STrengthening the REporting of Genetic Association Studies
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STrengthening the REporting of Genetic Association Studies
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
STREGA
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
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STrengthening the REporting of Genetic Association Studies
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
STREGA
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
Names
More detailed information about this field from each metasource.
STrengthening the REporting of Genetic Association Studies
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
STREGA
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
The STrengthening the REporting of Genetic Association studies (STREGA) initiative builds on the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement and provides additions to 12 of the 22 items on the STROBE checklist. The additions concern population stratification, genotyping errors, modelling haplotype variation, Hardy-Weinberg equilibrium, replication, selection of participants, rationale for choice of genes and variants, treatment effects in studying quantitative traits, statistical methods, relatedness, reporting of descriptive and outcome data, and the volume of data issues that are important to consider in genetic association studies.
Description
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The STrengthening the REporting of Genetic Association studies (STREGA) initiative builds on the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement and provides additions to 12 of the 22 items on the STROBE checklist. The additions concern population stratification, genotyping errors, modelling haplotype variation, Hardy-Weinberg equilibrium, replication, selection of participants, rationale for choice of genes and variants, treatment effects in studying quantitative traits, statistical methods, relatedness, reporting of descriptive and outcome data, and the volume of data issues that are important to consider in genetic association studies.
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
Webpage:
http://www.equator-network.org/reporting-guidelines/strobe-strega/Webpage
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http://www.equator-network.org/reporting-guidelines/strobe-strega/
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
Publications:
Publications
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STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement
PMID: 19192942
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
Publications
More detailed information about this field from each metasource.
STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement
PMID: 19192942
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
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STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement
PubMed citations: 144.
144 articles citing: STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement
Association of MTHFR Polymorphisms with H-Type Hypertension: A Systemic Review and Network Meta-Analysis of Diagnostic Test Accuracy. PMID:35360528
Nutrigenetics, omega-3 and plasma lipids/lipoproteins/apolipoproteins with evidence evaluation using the GRADE approach: a systematic review. PMID:35193914
Impact of Inherited Genetic Variants on Critically Ill Septic Children. PMID:35056044
Implications of OPRM1 and CYP2B6 variants on treatment outcomes in methadone-maintained patients in Ontario: Exploring sex differences. PMID:34910759
Replication of European hypertension associations in a case-control study of 9,534 African Americans. PMID:34793544
Association between IL-1B (-511)/IL-1RN (VNTR) polymorphisms and type 2 diabetes: a systematic review and meta-analysis. PMID:34754627
Clonal Hematopoiesis Is Associated With Higher Risk of Stroke. PMID:34743536
Putative Role of MCT1 rs1049434 Polymorphism in High-Intensity Endurance Performance: Concept and Basis to Understand Possible Individualization Stimulus. PMID:34678924
Common Statin Intolerance Variants in ABCB1 and LILRB5 Show Synergistic Effects on Statin Response: An Observational Study Using Electronic Health Records. PMID:34659336
GoodReports: developing a website to help health researchers find and use reporting guidelines. PMID:34657590
Association between Polymorphisms in Vitamin D Pathway-Related Genes, Vitamin D Status, Muscle Mass and Function: A Systematic Review. PMID:34578986
Genome-Wide Association Study of NAFLD Using Electronic Health Records. PMID:34535985
A Proposal for a Data-Driven Approach to the Influence of Music on Heart Dynamics. PMID:34490368
MICA and KIR: Immunogenetic Factors Influencing Left Ventricular Systolic Dysfunction and Digestive Clinical Form of Chronic Chagas Disease. PMID:34489964
Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans. PMID:34135450
Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. PMID:34098570
Artificial intelligence extension of the OSCAR-IB criteria. PMID:34008926
