Citation Impact
Citing Papers
NanoPack: visualizing and processing long-read sequencing data
2018 Standout
Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression
2014 StandoutNobel
Promoter Choice Determines Splice Site Selection in Protocadherin α and γ Pre-mRNA Splicing
2002 StandoutNobel
A survey of best practices for RNA-seq data analysis
2016 Standout
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Syndromes of disordered chromatin remodeling
2003
DNA methylation age of human tissues and cell types
2013 Standout
Genome-scale DNA methylation maps of pluripotent and differentiated cells
2008 StandoutNature
Lack of association of MYO9B genetic variants with coeliac disease in a British cohort
2006
Functions of DNA methylation: islands, start sites, gene bodies and beyond
2012 Standout
Structure and Function of Eukaryotic DNA Methyltransferases
2004
DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes
2001
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
2009 StandoutNobel
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
1999 Nature
The history of cancer epigenetics
2004 Standout
Overlap of expression Quantitative Trait Loci (eQTL) in human brain and blood
2014
Hippocampal Gene Expression Analysis Highlights Ly6a/Sca-1 as Candidate Gene for Previously Mapped Novelty Induced Behaviors in Mice
2011
DNA methylation patterns and epigenetic memory
2002 Standout
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Unravelling the pathogenesis of inflammatory bowel disease
2007 StandoutNature
Presynaptic Neurexin-3 Alternative Splicing trans-Synaptically Controls Postsynaptic AMPA Receptor Trafficking
2013 StandoutNobel
The Human Obesity Gene Map: The 2005 Update
2006
Hallmarks of aging: An expanding universe
2023 Standout
Quantifying transcription factor kinetics: At work or at play?
2013
The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease
2003
Cancer Epigenetics: From Mechanism to Therapy
2012 Standout
DNA methylation in health and disease
2000
Inflammatory Bowel Disease
2009 Standout
DNA methylation: roles in mammalian development
2013 Standout
Integrating single-cell transcriptomic data across different conditions, technologies, and species
2018 Standout
Single-Molecule Dynamics of Enhanceosome Assembly in Embryonic Stem Cells
2014 StandoutNobel
DNMT3B mutations and DNA methylation defect define two types of ICF syndrome
2004
Molecular Enzymology of the Catalytic Domains of the Dnmt3a and Dnmt3b DNA Methyltransferases
2002
Epigenetics in Cancer
2008 Standout
Neurexin 1 (NRXN1) Deletions in Schizophrenia
2009
Methylation matters
2001
Association between genetic variants in myosin IXB and Crohnʼs disease
2009
Rapid Single-Step Induction of Functional Neurons from Human Pluripotent Stem Cells
2013 StandoutNobel
The Mammalian Epigenome
2007 Standout
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
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome
2010
Charting the travels of copper in eukaryotes from yeast to mammals
2012
DNA methylation landscapes: provocative insights from epigenomics
2008 Standout
Causes and consequences of microRNA dysregulation in cancer
2009 Standout
Rethinking schizophrenia
2010 StandoutNature
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
Non-coding RNAs in human disease
2011 Standout
Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis
2008 Standout
The intestinal epithelial barrier: a therapeutic target?
2016 Standout
Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells
2002
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Imprinting Capacity of Gamete Lineages in Caenorhabditis elegans
2005 StandoutNobel
DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development
1999 Standout
Signatures of Archaic Adaptive Introgression in Present-Day Human Populations
2016
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
2016 Standout
Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort
2006
Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant
2000
Molecular pathogenesis of inflammatory bowel disease: Genotypes, phenotypes and personalized medicine
2007
The Genetics of Inflammatory Bowel Disease
2007
Modeling psychiatric disorders at the cellular and network levels
2012
Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease
2010
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
2012
Human DNA methylomes at base resolution show widespread epigenomic differences
2009 StandoutNature
Replication of genetic variation in the MYO9B gene in Crohn's disease
2011
The fundamental role of epigenetic events in cancer
2002 Standout
In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state
2007 StandoutNature
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
2013 Standout
The Human Obesity Gene Map: The 2004 Update
2005
DNA Hypomethylation, Cancer, the Immunodeficiency, Centromeric Region Instability, Facial Anomalies Syndrome and Chromosomal Rearrangements
2002
DNA methylation and human disease
2005 Standout
Global Properties and Functional Complexity of Human Gene Regulatory Variation
2013
The role of neurexins in schizophrenia and autistic spectrum disorder
2011
The DNA methyltransferases of mammals
2000 Standout
Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2
2000
A Fibrosis‐Independent Hepatic Transcriptomic Signature Identifies Drivers of Disease Progression in Primary Sclerosing Cholangitis
2020 StandoutNobel
Pathophysiology of Human Visceral Obesity: An Update
2013 Standout
Copper Stress Affects Iron Homeostasis by Destabilizing Iron-Sulfur Cluster Formation in Bacillus subtilis
2010
Zonulin Upregulation Is Associated With Increased Gut Permeability in Subjects With Type 1 Diabetes and Their Relatives
2006
Mice lacking myosin IXb, an inflammatory bowel disease susceptibility gene, have impaired intestinal barrier function and superficial ulceration in the ileum
2016
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
EUKARYOTIC CYTOSINE METHYLTRANSFERASES
2005 Standout
The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
1999
The PWWP Domain of Dnmt3a and Dnmt3b Is Required for Directing DNA Methylation to the Major Satellite Repeats at Pericentric Heterochromatin
2004
Diagnosing COVID-19: The Disease and Tools for Detection
2020 Standout
Epigenetic regulation in pluripotent stem cells: a key to breaking the epigenetic barrier
2012 StandoutNobel
Copper induces cell death by targeting lipoylated TCA cycle proteins
2022 StandoutScience
A fourth Denisovan individual
2017 StandoutNobel
The Role of DNA Methylation in Mammalian Epigenetics
2001 StandoutScience
A role for myosin IXb, a motor–RhoGAP chimera, in epithelial wound healing and tight junction regulation
2012
Abnormal methylation does not prevent X inactivation in ICF patients
1999
Zinc Pyrithione Inhibits Yeast Growth through Copper Influx and Inactivation of Iron-Sulfur Proteins
2011
Works of Eric Strengman being referenced
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
2012
Gene expression profiling in C57BL/6J and A/J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background
2010
Variance‐Component Analysis of Obesity in Type 2 Diabetes Confirms Loci on Chromosomes 1q and 11q
2003
Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients
2011
Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes
2012
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
2005
Genetic variation in ICF syndrome: Evidence for genetic heterogeneity
2000
Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping
1998
Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
2008
Gene expression profiling and phenotype analyses ofS. cerevisiaein response to changing copper reveals six genes with new roles in copper and iron metabolism
2005
Genetic variation in ICF syndrome: Evidence for genetic heterogeneity
2000