Citation Impact
Citing Papers
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
2015 StandoutNobel
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
2010 StandoutScience
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
2014 StandoutNobel
Scaling read aligners to hundreds of threads on general-purpose processors
2018
High burden and pervasive positive selection of somatic mutations in normal human skin
2015 StandoutScience
Detection of ultra-rare mutations by next-generation sequencing
2012
The Ensembl Variant Effect Predictor
2016 Standout
Improved metagenomic analysis with Kraken 2
2019 Standout
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
The impact of rare and low-frequency genetic variants in common disease
2017
The Date of Interbreeding between Neandertals and Modern Humans
2012 StandoutNobel
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
2018 StandoutNobel
Single-cell-resolution transcriptome map of human, chimpanzee, bonobo, and macaque brains
2020 StandoutNobel
Rewiring of the Fruit Metabolome in Tomato Breeding
2018 Standout
Large multiallelic copy number variations in humans
2015
Functional Analyses of Transcription Factor Binding Sites that Differ between Present-Day and Archaic Humans
2015 StandoutNobel
The Songbird as a Model for the Generation and Learning of Complex Sequential Behaviors
2010
Accelerated Recruitment of New Brain Development Genes into the Human Genome
2011
Double Digest RADseq: An Inexpensive Method for De Novo SNP Discovery and Genotyping in Model and Non-Model Species
2012 Standout
Human uniqueness: genome interactions with environment, behaviour and culture
2008
Rare-Variant Association Analysis: Study Designs and Statistical Tests
2014
Comparing a few SNP calling algorithms using low-coverage sequencing data
2013
FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution
2011
Comparative primate genomics: emerging patterns of genome content and dynamics
2014
Genome sequencing and population genomics in non-model organisms
2013
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
The single-cell transcriptional landscape of mammalian organogenesis
2019 StandoutNature
Distinguishing between Selective Sweeps from Standing Variation and from a De Novo Mutation
2012
Pro-inflammation Associated with a Gain-of-Function Mutation (R284S) in the Innate Immune Sensor STING
2018
Drug repurposing: progress, challenges and recommendations
2018 Standout
Musical Training as a Framework for Brain Plasticity: Behavior, Function, and Structure
2012 Standout
Liquid biopsies come of age: towards implementation of circulating tumour DNA
2017 Standout
Comprehensive variation discovery in single human genomes
2014
The evolving tumor microenvironment: From cancer initiation to metastatic outgrowth
2023 Standout
Humanized Foxp2 specifically affects cortico-basal ganglia circuits
2010 StandoutNobel
An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage
2014 Standout
A framework for variation discovery and genotyping using next-generation DNA sequencing data
2011 Standout
Single-Cell Transcriptomic Analysis of Primary and Metastatic Tumor Ecosystems in Head and Neck Cancer
2017 Standout
ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data
2012
Insights into the role of sialylation in cancer progression and metastasis
2020
Worldwide Distribution of the MYH9 Kidney Disease Susceptibility Alleles and Haplotypes: Evidence of Historical Selection in Africa
2010
A Recent Evolutionary Change Affects a Regulatory Element in the Human FOXP2 Gene
2012 StandoutNobel
ANGSD: Analysis of Next Generation Sequencing Data
2014 Standout
A comprehensive comparison of RNA-Seq-based transcriptome analysis from reads to differential gene expression and cross-comparison with microarrays: a case study in Saccharomyces cerevisiae
2012
Methods of integrating data to uncover genotype–phenotype interactions
2015
DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets
2017 Standout
Human Brain Evolution: Harnessing the Genomics (R)evolution to Link Genes, Cognition, and Behavior
2010
Bayesian inference of ancient human demography from individual genome sequences
2011
The Human Condition—A Molecular Approach
2014 StandoutNobel
40,000-Year-Old Individual from Asia Provides Insight into Early Population Structure in Eurasia
2017 StandoutNobel
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
MicroRNA-Driven Developmental Remodeling in the Brain Distinguishes Humans from Other Primates
2011 StandoutNobel
Minimap2: pairwise alignment for nucleotide sequences
2018 Standout
An Efficient Nonviral Method to Generate Integration-Free Human-Induced Pluripotent Stem Cells from Cord Blood and Peripheral Blood Cells
2012 StandoutNobel
Ancient Ethiopian genome reveals extensive Eurasian admixture in Eastern Africa
2015 StandoutScience
Lipid Nanoparticles Delivering Constitutively Active STING mRNA to Stimulate Antitumor Immunity
2022 StandoutNobel
De novo assembly of the Aedes aegypti genome using Hi-C yields chromosome-length scaffolds
2017 StandoutScience
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
The rise of “big data” on cloud computing: Review and open research issues
2014 Standout
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
2016 StandoutScienceNobel
The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote
2013 Standout
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
2013 StandoutNobel
Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations
2018 StandoutScienceNobel
deML: robust demultiplexing of Illumina sequences using a likelihood-based approach
2014
BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions
2012
MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis
2018 Standout
Searching for missing heritability: Designing rare variant association studies
2014
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
2011 Standout
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
Population Genetic Analysis of the N-Acylsphingosine Amidohydrolase Gene Associated With Mental Activity in Humans
2008
Twelve years of SAMtools and BCFtools
2021 Standout
In silico prediction of splice-altering single nucleotide variants in the human genome
2014
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
2013 Standout
Palaeoproteomic evidence identifies archaic hominins associated with the Châtelperronian at the Grotte du Renne
2016 StandoutNobel
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Chemical Glycoproteomics
2016 StandoutNobel
Works of Fuli Yu being referenced
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
2014
Extremely low-coverage whole genome sequencing in South Asians captures population genomics information
2017
Characterization of single-nucleotide variation in Indian-origin rhesus macaques (Macaca mulatta)
2011
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity
2016
Whole-genome sequence–based analysis of high-density lipoprotein cholesterol
2013
Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing
2010
An integrative variant analysis suite for whole exome next-generation sequencing data
2012
Positive Selection of a Pre-Expansion CAG Repeat of the Human SCA2 Gene
2005
An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data
2013
A SNP discovery method to assess variant allele probability from next-generation resequencing data
2009
Detecting natural selection by empirical comparison to random regions of the genome
2009
Comment on "Ongoing Adaptive Evolution of ASPM , a Brain Size Determinant in Homo sapiens "
2007 Science