Citation Impact
Citing Papers
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
2005 Standout
Receptor-Mediated Adenylyl Cyclase Activation Through XLαs, the Extra-Large Variant of the Stimulatory G Protein α-Subunit
2002
MutL traps MutS at a DNA mismatch
2015 StandoutNobel
Tet Proteins Can Convert 5-Methylcytosine to 5-Formylcytosine and 5-Carboxylcytosine
2011 StandoutScience
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
2009 StandoutScience
Cerebral cortex expansion and folding: what have we learned?
2016
Saccharomyces cerevisiae MutLα Is a Mismatch Repair Endonuclease
2007 StandoutNobel
Comprehensive molecular portraits of human breast tumours
2012 StandoutNature
Mismatch Repair-dependent Iterative Excision at Irreparable O6-Methylguanine Lesions in Human Nuclear Extracts
2006 StandoutNobel
The genomic basis of the Williams – Beuren syndrome
2008
Mechanisms in Eukaryotic Mismatch Repair
2006 StandoutNobel
β-Arrestin-dependent, G Protein-independent ERK1/2 Activation by the β2 Adrenergic Receptor
2005 StandoutNobel
A molecular portrait of microsatellite instability across multiple cancers
2017
Genome-scale DNA methylation maps of pluripotent and differentiated cells
2008 StandoutNature
Acromegaly
2006 Standout
Characterization of Human Retinal Fascin Gene (FSCN2) at 17q25: Close Physical Linkage of Fascin and Cytoplasmic Actin Genes
2000
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
2003
Epigenetics: A Landscape Takes Shape
2007 Standout
Gi-Coupled GPCR Signaling Controls the Formation and Organization of Human Pluripotent Colonies
2009 StandoutNobel
Modular regulatory principles of large non-coding RNAs
2012 StandoutNature
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Human ADAR1 Prevents Endogenous RNA from Triggering Translational Shutdown
2018 StandoutNobel
Cushing's syndrome
2015 Standout
Multiplex pairwise assembly of array-derived DNA oligonucleotides
2015 StandoutNobel
Molecular defects in the pathogenesis of pituitary tumours
2003
Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region
2009
Gestational trophoblastic disease
2010 Standout
Identification of SATB2 as the cleft palate gene on 2q32-q33
2003
Cancer Epigenetics: From Mechanism to Therapy
2012 Standout
Hydrolytic function of Exo1 in mammalian mismatch repair
2014 StandoutNobel
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
2008 StandoutNature
Endonucleolytic Function of MutLα in Human Mismatch Repair
2006 StandoutNobel
Imprints of disease at GNAS1
2001
Epigenetics in Cancer
2008 Standout
Mechanisms regulating imprinted genes in clusters
2007
Mechanisms of NAFLD development and therapeutic strategies
2018 Standout
Cleft lip and palate
2009 Standout
The Mammalian Epigenome
2007 Standout
Williams–Beuren Syndrome
2010 Standout
A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles
2007
Retinitis pigmentosa
2006 Standout
SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease
2004
X-inactivation profile reveals extensive variability in X-linked gene expression in females
2005 StandoutNature
Molecular Mechanisms of Long Noncoding RNAs
2011 Standout
High-Resolution Analysis of Cytosine Methylation in Ancient DNA
2012
Histone H3 lysine 9 and H4 lysine 20 trimethylation and the expression of Suv4-20h2 and Suv-39h1 histone methyltransferases in hepatocarcinogenesis induced by methyl deficiency in rats
2006
Evaluation of Factors Related to Late Recurrence - Later than 10 Years after the Initial Treatment - in Primary Breast Cancer
2013 Standout
TET enzymes, TDG and the dynamics of DNA demethylation
2013 StandoutNature
Universal sample preparation method for proteome analysis
2009 Standout
Genetics and Proteomics of Pituitary Tumors
2005
Genetic predisposition to colorectal cancer
2004
Communication by Extracellular Vesicles: Where We Are and Where We Need to Go
2016 Standout
Advances in understanding cancer genomes through second-generation sequencing
2010
Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB
2004
ECAT11/L1td1 Is Enriched in ESCs and Rapidly Activated During iPSCGeneration, but It Is Dispensable for the Maintenance and Induction of Pluripotency
