Standout Papers
Citation Impact
Citing Papers
Protein interaction networks revealed by proteome coevolution
2019 StandoutScienceNobel
DNA capture by a CRISPR-Cas9–guided adenine base editor
2020 StandoutScienceNobel
Nucleic acid detection with CRISPR-Cas13a/C2c2
2017 StandoutScience
A genomic region associated with protection against severe COVID-19 is inherited from Neandertals
2021 StandoutNobel
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
Sequencing and Analysis of Neanderthal Genomic DNA
2006 StandoutScienceNobel
Updated benchmarking of variant effect predictors using deep mutational scanning
2023
The Ensembl Variant Effect Predictor
2016 Standout
Genome-wide prediction of disease variant effects with a deep protein language model
2023
An integrated map of genetic variation from 1,092 human genomes
2012 StandoutNature
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
2016 Standout
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
2016 StandoutNature
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN
2021
Assembly of the Working Draft of the Human Genome with GigAssembler
2001
Phage-assisted evolution of an adenine base editor with improved Cas domain compatibility and activity
2020 StandoutNobel
Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants
2021
Genetic effects on gene expression across human tissues
2017 StandoutNature
Accurate classification of BRCA1 variants with saturation genome editing
2018 Nature
Human SNP variability and mutation rate are higher in regions of high recombination
2002
Sustained delivery of siRNA from dopamine-coated stainless steel surfaces
2013
Database resources of the National Center for Biotechnology Information
2000
The Pfam Protein Families Database
2002 Standout
Predicting the clinical impact of human mutation with deep neural networks
2018
The genomic landscape of Neanderthal ancestry in present-day humans
2014 StandoutNatureNobel
Methods and Applications of CRISPR-Mediated Base Editing in Eukaryotic Genomes
2017
Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis
2020
Progressive Loss of Striatal Neurons Causes Motor Dysfunction in MND2 Mutant Mice and Is Not Prevented by Bcl-2
2002
Human genome sequence variation and the influence of gene history, mutation and recombination
2002
Lysyl oxidases: A novel multifunctional amine oxidase family
2001
Predicting variant deleteriousness in non-human species: applying the CADD approach in mouse
2018
Evolved Cas9 variants with broad PAM compatibility and high DNA specificity
2018 Nature
CRISPR-Cas9 Circular Permutants as Programmable Scaffolds for Genome Modification
2019 StandoutNobel
Multiplex assessment of protein variant abundance by massively parallel sequencing
2018
Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
2005 StandoutNature
Comparative Recombination Rates in the Rat, Mouse, and Human Genomes
2004
Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data
2017
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage
2017 StandoutNature
Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction
2012 Standout
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
2016
PipMaker—A Web Server for Aligning Two Genomic DNA Sequences
2000
Database resources of the National Center for Biotechnology Information: update
2003 Standout
Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors
2016
RefSeq and LocusLink: NCBI gene-centered resources
2001
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Variant Interpretation: Functional Assays to the Rescue
2017
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
2014 Standout
The Rat Genome Database 2015: genomic, phenotypic and environmental variations and disease
2014
X-inactivation profile reveals extensive variability in X-linked gene expression in females
2005 StandoutNature
The impact of rare variation on gene expression across tissues
2017 Nature
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
IMHOTEP—a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants
2016
Search-and-replace genome editing without double-strand breaks or donor DNA
2019 StandoutNature
A high-resolution recombination map of the human genome
2002
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors
2020 Standout
The major genetic risk factor for severe COVID-19 is inherited from Neanderthals
2020 StandoutNatureNobel
Mutation effects predicted from sequence co-variation
2017
A New High-Energy Cathode for a Na-Ion Battery with Ultrahigh Stability
2013
Quantitative Missense Variant Effect Prediction Using Large-Scale Mutagenesis Data
2017
Uncovering disease mechanisms through network biology in the era of Next Generation Sequencing
2016
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
2006 StandoutNature
Predicting functional effect of missense variants using graph attention neural networks
2022
An SNP Resource for Rice Genetics and Breeding Based on SubspeciesIndicaandJaponicaGenome Alignments
