Citation Impact
Citing Papers
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
Prevalencia e incidencia de la enfermedad de Alzheimer en Europa: metaanálisis
2016 Standout
The UK Biobank resource with deep phenotyping and genomic data
2018 StandoutNature
The Ensembl Variant Effect Predictor
2016 Standout
Human Stem Cell Resources Are an Inroad to Neandertal DNA Functions
2020 StandoutNobel
The role of m6A RNA methylation in human cancer
2019 Standout
An Expanded View of Complex Traits: From Polygenic to Omnigenic
2017 Standout
Immunogenetics of systemic sclerosis: Defining heritability, functional variants and shared-autoimmunity pathways
2015
Effective water/wastewater treatment methodologies for toxic pollutants removal: Processes and applications towards sustainable development
2021 Standout
Genetic effects on gene expression across human tissues
2017 StandoutNature
Detection and interpretation of shared genetic influences on 42 human traits
2016
Genetics of inflammatory bowel disease: beyond NOD2
2017
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
2018 Standout
Impacts of Neanderthal-Introgressed Sequences on the Landscape of Human Gene Expression
2017
Systemic sclerosis
2017 Standout
Epidemiology of Prostate Cancer
2019 Standout
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
2015
An atlas of genetic correlations across human diseases and traits
2015 Standout
A general framework for estimating the relative pathogenicity of human genetic variants
2014 Standout
Reading Mendelian randomisation studies: a guide, glossary, and checklist for clinicians
2018 Standout
Genetic architecture of epigenetic and neuronal ageing rates in human brain regions
2017
A Review of Feature Selection Methods for Machine Learning-Based Disease Risk Prediction
2022
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
2016
Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection
2019
Multimodal biomedical AI
2022 Standout
Interpreting findings from Mendelian randomization using the MR-Egger method
2017 Standout
Tutorial: a guide to performing polygenic risk score analyses
2020
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
2018 Standout
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
2016
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
Revolutionizing healthcare: the role of artificial intelligence in clinical practice
2023 Standout
DNA methylation-based biomarkers and the epigenetic clock theory of ageing
2018 Standout
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Ulcerative colitis
2020 Standout
Reevaluation of SNP heritability in complex human traits
2017
Epidemiology and Natural History of Inflammatory Bowel Diseases
2011 Standout
Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits
2018
A global overview of pleiotropy and genetic architecture in complex traits
2019
The projected effect of risk factor reduction on Alzheimer's disease prevalence
2011 Standout
Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum
2016
Genetic Risk Profiling and Prediction of Disease Course in Crohn's Disease Patients
2009
CADD: predicting the deleteriousness of variants throughout the human genome
2018 Standout
DNA methylation GrimAge strongly predicts lifespan and healthspan
2019 Standout
Gene Polymorphism Association with Type 2 Diabetes and Related Gene-Gene and Gene-Environment Interactions in a Uyghur Population.
2016
Measuring missing heritability: Inferring the contribution of common variants
2014
Cigarette Smoking is a Risk Factor for Alzheimer's Disease: An Analysis Controlling for Tobacco Industry Affiliation
2010
Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator
2016 Standout
Religious Orders Study and Rush Memory and Aging Project
2018 Standout
Single and Multigenic Analysis of the Association between Variants in 12 Steroid Hormone Metabolism Genes and Risk of Prostate Cancer
2009
Interpreting non-coding variation in complex disease genetics
2012
Epigenetic age of the pre-frontal cortex is associated with neuritic plaques, amyloid load, and Alzheimer’s disease related cognitive functioning
2015
An epigenetic biomarker of aging for lifespan and healthspan
2018 Standout
Validity of polygenic risk scores: are we measuring what we think we are?
2019
Recent advances of 3D graphene-based adsorbents for sample preparation of water pollutants: A review
2020
Works of Guo‐Bo Chen being referenced
A Generalized Combinatorial Approach for Detecting Gene-by-Gene and Gene-by-Environment Interactions with Application to Nicotine Dependence
2007
Gene-Gene Interactions Among CHRNA4, CHRNB2, BDNF, and NTRK2 in Nicotine Dependence
2008
Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method
2017
Estimating heritability of complex traits from genome-wide association studies using IBS-based Haseman–Elston regression
2014
Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples
2014
3D graphene aerogel composite of 1D-2D Nb2O5-g-C3N4 heterojunction with excellent adsorption and visible-light photocatalytic performance
2019
Association of amyloid precursor protein-binding protein, family B, member 1 with nicotine dependence in African and European American smokers
2008
A Combinatorial Approach to Detecting Gene-Gene and Gene-Environment Interactions in Family Studies
2008
Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data
2014
EigenGWAS: finding loci under selection through genome-wide association studies of eigenvectors in structured populations
2016