2011 StandoutNobel
Mammalian G Proteins and Their Cell Type Specific Functions
2005
The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair
2006
The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles
2002
Role of Dietary Fructose and Hepatic De Novo Lipogenesis in Fatty Liver Disease
2016
lincRNAs act in the circuitry controlling pluripotency and differentiation
2011 StandoutNature
NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation
2008
Mammalian G-protein function in vivo: New insights through altered gene expression
2006
Comparative Analysis of Amino Acid Usage and Protein Length Distribution Between Alternatively and Non-alternatively Spliced Genes Across Six Eukaryotic Genomes
2003
Long non-coding RNAs: insights into functions
2009 Standout
The epidemiology and genetics of pituitary adenomas
2009
The ORF1 Protein Encoded by LINE‐1: Structure and Function During L1 Retrotransposition
2006
DNA methylation and human disease
2005 Standout
Isoforms of RNA-Editing Enzyme ADAR1 Independently Control Nucleic Acid Sensor MDA5-Driven Autoimmunity and Multi-organ Development
2015
Dosage‐dependent switch from G protein‐coupled to G protein‐independent signaling by a GPCR
2006 StandoutNobel
The Small Intestine Converts Dietary Fructose into Glucose and Organic Acids
2018
Lynch Syndrome Genes
2005
Diflunisal Analogues Stabilize the Native State of Transthyretin. Potent Inhibition of Amyloidogenesis
2003
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
EUKARYOTIC CYTOSINE METHYLTRANSFERASES
2005 Standout
Breast Cancer Treatment
2019 Standout
DNA Mismatch Repair: Functions and Mechanisms
2005 StandoutNobel
PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance
2010 StandoutNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
The function of non-coding RNAs in genomic imprinting
2009
Conservation and divergence of methylation patterning in plants and animals
2010 Standout
Familial recurrent hydatidiform mole: a review.
2004
Viruses transfer the antiviral second messenger cGAMP between cells
2015 Science
Aromatic Sulfonyl Fluorides Covalently Kinetically Stabilize Transthyretin to Prevent Amyloidogenesis while Affording a Fluorescent Conjugate
2013 StandoutNobel
Cancer Genome Landscapes
2013 StandoutScience
A High-Plex PCR Approach for Massively Parallel Sequencing
2013
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing
2010
Xist RNA and the Mechanism of X Chromosome Inactivation
2002
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination
2008
The Cerebellum-Specific Munc13 Isoform Munc13-3 Regulates Cerebellar Synaptic Transmission and Motor Learning in Mice
2001 StandoutNobel
Works of Bruce E. Hayward being referenced
SAMHD1‐dependent retroviral control and escape in mice
2013
Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23
1996
A global disorder of imprinting in the human female germ line
2002 Nature
Extensive gene conversion at thePMS2DNA mismatch repair locus
2007
Genetic diagnosis of familial breast cancer using clonal sequencing
2010
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
2010
Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline
2003
Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia
2009
Novel PMS2 Pseudogenes Can Conceal Recessive Mutations Causing a Distinctive Childhood Cancer Syndrome
2004
Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly
2001
An imprinted antisense transcript at the human GNAS1 locus
2000
Recombination Creates Novel L1 (LINE-1) Elements in Rattus norvegicus
1997
PMS2 Mutations in Childhood Cancer
2006
Tissue-Specific Expression of Antisense and Sense Transcripts at the Imprinted Gnas Locus
2000
Both isoforms of ketohexokinase are dispensable for normal growth and development
2010
Structure and alternative splicing of the ketohexokinase gene
1998
Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins
1998
The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
1998
Properties of Normal and Mutant Recombinant Human Ketohexokinases and Implications for the Pathogenesis of Essential Fructosuria
2003