| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | John Ioannidis | Q6251482 |
| P2093 | author name string | Fotini K Kavvoura | |
| P2860 | cites work | Why most published research findings are false | Q21092395 |
| Local literature bias in genetic epidemiology: an empirical evaluation of the Chinese literature | Q21563436 | ||
| ‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?* | Q22066036 | ||
| A comprehensive review of genetic association studies | Q22337119 | ||
| Design and analysis of admixture mapping studies | Q22337165 | ||
| Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease | Q22337234 | ||
| An exploratory test for an excess of significant findings | Q24273224 | ||
| The appropriateness of asymmetry tests for publication bias in meta-analyses: a large survey | Q24282603 | ||
| Selection in reported epidemiological risks: an empirical assessment | Q24288769 | ||
| Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study | Q24288773 | ||
| A Bayesian measure of the probability of false discovery in genetic epidemiology studies | Q24289227 | ||
| Sifting the evidence-what's wrong with significance tests? | Q24524896 | ||
| Genome-wide association study identifies novel breast cancer susceptibility loci | Q24645441 | ||
| A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity | Q24650037 | ||
| The case of the misleading funnel plot | Q24676535 | ||
| Bias in meta-analysis detected by a simple, graphical test | Q24685585 | ||
| The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer | Q24806109 | ||
| Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis | Q27860511 | ||
| Operating characteristics of a rank correlation test for publication bias | Q27860653 | ||
| Measuring inconsistency in meta-analyses | Q27860655 | ||
| Quantifying heterogeneity in a meta-analysis | Q27860672 | ||
| Meta-analysis in clinical trials | Q27860779 | ||
| Statistical aspects of the analysis of data from retrospective studies of disease | Q27860916 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| Meta-analysis of Observational Studies in Epidemiology: A Proposal for Reporting | Q27861077 | ||
| Misleading funnel plot for detection of bias in meta-analysis | Q28144453 | ||
| How should meta-regression analyses be undertaken and interpreted? | Q28193388 | ||
| Population stratification and spurious allelic association | Q28211105 | ||
| The path from genome-based research to population health: development of an international public health genomics network | Q28252405 | ||
| Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database | Q28280965 | ||
| Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research | Q28285027 | ||
| Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes | Q28680760 | ||
| Publication bias in clinical research | Q29541186 | ||
| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants | Q29547210 | ||
| Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels | Q29547214 | ||
| A modified test for small-study effects in meta-analyses of controlled trials with binary endpoints | Q29614902 | ||
| Replicating genotype-phenotype associations | Q29614919 | ||
| Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies | Q29614926 | ||
| Replication validity of genetic association studies | Q29615456 | ||
| Genome-wide association studies for common diseases and complex traits | Q29615822 | ||
| New models of collaboration in genome-wide association studies: the Genetic Association Information Network | Q29616279 | ||
| Assessing the probability that a positive report is false: an approach for molecular epidemiology studies | Q29616285 | ||
| Comparison of two methods to detect publication bias in meta-analysis | Q29617904 | ||
| Empirical evidence for selective reporting of outcomes in randomized trials: comparison of protocols to published articles | Q29618882 | ||
| The hazards of scoring the quality of clinical trials for meta-analysis | Q29619369 | ||
| Assessing heterogeneity in meta-analysis: Q statistic or I2 index? | Q29619545 | ||
| Effects of CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on HIV-1 disease progression: An international meta-analysis of individual-patient data. | Q30664904 | ||
| To IPD or not to IPD? Advantages and disadvantages of systematic reviews using individual patient data | Q30676636 | ||
| Commentary: meta-analysis of individual participants' data in genetic epidemiology | Q30707324 | ||
| Genetic variation and willingness to participate in epidemiologic research: data from three studies | Q31010279 | ||
| Early extreme contradictory estimates may appear in published research: the Proteus phenomenon in molecular genetics research and randomized trials | Q31170846 | ||
| Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations | Q33184110 | ||
| Sources of evidence for systematic reviews of interventions in diabetes | Q33223698 | ||
| Family-based versus unrelated case-control designs for genetic associations | Q33253242 | ||
| The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note | Q33260566 | ||
