Citation Impact
Citing Papers
Distinctive patterns of microRNA expression in primary muscular disorders
2007
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
The segment polarity gene armadillo encodes a functionally modular protein that is the Drosophila homolog of human plakoglobin
1990
The RNA Binding Protein Quaking Regulates Formation of circRNAs
2015 Standout
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
The light response of drosophila photoreceptors is accompanied by an increase in cellular calcium: Effects of specific mutations
1994
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
1998
Disease-Specific Induced Pluripotent Stem Cells
2008 Standout
mRNA vaccines — a new era in vaccinology
2018 StandoutNobel
Direct Interaction of Alzheimer's Disease-related Presenilin 1 with Armadillo Protein p0071
1999 StandoutNobel
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
1993 StandoutNature
The trp gene is essential for a light-activated Ca2+ channel in Drosophila photoreceptors
1992
Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy
2002
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
1989
Identification and characterization of a spinal muscular atrophy-determining gene
1995 Standout
WT-1 is required for early kidney development
1993 Standout
Screening for antisense modulation of dystrophin pre-mRNA splicing
2002
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
An mRNA Vaccine Encoding Rabies Virus Glycoprotein Induces Protection against Lethal Infection in Mice and Correlates of Protection in Adult and Newborn Pigs
2016
The muscular dystrophies
2002 Standout
The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers
1996 Standout
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
1990
Exon Skipping and Duchenne Muscular Dystrophy Therapy: Selection of the Most Active U1 snRNA Antisense Able to Induce Dystrophin Exon 51 Skipping
2010
Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: Implications for cell and gene therapy
1990
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
2006 StandoutNobel
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14
1990
A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome
1989
A Long Noncoding RNA Controls Muscle Differentiation by Functioning as a Competing Endogenous RNA
2011 Standout
Enantioselective Synthesis of Tertiary and Quaternary Stereogenic Centers: Copper/Phosphoramidite‐Catalyzed Allylic Alkylation with Organolithium Reagents
2012 StandoutNobel
Exon–Intron Organization of the Human Dystrophin Gene
1997
The structural and functional diversity of dystrophin
1993
Targeted Exon Skipping in Transgenic hDMD Mice: A Model for Direct Preclinical Screening of Human-Specific Antisense Oligonucleotides
2004
Cytosolic calcium transients: Spatial localization and role in drosophila photoreceptor cell function
1994 StandoutNobel
Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy
2002
Environmental fate processes and biochemical transformations of chiral emerging organic pollutants
2006
Muscular dystrophy into the new millennium
2002
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
2003
Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy
1999
Circulating Endothelial Progenitor Cells, Vascular Function, and Cardiovascular Risk
2003 Standout
A thermostable Cas9 with increased lifetime in human plasma
2017 StandoutNobel
Synaptotagmins: Why So Many?
2002 StandoutNobel
Structure of a Pestivirus Envelope Glycoprotein E2 Clarifies Its Role in Cell Entry
2012
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
1990 Nature
Understanding the hepatitis C virus life cycle paves the way for highly effective therapies
2013 StandoutNobel
Muscular dystrophies: genes to pathogenesis
2003
The C. elegans gene lin-44, which controls the polarity of certain asymmetric cell divisions, encodes a Wnt protein and acts cell nonautonomously
1995 StandoutNobel
Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy
1993
Emerging Strategies in the Treatment of Duchenne Muscular Dystrophy
2018
Physical linkage of the fragile site FRA11B and a Jacobsen Syndrome chromosome deletion breakpoint in 11q23. 3
1994
Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens
1995 Standout
Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse
2003
Experience and Strategy for the Molecular Testing of Duchenne Muscular Dystrophy
2005
Lysosomal storage diseases
1995
In Vivo and in Vitro Correction of the mdx Dystrophin Gene Nonsense Mutation by Short-Fragment Homologous Replacement
2001
Molecular analysis of the armadillo locus: uniformly distributed transcripts and a protein with novel internal repeats are associated with a Drosophila segment polarity gene.
