Citation Impact
Citing Papers
Variation in Transcription Factor Binding Among Humans
2010 Science
rMATS: Robust and flexible detection of differential alternative splicing from replicate RNA-Seq data
2014 Standout
The human splicing code reveals new insights into the genetic determinants of disease
2014 Science
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
2009 Standout
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
Sex Differences in the Gut Microbiome Drive Hormone-Dependent Regulation of Autoimmunity
2013 StandoutScience
The Ensembl Regulatory Build
2015
Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins
2014
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Differential expression analysis for sequence count data
2010 Standout
Evaluation of affinity-based genome-wide DNA methylation data: Effects of CpG density, amplification bias, and copy number variation
2010
Defibrotide reduces procoagulant activity and increases fibrinolytic properties of endothelial cells
2003
Gemtuzumab ozogamicin: promise and challenge in patients with acute myeloid leukemia
2002
A penalized matrix decomposition, with applications to sparse principal components and canonical correlation analysis
2009
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
2012 StandoutNature
Genetic effects on gene expression across human tissues
2017 StandoutNature
Gemtuzumab ozogamicin in the treatment of acute myeloid leukemia
2003
Prevalence of Obesity and Trends in the Distribution of Body Mass Index Among US Adults, 1999-2010
2012 Standout
Chemotherapy for malignant gliomas
1988
A HapMap harvest of insights into the genetics of common disease
2008
Alternative isoform regulation in human tissue transcriptomes
2008 StandoutNature
Multi-institutional use of defibrotide in 88 patients after stem cell transplantation with severe veno-occlusive disease and multisystem organ failure: response without significant toxicity in a high-risk population and factors predictive of outcome
2002
Cytochrome P-450 Polymorphisms and Response to Clopidogrel
2008 Standout
Pathogenesis of Shiga Toxin-Associated Hemolytic Uremic Syndrome
2001
Macrophages in the Pathogenesis of Atherosclerosis
2011 Standout
Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
2005 Standout
The role of regulatory variation in complex traits and disease
2015
Inflammatory Bowel Disease
2009 Standout
Integrating single-cell transcriptomic data across different conditions, technologies, and species
2018 Standout
WGAViewer: Software for genomic annotation of whole genome association studies: Figure 1.
2008
Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic and clinical aspects
2007
Autophagy: Renovation of Cells and Tissues
2011 Standout
Mapping and analysis of chromatin state dynamics in nine human cell types
2011 StandoutNature
Vascular disorders of the liver # †
2008 Standout
Human nutrition, the gut microbiome and the immune system
2011 StandoutNature
Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans
2015
Cis and Trans Effects of Human Genomic Variants on Gene Expression
2014
Hypoxia and the extracellular matrix: drivers of tumour metastasis
2014 StandoutNobel
Prevention of veno-occlusive disease with defibrotide after allogeneic stem cell transplantation
2004
Blinded by the Light: The Growing Complexity of p53
2009 Standout
Dissecting the genetics of the human transcriptome identifies novel trait-relatedtrans-eQTLs and corroborates the regulatory relevance of non-protein coding loci
2015
Population genomics of human gene expression
2007
Identification and validation of genes involved in cervical tumourigenesis
2011
High-Resolution Mapping of Expression-QTLs Yields Insight into Human Gene Regulation
2008
Molecular chaperones in protein folding and proteostasis
2011 StandoutNature
MCScanX: a toolkit for detection and evolutionary analysis of gene synteny and collinearity
2012 Standout
On the Dependency of Cellular Protein Levels on mRNA Abundance
2016 Standout
Rethinking schizophrenia
2010 StandoutNature
Malignant Gliomas in Adults
2008 Standout
Reduced Mortality after Allogeneic Hematopoietic-Cell Transplantation
2010 Standout
Meta-analysis of radiation therapy with and without adjuvant chemotherapy for malignant gliomas in adults
1993
Programmed Cell Senescence during Mammalian Embryonic Development
2013 Standout
Sex-specific genetic architecture of human disease
2008
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance
2009 StandoutNature
Deep learning
2015 StandoutNatureNobel
Radiotherapy plus Concomitant and Adjuvant Temozolomide for Glioblastoma
