: et al.
Source: Cardiovascular Research. 120:95-107
Subject Terms: Heart Failure, Myocardial Infarction, Mendelian Randomization Analysis/methods, Heart failure, Single Nucleotide, Aortic Valve Stenosis, Aortic valve stenosis, Mendelian Randomization Analysis, Genetic polymorphisms, Atrial fibrillation, Polymorphism, Single Nucleotide, 3. Good health, Adiponectin/genetics, Heart Failure/diagnosis, Myocardial infarction, Risk Factors, Atrial Fibrillation, Atrial Fibrillation/diagnosis, Humans, Adiponectin, Myocardial Infarction/diagnosis, Polymorphism, Aortic Valve Stenosis/epidemiology, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/37897683
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9
Authors:
Source: Lipids Health Dis
Lipids in Health and Disease, Vol 23, Iss 1, Pp 1-4 (2024)
Stender, S, Gellert-Kristensen, H & Smith, G D 2024, ' Reclaiming mendelian randomization from the deluge of papers and misleading findings ', Lipids in Health and Disease, vol. 23, no. 1, 286 . https://doi.org/10.1186/s12944-024-02284-wSubject Terms: UK Biobank, RC620-627, Epidemiology, 2SMR, Comment, Mendelian Randomization Analysis/methods, Nonlinear MR, Mendelian Randomization Analysis, Genome-Wide Association Study/methods, Mendelian randomization, Humans, Vitamin D, name=Bristol Population Health Science Institute, Nutritional diseases. Deficiency diseases, Genome-Wide Association Study
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10
Authors:
Source: Bioinformatics
Bioinformatics, vol. 40, no. 8Subject Terms: 0301 basic medicine, Mendelian Randomization Analysis/methods, Transcriptome/genetics, Polymorphism, Single Nucleotide, Software, Algorithms, Humans, Applications Note, 0303 health sciences, 03 medical and health sciences, Mendelian Randomization Analysis, Transcriptome
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11
Authors: et al.
Source: Eur Heart J
Siedlinski, M, Carnevale, L, Xu, X, Carnevale, D, Evangelou, E, Caulfield, M J, Maffia, P, Wardlaw, J, Samani, N J, Tomaszewski, M, Lembo, G, Holmes, M V & Guzik, T J 2023, ' Genetic analyses identify brain structures related to cognitive impairment associated with elevated blood pressure ', European Heart Journal . https://doi.org/10.1093/eurheartj/ehad101
Siedlinski, M, Carnevale, L, Xu, X, Carnevale, D, Evangelou, E, Caulfield, M J, Maffia, P, Wardlaw, J, Samani, N J, Tomaszewski, M, Lembo, G, Holmes, M V & Guzik, T J 2023, 'Genetic analyses identify brain structures related to cognitive impairment associated with elevated blood pressure', European Heart Journal, vol. 44, no. 23, pp. 2114-2125. https://doi.org/10.1093/eurheartj/ehad101
European Heart JournalSubject Terms: Genome-wide association study, hypertension, brain, Mendelian Randomization Analysis/methods, Blood Pressure, Cognitive Dysfunction/genetics, Polymorphism, Single Nucleotide, blood pressure, cognitive function, genome-wide association study, mendelian randomisation, Hypertension/complications, Humans, Fast Track Translational Research, Cognitive Dysfunction, Polymorphism, Mendelian randomisation, Brain, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide/genetics, Blood pressure, Cognitive function, Hypertension, Single Nucleotide/genetics, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/36972688
https://research.manchester.ac.uk/en/publications/c67a94e1-d53d-43c3-ac99-0efe8d03f6b0
https://doi.org/10.1093/eurheartj/ehad101
https://hdl.handle.net/11588/980703
https://academic.oup.com/eurheartj/article/44/23/2114/7081391?login=true
https://academic.oup.com/eurheartj/advance-article/doi/10.1093/eurheartj/ehad101/7081391
https://doi.org/10.1093/eurheartj/ehad101
https://hdl.handle.net/20.500.11820/a3245853-db77-4ac4-9cad-1c31f4ffef19
https://www.pure.ed.ac.uk/ws/files/337653504/ehad101.pdf