A Scoping Review of the Methodology Used in Studies of Genetic Influences on the Development of Keloid or Hypertrophic Scarring in Adults and Children After Acute Wounding. PMID:33975469
Defining functional variants associated with Alzheimer's disease in the induced immune response. PMID:33959712
Genetic polymorphisms as multi-biomarkers in severe acute respiratory syndrome (SARS) by coronavirus infection: A systematic review of candidate gene association studies. PMID:33933633
Expanding the Genotypic Spectrum of Congenital Sensory and Autonomic Neuropathies Using Whole-Exome Sequencing. PMID:33884296
Meta-Analysis of ABCG2 and ABCB1 Polymorphisms With Sunitinib-Induced Toxicity and Efficacy in Renal Cell Carcinoma. PMID:33762959
Improving reporting standards for polygenic scores in risk prediction studies. PMID:33692554
Gene Sequencing for Pathogenic Variants Among Adults With Breast and Ovarian Cancer in the Caribbean. PMID:33646313
The ACE and ACTN3 polymorphisms in female soccer athletes. PMID:33602343
CD38 is associated with bonding-relevant cognitions and relationship satisfaction over the first 3 years of marriage. PMID:33536489
Clustering suicidal phenotypes and genetic associations with brain-derived neurotrophic factor in patients with substance use disorders. PMID:33479229
Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study. PMID:33445220
A review found inadequate reporting of case-control studies of risk factors for pancreatic cancer. PMID:33359318
An ontology-based documentation of data discovery and integration process in cancer outcomes research. PMID:33317497
A brief guide to the science and art of writing manuscripts in biomedicine. PMID:33167977
Better reporting quality for improved pediatric investigation: Application of health research reporting guidelines. PMID:32851210
Association of matrix metalloproteinase-12 polymorphisms with chronic obstructive pulmonary disease risk: A protocol for systematic review and meta analysis. PMID:32756209
Detection of somatic TP53 mutation in surgically resected small-cell lung cancer by targeted exome sequencing: association with longer relapse-free survival. PMID:32685741
Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease. PMID:32568366
Association of NOD2 and IFNG single nucleotide polymorphisms with leprosy in the Amazon ethnic admixed population. PMID:32433683
Reporting guideline checklists are not quality evaluation forms: they are guidance for writing. PMID:32373717
Wound care practices across two acute care settings: A comparative study. PMID:31820850
The Variant at TGFBRAP1 but Not TGFBR2 Is Associated with Antituberculosis Drug-Induced Liver Injury. PMID:31534460
Genetic polymorphisms in PXR and NF-κB1 influence susceptibility to anti-tuberculosis drug-induced liver injury. PMID:31490979
Identification of HLA-DRB1*04:10 allele as risk allele for Japanese moyamoya disease and its association with autoimmune thyroid disease: A case-control study. PMID:31412073
Single nucleotide polymorphisms of the genes IL-2, IL-2RB, and JAK3 in patients with cutaneous leishmaniasis caused by Leishmania (V.) guyanensis in Manaus, Amazonas, Brazil. PMID:31393896
Biological predictors of chemotherapy-induced peripheral neuropathy (CIPN): MASCC neurological complications working group overview. PMID:31363906
Prioritization of Variants for Investigation of Genotype-Directed Nutrition in Human Superpopulations. PMID:31323740
A systematic review of the prevalence of DNA damage response gene mutations in prostate cancer. PMID:31322208
Single Nucleotide Polymorphisms and Post-operative Complications Following Major Gastrointestinal Surgery: a Systematic Review and Meta-analysis. PMID:31270721
Functional polymorphisms of the receptor for the advanced glycation end product promoter gene in inflammatory bowel disease: a case-control study. PMID:31175506
Effect of Fc Receptor Genetic Diversity on HIV-1 Disease Pathogenesis. PMID:31143176
Genetic study in patients operated dentally and anesthetized with articaine-epinephrine. PMID:31118755
Ten simple rules for carrying out and writing meta-analyses. PMID:31095553
Association of Economic Status and Educational Attainment With Posttraumatic Stress Disorder: A Mendelian Randomization Study. PMID:31050786
The role of FAS, FAS-L, BAX, and BCL-2 gene polymorphisms in determining susceptibility to unexplained recurrent pregnancy loss. PMID:30937706
Persistence of chloroquine resistance alleles in malaria endemic countries: a systematic review of burden and risk factors. PMID:30871535
K13-propeller gene polymorphisms in Plasmodium falciparum parasite population in malaria affected countries: a systematic review of prevalence and risk factors. PMID:30846002
Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk. PMID:30845235
Smoking Cessation Pharmacotherapy Based on Genetically-Informed Biomarkers: What is the Evidence? PMID:30690475
High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report. PMID:30592451
K13-propeller gene polymorphisms in Plasmodium falciparum parasite population: a systematic review protocol of burden and associated factors. PMID:30447701
