Citation Impact
Citing Papers
Nod1 Detects a Unique Muropeptide from Gram-Negative Bacterial Peptidoglycan
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Innate and Adaptive Immunity Cooperate Flexibly to Maintain Host-Microbiota Mutualism
2009 StandoutScienceNobel
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
2009 StandoutScience
Selective blockade of inhibitory Fcγ receptor enables human dendritic cell maturation with IL-12p70 production and immunity to antibody-coated tumor cells
2005 StandoutNobel
Leukemia in twins: lessons in natural history
2003
Meta-Analysis of GJB2 Mutation 35delG Frequencies in Europe
2001
The Molecular Genetics of Human Hemoglobin
1984
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
2024 StandoutNobel
Molecular epidemiology of DFNB1 deafness in France
2004
GJB2 mutations: Passage through Iran
2005
Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness
2000
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment
2001
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Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
2001
Sorting points into neighborhoods (SPIN): data analysis and visualization by ordering distance matrices
2005
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2006
Unravelling the pathogenesis of inflammatory bowel disease
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Unrepaired DNA Breaks in p53-Deficient Cells Lead to Oncogenic Gene Amplification Subsequent to Translocations
2002
High-Resolution Profiling of Histone Methylations in the Human Genome
2007 Standout
AID Is Required for c-myc/IgH Chromosome Translocations In Vivo
2004 StandoutNobel
A genotype-phenotype correlation for GJB2 (connexin 26) deafness
2004
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
2001 StandoutNature
Cells on chips
2006 StandoutNature
Genomewide Search in Canadian Families with Inflammatory Bowel Disease Reveals Two Novel Susceptibility Loci
2000
Collagen stimulates tyrosine phosphorylation of phospholipase C‐γ2 but not phospholipase C‐γ1 in human platelets
1994
Mediator and cohesin connect gene expression and chromatin architecture
2010 Nature
Id proteins in development, cell cycle and cancer
2003
Mechanisms of therapy-related carcinogenesis
2005
Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness
1998
DNA topoisomerase II, genotoxicity, and cancer
2007
Mouse models of human AML accurately predict chemotherapy response
2009
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins
2000
Connexin26 gene (GJB2): prevalence of mutations in the Chinese population
2002
Sensorineural hearing loss in children
2005 Standout
Nanoparticles functionalised with reversible molecular and supramolecular switches
2010 StandoutNobel
The Molecular Basis of Leukemia
2004
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
2001 StandoutNature
The frequency of illegitimate V(D)J recombinase-mediated mutations in children treated with etoposide-containing antileukemic therapy
1998
Plant pathogens and integrated defence responses to infection
2001 StandoutNature
A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment
2002
Rethinking schizophrenia
2010 StandoutNature
Human Fc gamma RII, in the absence of other Fc gamma receptors, mediates a phagocytic signal.
1991
A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression
2011 StandoutNature
TET enzymes, TDG and the dynamics of DNA demethylation
2013 StandoutNature
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
GJB2: The spectrum of deafness-causing allele variants and their phenotype
2004
Enhanced Phagocytosis through Inhibition of de Novo Ceramide Synthesis
2003 StandoutNobel
Consanguinity and endogamy in Northern Tunisia and its impact on non‐syndromic deafness
2004
Neuroblastoma
2007 Standout
Genomic Rearrangements and Gene Copy-Number Alterations as a Cause of Nervous System Disorders
2006
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia
2010
The Inflammasomes
2010 Standout
Molecular genetics, natural history and the demise of childhood leukaemia
1999
DNA-PKcs has KU-dependent function in rRNA processing and haematopoiesis
2020 StandoutNatureNobel
The role of senescent cells in ageing
2014 StandoutNature
Microfluidic chips for clinical and forensic analysis
2002
Clonal evolution in cancer
2012 StandoutNature
Points of control in inflammation
2002 StandoutNature
DNA Topoisomerases and Their Poisoning by Anticancer and Antibacterial Drugs
2010 Standout
Genes that mediate breast cancer metastasis to lung
2005 StandoutNature
Topological domains in mammalian genomes identified by analysis of chromatin interactions
2012 StandoutNature
22q11.2 deletion syndrome
2015 Standout
Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease
2000
International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16
2001
High-Density Genome Scan in Crohn Disease Shows Confirmed Linkage to Chromosome 14q11-12
2000
Spatial partitioning of the regulatory landscape of the X-inactivation centre
2012 StandoutNature
Photoinduced Conversion of Silver Nanospheres to Nanoprisms
2001 StandoutScience
Selective Colorimetric Detection of Polynucleotides Based on the Distance-Dependent Optical Properties of Gold Nanoparticles
1997 StandoutScience
Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss
1999
Association of CYP 3 A 4 genotype with treatment-related leukemia
1998
Scanometric DNA Array Detection with Nanoparticle Probes
2000 StandoutScience
Gold Nanoparticles: Assembly, Supramolecular Chemistry, Quantum-Size-Related Properties, and Applications toward Biology, Catalysis, and Nanotechnology
2003 Standout
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
Interactions Between the Microbiota and the Immune System
2012 StandoutScience
Abrogation of the Fc gamma receptor IIA-mediated phagocytic signal by stem-loop Syk antisense oligonucleotides.