| The publication process itself was the major cause of publication bias in genetic epidemiology | Q33263359 | ||
| Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease | Q33276409 | ||
| Genetics of ischaemic stroke among persons of non-European descent: a meta-analysis of eight genes involving approximately 32,500 individuals | Q33282647 | ||
| Heterogeneity in meta-analyses of genome-wide association investigations | Q33297003 | ||
| Glutathione S-transferase polymorphisms and colorectal cancer: a HuGE review | Q33810936 | ||
| N-acetyltransferase polymorphisms and colorectal cancer: a HuGE review | Q33900247 | ||
| 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review | Q33900252 | ||
| Association mapping in structured populations | Q33903172 | ||
| Recent developments in genomewide association scans: a workshop summary and review | Q34021104 | ||
| A road map for efficient and reliable human genome epidemiology | Q42680046 | ||
| How vague is vague? A simulation study of the impact of the use of vague prior distributions in MCMC using WinBUGS. | Q44569346 | ||
| Common genetic variants for breast cancer: 32 largely refuted candidates and larger prospects | Q44834778 | ||
| Homocysteine and stroke: evidence on a causal link from mendelian randomisation | Q45225758 | ||
| Invited commentary: a critical look at some popular meta-analytic methods | Q46474567 | ||
| Welcome to the genomic era. | Q51828703 | ||
| Bayesian meta-analysis and meta-regression for gene-disease associations and deviations from Hardy-Weinberg equilibrium. | Q51942147 | ||
| In an empirical evaluation of the funnel plot, researchers could not visually identify publication bias. | Q51967379 | ||
| Estimation of magnitude in gene-environment interactions in the presence of measurement error. | Q52001293 | ||
| Summing up evidence: one answer is not always enough. | Q52900179 | ||
| Random-effects meta-analyses are not always conservative. | Q52915135 | ||
| Joint effect of genes and environment distorted by selection biases: implications for hospital-based case-control studies. | Q52942908 | ||
| Selection bias in the assessment of gene-environment interaction in case-control studies. | Q52953340 | ||
| Journals should publish all "null" results and should sparingly publish "positive" results. | Q52998122 | ||
| Language bias in randomised controlled trials published in English and German. | Q53358085 | ||
| Counterpoint: bias from population stratification is not a major threat to the validity of conclusions from epidemiological studies of common polymorphisms and cancer. | Q55035893 | ||
| The Emergence of Networks in Human Genome Epidemiology | Q56828411 | ||
| Make it HuGE: human genome epidemiology reviews, population health, and the IJE | Q57109370 | ||
| A candidate gene approach to searching for low-penetrance breast and prostate cancer genes | Q57306192 | ||
| Turning the Pump Handle: Evolving Methods for Integrating the Evidence on Gene-Disease Association | Q57542900 | ||
| Mendelian randomisation: a new spin or real progress? | Q64134143 | ||
| Are vitamin D receptor polymorphisms associated with bone mineral density? A meta-analysis | Q71908632 | ||
| Population stratification in epidemiologic studies of common genetic variants and cancer: quantification of bias | Q74028329 | ||
| Effect of the statistical significance of results on the time to completion and publication of randomized efficacy trials | Q74121809 | ||
| Genetic effects on HIV disease progression | Q74539570 | ||
| Detecting and describing heterogeneity in meta-analysis | Q74573466 | ||
| The Human Genome Epidemiology Network | Q74776633 | ||
| Clinical epidemiological quality in molecular genetic research: the need for methodological standards | Q77816185 | ||
| An empirical evaluation of multifarious outcomes in pharmacogenetics: beta-2 adrenoceptor gene polymorphisms in asthma treatment | Q79138082 | ||
| Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis | Q79435087 | ||
| Genetic effects versus bias for candidate polymorphisms in myocardial infarction: case study and overview of large-scale evidence | Q79758514 | ||
| Selective reporting biases in cancer prognostic factor studies | Q80395257 | ||
| Case-control association tests correcting for population stratification | Q82399033 | ||
| Accounting for unmeasured population substructure in case-control studies of genetic association using a novel latent-class model | Q34044226 | ||
| Meta-analysis of the literature or of individual patient data: is there a difference? | Q34334544 | ||
| Identifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors | Q34389549 | ||
| Gene-environment interactions in human diseases | Q34407923 | ||
| Statistical heterogeneity in systematic reviews of clinical trials: a critical appraisal of guidelines and practice. | Q34513646 | ||
| Genomic control, a new approach to genetic-based association studies | Q34539204 | ||
| Beta blockade during and after myocardial infarction: an overview of the randomized trials | Q34557544 | ||
