Citation Impact
Citing Papers
CLEVER: clique-enumerating variant finder
2012
Infrared molecular fingerprinting of blood-based liquid biopsies for the detection of cancer
2021 StandoutNobel
Four-component protein nanocages designed by programmed symmetry breaking
2024 StandoutNatureNobel
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
2016 StandoutNobel
An integrative probabilistic model for identification of structural variation in sequencing data
2012
LUMPY: a probabilistic framework for structural variant discovery
2014
Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement
2014 Standout
A view on drug resistance in cancer
2019 StandoutNature
Induced Pluripotent Stem Cells: Past, Present, and Future
2012 StandoutNobel
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
Clonal Heterogeneity and Tumor Evolution: Past, Present, and the Future
2017 Standout
SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations
2013
From human genome to cancer genome: The first decade
2013
CRISPR-mediated genotypic and phenotypic correction of a chronic granulomatous disease mutation in human iPS cells
2015
ChopSticks: High-resolution analysis of homozygous deletions by exploiting concordant read pairs
2012
The Cancer Genome Atlas Pan-Cancer analysis project
2013 Standout
Cancer stem cells revisited
2017 Standout
Expanding the computational toolbox for mining cancer genomes
2014
Antiviral resistance of stem cells
2018 StandoutNobel
PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data
2013
Short- and long-term effects of chromosome mis-segregation and aneuploidy
2015
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
2020 Standout
Reprogramming Factor Stoichiometry Influences the Epigenetic State and Biological Properties of Induced Pluripotent Stem Cells
2011
Replication Catastrophe: When a Checkpoint Fails because of Exhaustion
2017
The pangenome of an agronomically important crop plant Brassica oleracea
2016 Standout
Genetic and Epigenetic Variations in iPSCs: Potential Causes and Implications for Application
2013
Engineered virus-like particles for efficient in vivo delivery of therapeutic proteins
2022
Long-Term Expansion of Functional Mouse and Human Hepatocytes as 3D Organoids
2018 StandoutNobel
Genome-wide Translocation Sequencing Reveals Mechanisms of Chromosome Breaks and Rearrangements in B Cells
2011
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology
2022 Standout
Genome structural variation discovery and genotyping
2011
Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data
2013 Standout
Primate iPS cells as tools for evolutionary analyses
2014 StandoutNobel
The molecular landscape of head and neck cancer
2018 Standout
Loss of transcriptional control over endogenous retroelements during reprogramming to pluripotency
2014
Genetic and epigenetic stability of human pluripotent stem cells
2012
Chromatin remodeller SMARCA4 recruits topoisomerase 1 and suppresses transcription-associated genomic instability
2016 StandoutNobel
The PI3K Pathway in Human Disease
2017 Standout
Genomics of uterine leiomyomas: insights from high-throughput sequencing
2014
TIGRA: A targeted iterative graph routing assembler for breakpoint assembly
2013
Maftools: efficient and comprehensive analysis of somatic variants in cancer
2018 Standout
Exploration of the gene fusion landscape of glioblastoma using transcriptome sequencing and copy number data
2013
Identification of copy number variants in whole-genome data using Reference Coverage Profiles
2015 StandoutNobel
Management of glioblastoma: State of the art and future directions
2020 Standout
TIMER2.0 for analysis of tumor-infiltrating immune cells
2020 Standout
Epithelial Mesenchymal Transition in Tumor Metastasis
2018 Standout
Statistical challenges associated with detecting copy number variations with next-generation sequencing
2012
Reference-guided assembly of four diverse Arabidopsis thaliana genomes
2011
Longer metaphase and fewer chromosome segregation errors in modern human than Neanderthal brain development
2022 StandoutNobel
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery
2010
Artificial intelligence in cancer imaging: Clinical challenges and applications
2019 Standout
DELLY: structural variant discovery by integrated paired-end and split-read analysis
2012
Epigenetic regulation in pluripotent stem cells: a key to breaking the epigenetic barrier
2012 StandoutNobel
Wound Healing: A Cellular Perspective
2018 Standout
Epidemiology of uterine fibroids: a systematic review
2017 Standout
Characterization of structural variants with single molecule and hybrid sequencing approaches
2014
Redox Signaling by Reactive Electrophiles and Oxidants
2018
Works of Mitchell L. Leibowitz being referenced
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
2010
Chromothripsis as an on-target consequence of CRISPR–Cas9 genome editing
2021
Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
2013
Genome Sequencing of Mouse Induced Pluripotent Stem Cells Reveals Retroelement Stability and Infrequent DNA Rearrangement during Reprogramming
2011
Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangements
2013
Chromothripsis: A New Mechanism for Rapid Karyotype Evolution
2015