2005 Standout
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
2009
Genetics and pathogenesis of inflammatory bowel disease
2011 StandoutNature
Hepatic Venoocclusive Disease in Blood and Bone Marrow Transplantation in Children and Young Adults: Incidence, Risk Factors, and Outcome in a Cohort of 241 Patients
2002
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
2010 Standout
Transcriptome genetics using second generation sequencing in a Caucasian population
2010 Nature
Systematic Review of Controlled Clinical Trials on the Use of Ursodeoxycholic Acid for the Prevention of Hepatic Veno-occlusive Disease in Hematopoietic Stem Cell Transplantation
2007
Gene Copy-Number Alterations: A Cost-Benefit Analysis
2013
Integrative Modeling of eQTLs and Cis-Regulatory Elements Suggests Mechanisms Underlying Cell Type Specificity of eQTLs
2013
Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease
2010
Diet and the evolution of human amylase gene copy number variation
2007
Intrinsic Protein Disorder and Interaction Promiscuity Are Widely Associated with Dosage Sensitivity
2009
Genome-wide analysis of transcript isoform variation in humans
2008
Characterization of genome-wide p53-binding sites upon stress response
2008
Comprehensive Integration of Single-Cell Data
2019 Standout
phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data
2013 Standout
Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals
2013
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
2010 Standout
The Human Condition—A Molecular Approach
2014 StandoutNobel
Noncanonical DNA Motifs as Transactivation Targets by Wild Type and Mutant p53
2008
Serum bilirubin levels and mortality after myeloablative allogeneic hematopoietic cell transplantation†
2005
Brain Tumors
2001 Standout
The evolution of gene expression levels in mammalian organs
2011 StandoutNatureNobel
Sequencing technologies — the next generation
2009 Standout
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
2008
Alternative splicing and evolution: diversification, exon definition and function
2010
Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19
2020 Standout
Prior gemtuzumab ozogamicin exposure significantly increases the risk of veno-occlusive disease in patients who undergo myeloablative allogeneic stem cell transplantation
2003
Genetic structure and domestication history of the grape
2011 Standout
Antitumor Antibiotics: Bleomycin, Enediynes, and Mitomycin
2005 Standout
Leukocytosis and Ischemic Vascular Disease Morbidity and Mortality
2005
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
2008
Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation
2012 Standout
Chemotherapy in adult high-grade glioma: a systematic review and meta-analysis of individual patient data from 12 randomised trials
2002
Classification of Intrinsically Disordered Regions and Proteins
2014 Standout
Is Obesity Our Genetic Legacy?
2008
Breeding Technologies to Increase Crop Production in a Changing World
2010 StandoutScience
Genomic Selection for Crop Improvement
2009
Platelet activation by Shiga toxin and circulatory factors as a pathogenetic mechanism in the hemolytic uremic syndrome
2001
The Chemistry of Neutron Capture Therapy
1998 Standout
Ursodeoxycholic acid for the prevention of hepatic complications in allogeneic stem cell transplantation
2002
Promotion of direct reprogramming by transformation-deficient Myc
2010 StandoutNobel
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
2013 Standout
Defibrotide in the treatment of children with veno-occlusive disease (VOD): a retrospective multicentre study demonstrates therapeutic efficacy upon early intervention
2003
Works of Anna Grassi being referenced
Defibrotide for the treatment of hepatic veno-occlusive disease: results of the European compassionate-use study
2000
Evolution, structure and function of mitochondrial carriers: a review with new insights
2011
Tandem repeats modify the structure of human genes hosted in segmental duplications
2009
p53FamTaG: a database resource of human p53, p63 and p73 direct target genes combining in silico prediction and microarray data
2007
Thrombosis in Cancer Patients Treated with Hematopoietic Growth Factors - A Meta-Analysis
1996
Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes
2007 Science
CCNU-chemotherapy of hemispheric supratentorial glioblastoma multiforme
1980
Defibrotide for the treatment of hepatic veno‐occlusive disease: results of the European compassionate‐use study
2000
Platelet-derived Microvesicles in Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic Syndrome
1996