https://ruj.uj.edu.pl/xmlui/handle/item/310461
https://academic.oup.com/eurheartj/advance-article/doi/10.1093/eurheartj/ehad101/7081391
https://hdl.handle.net/11588/980703
https://doi.org/10.1093/eurheartj/ehad101
https://academic.oup.com/eurheartj/article/44/23/2114/7081391?login=true
https://research.manchester.ac.uk/en/publications/c67a94e1-d53d-43c3-ac99-0efe8d03f6b0
http://www.scopus.com/inward/record.url?scp=85163892242&partnerID=8YFLogxK
https://www.mendeley.com/catalogue/3cfd4945-f251-3228-b88d-94efe3391660/
https://doi.org/10.1093/eurheartj/ehad101 -
12
Authors:
Source: Alton, P, Hughes, D M & Zhao, S S 2023, 'Cardiovascular safety of genetically proxied interleukin-5 inhibition : A mendelian randomization study', Respiratory Investigation, vol. 61, no. 2, pp. 149-152. https://doi.org/10.1016/j.resinv.2022.12.004
Subject Terms: 0301 basic medicine, 0303 health sciences, Mendelian Randomization Analysis/methods, Single Nucleotide, Venous Thromboembolism, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide, 3. Good health, Stroke, 03 medical and health sciences, Stroke/genetics, Cardiovascular Diseases, Humans, Polymorphism, Interleukin-5, Genome-Wide Association Study
Access URL: https://pubmed.ncbi.nlm.nih.gov/36682083
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13
Authors:
Source: Psychiatr Genet
Subject Terms: Psychiatry, 0301 basic medicine, Depressive Disorder, Major, Reproducibility of Results, Review Article, Mendelian Randomization Analysis, 3. Good health, Causality, 03 medical and health sciences, 0302 clinical medicine, Mendelian Randomization Analysis / methods, 616.89, Humans
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14
Authors: et al.
Contributors: et al.
Source: BMC Res Notes
BMC Research Notes, Vol 17, Iss 1, Pp 1-6 (2024)Subject Terms: Science (General), QH301-705.5, Two-sample Mendelian randomisation, Mendelian Randomization Analysis/methods, Mendelian Randomization Analysis, Population homogeneity, 3. Good health, Causality, Q1-390, Research Note, Phenotype, Genome-Wide Association Study/methods, Medicine, Biology (General), Sensitivity analysis, Genetic Association Studies, Genome-Wide Association Study
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15
Authors: et al.
Source: BMC Pregnancy Childbirth
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-11 (2024)
Thompson, WD, Reynolds, RM, Beaumont, RN, Warrington, NM, Tyrrell, J, Wood, AR, Evans, DM, Mcdonald, TJ, Hattersley, AH, Freathy, RM, Lawlor, DA & Borges, MC 2024, ' Maternal plasma cortisol’s effect on offspring birth weight: a Mendelian Randomisation study ', BMC pregnancy and childbirth, vol. 24, no. 1 . https://doi.org/10.1186/s12884-024-06250-3
BMC Pregnancy and ChildbirthSubject Terms: 0301 basic medicine, UK Biobank, Genotype, Hydrocortisone, Birth Weight/genetics, Mendelian Randomization Analysis/methods, Polymorphism, Single Nucleotide, Cortisol, 03 medical and health sciences, 0302 clinical medicine, Birth weight, Mendelian Randomization, Pregnancy, Humans, Birth Weight, Polymorphism, Efsoch, Research, Infant, Newborn, Infant, Single Nucleotide, Gynecology and obstetrics, Mendelian Randomization Analysis, Newborn, 3. Good health, Causality, RG1-991, Female, name=Bristol Population Health Science Institute, EFSOCH, Genome-Wide Association Study
File Description: application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/38225564
https://doaj.org/article/184b224809554cf29e490e6fb1d795b3
https://www.pure.ed.ac.uk/ws/files/413971339/Effect_of_maternal_pregnancy_cortisol_on_offspring_birth_weight_BMC_accepted.docx
https://hdl.handle.net/20.500.11820/79342381-6c79-4be6-99fd-382b951cc939
https://hdl.handle.net/11250/3189160 -
16
Authors: et al.
Contributors: et al.
