Citation Impact
Citing Papers
Fast and efficient QTL mapper for thousands of molecular phenotypes
2015
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
RNA splicing is a primary link between genetic variation and disease
2016 Science
A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae
2020 Standout
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
The UK Biobank resource with deep phenotyping and genomic data
2018 StandoutNature
Genetic manipulation of Patescibacteria provides mechanistic insights into microbial dark matter and the epibiotic lifestyle
2023 StandoutNobel
Autoimmune Th17 Cells Induced Synovial Stromal and Innate Lymphoid Cell Secretion of the Cytokine GM-CSF to Initiate and Augment Autoimmune Arthritis
2018 StandoutNobel
A survey of best practices for RNA-seq data analysis
2016 Standout
The Ensembl Variant Effect Predictor
2016 Standout
cis-Acting Complex-Trait-Associated lincRNA Expression Correlates with Modulation of Chromosomal Architecture
2017
Improved metagenomic analysis with Kraken 2
2019 Standout
High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries
2018 Standout
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
Chromosome-scale and haplotype-resolved genome assembly of a tetraploid potato cultivar
2022
Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study
2016
An Expanded View of Complex Traits: From Polygenic to Omnigenic
2017 Standout
Elements of cancer immunity and the cancer–immune set point
2017 StandoutNature
Systematic identification of genetic influences on methylation across the human life course
2016
Insights into TREM2 biology by network analysis of human brain gene expression data
2013
Rheumatoid arthritis
2018 Standout
Genetic effects on gene expression across human tissues
2017 StandoutNature
Toward the Development of a Global Induced Pluripotent Stem Cell Library
2013 Nobel
Research gaps in psoriasis: Opportunities for future studies
2013
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
2018 Standout
The evolving landscape of biomarkers for checkpoint inhibitor immunotherapy
2019 Standout
Stem Cell Therapies in Clinical Trials: Progress and Challenges
2015 Standout
The multidimensional mechanisms of long noncoding RNA function
2017 Standout
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype
2019 Standout
Effective gene expression prediction from sequence by integrating long-range interactions
2021 StandoutNobel
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
2014 Standout
Five Years of GWAS Discovery
2012 Standout
The role of regulatory variation in complex traits and disease
2015
An atlas of genetic correlations across human diseases and traits
2015 Standout
Current and future perspectives of liquid biopsies in genomics-driven oncology
2018 Standout
Chromatin marks identify critical cell types for fine mapping complex trait variants
2012
MAGMA: Generalized Gene-Set Analysis of GWAS Data
2015 Standout
Psoriasis
2015 Standout
High-performance medicine: the convergence of human and artificial intelligence
2018 Standout
Non-alcoholic fatty liver disease
2021 Standout
Multimodal biomedical AI
2022 Standout
Trycycler: consensus long-read assemblies for bacterial genomes
2021
Drug repurposing: progress, challenges and recommendations
2018 Standout
Genetic regulation of gene expression in the epileptic human hippocampus
2017
Genetic variation and the de novo assembly of human genomes
2015
Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23
2016
Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens
2013
Genetic variability in the regulation of gene expression in ten regions of the human brain
2014
The major genetic risk factor for severe COVID-19 is inherited from Neanderthals
2020 StandoutNatureNobel
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
Archaic Hominin Admixture Facilitated Adaptation to Out-of-Africa Environments
2016
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Toward Genetic Prediction of Nonalcoholic Fatty Liver Disease Trajectories: PNPLA3 and Beyond
2020
High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case–parent trio study
2014
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
2016 Standout
Towards precision medicine
2016
Modelling local gene networks increases power to detect trans-acting genetic effects on gene expression
2016
The immunopathology of sepsis and potential therapeutic targets
2017 Standout
Integrative Modeling of eQTLs and Cis-Regulatory Elements Suggests Mechanisms Underlying Cell Type Specificity of eQTLs
2013
TBtools-II: A “one for all, all for one” bioinformatics platform for biological big-data mining
2023 Standout
Regulatory T Cell-Specific Epigenomic Region Variants Are a Key Determinant of Susceptibility to Common Autoimmune Diseases
2020 StandoutNobel
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association
2017 Standout
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
2013
Validating therapeutic targets through human genetics
2013
Gene regulation by long non-coding RNAs and its biological functions
2020 Standout
Global Properties and Functional Complexity of Human Gene Regulatory Variation
2013
Kourami: graph-guided assembly for novel human leukocyte antigen allele discovery
2018
Genetic insights into common pathways and complex relationships among immune-mediated diseases
2013
Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk
2018
The amyloid hypothesis of Alzheimer's disease at 25 years
2016 Standout
CADD: predicting the deleteriousness of variants throughout the human genome
2018 Standout
Innate Immune Activity Conditions the Effect of Regulatory Variants upon Monocyte Gene Expression
2014 Science
Software Application Profile: PHESANT: a tool for performing automated phenome scans in UK Biobank
2017
GTDB-Tk: a toolkit to classify genomes with the Genome Taxonomy Database
2019 Standout
Regulatory T Cells and Human Disease
2020 StandoutNobel
Familial predisposition and genetic risk factors for lymphoma
2015
2016 US lymphoid malignancy statistics by World Health Organization subtypes
2016 Standout
Molecular control of regulatory T cell development and function
2017 StandoutNobel
Extending reference assembly models
2015
Genome-wide association studies
2021
Statistical Testing of Shared Genetic Control for Potentially Related Traits
2013
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Interferon regulatory factor 2 protects mice from lethal viral neuroinvasion
2016 StandoutNobel
Works of Alexander Dilthey being referenced
Multi-Population Classical HLA Type Imputation
2013
Imputation of KIR Types from SNP Variation Data
2015
Improved genome inference in the MHC using a population reference graph
2015
Psoriasis Patients Are Enriched for Genetic Variants That Protect against HIV-1 Disease
2012
De novo assembly of haplotype-resolved genomes with trio binning
2018
Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank
2017
High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs
2016
Genetics of gene expression in primary immune cells identifies cell type–specific master regulators and roles of HLA alleles
2012
A Fast Approximate Algorithm for Mapping Long Reads to Large Reference Databases
2018
HLA*IMP—an integrated framework for imputing classical HLA alleles from SNP genotypes
2011
Multiple Hodgkin lymphoma–associated loci within the HLA region at chromosome 6p21.3
2011