Citation Impact
Citing Papers
Comprehensive molecular portraits of human breast tumours
2012 StandoutNature
Molecular Genetic Approaches to the Analysis and Diagnosis of Human Inherited Disease: An Overview
1992
Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation
1992 Nature
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
1989 StandoutNobel
Cell interactions coordinate the development of the C. elegans egg-laying system
1990 StandoutNobel
On the Role of RNA Amplification in dsRNA-Triggered Gene Silencing
2001 StandoutNobel
A community effect in animal development
1988 StandoutNatureNobel
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
1997
Disease-Specific Induced Pluripotent Stem Cells
2008 Standout
Expression cloning of Siamois, a xenopus homeobox gene expressed in dorsal-vegetal cells of blastulae and able to induce a complete secondary axis
1995 StandoutNobel
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
1989
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
Chapter 20 Assays for Gene Function in Developing Xenopus Embryos
1991
A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crest
1989 StandoutNobel
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
2000 Standout
The generation of diversity and pattern in animal development
1992 StandoutNobel
Community effects and related phenomena in development
1993 StandoutNobel
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
1988
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 Standout
Pax7 Is Required for the Specification of Myogenic Satellite Cells
2000 Standout
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
1990
Activation of muscle genes without myogenesis by ectopic expression of MyoD in frog embryo cells
1990 StandoutNatureNobel
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1991 StandoutNature
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
1996
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
2006 StandoutNobel
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
2001 StandoutNobel
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Dystrophin: The protein product of the duchenne muscular dystrophy locus
1987 Standout
Mechanisms of asymmetric cell division: Two Bs or not two Bs, that is the question
1992 StandoutNobel
The molecular basis of common and rare fragile sites
2005
The structural and functional diversity of dystrophin
1993
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
Mouse X chromosome
1997
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
1994
Xsox17α and -β Mediate Endoderm Formation in Xenopus
1997
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Transposon-induced deletions in unc-22 of C. elegans associated with almost normal gene activity
1988 Nature
Multiple intercellular signalling systems control the development of the Caenorhabditis elegans vulva
1991 StandoutNatureNobel
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs
1991 Nature
A phenotypic and molecular characterization of the fmr1‐tm1Cgr Fragile X mouse
2004
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
1990 Nature
Clonal evolution in cancer
2012 StandoutNature
Persistence and replication of plasmid DNA microinjected into early embryos of Xenopus laevis
1988
Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy
1993
Three novel TBX5 mutations in Chinese patients with Holt-Oram syndrome
2000
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome
1987
Experience and Strategy for the Molecular Testing of Duchenne Muscular Dystrophy
2005
The Fragile X Mental Retardation Protein in Circadian Rhythmicity and Memory Consolidation
2009
The molecular genetics of Duchenne muscular dystrophy: the beginning of the end?
1988
Holt-Oram syndrome: a clinical genetic study.
1996
Embryonic induction and muscle gene activation
1989 StandoutNobel
The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)
2016 Standout
Tissue Engineering
1993 StandoutScience
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
1988
Single-cell transplantation determines the time when Xenopus muscle precursor cells acquire a capacity for autonomous differentiation.
1993 StandoutNobel
Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor
1990 Standout
The CArG promoter sequence is necessary for muscle-specific transcription of the cardiac actin gene in Xenopus embryos.
1989 StandoutNobel
A homeobox-containing marker of posterior neural differentiation shows the importance of predetermination in neural induction
1987 StandoutNobel
The Molecular Basis of Muscular Dystrophy in the mdx Mouse: a Point Mutation
1989 Science
Nuclear reprogramming and stem cell creation
2003 StandoutNobel
Functional Coherence of the Human Y Chromosome
1997 StandoutScience
A stoichiometric complex of neurexins and dystroglycan in brain
2001 StandoutNobel
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
1989 Standout
Stability of RNA in developing Xenopus embryos and identification of a destabilizing sequence in TFIIIA messenger RNA
1988
High-frequency germ-line transmission of plasmid DNA sequences injected into fertilized zebrafish eggs.
1991 StandoutNobel
Neural Science
2000 StandoutNobel
Genetic analysis of the mouse using interspecific crosses
1988
Replication, integration and stable germ-line transmission of foreign sequences injected into early zebrafish embryos
1988
Controlling mRNA lifespan
1988 StandoutNatureNobel
Xenopus embryos contain a somite-specific, MyoD-like protein that binds to a promoter site required for muscle actin expression.
1991 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Heterologous Protection Against Influenza by Injection of DNA Encoding a Viral Protein
1993 StandoutScience
Muscle-specific (CArG) and serum-responsive (SRE) promoter elements are functionally interchangeable inXenopusembryos and mouse fibroblasts
1989
Embryonic induction - molecular prospects
1987 StandoutNobel
Mendelian Inheritance in Man
1991
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.
1991 StandoutNobel
Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome
2006 StandoutScience
Developing a New Definition and Assessing New Clinical Criteria for Septic Shock
2016 Standout
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Works of Gareth Cross being referenced
Differential Impact of the FMR-1 Full Mutation on Memory and Attention Functioning: A Neuropsychological Perspective
2001
Holt–Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q
1994
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
1988
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter
1994
Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5′ end of the gene
1987
EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY
1987
The Epidemiology of Sepsis during Rapid Response Team Reviews in a Teaching Hospital
2015
The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome
1987 Nature
Tissue-specific expression of actin genes injected into Xenopus embryos
1986
Preferential deletion of exons in Duchenne and Becker muscular dystrophies
1987 Nature
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.
1987