Citation Impact
Citing Papers
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
2005 Standout
Unusual DNA Structures Associated With Germline Genetic Activity in Caenorhabditis elegans
2006 StandoutNobel
Hippo signaling disruption and Akt stimulation of ovarian follicles for infertility treatment
2013 Standout
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
HIF prolyl and asparaginyl hydroxylases in the biological response to intracellular O2 levels
2003 StandoutNobel
Treatment of kidney cancer
2009 StandoutNobel
Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes
2009
Cell mechanics and the cytoskeleton
2010 StandoutNature
Regulation and Destabilization of HIF-1α by ARD1-Mediated Acetylation
2002
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
1998
Filamins as integrators of cell mechanics and signalling
2001
The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein
1996
Life at the edge: the nuclear envelope and human disease
2002
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
Targeting HIF-1 for cancer therapy
2003 StandoutNobel
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
1999
Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis
2007 StandoutNobel
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
2004 StandoutNature
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
2007 StandoutNobel
Transcriptional Repressor Germ Cell-less (GCL) and Barrier to Autointegration Factor (BAF) Compete for Binding to Emerin in Vitro
2003
Challenges in Duchenne muscular dystrophy1This review is based on the first Alan Emery lecture given at Green College, Oxford, on 11th March 1997.1
1997
Hallmarks of aging: An expanding universe
2023 Standout
Nuclear lamins and laminopathies
2011
The muscular dystrophies
2002 Standout
Sec24p and Sec16p cooperate to regulate the GTP cycle of the COPII coat
2011 StandoutNobel
A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated
1998 Nature
Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells
2001 StandoutNature
Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons
2006
Molecular Cloning and Identification of -Acyl-D-glucosamine 2-Epimerase from Porcine Kidney as a Renin-binding Protein
1996
Interaction of the Calcium-sensing Receptor and Filamin, a Potential Scaffolding Protein
2001
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
2008 StandoutNature
A Human Homologue of the Drosophila melanogaster diaphanous Gene Is Disrupted in a Patient with Premature Ovarian Failure: Evidence for Conserved Function in Oogenesis and Implications for Human Sterility
1998
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Degradation of the E7 human papillomavirus oncoprotein by the ubiquitin-proteasome system: targeting via ubiquitination of the N-terminal residue
2000 StandoutNobel
Integrated control of lung fluid balance
2004
Muscular dystrophies, the cytoskeleton and cell adhesion
2002
Actin Filament Crosslinking by Chicken Gizzard Filamin Is Regulated by Phosphorylation in Vitro
1995
Telomerase RNA structure and function: implications for dyskeratosis congenita
2004 StandoutNobel
Sulfation of N-Acetylglucosamine by Chondroitin 6-Sulfotransferase 2 (GST-5)
2000 StandoutNobel
X-inactivation profile reveals extensive variability in X-linked gene expression in females
2005 StandoutNature
Review: Nuclear Lamins—Structural Proteins with Fundamental Functions
2000
Fluorescence in situ hybridization to chromosomes as a tool to understand human and primate genome evolution
2004
Identification and specificities of N-terminal acetyltransferases from Saccharomyces cerevisiae
1999
Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity
2007
GlcNAc 2-Epimerase Can Serve a Catabolic Role in Sialic Acid Metabolism
2003 StandoutNobel
The role of the nuclear envelope in Emery–Dreifuss muscular dystrophy
2001
Synaptotagmins: Why So Many?