Source: Int J Cancer
Zhou, X, Wang, L, Xiao, J, Sun, J, Yu, L, Zhang, H, Meng, X, Yuan, S, Timofeeva, M, Law, P J, Houlston, R S, Ding, K, Dunlop, M G, Theodoratou, E & Li, X 2022, ' Alcohol consumption, DNA methylation and colorectal cancer risk : Results from pooled cohort studies and Mendelian randomization analysis ', International Journal of Cancer, vol. 151, no. 1, pp. 83-94 . https://doi.org/10.1002/ijc.33945Subject Terms: 0301 basic medicine, Alcohol Drinking, colorectal cancer, Mendelian Randomization Analysis/methods, Polymorphism, Single Nucleotide, Cancer Genetics and Epigenetics, Alcohol Drinking/epidemiology, Cohort Studies, 03 medical and health sciences, Neoplasm Proteins/genetics, Mendelian randomization, Humans, Polymorphism, Colorectal Neoplasms/epidemiology, 0303 health sciences, DNA methylation, alcohol, Single Nucleotide, DNA Methylation, Mendelian Randomization Analysis, Neoplasm Proteins, 3. Good health, Colorectal Neoplasms, Genome-Wide Association Study
File Description: application/pdf; Print-Electronic
Access URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.33945
https://pubmed.ncbi.nlm.nih.gov/35102554
https://hdl.handle.net/20.500.11820/df01f2d1-dcc2-408e-9fa9-6bb5b0d8f4a2
https://www.pure.ed.ac.uk/ws/files/252720936/Alcohol_consumption_DNA_methylation_and_colorectal_cancer_risk_Results_from_pooled_cohort_studies_and_Mendelian_randomization_analysis.pdf -
17
Authors: et al.
Source: Nature communications, vol. 15, no. 1, pp. 1420
Subject Terms: Humans, Child, Genome-Wide Association Study/methods, Mendelian Randomization Analysis/methods, Obesity/epidemiology, Obesity/genetics, Risk Factors, Educational Status, Polymorphism, Single Nucleotide
File Description: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/38360877; info:eu-repo/semantics/altIdentifier/eissn/2041-1723; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_606B3CD782342; https://serval.unil.ch/notice/serval:BIB_606B3CD78234; https://serval.unil.ch/resource/serval:BIB_606B3CD78234.P001/REF.pdf
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18
Authors: et al.
Source: Munafo, M R, Brown, J, Hefler, M & Davey Smith, G 2024, 'Managing the exponential growth of mendelian randomization studies', Tobacco Control, vol. 33, no. 5, pp. 559-560. https://doi.org/10.1136/tc-2024-058987
Subject Terms: /dk/atira/pure/core/keywords/targ, name=TARG, Humans, Mendelian Randomization Analysis/methods, Research Design
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19
Authors: et al.
Source: Munafò, M, Brown, J, Hefler, M & Davey Smith, G 2024, 'Managing the Exponential Growth of Mendelian Randomization Studies', Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco, vol. 26, no. 10, pp. 1273-1275. https://doi.org/10.1093/ntr/ntae165
Subject Terms: /dk/atira/pure/core/keywords/targ, name=TARG, Mendelian Randomization Analysis/methods
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20
Authors:
Source: Genetic epidemiology, vol. 47, no. 4, pp. 314-331
Subject Terms: 0301 basic medicine, 0303 health sciences, 03 medical and health sciences, Phenotype, Bias, Humans, Genome-Wide Association Study, Mendelian Randomization Analysis/methods, Polymorphism, Single Nucleotide, Mendelian randomization, sample overlap, weak instrument bias, winner's curse, Mendelian Randomization Analysis
File Description: application/pdf
Access URL: https://www.biorxiv.org/content/biorxiv/early/2021/03/28/2021.03.26.437168.full.pdf
https://pubmed.ncbi.nlm.nih.gov/37036286
https://europepmc.org/article/PPR/PPR304210
https://biorxiv.org/content/10.1101/2021.03.26.437168v1.full.pdf
https://www.biorxiv.org/content/10.1101/2021.03.26.437168v1
https://serval.unil.ch/resource/serval:BIB_F65931571130.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_F65931571130
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_F659315711301
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