Citation Impact
Citing Papers
The Xist RNA Gene Evolved in Eutherians by Pseudogenization of a Protein-Coding Gene
2006 Science
PhyloWGS: Reconstructing subclonal composition and evolution from whole-genome sequencing of tumors
2015
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
2003 Standout
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
2014 Standout
High-Definition Reconstruction of Clonal Composition in Cancer
2014
Adaptive evolution of SCML1 in primates, a gene involved in male reproduction
2008
Depression
2018 Standout
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
2005 Standout
lincRNAs: Genomics, Evolution, and Mechanisms
2013 Standout
Identification of Genes Associated with the Corticotroph Phenotype in Bronchial Carcinoid Tumors
2002
A microRNA family exerts maternal control on sex determination in C. elegans
2017 StandoutNobel
A Scan for Positively Selected Genes in the Genomes of Humans and Chimpanzees
2005
Genetic effects on gene expression across human tissues
2017 StandoutNature
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
1992 Standout
Modular regulatory principles of large non-coding RNAs
2012 StandoutNature
Polycomb group protein complexes: do different complexes regulate distinct target genes?
1999
Landscape of X chromosome inactivation across human tissues
2017 Nature
Single-Cell Resolution of Temporal Gene Expression during Heart Development
2016
Cushing's syndrome
2015 Standout
Clonal Heterogeneity and Tumor Evolution: Past, Present, and the Future
2017 Standout
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1995 Standout
Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias
2016
X inactivation Xplained
2007
The GPR54 Gene as a Regulator of Puberty
2003 Standout
Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons
2006
The Molecular Genetics of Crop Domestication
2006 Standout
Synaptic transmission: A bidirectional and self-modifiable form of cell-cell communication
1993 StandoutNobel
A Genomic and Functional Inventory of Deubiquitinating Enzymes
2005 Standout
Integrating single-cell transcriptomic data across different conditions, technologies, and species
2018 Standout
Fumarate and Succinate Regulate Expression of Hypoxia-inducible Genes via TET Enzymes
2015 StandoutNobel
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
2001
Sex and gender: modifiers of health, disease, and medicine
2020 Standout
Cleft lip and palate
2009 Standout
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
2001 StandoutNature
The X chromosome in immune functions: when a chromosome makes the difference
2010
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
1991 Nature
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
The polycomb group protein EZH2 is involved in progression of prostate cancer
2002 StandoutNature
Multiple small RNA pathways regulate the silencing of repeated and foreign genes in C. elegans
2013 StandoutNobel
Tumour heterogeneity and cancer cell plasticity
2013 StandoutNature
Dynamics of DNA Methylation in Recent Human and Great Ape Evolution
2013
Epigenetic memory of an active gene state depends on histone H3.3 incorporation into chromatin in the absence of transcription
2007 StandoutNobel
The Long Noncoding RNA, Jpx, Is a Molecular Switch for X Chromosome Inactivation
2010
Choice of enzymes for mapping based on CpG islands in the human genome
1992
Epigenetics of Stress-Related Psychiatric Disorders and Gene × Environment Interactions
2015
X‐chromosome inactivation in development and cancer
2014
Epigenetic Patterns Maintained in Early Caenorhabditis elegans Embryos Can Be Established by Gene Activity in the Parental Germ Cells
2011
Sex and inflammation in respiratory diseases: a clinical viewpoint
2013
2-D Structure of the A Region of Xist RNA and Its Implication for PRC2 Association
2010
The Number of X Chromosomes Causes Sex Differences in Adiposity in Mice
2012
Polycomb-group genes as regulators of mammalian lymphopoiesis
2001
Single-Cell Transcriptomic Analysis of Primary and Metastatic Tumor Ecosystems in Head and Neck Cancer
2017 Standout
Construction of a BAC Contig Map of Chromosome 16q by Two-Dimensional Overgo Hybridization
2000
Genomic Rearrangements and Gene Copy-Number Alterations as a Cause of Nervous System Disorders
2006
Stem Cells and Cancer
2004 Standout
A human chromosome 7 yeast artificial chromosome (YAC) resource: construction, characterization, and screening
1995
5-hydroxymethylcytosine in cancer: significance in diagnosis and therapy
2015
PAML 4: Phylogenetic Analysis by Maximum Likelihood
2007 Standout
Sex differences in immune responses
2016 Standout
Cushing's syndrome
2006 Standout
A condensin-like dosage compensation complex acts at a distance to control expression throughout the genome
2009
A Dual Origin of the Xist Gene from a Protein-Coding Gene and a Set of Transposable Elements
2008
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes
2007
Evolution and Functions of Long Noncoding RNAs
2009 Standout
Maintenance of gene expression patterns
2005
dbSNP: the NCBI database of genetic variation
2001 Standout
Long Noncoding RNAs: Cellular Address Codes in Development and Disease
2013 Standout
Evolution of primate gene expression
2006 StandoutNobel
The Polycomb complex PRC2 and its mark in life
2011 StandoutNature
Gene regulation by long non-coding RNAs and its biological functions
2020 Standout
CTCF: Master Weaver of the Genome
2009 Standout
High throughput analysis of differential gene expression
1998
The evolution of gene expression levels in mammalian organs
2011 StandoutNatureNobel
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Genome Regulation by Long Noncoding RNAs
2012 Standout
Structure of the STRA6 receptor for retinol uptake
2016 StandoutScienceNobel
A powerful and flexible approach to the analysis of RNA sequence count data
2011
Policy: NIH to balance sex in cell and animal studies
2014 StandoutNature
Histone variant macroH2A confers resistance to nuclear reprogramming
2011 StandoutNobel
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
TheCaenorhabditis elegans spalt-like genesem-4restricts touch cell fate by repressing the selector Hox geneegl-5and the effector genemec-3
2003 StandoutNobel
Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation
2012 Standout
A General Mechanism for Network-Dosage Compensation in Gene Circuits
2010 StandoutScienceNobel
Structural and functional characterization of the USP11 deubiquitinating enzyme, which interacts with the RanGTP-associated protein RanBPM
2002
Anchoring 9,371 Maize Expressed Sequence Tagged Unigenes to the Bacterial Artificial Chromosome Contig Map by Two-Dimensional Overgo Hybridization
2004
X Chromosome Dosage Compensation: How Mammals Keep the Balance
2008
The Molecular Biology of Axon Guidance
1996 StandoutScience
Targeted Investigation of the Neandertal Genome by Array-Based Sequence Capture
2010 StandoutScienceNobel
Works of Mark T. Ross being referenced
Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2
2013
Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination
2005
Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22
1999
Identification and Characterization of KLHL4, a Novel Human Homologue of the Drosophila Kelch Gene That Maps within the X-Linked Cleft Palate and Ankyloglossia (CPX) Critical Region
2001
Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials
2007
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2
1998
Large-Scale Population Study of Human Cell Lines Indicates that Dosage Compensation Is Virtually Complete
2008
Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region
2001
Characterization ofSCML1,a New Gene in Xp22, with Homology to Developmental Polycomb Genes
1998
Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals
2005
Selection of a human chromosome 21 enriched YAC sub–library using a chromosome–specific composite probe
1992
A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa
1995
Long-range physical mapping around the human steroid sulfatase locus
1990
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns
2012
Progressive proximal expansion of the primate X chromosome centromere
2005
Screening Large‐Insert Libraries by Hybridization
1999