2004
A Populationwide Coalescent Analysis of Icelandic Matrilineal and Patrilineal Genealogies: Evidence for a Faster Evolutionary Rate of mtDNA Lineages than Y Chromosomes
2003
Efficient generation of mouse models of human diseases via ABE- and BE-mediated base editing
2018 Standout
GAVIN: Gene-Aware Variant INterpretation for medical sequencing
2017
A Neutral Explanation for the Correlation of Diversity with Recombination Rates in Humans
2003 StandoutNobel
Linkage Disequilibrium in Humans: Models and Data
2001
Analysis of one million base pairs of Neanderthal DNA
2006 StandoutNatureNobel
A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase
2020
Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines
2017
The map-based sequence of the rice genome
2005 StandoutNature
CADD: predicting the deleteriousness of variants throughout the human genome
2018 Standout
“Turn-On” Protein Fluorescence: In Situ Formation of Cyanine Dyes
2014
Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6
2018 StandoutScience
Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy
2007 Standout
Sequence variations in the public human genome data reflect a bottlenecked population history
2002
Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization
2015
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
2005 Science
Hypoxia-inducible factor 1 is a master regulator of breast cancer metastatic niche formation
2011 StandoutNobel
Bio‐inspired Immobilization of Cell‐Adhesive Ligands on Electrospun Nanofibrous Patches for Cell Delivery
2012
Prioritizing genes for systematic variant effect mapping
2020
Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields
2014 Standout
STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets
2018 Standout
De novo design of small beta barrel proteins
2023 StandoutNobel
Database resources of the National Center for Biotechnology Information
2013
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome
2004 Science
dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs
2015
Ion-Catalyzed Synthesis of Microporous Hard Carbon Embedded with Expanded Nanographite for Enhanced Lithium/Sodium Storage
2016 StandoutNobel
Genomic analysis of orthologous mouse and human olfactory receptor loci
2001 StandoutNobel
Sequence analysis of mouse vomeronasal receptor gene clusters reveals common promoter motifs and a history of recent expansion
2001 StandoutNobel
Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis
2000
A yeast‐based complementation assay elucidates the functional impact of 200 missense variants in human PSAT1
2020
A Deep Neural Network for Predicting and Engineering Alternative Polyadenylation
2019
Arylfluorosulfates Inactivate Intracellular Lipid Binding Protein(s) through Chemoselective SuFEx Reaction with a Binding Site Tyr Residue
2016 StandoutNobel
CRISPR-Cas guides the future of genetic engineering
2018 StandoutScienceNobel
Characterization of Mammalian Selenoproteomes
2003 StandoutScience
Using deep mutational scanning to benchmark variant effect predictors and identify disease mutations
2020
Palaeoproteomic evidence identifies archaic hominins associated with the Châtelperronian at the Grotte du Renne
2016 StandoutNobel
The Structure of Haplotype Blocks in the Human Genome
2002 StandoutScience
Polydopamine-Assisted Osteoinductive Peptide Immobilization of Polymer Scaffolds for Enhanced Bone Regeneration by Human Adipose-Derived Stem Cells
2013
Generation times in wild chimpanzees and gorillas suggest earlier divergence times in great ape and human evolution
2012 StandoutNobel
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Targeted Investigation of the Neandertal Genome by Array-Based Sequence Capture
2010 StandoutScienceNobel
Environment-friendly facile synthesis of Pt nanoparticles supported on polydopamine modified carbon materials
2013
Estimating Ancestral Population Sizes and Divergence Times
2003
Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes
2005
Works of Wonhee Jang being referenced
Chemical biology-based approaches on fluorescent labeling of proteins in live cells
2012
Making effective use of human genomic sequence data
1999
Mussel-Inspired Immobilization of Vascular Endothelial Growth Factor (VEGF) for Enhanced Endothelialization of Vascular Grafts
2012
ClinVar: public archive of relationships among sequence variation and human phenotype
2013 Standout
Comparison of human genetic and sequence-based physical maps
2001 Nature
ClinVar: public archive of interpretations of clinically relevant variants
2015 Standout
High-Resolution Genetic, Physical, and Transcript Map of themnd2Region of Mouse Chromosome 6
1998
A web server for performing electronic PCR
2004
Comparative Sequence of Human and Mouse BAC Clones from the mnd2 Region of Chromosome 2p13
1999
Study on structure and electrochemical properties of carbon-coated monoclinic Li3V2(PO4)3 using synchrotron based in situ X-ray diffraction and absorption
2013