Association of tumour necrosis factor-α (TNF-α) gene polymorphisms (-308 G>A and -238 G>A) and the risk of severe dengue: A meta-analysis and trial sequential analysis. PMID:30300401
Reported use of reporting guidelines among JNCI: Journal of the National Cancer Institute authors, editorial outcomes, and reviewer ratings related to adherence to guidelines and clarity of presentation. PMID:30275983
Prevalence of chloroquine resistance alleles among Plasmodium falciparum parasites in countries affected by malaria disease since change of treatment policy: a systematic review protocol. PMID:30053912
The STROBE Extensions: Considerations for Development. PMID:30052544
Genetic polymorphisms of organic cation transporters 1 (OCT1) and responses to metformin therapy in individuals with type 2 diabetes mellitus: a systematic review protocol. PMID:30041690
Genetic studies of gestational duration and preterm birth. PMID:30007778
Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility. PMID:29979793
A Common Variation in the Caveolin 1 Gene Is Associated with High Serum Triglycerides and Metabolic Syndrome in an Admixed Latin American Population. PMID:29762069
Frequency of common polymorphisms in Caveolin 1 ( CAV1 ) gene in adults with high serum triglycerides from Colombian Caribbean Coast. PMID:29662258
Recipient rs1045642 Polymorphism Is Associated With Office Blood Pressure at 1-Year Post Kidney Transplantation: A Single Center Pharmacogenetic Cohort Pilot Study. PMID:29556197
Inter-individual variation in health and disease associated with pulmonary infectious agents. PMID:29353387
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis. PMID:29324865
Variations in ADIPOR1 But Not ADIPOR2 are Associated With Hypertriglyceridemia and Diabetes in an Admixed Latin American Population. PMID:29145541
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research. PMID:29062538
A haplotypic variant at the IRGM locus and rs11747270 are related to the susceptibility for chronic periodontitis. PMID:28983640
Genetic polymorphisms predict response to anti-tumor necrosis factor treatment in Crohn's disease. PMID:28785150
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research. PMID:28768629
Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis. PMID:28552956
Positive association between ALDH2 rs671 polymorphism and essential hypertension: A case-control study and meta-analysis. PMID:28472173
Association between ErbB4 single nucleotide polymorphisms and susceptibility to schizophrenia: A meta-analysis of case-control studies. PMID:28225484
Medicine, medical writing, and India. PMID:28066014
Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study. PMID:28030616
Interpretation of gene associations with risk of acute respiratory distress syndrome: P values, Bayes factors, positive predictive values, and need for replication. PMID:27998281
The AGT Gene M235T Polymorphism and Response of Power-Related Variables to Aerobic Training. PMID:27928207
Ocular toxoplasmosis: susceptibility in respect to the genes encoding the KIR receptors and their HLA class I ligands. PMID:27827450
Genomic analyses of early peri-implant bone healing in humans: a systematic review. PMID:27747627
How to Write a Scientific Paper: Practical Guidelines. PMID:27683473
Host genetics and susceptibility to congenital and childhood cytomegalovirus infection: a systematic review. PMID:27586547
Matrix Metalloproteinase-2 Polymorphisms in Chronic Heart Failure: Relationship with Susceptibility and Long-Term Survival. PMID:27551966
CONSISE statement on the reporting of Seroepidemiologic Studies for influenza (ROSES-I statement): an extension of the STROBE statement. PMID:27417916
Association of PDE4B Polymorphisms with Susceptibility to Schizophrenia: A Meta-Analysis of Case-Control Studies. PMID:26756575
A meta-analysis of the associations between the Q141K and Q126X ABCG2 gene variants and gout risk. PMID:26617691
Considerations for Using Genetic and Epigenetic Information in Occupational Health Risk Assessment and Standard Setting. PMID:26583908
The role of host genetic factors in respiratory tract infectious diseases: systematic review, meta-analyses and field synopsis. PMID:26524966
Effect of follicle-stimulating hormone receptor Asn680Ser polymorphism on the outcomes of controlled ovarian hyperstimulation: an updated meta-analysis of 16 cohort studies. PMID:26481502
Genetic epistasis between killer immunoglobulin-like receptors and human leukocyte antigens in Kawasaki disease susceptibility. PMID:26335810
Epidemiology of HEV in the Mediterranean basin: 10-year prevalence in Italy. PMID:26173715
Identification of genetic variants in the TNF promoter associated with COPD secondary to tobacco smoking and its severity. PMID:26170653
Mitochondrial DNA Haplogroups and Neurocognitive Impairment During HIV Infection. PMID:26129753
The SNP rs931794 in 15q25.1 Is Associated with Lung Cancer Risk: A Hospital-Based Case-Control Study and Meta-Analysis. PMID:26079375
Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis. PMID:26077880
Effects of the CYP3A4*1B Genetic Polymorphism on the Pharmacokinetics of Tacrolimus in Adult Renal Transplant Recipients: A Meta-Analysis. PMID:26039043