| The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis | Q34569981 | ||
| Meta-analyses of molecular association studies: methodologic lessons for genetic epidemiology | Q35136177 | ||
| Flexible design for following up positive findings | Q35946307 | ||
| Relative citation impact of various study designs in the health sciences | Q36130841 | ||
| Dose-related association of MTHFR 677T allele with risk of ischemic stroke: evidence from a cumulative meta-analysis | Q36157785 | ||
| CTLA-4 gene polymorphisms and susceptibility to type 1 diabetes mellitus: a HuGE Review and meta-analysis | Q36165718 | ||
| A network of investigator networks in human genome epidemiology | Q36193157 | ||
| Genotyping errors: causes, consequences and solutions | Q36320430 | ||
| Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls. | Q36356533 | ||
| Commentary: grading the credibility of molecular evidence for complex diseases | Q36422605 | ||
| Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database | Q36461180 | ||
| Factors influencing publication of research results. Follow-up of applications submitted to two institutional review boards | Q36728722 | ||
| Data trawling: to fish or not to fish | Q36829063 | ||
| Non-replication and inconsistency in the genome-wide association setting | Q36841272 | ||
| Uncertainty in heterogeneity estimates in meta-analyses | Q36987539 | ||
| Establishment of genetic associations for complex diseases is independent of early study findings | Q39218509 | ||
| Molecular evidence-based medicine: evolution and integration of information in the genomic era. | Q40219317 | ||
| Sample bias among women with retained DNA samples for future genetic studies | Q40273882 | ||
| Assessing publication bias in genetic association studies: evidence from a recent meta-analysis. | Q40464249 | ||
| Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. | Q40469466 | ||
| Cumulative meta-analysis of clinical trials builds evidence for exemplary medical care. | Q40590984 | ||
| Association of collagen Ialpha 1 Sp1 polymorphism with the risk of prevalent fractures: a meta-analysis. | Q40687589 | ||
| Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations | Q40718941 | ||
| Misclassification of genetic susceptibility biomarkers: implications for case-control studies and cross-population comparisons. | Q41074667 | ||
| P433 | issue | 1 | |
| P921 | main subject | meta-analysis | Q815382 |
| P304 | page(s) | 1-14 | |
| P577 | publication date | 2007-11-17 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Methods for meta-analysis in genetic association studies: a review of their potential and pitfalls | |
| P478 | volume | 123 |
| Q52673305 | A Bayesian Framework for Generalized Linear Mixed Modeling Identifies New Candidate Loci for Late-Onset Alzheimer's Disease. |
| Q55332313 | A data mining paradigm for identifying key factors in biological processes using gene expression data. |
| Q51955888 | A drug transporter for all ages? ABCB1 and the developmental pharmacogenetics of cyclosporine. |
| Q37738889 | A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. |
| Q34130800 | A functional variant in ERAP1 predisposes to multiple sclerosis |
| Q35150211 | A meta-analysis of gene expression quantitative trait loci in brain |
| Q30541742 | A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability |
| Q53072839 | A1166C genetic variation of the angiotensin II type I receptor gene and susceptibility to coronary heart disease: Collaborative of 53 studies with 20,435 cases and 23,674 controls |
| Q34696368 | Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures |
| Q38170153 | Adoptive infusion of tolerance dendritic cells prolongs survival of small intestine allografts in rats: systematic review and meta-analysis |
| Q34709103 | An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs |
| Q38376456 | Association Between the IL-6 rs1800795 Polymorphism and the Risk of Cervical Cancer: A Meta-Analysis of 1210 Cases and 1525 Controls |
| Q26864806 | Association between CC10 +38A/G polymorphism and asthma risk: A meta-analysis |
| Q35112796 | Association between polymorphisms in lysyl oxidase-like 1 and susceptibility to pseudoexfoliation syndrome and pseudoexfoliation glaucoma |
| Q37500050 | Association between the IL1B (-511), IL1B (+3954), IL1RN (VNTR) polymorphisms and Graves' disease risk: a meta-analysis of 11 case-control studies |
| Q35623721 | Association between toll-like receptors 9 (TLR9) gene polymorphism and risk of pulmonary tuberculosis: meta-analysis |
| Q33571844 | Association of IL4, IL13, and IL4R polymorphisms with gastrointestinal cancer risk: A meta-analysis |
| Q35203432 | Association of TPH-1 and TPH-2 gene polymorphisms with suicidal behavior: a systematic review and meta-analysis |
| Q30981985 | Association of matrix metalloproteinase family gene polymorphisms with lung cancer risk: logistic regression and generalized odds of published data |
| Q34545613 | Association of the 5HTR2A gene with suicidal behavior: case-control study and updated meta-analysis. |