1996
Molecular-Mechanical Switching at the Nanoparticle−Solvent Interface: Practice and Theory
2010 StandoutNobel
Self-Assembly of CdSe−ZnS Quantum Dot Bioconjugates Using an Engineered Recombinant Protein
2000 StandoutNobel
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands
2003
A General Mechanism for Network-Dosage Compensation in Gene Circuits
2010 StandoutScienceNobel
Nod2-Dependent Regulation of Innate and Adaptive Immunity in the Intestinal Tract
2005 StandoutScience
Integrins and Signal Transduction Pathways: the Road Taken
1995 StandoutScience
Illegitimate Cre-dependent chromosome rearrangements in transgenic mouse spermatids
2000 StandoutNobel
Prevalent connexin 26 gene (GJB2) mutations in Japanese
2000
LCX, leukemia-associated protein with a CXXC domain, is fused to MLL in acute myeloid leukemia with trilineage dysplasia having t(10;11)(q22;q23).
2002
Roles of DNA topoisomerase II isozymes in chemotherapy and secondary malignancies
2007
Semiconductor Nanocrystals as Fluorescent Biological Labels
1998 StandoutScience
FcγRIIa Is Expressed on Natural IFN-α-Producing Cells (Plasmacytoid Dendritic Cells) and Is Required for the IFN-α Production Induced by Apoptotic Cells Combined with Lupus IgG
2003
The molecular dissection of Fc gamma receptor mediated phagocytosis
1995
One-Pot Colorimetric Differentiation of Polynucleotides with Single Base Imperfections Using Gold Nanoparticle Probes
1998 Standout
Oligonucleotide-Modified Gold Nanoparticles for Intracellular Gene Regulation
2006 StandoutScience
Pharmacogenomics: Translating Functional Genomics into Rational Therapeutics
1999 StandoutScience
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Structural Basis of Type II Topoisomerase Inhibition by the Anticancer Drug Etoposide
2011 StandoutScience
The Structure of Haplotype Blocks in the Human Genome
2002 StandoutScience
Global and Hox-specific roles for the MLL1 methyltransferase
2005
Works of Eric Rappaport being referenced
MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site
2002
Primary Respiratory Chain Disease Causes Tissue-Specific Dysregulation of the Global Transcriptome and Nutrient-Sensing Signaling Network
2013
Connexin-26 mutations in sporadic and inherited sensorineural deafness
1998
Potential role for wild-type p53 in leukemias with MLL gene translocations
1998
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study
1999
Proline Affects Brain Function in 22q11DS Children with the Low Activity COMT158 Allele
2008
Parallel molecular genetic analysis
1998
Modulation of human mononuclear phagocyte FcγRII mRNA and protein
1989
Differential expression of Fcγ RIIA, Fcγ RIIB and Fcγ RIIC in hematopoietic cells: Analysis of transcripts
1993
Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform
2005
Reciprocal DNA topoisomerase II cleavage events at 5′-TATTA-3′ sequences in MLL and AF-9 create homologous single-stranded overhangs that anneal to form der(11) and der(9) genomic breakpoint junctions in treatment-related AML without further processing
2003
Nucleic acid detection using non-radioactive labelling methods
1995
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss
2002
Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells
2009
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays
2006
MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q
2006
Panhandle PCR for cDNA: A rapid method for isolation of MLL fusion transcripts involving unknown partner genes
2000
Etoposide Metabolites Enhance DNA Topoisomerase II Cleavage near Leukemia-Associated MLL Translocation Breakpoints
2001
Alpha-gene deletions in black newborn infants with Hb Bart's
1980
Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions ofMLLtranslocations and identify complex translocation ofMLL,AF-4, andCDK6
2002
Panhandle PCR strategy to amplify MLL genomic breakpoints in treatment-related leukemias
1997
Detection of leukemia-associated MLL-GAS7 translocation early during chemotherapy with DNA topoisomerase II inhibitors
2000
t(11;22)(q23;q11.2) in acute myeloid leukemia of infant twins fuses MLL with hCDC rel , a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes
1998
Panhandle Polymerase Chain Reaction Amplifies MLL Genomic Translocation Breakpoint Involving Unknown Partner Gene
1997
Expression profiles of acute lymphoblastic and myeloblastic leukemias with ALL-1 rearrangements
2003
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation
2001
ID2 expression is not associated with MYCN amplification or expression in human neuroblastomas.
2003