Assessing the quality of published genetic association studies in meta-analyses: the quality of genetic studies (Q-Genie) tool. PMID:25975208
Genetics of diabetic nephropathy: a long road of discovery. PMID:25971618
Should we have blind faith in bioinformatics software? Illustrations from the SNAP web-based tool. PMID:25742008
Incorporation of personal single nucleotide polymorphism (SNP) data into a national level electronic health record for disease risk assessment, part 1: an overview of requirements. PMID:25599712
Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD): the TRIPOD Statement. PMID:25563062
Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD): the TRIPOD statement. PMID:25562432
Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD): the TRIPOD statement. The TRIPOD Group. PMID:25561516
Association of vWA and TPOX polymorphisms with venous thrombosis in Mexican mestizos. PMID:25250329
Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations? PMID:25145545
Relation of completeness of reporting of health research to journals' endorsement of reporting guidelines: systematic review. PMID:24965222
Maternal Characteristics of Women Exposed to Hypnotic Benzodiazepine Receptor Agonist during Pregnancy. PMID:24817891
Association between vitamin D receptor gene polymorphisms and breast cancer risk: a meta-analysis of 39 studies. PMID:24769568
The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research. PMID:24435092
RsaI but not DraI polymorphism in CYP2E1 gene increases the risk of gastrointestinal cancer in Malaysians: a case-control study. PMID:24394801
APOE associations with severe CAA-associated vasculopathic changes: collaborative meta-analysis. PMID:24163429
Better reporting of scientific studies: why it matters. PMID:24013839
A SNP resource for Douglas-fir: de novo transcriptome assembly and SNP detection and validation. PMID:23445355
Setting the RECORD straight: developing a guideline for the REporting of studies Conducted using Observational Routinely collected Data. PMID:23413321
Reporting genetic association studies: the roadblocks and guiding rules for robust results. PMID:23053565
Reporting guidelines: optimal use in preventive medicine and public health. PMID:22992369
Influence of CYP2C9 and VKORC1 on patient response to warfarin: a systematic review and meta-analysis. PMID:22952875
Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction. PMID:22876292
Genetics and genomics in pediatric septic shock. PMID:22511139
The tension between data sharing and the protection of privacy in genomics research. PMID:22404490
Genetic epidemiology with a capital E: where will we be in another 10 years? PMID:22311722
STROBE-ME too! PMID:22076058
Developing risk prediction models for type 2 diabetes: a systematic review of methodology and reporting. PMID:21902820
Ethical aspects of human biobanks: a systematic review. PMID:21674823
Genetics of rhinosinusitis. PMID:21499907
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement. PMID:21431409
Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration. PMID:21424820
Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement. PMID:21423587
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement. PMID:21411493
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement. PMID:21410995
Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration. PMID:21407270
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement. PMID:21407265
Genetic polymorphisms in homocysteine metabolism and response to folate intake: a comprehensive strategy to elucidate useful genetic information. PMID:20571252
Replication in genome-wide association studies. PMID:20454541
Selection of extreme phenotypes: the role of clinical observation in translational research. PMID:20231122
Guidance for developers of health research reporting guidelines. PMID:20169112
Common genetic variation and the control of HIV-1 in humans. PMID:20041166
Eating disorders: the current status of molecular genetic research. PMID:20033240
Reporting experiments in homeopathic basic research (REHBaR)--a detailed guideline for authors. PMID:19945681
Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how? PMID:19936793
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deoxyribonucleic acid
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
genome-wide association study
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
phenotype
metasource: Fairsharing.org
version: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
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More detailed information about this field from each metasource.
deoxyribonucleic acid
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
genome-wide association study
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
phenotype
metasource: Fairsharing.orgversion: FAIRsharing.org: STREGA; STrengthening the REporting of Genetic Association Studies; DOI: https://doi.org/10.25504/FAIRsharing.m21pn; Last edited: Jan. 8, 2019, 1:38 p.m.; Last accessed: Jan 03 2022 7:13 p.m.
dna genome-wide association study phenotype
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