| Q37141573 | Association of the GNAS locus with severe malaria |
| Q38255387 | Association of vitamin D receptor gene polymorphisms with asthma risk: systematic review and updated meta-analysis of case-control studies |
| Q37599326 | Bayesian statistical methods for genetic association studies |
| Q35566722 | Big data challenges in bone research: genome-wide association studies and next-generation sequencing |
| Q37320809 | Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants. |
| Q50083309 | Common genetic variant rs3802842 in 11q23 contributes to colorectal cancer risk in Chinese population |
| Q41913384 | Credible genetic associations? |
| Q49587994 | Cross-Phenotype Association Analysis Using Summary Statistics from GWAS. |
| Q34663979 | Detection of ancestry informative HLA alleles confirms the admixed origins of Japanese population. |
| Q92701923 | Do Genomic Factors Play a Role in Diabetic Retinopathy? |
| Q90682049 | Effect of Autologous Bone Marrow Stem Cell Therapy in Patients with Liver Cirrhosis: A Meta-analysis |
| Q33595844 | Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies |
| Q33926033 | FTO gene polymorphisms and obesity risk: a meta-analysis |
| Q36470668 | Gamma-ray-induced mutagen sensitivity and risk of sporadic breast cancer in young women: a case-control study |
| Q37143708 | Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes |
| Q57313776 | Genetic Polymorphisms Associated with Retinal Vein Occlusion: A Greek Case-control Study and Meta-analysis |
| Q43031194 | Genetic determinants of treatment benefit of the angiotensin-converting enzyme-inhibitor perindopril in patients with stable coronary artery disease |
| Q53091314 | Genetic polymorphisms of UGT1A7 and cancer risk: evidence from 21 case-control studies. |
| Q45905242 | Genetic, epidemiological and biological analysis of interleukin-10 promoter single-nucleotide polymorphisms suggests a definitive role for -819C/T in leprosy susceptibility. |
| Q37074094 | Genetics and women's health issues--the commitment of EMS to women scientists and gender-associated disease topics |
| Q37681343 | Genetics of osteoporosis: accelerating pace in gene identification and validation |
| Q33526292 | Genome wide association for addiction: replicated results and comparisons of two analytic approaches |
| Q41894157 | Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies |
| Q33982372 | Impact of CYP2C19 variant genotypes on clinical efficacy of antiplatelet treatment with clopidogrel: systematic review and meta-analysis |
| Q36725968 | Impact of phenotype definition on genome-wide association signals: empirical evaluation in human immunodeficiency virus type 1 infection |
| Q35007657 | Imputation aware meta-analysis of genome-wide association studies |
| Q42945109 | Increased risk of major depression by childhood abuse is not modified by CNR1 genotype |
| Q30374387 | Interferon-Inducible Transmembrane Protein 3 Genetic Variant rs12252 and Influenza Susceptibility and Severity: A Meta-Analysis. |
| Q35547835 | Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand |
| Q33571814 | Leveraging genetic variability across populations for the identification of causal variants. |
| Q35753091 | Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challenges |
| Q37642504 | Meta-analysis for genome-wide association studies using case-control design: application and practice |
| Q24273398 | Meta-analysis in genome-wide association studies |
| Q35986264 | Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia |
| Q38105261 | Meta-analysis methods for genome-wide association studies and beyond |
| Q35299817 | Meta-analysis of diabetic nephropathy associated genetic variants in inflammation and angiogenesis involved in different biochemical pathways |
| Q42412705 | Meta-analysis of genetic association studies under heterogeneity |
| Q37620160 | Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse |
| Q28749593 | Meta-analysis of genome-wide association studies with overlapping subjects |
| Q28660901 | Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data |
| Q38779634 | Meta-analysis of the serotonin transporter promoter variant (5-HTTLPR) in relation to adverse environment and antisocial behavior. |
| Q46784510 | Methodological remarks concerning a recent meta-analysis on XPG Asp1104His and XPF Arg415Gln polymorphisms and breast cancer risk |
| Q34328854 | Microsomal epoxide hydrolase gene polymorphisms and risk of chronic obstructive pulmonary disease: A comprehensive meta-analysis |
| Q34026890 | No association between COMT val158met polymorphism and suicidal behavior: meta-analysis and new data |
| Q37990826 | No association between the HTR1A gene and suicidal behavior: a meta-analysis |
| Q35333890 | No association of functional polymorphisms in methlylenetetrahydrofolate reductase and the risk and minor physical anomalies of schizophrenia in Korean population |
| Q89786300 | Non-significant association between - 330 T/G polymorphism in interleukin-2 gene and chronic periodontitis: findings from a meta-analysis |
