Citation Impact
Citing Papers
Probing mucin-type O-linked glycosylation in living animals
2006 StandoutNobel
Epigenetic memory of active gene transcription is inherited through somatic cell nuclear transfer
2005 StandoutNobel
Identification of Novel Genes Coding for Small Expressed RNAs
2001 StandoutScience
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
2009 StandoutScience
A target selection of somatic hypermutations is regulated similarly between T and B cells upon activation-induced cytidine deaminase expression
2005 StandoutNobel
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
2009 StandoutScience
A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation
2003 StandoutNobel
X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C
2011 StandoutNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Sequence- and Structure-Specific RNA Processing by a CRISPR Endonuclease
2010 StandoutScienceNobel
Epigenetic regulation of hypoxic sensing disrupts cardiorespiratory homeostasis
2012 StandoutNobel
Epigenetic Variation Illustrated by DNA Methylation Patterns of the Fragile-X Gene FMR1
1997
Distinct phenotypes distinguish the molecular classes of Angelman syndrome
2001
Phenotypic plasticity and the epigenetics of human disease
2007 Nature
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
1997
A 3-Mb Map of a Large Segmental Duplication Overlapping the α7-Nicotinic Acetylcholine Receptor Gene (CHRNA7) at Human 15q13–q14
2002
Transcriptional fates of human-specific segmental duplications in brain
2018
Identification of Tissue-Specific MicroRNAs from Mouse
2002 Standout
Chromosome Territories
2010
MicroRNAs
2004 Standout
The nuclear RNase III Drosha initiates microRNA processing
2003 StandoutNature
Chemical Technologies for Probing Glycans
2006 StandoutNobel
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
DNA methylation patterns and epigenetic memory
2002 Standout
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment
2003
Disruption of imprinting caused by deletion of the H19 gene region in mice
1995 Nature
Post-transcriptional gene regulation by mRNA modifications
2016 Standout
Nicotinic acetylcholine receptor α7 subunit is an essential regulator of inflammation
2002 StandoutNature
Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
2009 StandoutNature
Prokaryote and eukaryote evolvability
2003
Allele-specific replication timing of imprinted gene regions
1993 Nature
Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
2005 StandoutNature
Genes Expressed in Neurons of Adult Male Drosophila
1997 StandoutNobel
Identification of novel non‐coding RNAs as potential antisense regulators in the archaeon Sulfolobus solfataricus
2004
The expanding snoRNA world
2002
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function
2005
Methylation matters
2001
Gene Switching and the Stability of Odorant Receptor Gene Choice
2004 StandoutNobel
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects
2002
UBE3A/E6-AP mutations cause Angelman syndrome
1997
The MicroRNA miR-1 Regulates a MEF-2-Dependent Retrograde Signal at Neuromuscular Junctions
2008 StandoutNobel
CTCF Elements Direct Allele-Specific Undermethylation at the Imprinted H19 Locus
2004
Novel small RNA-encoding genes in the intergenic regions of Escherichia coli
2001
RNA-guided genetic silencing systems in bacteria and archaea
2012 StandoutNatureNobel
Maternal nutritional status, C1metabolism and offspring DNA methylation: a review of current evidence in human subjects
2011
Generation of germline-competent induced pluripotent stem cells
2007 StandoutNatureNobel
Non–coding RNA genes and the modern RNA world
2001
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
2001
The novel BORIS + CTCF gene family is uniquely involved in the epigenetics of normal biology and cancer
2002
Polycomb Silencing and the Maintenance of Stable Chromatin States
1999
Small Nucleolar RNAs
2002
Direct and site-specific quantification of RNA 2′-O-methylation by PCR with an engineered DNA polymerase
2016
RNomics: an experimental approach that identifies 201 candidates for novel, small, non-messenger RNAs in mouse
2001
Imprinting and the Initiation of Gene Silencing in the Germ Line
1998
Noncoding RNA genes
1999
Non-coding RNAs: lessons from the small nuclear and small nucleolar RNAs
2007
Creation of genomic methylation patterns
1996
Revealing the world of RNA interference
2004 StandoutNatureNobel
MicroRNA expression profiles classify human cancers
2005 StandoutNatureNobel
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
1994
Profiling of Ribose Methylations in RNA by High‐Throughput Sequencing
2014
Chemical pulldown reveals dynamic pseudouridylation of the mammalian transcriptome
2015
Imprinted expression of the Igf2r gene depends on an intronic CpG island
1997 Nature
Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing to Prader-Willi Syndrome
1999
Genomic imprinting: parental influence on the genome
2001 Standout
Allelic inactivation regulates olfactory receptor gene expression
1994 StandoutNobel
Topological domains in mammalian genomes identified by analysis of chromatin interactions
2012 StandoutNature
Imprinting and disease
2003
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A
2001
microRNAs
2001 StandoutNobel
The functions of animal microRNAs
2004 StandoutNatureNobel
DNA methylation and human disease
2005 Standout
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
A catalogue of imprinted genes and parent-of-origin effects in humans and animals
1998
Methylation Dynamics, Epigenetic Fidelity and X Chromosome Structure
2007
A Genetic Approach to Mammalian Glycan Function
2003
A segment of cold shock protein directs the folding of a combinatorial protein
2005 StandoutNobel
Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes
2001
RNA–protein analysis using a conditional CRISPR nuclease
2013 StandoutNobel
DNA Methylation Is Linked to Deacetylation of Histone H3, but Not H4, on the Imprinted Genes Snrpnand U2af1-rs1
2001
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.
