Citation Impact
Citing Papers
Localized Dimerization and Nucleoid Binding Drive Gradient Formation by the Bacterial Cell Division Inhibitor MipZ
2012
Evolutionary history of Tibetans inferred from whole-genome sequencing
2017 StandoutNobel
The Ensembl Variant Effect Predictor
2016 Standout
In silico prediction of protein-protein interactions in human macrophages
2014 Standout
The impact of rare and low-frequency genetic variants in common disease
2017
Network‐based prediction of protein function
2007
An integrated map of genetic variation from 1,092 human genomes
2012 StandoutNature
Genetic contributions to NAFLD: leveraging shared genetics to uncover systems biology
2019
Benefits and limitations of genome-wide association studies
2019
Genetic effects on gene expression across human tissues
2017 StandoutNature
Long-Term Balancing Selection in LAD1 Maintains a Missense Trans-Species Polymorphism in Humans, Chimpanzees, and Bonobos
2015 StandoutNobel
Combinatorial network of primary and secondary microRNA-driven regulatory mechanisms
2009
Predicting biological networks from genomic data
2008
The genomic landscape of Neanderthal ancestry in present-day humans
2014 StandoutNatureNobel
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype
2019 Standout
STRING v10: protein–protein interaction networks, integrated over the tree of life
2014 Standout
agriGO v2.0: a GO analysis toolkit for the agricultural community, 2017 update
2017 Standout
Rare-Variant Association Analysis: Study Designs and Statistical Tests
2014
The changing landscape of atherosclerosis
2021 StandoutNature
Genetic Variation and Response to Neurocritical Illness: a Powerful Approach to Identify Novel Pathophysiological Mechanisms and Therapeutic Targets
2020
Psoriasis
2021 Standout
ClinVar: public archive of relationships among sequence variation and human phenotype
2013 Standout
The STRING database in 2017: quality-controlled protein–protein association networks, made broadly accessible
2016 Standout
Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism
2016 StandoutNobel
A general framework for estimating the relative pathogenicity of human genetic variants
2014 Standout
Life’s Essential 8: Updating and Enhancing the American Heart Association’s Construct of Cardiovascular Health: A Presidential Advisory From the American Heart Association
2022 Standout
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
2015 Standout
Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond
2014
Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study
2014
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
2008 Standout
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
A Novel Heuristic for Local Multiple Alignment of Interspersed DNA Repeats
2009
Non-alcoholic fatty liver disease
2021 Standout
Obesity and Cardiovascular Disease: A Scientific Statement From the American Heart Association
2021 Standout
Multimodal biomedical AI
2022 Standout
Privacy in the age of medical big data
2018 Standout
Axes of a revolution: challenges and promises of big data in healthcare
2020
Type 2 diabetes
2017 Standout
Effective Identification of Conserved Pathways in Biological Networks Using Hidden Markov Models
2009
progressiveMauve: Multiple Genome Alignment with Gene Gain, Loss and Rearrangement
2010 Standout
MicroRNA Expression and Regulation in Human, Chimpanzee, and Macaque Brains
2011 StandoutNobel
Global aetiology and epidemiology of type 2 diabetes mellitus and its complications
2017 Standout
Integrative omics for health and disease
2018
Toward the dynamic interactome: it's about time
2010
An early modern human from Romania with a recent Neanderthal ancestor
2015 StandoutNatureNobel
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
The integrative biology of type 2 diabetes
2019 Nature
FunCoup 3.0: database of genome-wide functional coupling networks
2013
Melanoma-intrinsic β-catenin signalling prevents anti-tumour immunity
2015 StandoutNature
Most genetic risk for autism resides with common variation
2014
Regulatory T Cell-Specific Epigenomic Region Variants Are a Key Determinant of Susceptibility to Common Autoimmune Diseases
2020 StandoutNobel
Use and misuse of the gene ontology annotations
2008
STRING 8--a global view on proteins and their functional interactions in 630 organisms
2008 Standout
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
2014 Standout
The Human Condition—A Molecular Approach
2014 StandoutNobel
70-year legacy of the Framingham Heart Study
2019
Gut microbiota in human metabolic health and disease
2020 Standout
A Survey of Statistical Network Models
2010
Identifying functional modules in protein–protein interaction networks: an integrated exact approach
2008
EDC-2: The Endocrine Society's Second Scientific Statement on Endocrine-Disrupting Chemicals
2015 Standout
Exposing the exposures responsible for type 2 diabetes and obesity
2016 Science
Chronic Kidney Disease Diagnosis and Management
2019 Standout
Psoriasis and Genetics
2020
Race, APOL1 Risk, and eGFR Decline in the General Population
2016
Bacterial scaffold directs pole-specific centromere segregation
2014 StandoutNobel
2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
2019 Standout
Rational HIV Immunogen Design to Target Specific Germline B Cell Receptors
2013 StandoutScienceNobel
Exactp-Values for Network Interference
2016 StandoutNobel
Second-generation PLINK: rising to the challenge of larger and richer datasets
2015 Standout
Pathophysiology of Type 2 Diabetes Mellitus
2020 Standout
A fourth Denisovan individual
2017 StandoutNobel
Temporal networks
2012 Standout
Nuclear and mitochondrial DNA sequences from two Denisovan individuals
2015 StandoutNobel
Cardiovascular Health in African Americans: A Scientific Statement From the American Heart Association
2017
Metabolomics for Investigating Physiological and Pathophysiological Processes
2019
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Fast and accurate imputation of summary statistics enhances evidence of functional enrichment
2014
How important are rare variants in common disease?
2014
2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
2019 Standout
MetaboAnalyst 5.0: narrowing the gap between raw spectra and functional insights
2021 Standout
Works of Jason Flannick being referenced
Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants
2013
Genetic and Computational Identification of a Conserved Bacterial Metabolic Module
2008
Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation
2012
Evaluating empirical bounds on complex disease genetic architecture
2013
Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose
2018
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis
2018
Current progress in network research: toward reference networks for key model organisms
2007
The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease
2015
Græmlin: General and robust alignment of multiple large interaction networks
2006
Type 2 diabetes: genetic data sharing to advance complex disease research
2016
Using multiple alignments to improve seeded local alignment algorithms
2005
Automatic Parameter Learning for Multiple Local Network Alignment
2009
Cerebrovascular Disease Knowledge Portal
2018