2002 StandoutNobel
Laminopathies and the long strange trip from basic cell biology to therapy
2009
Rho and Rac Take Center Stage
2004 Standout
Molecular mechanisms of muscular dystrophies: old and new players
2006
The von Hippel–Lindau protein, HIF hydroxylation, and oxygen sensing
2005 StandoutNobel
Signalling hypoxia by HIF hydroxylases
2005 StandoutNobel
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Molecular basis of muscular dystrophies
2000
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
2009
Muscular dystrophies: genes to pathogenesis
2003
The Hallmarks of Aging
2013 Standout
The Ig-like Structure of the C-Terminal Domain of Lamin A/C, Mutated in Muscular Dystrophies, Cardiomyopathy, and Partial Lipodystrophy
2002
A mutation in the X-linked Emery–Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy
2001
Nuclear lamina at the crossroads of the cytoplasm and nucleus
2011
Analysis of ARD1 Function in Hypoxia Response Using Retroviral RNA Interference
2005
Nuclear lamins: building blocks of nuclear architecture
2002
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
1999
A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila
2007 StandoutNobel
The apparent absence of lamin B1 and emerin in many tissue nuclei is due to epitope masking
2005
Signalling via the hypoxia-inducible factor-1α requires multiple posttranslational modifications
2004
Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
2000
Evolution of primate gene expression
2006 StandoutNobel
Gene regulation by long non-coding RNAs and its biological functions
2020 Standout
Structure of the Globular Tail of Nuclear Lamin
2002
Identification of essential genes in cultured mammalian cells using small interfering RNAs
2001
Heterogeneous gene expression from the inactive X chromosome: An X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others
1999
Nuclear Membrane Proteins with Potential Disease Links Found by Subtractive Proteomics
2003 Science
Nuclear Membrane Dynamics and Reassembly in Living Cells: Targeting of an Inner Nuclear Membrane Protein in Interphase and Mitosis
1997
Molecular Pathology of Laminopathies
2021
A first-generation X-inactivation profile of the human X chromosome
1999
Cytoskeletal Protein ABP-280 Directs the Intracellular Trafficking of Furin and Modulates Proprotein Processing in the Endocytic Pathway
1997 StandoutNobel
The muscular dystrophies
2012
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
The future of cloning
1999 StandoutNatureNobel
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
2012 Standout
The Caenorhabditis elegans Heterochronic Regulator LIN-14 Is a Novel Transcription Factor That Controls the Developmental Timing of Transcription from the Insulin/Insulin-Like Growth Factor Gene ins-33 by Direct DNA Binding
2005 StandoutNobel
Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy
1999
A novel hnRNP protein (HAP/SAF-B) enters a subset of hnRNP complexes and relocates in nuclear granules in response to heat shock
1999
A stoichiometric complex of neurexins and dystroglycan in brain
2001 StandoutNobel
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
2000 Standout
Regulation of G Protein–Coupled Receptor Signaling by Scaffold Proteins
2002 StandoutNobel
Sudden Cardiac Death
1998 Standout
Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies
2008
X-CHROMOSOME INACTIVATION IN MAMMALS
1997
The Nuclear Envelope and Human Disease
2004
The Function of Nuclear Architecture: A Genetic Approach
2003
BRCA1-IRIS promotes human tumor progression through PTEN blockade and HIF-1α activation
2018 StandoutNobel
Clinical Approach to Genetic Cardiomyopathy in Children
1996
An Isolated Cardiac Conduction Disease Maps to Chromosome 19q
1995
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
C. elegansNuclear Envelope Proteins Emerin, MAN1, Lamin, and Nucleoporins Reveal Unique Timing of Nuclear Envelope Breakdown during Mitosis
2000
Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF
2001
A DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation
2006 StandoutNobel
Generation of skeletal muscle stem/progenitor cells from murine induced pluripotent stem cells
2010 StandoutNobel
unc-83encodes a novel component of the nuclear envelope and is essential for proper nuclear migration
2001 StandoutNobel
The small GTPase RalA targets filamin to induce filopodia
1999
Nanotoxicology: An Emerging Discipline Evolving from Studies of Ultrafine Particles
2005 Standout
Works of Mita Mancini being referenced
Genomic organization and transcriptional analysis of the human genes coding for caveolin-1 and caveolin-2
2000
Molecular Cytogenetic Resources for Chromosome 4 and Comparative Analysis of Phylogenetic Chromosome IV in Great Apes
2000
Mapping of two genes encoding isoforms of the actin binding protein ABP-280, a dystrophin like protein, to Xq28 and to chromosome 7
1993
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
1994
Methylation and sequence analysis around Eagi sites: identification of 28 new CpG islands in XQ24-XQ28
1992
Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiae
1994
The Exon-Intron Organization of the Human X-Linked Gene (FLN1) Encoding Actin-Binding Protein 280
1994