1993
Role of MicroRNAs in Plant and Animal Development
2003 StandoutScienceNobel
NONCODING RNAS IN THE MAMMALIAN CENTRAL NERVOUS SYSTEM
2006
The future of cloning
1999 StandoutNatureNobel
Developmental potential of mouse primordial germ cells
1999
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
Introns in gene evolution
2003
A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice
1998
Cutadapt removes adapter sequences from high-throughput sequencing reads
2011 Standout
Imprinting disorders: non-Mendelian mechanisms affecting growth.
2002
Imprinting and the Epigenetic Asymmetry Between Parental Genomes
2001 Science
Profiling of Ribose Methylations in RNA by High‐Throughput Sequencing
2014
BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regions
2012
X-CHROMOSOME INACTIVATION IN MAMMALS
1997
Association between active genes occurs at nuclear speckles and is modulated by chromatin environment
2008
Introns in Gene Evolution
2003
Translating the Histone Code
2001 StandoutScience
HEAT-SHOCK PROTEINS, MOLECULAR CHAPERONES, AND THE STRESS RESPONSE: Evolutionary and Ecological Physiology
1999 Standout
Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase
2010 StandoutNobel
Identification of many microRNAs that copurify with polyribosomes in mammalian neurons
2003 StandoutNobel
A DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation
2006 StandoutNobel
THE UBIQUITIN SYSTEM
1998 StandoutNobel
The first half-century of nuclear transplantation
2003 StandoutNobel
ATM mutations are associated with inactivation of theARF-TP53 tumor suppressor pathway in diffuse large B-cell lymphoma
2002
An Expanding Universe of Noncoding RNAs
2002 Science
Trimmomatic: a flexible trimmer for Illumina sequence data
2014 Standout
Works of Karin Buiting being referenced
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
2000
Balanced Translocation 46, XY, t(2;15)(q37.2;q11.2) Associated with Atypical Prader-Willi Syndrome
1997
Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method
1997
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
2001
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
1996
Identification of a Testis-Specific Gene (C15orf2) in the Prader–Willi Syndrome Region on Chromosome 15
2000
Identification of Novel Exons 3′ to the HumanSNRPNGene
1997
Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome
2001
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11→q13
1999
Molecular Mechanism of Angelman Syndrome in Two Large Families Involves an Imprinting Mutation
1999
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene
1993
Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
2003
Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7)
1998
Imprinting defects on human chromosome 15
2006
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
1992
Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15
2001
Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
1995
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp
1999
Characterization of a methylation imprint in the Prader — Willi syndrome chromosome region
1993
The murine <i>Ext1</i> gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15
1997
Imprinting-Mutation Mechanisms in Prader-Willi Syndrome
1999
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete
2009
Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenicDrosophila
1998
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation
1997
Maintenance of imprinting and nuclear architecture in cycling cells
2007
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
1994
Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation
1997
A Single-Tube PCR Test for the Diagnosis of Angelman and Prader-Willi Syndrome Based on Allelic Methylation Differences at the SNRPN Locus
1997
The imprinting box of the Prader-Willi/Angelman syndrome domain
2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp
1999
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
1996
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.
1992
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
2000
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus.
1997