Citation Impact
Citing Papers
Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate
2019 StandoutScienceNobel
Hypoxia Induces Trimethylated H3 Lysine 4 by Inhibition of JARID1A Demethylase
2010
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
2014 StandoutNobel
A Neural Circuit for Memory Specificity and Generalization
2013 StandoutScienceNobel
Integration of over 9,000 mass spectrometry experiments builds a global map of human protein complexes
2017
Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness
2017 Standout
Hierarchical Mechanisms for Direct Reprogramming of Fibroblasts to Neurons
2013 StandoutNobel
NSun2-Mediated Cytosine-5 Methylation of Vault Noncoding RNA Determines Its Processing into Regulatory Small RNAs
2013
RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome
2011 Standout
Bacterial glycosyltransferase-mediated cell-surface chemoenzymatic glycan modification
2019 StandoutNobel
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
2024 StandoutNobel
MCPH1 Functions in an H2AX-dependent but MDC1-independent Pathway in Response to DNA Damage
2007
Autism‐associated familial microdeletion of Xp11.22
2008
Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge
2013
Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology
2017
PI3Kδ and primary immunodeficiencies
2016
A novel mutation in JARID1C gene associated with mental retardation
2006
TRAPP complexes in membrane traffic: convergence through a common Rab
2010
Physical Principles of Membrane Shape Regulation by the Glycocalyx
2019 StandoutNobel
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage ofXLMRgenes
2007
Accurate and comprehensive sequencing of personal genomes
2011
RBP2 Belongs to a Family of Demethylases, Specific for Tri-and Dimethylated Lysine 4 on Histone 3
2007
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
Chromatin Modifications and Their Function
2007 Standout
Neuroligin 2 Drives Postsynaptic Assembly at Perisomatic Inhibitory Synapses through Gephyrin and Collybistin
2009
High-Resolution Mapping Reveals a Conserved, Widespread, Dynamic mRNA Methylation Program in Yeast Meiosis
2013 StandoutNobel
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
2010 Standout
Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
2008
Associations of genetic polymorphisms of Siglecs with human diseases
2014
Physical and Functional Association of a Trimethyl H3K4 Demethylase and Ring6a/MBLR, a Polycomb-like Protein
2007
N6-methyladenosine Modulates Messenger RNA Translation Efficiency
2015 Standout
Pathogenesis and therapy of psoriasis
2007 StandoutNature
The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation
2007 Nature
Nomenclature of the ARID family of DNA-binding proteins
2005
PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase
2009 StandoutNobel
What primary microcephaly can tell us about brain growth
2006
Role of tRNA modifications in human diseases
2014
The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4 Demethylases
2007
A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation
2013
The Role of Ionotropic Glutamate Receptors in Childhood Neurodevelopmental Disorders: Autism Spectrum Disorders and Fragile X Syndrome
2014
Annotating genomes with massive-scale RNA sequencing
2008
A de novo paradigm for mental retardation
2010
The molecular landscape of ASPM mutations in primary microcephaly
2008
Dynamic Regulation of Histone Lysine Methylation by Demethylases
2007
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
The complex language of chromatin regulation during transcription
2007 StandoutNature
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
Dynamic RNA Modifications in Gene Expression Regulation
2017 Standout
The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia
2006
Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling
2013 StandoutNobel
Wnt/β-Catenin Signaling and Disease
2012 Standout
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
2010 Standout
The Adaptor Function of TRAPPC2 in Mammalian TRAPPs Explains TRAPPC2-Associated SEDT and TRAPPC9-Associated Congenital Intellectual Disability
2011
The Impact of the Gut Microbiota on Human Health: An Integrative View
2012 Standout
Phase transitions in the assembly of multivalent signalling proteins
2012 StandoutNature
A Chromatin-Mediated Reversible Drug-Tolerant State in Cancer Cell Subpopulations
2010 Standout
RazerS—fast read mapping with sensitivity control
2009
Mechanisms involved in the regulation of histone lysine demethylases
2008
Next-generation DNA sequencing
2008 Standout
Psoriasis: genetic associations and immune system changes
2006
Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies
2010
Fast gapped-read alignment with Bowtie 2
2012 Standout
CASK Functions as a Mg2+-Independent Neurexin Kinase
2008 StandoutNobel
The histone demethylase Dmel\Kdm4A controls genes required for life span and male-specific sex determination in Drosophila
2009
Twitter evolution: converging mechanisms in birdsong and human speech
2010
Cerebral organoids model human brain development and microcephaly
2013 StandoutNature
The PI3K Pathway in Human Disease
2017 Standout
The Retinoblastoma Binding Protein RBP2 Is an H3K4 Demethylase
2007 StandoutNobel
Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes
2017 StandoutNobel
Identification of direct targets and modified bases of RNA cytosine methyltransferases
2013
lincRNAs act in the circuitry controlling pluripotency and differentiation
2011 StandoutNature
Stem cell function and stress response are controlled by protein synthesis
2016 Nature
Protein Sequence Editing of SKN-1A/Nrf1 by Peptide:N-Glycanase Controls Proteasome Gene Expression
2019 StandoutNobel
Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site
2012 StandoutNobel
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Autochthonous tumors driven by Rb1 loss have an ongoing requirement for the RBP2 histone demethylase
2018 StandoutNobel
Elucidation of AMPA receptor–stargazin complexes by cryo–electron microscopy
2016 StandoutScienceNobel
Role of Rab GTPases in Membrane Traffic and Cell Physiology
2011
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex
2010
Characterizing 5-methylcytosine in the mammalian epitranscriptome
2013
Chromatin and oxygen sensing in the context of JmjC histone demethylases
2014
Profiling the HeLa S3 Transcriptome using Randomly Primed cDNA and Massively Parallel Short-Read Sequencing
2008
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
2013 StandoutNobel
Fast and accurate short read alignment with Burrows–Wheeler transform
2009 Standout
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
2009 Standout
Canonical and noncanonical intraflagellar transport regulates craniofacial skeletal development
2016
STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets
2018 Standout
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
2018
Oligosaccharyltransferase: the central enzyme of N‐linked protein glycosylation
2011
Histone demethylase JMJD2C is a coactivator for hypoxia-inducible factor 1 that is required for breast cancer progression
2012 StandoutNobel
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
2010 StandoutNobel
Sudestada1, a Drosophila ribosomal prolyl-hydroxylase required for mRNA translation, cell homeostasis, and organ growth
2014 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Neurological Aspects of Human Glycosylation Disorders
2015
Coordinated repression of cell cycle genes by KDM5A and E2F4 during differentiation
2012 StandoutNobel
The emerging functions of histone demethylases
2008
Works of Andreas Tzschach being referenced
Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation
2009
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11
2006
A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation
2007
NovelJARID1C/SMCX mutations in patients with X-linked mental retardation
2006
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants ofCOH1
2008
A Novel MGST2 Non-Synonymous Mutation in a Chinese Pedigree with Psoriasis Vulgaris
2006
Mapping translocation breakpoints by next-generation sequencing
2008
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation
2007
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
2005
ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions
2011
Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay
2006
Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
2010
A balanced chromosomal translocation disruptingARHGEF9is associated with epilepsy, anxiety, aggression, and mental retardation
2008
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
2012
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly
2005
A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation
2008
2013
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability
2017