Citation Impact
Citing Papers
Characterizing and explaining the impact of disease-associated mutations in proteins without known structures or structural homologs
2022 StandoutNobel
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect
2019
The evolutionary history of human spindle genes includes back-and-forth gene flow with Neandertals
2022 StandoutNobel
Zero‐shot mutation effect prediction on protein stability and function using RoseTTAFold
2023 StandoutNobel
Predicting mRNA Abundance Directly from Genomic Sequence Using Deep Convolutional Neural Networks
2020
A CRISPR-based base-editing screen for the functional assessment of BRCA1 variants
2019
Engineered receptors for soluble cellular communication and disease sensing
2024 StandoutNatureNobel
Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives
2019
Learning the protein language: Evolution, structure, and function
2021
Deep generative models of genetic variation capture the effects of mutations
2018
Effective gene expression prediction from sequence by integrating long-range interactions
2021 StandoutNobel
High-performance medicine: the convergence of human and artificial intelligence
2018 Standout
Multimodal biomedical AI
2022 Standout
Search-and-replace genome editing without double-strand breaks or donor DNA
2019 StandoutNature
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors
2020 Standout
Dictionary learning for integrative, multimodal and scalable single-cell analysis
2023 Standout
Pooled Knockin Targeting for Genome Engineering of Cellular Immunotherapies
2020
Towards a comprehensive catalogue of validated and target-linked human enhancers
2020
Cancer genetics, precision prevention and a call to action
2018
Activity-by-contact model of enhancer–promoter regulation from thousands of CRISPR perturbations
2019
Chromatin Potential Identified by Shared Single-Cell Profiling of RNA and Chromatin
2020
A new era in functional genomics screens
2021
Identification of discriminative gene-level and protein-level features associated with pathogenic gain-of-function and loss-of-function variants
2021
Development of hRad51–Cas9 nickase fusions that mediate HDR without double-stranded breaks
2019
Key challenges for delivering clinical impact with artificial intelligence
2019 Standout
CADD: predicting the deleteriousness of variants throughout the human genome
2018 Standout
Disease variant prediction with deep generative models of evolutionary data
2021 Nature
Traditional Chinese medicine as a cancer treatment: Modern perspectives of ancient but advanced science
2019 Standout
Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants
2020
Genome-wide association studies
2021
Evolutionary-scale prediction of atomic-level protein structure with a language model
2023 StandoutScience
The STRING database in 2023: protein–protein association networks and functional enrichment analyses for any sequenced genome of interest
2022 Standout
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Works of Anh Leith being referenced
Accurate classification of BRCA1 variants with saturation genome editing
2018 Nature
A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens
2019