OOIR: Observatory of International Research

Papers

(The TQCC of Genetic Epidemiology is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)

Article	Citations
A comparison of robust Mendelian randomization methods using summary data	277
A principal component approach to improve association testing with polygenic risk scores	54
Bias correction for inverse variance weighting Mendelian randomization	48
The X factor: A robust and powerful approach to X‐chromosome‐inclusive whole‐genome association studies	28
Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations	28
Fine‐mapping and QTL tissue‐sharing information improves the reliability of causal gene identification	27
Statistical methods for cis‐Mendelian randomization with two‐sample summary‐level data	27
A comprehensive genetic and epidemiological association analysis of vitamin D with common diseases/traits in the UK Biobank	24
Efficient gene–environment interaction tests for large biobank‐scale sequencing studies	15
SNP‐HLA Reference Consortium (SHLARC): HLA and SNP data sharing for promoting MHC‐centric analyses in genomics	15
Mendelian randomisation with coarsened exposures	14
Caution against examining the role of reverse causality in Mendelian Randomization	14
FAT4 identified as a potential modifier of orofacial cleft laterality	13
Post hoc power is not informative	11
Genome‐wide association analysis of COVID‐19 mortality risk in SARS‐CoV‐2 genomes identifies mutation in the SARS‐CoV‐2 spike protein that colocalizes with P.1 of the Brazilian strain	11
Testing and estimation of X‐chromosome SNP effects: Impact of model assumptions	11
TWO‐SIGMA: A novel two‐component single cell model‐based association method for single‐cell RNA‐seq data	10
Chances and challenges of machine learning‐based disease classification in genetic association studies illustrated on age‐related macular degeneration	10
A robust two‐sample transcriptome‐wide Mendelian randomization method integrating GWAS with multi‐tissue eQTL summary statistics	10
Including diverse and admixed populations in genetic epidemiology research	10
A fast and powerful eQTL weighted method to detect genes associated with complex trait using GWAS summary data	9
A general framework for integrative analysis of incomplete multiomics data	9
Novel score test to increase power in association test by integrating external controls	9
Penalized models for analysis of multiple mediators	9
Multitrait transcriptome‐wide association study (TWAS) tests	9

Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z‐scores improves detection and reliability	8
Truncated tests for combining evidence of summary statistics	8
Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals	8
Integration of multiomic annotation data to prioritize and characterize inflammation and immune‐related risk variants in squamous cell lung cancer	7
Multi‐tissue transcriptome‐wide association studies	7
A novel Mendelian randomization method with binary risk factor and outcome	7
Joint testing of donor and recipient genetic matching scores and recipient genotype has robust power for finding genes associated with transplant outcomes	7
Dissecting the genetic overlap of smoking behaviors, lung cancer, and chronic obstructive pulmonary disease: A focus on nicotinic receptors and nicotine metabolizing enzyme	7
locStra: Fast analysis of regional/global stratification in whole‐genome sequencing studies	7
Genetic heterogeneity: Challenges, impacts, and methods through an associative lens	7
Genome‐wide association studies of 27 accelerometry‐derived physical activity measurements identified novel loci and genetic mechanisms	7
Incorporating European GWAS findings improve polygenic risk prediction accuracy of breast cancer among East Asians	7
Disentangling the effects of traits with shared clustered genetic predictors using multivariable Mendelian randomization	7
Supervariants identification for breast cancer	6
Polygenic modelling of treatment effect heterogeneity	6
Adjusting for collider bias in genetic association studies using instrumental variable methods	6
Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study	6
Mendelian randomization analysis with survival outcomes	6
The influence of unmeasured confounding on the MR Steiger approach	6
Assumptions about frequency‐dependent architectures of complex traits bias measures of functional enrichment	5
Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms	5
Inverse probability weighting is an effective method to address selection bias during the analysis of high dimensional data	5
Statistical methods with exhaustive search in the identification of gene–gene interactions for colorectal cancer	5
Validating the doubly weighted genetic risk score for the prediction of type 2 diabetes in the Lifelines and Estonian Biobank cohorts	5
Group analysis of distance matrices	5
Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes	5
Block coordinate descent algorithm improves variable selection and estimation in error‐in‐variables regression	4
Detecting X‐linked common and rare variant effects in family‐based sequencing studies	4
	4
Assessing exposure effects on gene expression	4
Novel HLA associations with outcomes of Mycobacterium tuberculosis exposure and sarcoidosis in individuals of African ancestry using nearest‐neighbor feature selection	4
Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function	4
Unsupervised cluster analysis of SARS‐CoV‐2 genomes reflects its geographic progression and identifies distinct genetic subgroups of SARS‐CoV‐2 virus	4
Statistical learning for sparser fine‐mapped polygenic models: The prediction of LDL‐cholesterol	4
A two‐sample robust Bayesian Mendelian Randomization method accounting for linkage disequilibrium and idiosyncratic pleiotropy with applications to the COVID‐19 outcomes	4
Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network	4
InTACT: An adaptive and powerful framework for joint‐tissue transcriptome‐wide association studies	4
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes	4
Genome‐wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores	4
Statistical power of transcriptome‐wide association studies	4