Citation Impact
Citing Papers
Epigenetic memory of active gene transcription is inherited through somatic cell nuclear transfer
2005 StandoutNobel
Induction of Tumors in Mice by Genomic Hypomethylation
2003 Science
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
2009 StandoutScience
Jinx , an MCMV susceptibility phenotype caused by disruption of Unc13d : a mouse model of type 3 familial hemophagocytic lymphohistiocytosis
2007 StandoutNobel
Predominant Autoantibody Production by Early Human B Cell Precursors
2003 StandoutScience
Disruption of MyD88 signaling suppresses hemophagocytic lymphohistiocytosis in mice
2011 StandoutNobel
Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA
2011 StandoutScience
Promoter Choice Determines Splice Site Selection in Protocadherin α and γ Pre-mRNA Splicing
2002 StandoutNobel
Recombinant Human DNA (Cytosine-5) Methyltransferase
1999 Nobel
Genome-scale DNA methylation maps of pluripotent and differentiated cells
2008 StandoutNature
Modern management of children with haemophagocytic lymphohistiocytosis
2003
Association between presence of HLA-B*5701, HLA-DR7 , and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir
2002 Standout
Combined Immunodeficiencies with Nonfunctional T Lymphocytes
2014
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
1999 Nature
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.
1994 StandoutNobel
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
Regulatory T cells exert checks and balances on self tolerance and autoimmunity
2009 StandoutNobel
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
DNA methylation patterns and epigenetic memory
2002 Standout
The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans
2002 StandoutNobel
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
2007 StandoutNobel
Interleukin-10-Producing Plasmablasts Exert Regulatory Function in Autoimmune Inflammation
2014 StandoutNobel
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
1995
Juvenile idiopathic arthritis
2007 Standout
The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease
2003
Cancer Epigenetics: From Mechanism to Therapy
2012 Standout
Mitochondrial toxicity and HIV therapy
2001
DNA methylation in health and disease
2000
HLH‐2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
2006 Standout
Tolerance and Autoimmunity: Lessons at the Bedside of Primary Immunodeficiencies
2007
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
2005
FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
1998
Reactive haemophagocytic syndrome in children with inflammatory disorders. A retrospective study of 24 patients
2001
Primary immunodeficiencies associated with pneumococcal disease
2003
Epigenetics in Cancer
2008 Standout
Dnmt3a and Dnmt3b Are Transcriptional Repressors That Exhibit Unique Localization Properties to Heterochromatin
2001
Mitochondria: In Sickness and in Health
2012 Standout
The complex language of chromatin regulation during transcription
2007 StandoutNature
Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial
2010 Standout
Macrophage activation syndrome in Kawasaki Disease: More common than we thought?
2014
Methylation matters
2001
The Calcium Sensors STIM1 and STIM2 Control B Cell Regulatory Function through Interleukin-10 Production
2011
Immunoglobulin heavy chain expression shapes the B cell receptor repertoire in human B cell development
2001
The Mammalian Epigenome
2007 Standout
Regulation and function of DNA methylation in plants and animals
2011
STIMulating store-operated Ca2+ entry
2009
Multiple Deletions Are Detectable in Mitochondrial DNA of Aging Mice
1995
Hypomethylation of pericentromeric DNA in breast adenocarcinomas
1998
Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene
2001
A congenital mutation of the novel gene LRRC8 causes agammaglobulinemia in humans
2003
Histiocyte disorders
2004
Gene Silencing in Cancer in Association with Promoter Hypermethylation
2003 Standout
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
2003 Standout
Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis
1997
DNA demethylation and pericentromeric rearrangements of chromosome 1
1997
Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis
2008 Standout
DNA hypomethylation leads to elevated mutation rates
1998 Nature
An outbreak of severe Kawasaki-like disease at the Italian epicentre of the SARS-CoV-2 epidemic: an observational cohort study
2020 Standout
Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene
1997
SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel
2014 StandoutNobel
Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
2002
The Polycomb group protein EZH2 directly controls DNA methylation
2005 StandoutNature
Insights into social insects from the genome of the honeybee Apis mellifera
2006 StandoutNature
DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development
1999 Standout
Genomic instability and the selection of treatments for cancer
2009
Improved outcome in haemophagocytic lymphohistiocytosis after bone marrow transplantation from related and unrelated donors: a single‐centre experience of 12 patients
1999
Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant
2000
A Dominant Complement Fixation Pathway for Pneumococcal Polysaccharides Initiated by SIGN-R1 Interacting with C1q
2006 StandoutNobel
Hemophagocytic Syndromes and Infection
2000
Protein Tyrosine Phosphatases in the Human Genome
2004 Standout
HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis
1997
ICF syndrome: a new case and review of the literature
1994
Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification
2010 StandoutNature
Human DNA methylomes at base resolution show widespread epigenomic differences
2009 StandoutNature
In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state
2007 StandoutNature
Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping
1998
The DNA methyltransferases of mammals
2000 Standout
Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis
2005
Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2
2000
Repair of oxidative damage within the mitochondrial DNA of RINr 38 cells.
1993
Efficacy of cyclosporine A in the treatment of macrophage activation syndrome in juvenile arthritis: Report of five cases
1996
Regulatory T Cells and Human Disease
2020 StandoutNobel
Hematopoietic Stem Cell Transplantation in Hemophagocytic Lymphohistiocytosis: A Single-Center Report of 48 Patients
2006
Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction
2009
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
A Deletion in the Gene Encoding the CD45 Antigen in a Patient with SCID
2001
Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis
2005
Cytokine Storm
2020 Standout
Frequency and Severity of Central Nervous System Lesions in Hemophagocytic Lymphohistiocytosis
1997
Mitochondrial Diseases in Man and Mouse
1999 StandoutScience
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.
1991
The Role of DNA Methylation in Mammalian Epigenetics
2001 StandoutScience
Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress
1997 Standout
Bradykinin B1 and B2 receptors both have protective roles in renal ischemia/reperfusion injury
2007 StandoutNobel
Treatment of Familial Hemophagocytic Lymphohistiocytosis With Bone Marrow Transplantation From HLA Genetically Nonidentical Donors
1997
A DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation
2006 StandoutNobel
Bone Marrow Failure Syndromes
1999
Abnormal methylation does not prevent X inactivation in ICF patients
1999
Works of F Ledeist being referenced
Prevention of graft failure by an anti human leukocyte functional antigen 1 monoclonal antibody in hla mismatched bone marrow transplantation
1986
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome
1993
Multibranched chromosomes in the ICF syndrome: Immunodeficiency, centromeric instability, and facial anomalies
1989
A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case
1997
Major histocompatibility complex class II deficiency: Clinical manifestations, immunologic features, and outcome
1993
A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stage.
1996
STIM1 Mutation Associated with a Syndrome of Immunodeficiency and Autoimmunity
2009
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia
2009
Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.
1990
Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A
1993
Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A
1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
1993