| Q28392036 | On individual genome-wide association studies and their meta-analysis |
| Q34437384 | On the relative efficiency of using summary statistics versus individual-level data in meta-analysis |
| Q37739305 | Phenotyping and genotyping neuropathic pain |
| Q28390545 | Pleiotropy in complex traits: challenges and strategies |
| Q24648412 | Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women |
| Q38178347 | Polymorphisms in a disintegrin and metalloprotease 33 gene and the risk of chronic obstructive pulmonary disease: a meta-analysis |
| Q47658702 | Polymorphisms in interleukins 17A and 17F genes and periodontitis: results from a meta-analysis. |
| Q36046178 | Polymorphisms in the nuclear excision repair gene ERCC2/XPD and susceptibility to cutaneous basal cell carcinoma. |
| Q28749837 | Practical aspects of imputation-driven meta-analysis of genome-wide association studies |
| Q30827855 | Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures |
| Q24288830 | Replication in Genome-Wide Association Studies |
| Q36619207 | Rs143383 in the growth differentiation factor 5 (GDF5) gene significantly associated with osteoarthritis (OA)-a comprehensive meta-analysis |
| Q41093157 | SMAD7 rs4939827 variant contributes to colorectal cancer risk in Chinese population |
| Q37483108 | Searching for genes that matter in acute kidney injury: a systematic review. |
| Q50094098 | Statistical Analysis of Multiple Phenotypes in Genetic Epidemiological Studies:From Cross-Phenotype Associations to Pleiotropy |
| Q30665298 | Statistical Approaches to Combine Genetic Association Data |
| Q92591104 | Statistical Methods and Software for Substance Use and Dependence Genetic Research |
| Q38536598 | Statistical and Computational Methods for Genetic Diseases: An Overview |
| Q38887464 | Statistical controversies in clinical research: overlap and errors in the meta-analyses of microRNA genetic association studies in cancers. |
| Q28294975 | Statistical significance in genetic association studies |
| Q24289342 | Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression |
| Q55345267 | Systematic reviews and cancer research: a suggested stepwise approach. |
| Q30547519 | Systematic reviews and meta-analyses of home telemonitoring interventions for patients with chronic diseases: a critical assessment of their methodological quality |
| Q33414801 | Systematic reviews of genetic association studies. Human Genome Epidemiology Network |
| Q38372330 | T1 polymorphism in a disintegrin and metalloproteinase 33 (ADAM33) gene may contribute to the risk of childhood asthma in Asians |
| Q33656600 | Targeted Therapy Database (TTD): a model to match patient's molecular profile with current knowledge on cancer biology |
| Q92074429 | Ten simple rules for carrying out and writing meta-analyses |
| Q34407953 | The VNTR polymorphism of the DC-SIGNR gene and susceptibility to HIV-1 infection: a meta-analysis |
| Q54117583 | The association between milk consumption and bladder cancer risk: appraisal of a recent meta-analysis. |
| Q24288684 | The common variant rs4444235 near BMP4 confers genetic susceptibility of colorectal cancer: an updated meta-analysis based on a comprehensive statistical strategy |
| Q44373114 | The evaporation of positive genetic association findings. When time has come to go |
| Q53089193 | The impact of MTHFR 677 C/T genotypes on folate status markers: a meta-analysis of folic acid intervention studies. |
| Q28259199 | The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009 |
| Q34230133 | The impact of imputation on meta-analysis of genome-wide association studies |
| Q39157253 | The role of brain-derived neurotrophic factor (BDNF) Val66Met genetic polymorphism in bipolar disorder: a case-control study, comorbidities, and meta-analysis of 16,786 subjects. |
| Q36182582 | The role of gene variants of the inflammatory markers CRP and TNF-α in cardiovascular heart disease: systematic review and meta-analysis |
| Q24289552 | The serotonin transporter promoter variant (5-HTTLPR), stress, and depression meta-analysis revisited: evidence of genetic moderation |
| Q28385221 | Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation |
| Q38130427 | To replicate or not to replicate: the case of pharmacogenetic studies: Establishing validity of pharmacogenomic findings: from replication to triangulation. |
| Q40369426 | Toll-like receptor 4 polymorphisms to determine acute pancreatitis susceptibility and severity: a meta-analysis |
| Q34976245 | Validating, augmenting and refining genome-wide association signals |
| Q58701309 | Vitamin D receptor FokI polymorphism and the risks of colorectal cancer, inflammatory bowel disease, and colorectal adenoma |
| Q35229748 | What did we learn from the genome-wide association study for tuberculosis susceptibility? |
| Q35791662 | XPC Ala499Val and XPG Asp1104His polymorphisms and digestive system cancer risk: a meta-analysis based on model-free approach |
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