Citation Impact
Citing Papers
DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome
2021
KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD)
2009 Standout
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
The Ensembl Variant Effect Predictor
2016 Standout
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Single-cell transcriptome landscape of circulating CD4+ T cell populations in autoimmune diseases
2024 StandoutNobel
The Genetics of Major Depression
2014
Depression
2018 Standout
Major depressive disorder
2016 Standout
Further evidence for the existence of major susceptibility of nasopharyngeal carcinoma in the region near HLA-A locus in Southern Chinese
2012
Phenotype ontologies: the bridge between genomics and evolution
2007
Estrogen receptors and human disease
2006 Standout
Mechanics and biology in intervertebral disc degeneration: a vicious circle
2015 Standout
Rewiring of the Fruit Metabolome in Tomato Breeding
2018 Standout
Vascular dementia
2015 Standout
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
2018 Standout
Fast and Rigorous Computation of Gene and Pathway Scores from SNP-Based Summary Statistics
2016
De novo domestication of wild tomato using genome editing
2018 Standout
Root traits contributing to plant productivity under drought
2013 Standout
Performance Characteristics According to Playing Position in Elite Soccer
2007 Standout
Effective gene expression prediction from sequence by integrating long-range interactions
2021 StandoutNobel
Genetic Variation and Physical Performance
2004
Nasopharyngeal carcinoma
2019 Standout
Practical aspects of imputation-driven meta-analysis of genome-wide association studies
2008
The mechanisms of action of metformin
2017 Standout
Variation in femoral length is associated with polymorphisms in RUNX2 gene
2005
The STRING database in 2017: quality-controlled protein–protein association networks, made broadly accessible
2016 Standout
Integrating single-cell transcriptomic data across different conditions, technologies, and species
2018 Standout
MAGMA: Generalized Gene-Set Analysis of GWAS Data
2015 Standout
Skeletal remodeling in health and disease
2007 Standout
Evaluation of Human Leukocyte Antigen-A (HLA-A), Other Non-HLA Markers on Chromosome 6p21 and Risk of Nasopharyngeal Carcinoma
2012
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
2014 Standout
Comprehensive literature review and statistical considerations for microarray meta-analysis
2012
Type 2 diabetes
2017 Standout
Nasopharyngeal carcinoma
2015 Standout
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
2018 Standout
Age-related macular degeneration
2018 Standout
Cystic fibrosis genetics: from molecular understanding to clinical application
2014 Standout
Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis
2013 StandoutNobel
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
Clinical application of exome sequencing in undiagnosed genetic conditions
2012
Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression
2018
Dissecting the genetics of complex traits using summary association statistics
2016
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Estrogen Receptor Gene Polymorphisms and the Genetics of Osteoporosis: A HuGE Review
2005
The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration
2007 Standout
Metformin and the gastrointestinal tract
2016
Type 2 diabetes mellitus
2015 Standout
The pharmacogenetics of metformin
2017
Genetics of osteoporosis: accelerating pace in gene identification and validation
2009
Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities
2013
Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits
2018
Rare and common variants: twenty arguments
2012
Osteoporosis in the elderly with chronic kidney disease
2006
Genetic susceptibility to the endemic form of NPC
2016
Genetic predisposition factors and nasopharyngeal carcinoma risk: A review of epidemiological association studies, 2000–2011
2012
Lumbar disc degeneration and genetic factors are the main risk factors for low back pain in women: the UK Twin Spine Study
2011
Age-Related Macular Degeneration: Genetics and Biology Coming Together
2014
Marker‐Assisted Selection in Plant Breeding: From Publications to Practice
2008
Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases
2014
Pathophysiology of Type 2 Diabetes Mellitus
2020 Standout
Turmeric (Curcuma longa) and its major constituent (curcumin) as nontoxic and safe substances: Review
2018 Standout
Learning from class-imbalanced data: Review of methods and applications
2016 Standout
MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis
2018 Standout
Endometriosis
2020 Standout
METAL: fast and efficient meta-analysis of genomewide association scans
2010 Standout
The Evaluation of Tools Used to Predict the Impact of Missense Variants Is Hindered by Two Types of Circularity
2015
The Time Is Right for a New Classification System for Diabetes: Rationale and Implications of the β-Cell–Centric Classification Schema
2016
Genotype-based treatment of type 2 diabetes with an α2A-adrenergic receptor antagonist
2014
Effects of Curcumin on Tobacco Smoke-induced Hepatic MAPK Pathway Activation and Epithelial-Mesenchymal TransitionIn Vivo
2017
A chemical genetic roadmap to improved tomato flavor
2017 Science
Network-assisted analysis to prioritize GWAS results: principles, methods and perspectives
2013
The revival of the Gini importance?
2018 Standout
dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations
2013
An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data
2012
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
ACID: Association Correction for Imbalanced Data in GWAS
2016
Works of Miaoxin Li being referenced
Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets
2011
Predicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studies
2013
The −1997 G/T Polymorphism in the COLIA1 Upstream Regulatory Region is Associated with Hip Bone Mineral Density (BMD) in Chinese Nuclear Families
2004
Tests of linkage and association of the COL1A2 gene with bone phenotypes’ variation in Chinese nuclear families
2003
SNPP: automating large-scale SNP genotype data management
2004
Genetic determination and correlation of body mass index and bone mineral density at the spine and hip in Chinese Han ethnicity
2005
No Evidence for Linkage and/or Association of Human Alpha2-HS Glycoprotein Gene with Bone Mineral Density Variation in Chinese Nuclear Families
2003
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese
2013
Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study
2011
Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis
2014
Bone mineral density in elderly Chinese: effects of age, sex, weight, height, and body mass index
2004
Cigarette smoking and gastrointestinal diseases: The causal relationship and underlying molecular mechanisms (Review)
2014
HYST: A Hybrid Set-Based Test for Genome-wide Association Studies, with Application to Protein-Protein Interaction-Based Association Analysis
2012
GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure
2011
Identification of Genes with Allelic Imbalance on 6p Associated with Nasopharyngeal Carcinoma in Southern Chinese
2011
PhD: a web database application for phenotype data management
2005
IGG3: a tool to rapidly integrate large genotype datasets for whole-genome imputation and individual-level meta-analysis
2009
Genome scan for QTLs underlying bone size variation at 10 refined skeletal sites: genetic heterogeneity and the significance of phenotype refinement
2004
SNPTracker: A Swift Tool for Comprehensive Tracking and Unifying dbSNP rs IDs and Genomic Coordinates of Massive Sequence Variants
2015
Estrogen Receptor α Gene Polymorphisms and Peak Bone Density in Chinese Nuclear Families
2003
IGG: A tool to integrate GeneChips for genetic studies
2007
Predicting regulatory variants with composite statistic
2016
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases
2012