1989 StandoutNobel
A high resolution vibrational spectroscopic study of CO/K coadsorption on Pt{111}
1993
Identification of the "Active Sites" of a Surface-Catalyzed Reaction
1996 StandoutScienceNobel
Tissue Engineering
1993 StandoutScience
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
1988
Tunneling ionization of noble gases in a high-intensity laser field
1989 StandoutNobel
Alkali-metal-affected adsorption of molecules on metal surfaces
1988
Enantioselective catalysis for agrochemicals. The case histories of (S)–metolachlor, (R)–metalaxyl and clozylacon
1997
Glycosphingolipid degradation and animal models of GM2‐gangliosidoses
1998
Late changes in spliceosomal introns define clades in vertebrate evolution
1999 StandoutNobel
Coverage, lateral order, and vibrations of atomic nitrogen on Ru(0001)
1996 StandoutNobel
Dissociative chemisorption of nitrogen on Ru(0001)
1993 StandoutNobel
Vibrational and structural properties of OH adsorbed on Pt(111)
1999 StandoutNobel
Photoemission of molecular adsorbates
1988
Genomes in Focus: Development and Applications of CRISPR‐Cas9 Imaging Technologies
2017 StandoutNobel
Theory and applications of ion-selective electrodes. Part 8
1990
A stoichiometric complex of neurexins and dystroglycan in brain
2001 StandoutNobel
Evidence for physisorbed N2 in the monolayer on Ru(001) at 40 K
1992
The interaction range in alkali metal-promoted systems
1988
Interactions of CO + K on Ru(001): Structure and bonding
1985
The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types
2002 StandoutNobel
Sticking coefficient for dissociative adsorption of N2 on Ru single-crystal surfaces
1996 StandoutNobel
Neural Science
2000 StandoutNobel
Inverse photoemission from CO co-adsorbed with K on Pt(111)
1987
The adsorption of N2 on Fe(111): Angle resolved photoemission and theoretical model studies
1987
De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies
1994 Science
Effect of Ligand Structure in the Bisoxazoline Mediated Asymmetric Addition of Methyllithium to Imines
2000
Intra- and Extracellular Use and Evaluation of Ammonium-Selective Microelectrodes
1991
Cryobiology: The Freezing of Biological Systems
1970 StandoutScience
Novel Diphosphinoiridium Catalysts for the Enantioselective Hydrogenation of N‐Arylketimines
1990
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Adsorption of molecular nitrogen on clean and modified Ru(001) surfaces: The role ofσbonding
1987
Vibrations, coverage, and lateral order of atomic nitrogen and formation of NH3 on Ru(1010)
1997 StandoutNobel
Interaction of hydrogen with nitrogen atoms chemisorbed on a Ru(0001) surface
1995 StandoutNobel
The vertebrate adhesive junction proteins beta-catenin and plakoglobin and the Drosophila segment polarity gene armadillo form a multigene family with similar properties.
1992 StandoutNobel
Structural analyses of Cs+CO coadsorbed on Ru(0001)
1995 StandoutNobel
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes.
1991
Cross sections and NO product state distributions resulting from substrate mediated photodissociation of NO2 adsorbed on Pd(111)
1990 StandoutNobel
New Chiral Phosphorus Ligands for Enantioselective Hydrogenation
2003 Standout
Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis
1993
Pharmaceuticals of Emerging Concern in Aquatic Systems: Chemistry, Occurrence, Effects, and Removal Methods
2019 Standout
MicroRNA-mediated repression of nonsense mRNAs
2014
Light-induced extracellular calcium and sodium concentration changes in the retina of Calliphora: involvement in the mechanism of light adaptation
1991
Screening Effects in Multielectron Ionization of Heavy Atoms in Intense Laser Fields
1986 StandoutNobel
Electrostatic effects between adsorbed species—the K … Co interaction on Ni(111) as studied by infrared reflection-absorption spectroscopy
1986
Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention
1984
Collision-free multiple photon ionization of atoms and molecules at 193 nm
1985
Carrier-Based Ion-Selective Electrodes and Bulk Optodes. 2. Ionophores for Potentiometric and Optical Sensors
1998 Standout
Structure Determination of an Alkali Metal–CO Coadsorption Phase: Ni(111)-K/
1995 StandoutNobel
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse
2000
Muscular dystrophy in girls with X;autosome translocations.
1986
Localization of some phosphatases in yeast
1963
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
The interaction of carbon monoxide with a ruthenium(100) surface
1989
Unusual type of benign x-linked muscular dystrophy.
1966
Diffusion and Atomic Hopping of N Atoms on Ru(0001) Studied by Scanning Tunneling Microscopy
1996 StandoutNobel
Catalytic Promotion and Poisoning: All-Electron Local-Density-Functional Theory of CO on Ni(001) Surfaces Coadsorbed with K or S
1985
Works of Hans Moser being referenced
[PROGRESSIVE MUSCULAR DYSTROPHY. VI. INCIDENCE, CLINICAL ASPECTS AND GENETICS OF THE DUCHENNE TYPE].
1964
[Carrier detection and genetic counselling in duchenne muscular dystrophy (author's transl)].
1977
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
1988
Molecular deletion patterns in Duchenne and Becker type muscular dystrophy
1989
The 1997–1998 epidemic of classical swine fever in the Netherlands
2000
Intracellular calcium changes in Balanus photoreceptor. A study with calcium ion-selective electrodes and Arsenazo III
1988
Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations
1992
FOLLOW-UP STUDY OF SERUM-CREATINE-KINASE IN CARRIERS OF DUCHENNE MUSCULAR DYSTROPHY
1974
Characterization off
1984
Molecule-molecule and molecule-metal interactions of CO/Ru(001) and N2/Ru(001) studied by angle-resolved photoemission
1985
[Determination of the probability of being heterozygote among relatives of sporadic cases of sex-linked recessive diseases (author's transl)].
1980
Progressive Muskeldystrophie VII. Die Erfassung von Heterozygoten der Duchenne-Muskeldystrophie durch Messung der Serum-Kreatin-Kinase unter lokalisierter Arbeitsbelastung in Anoxie
1965
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease.
1993
The manifesting carrier in Duchenne muscular dystrophy
1974
New Look at the Mechanism for Alkali-Metal Promotion
1985
Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.
1977
Der Einfluß von Atropisomerie und chiralem Zentrum auf die biologische Aktivität des Metolachlor / The Influence of Atropisomerism and Chiral Centre on the Biological Activity of Metolachlor
1982
Summary Abstract: Potassium induced modification of the Ru(001) surface electronic structure
1985
Electrophysiological evidence for ammonium as a substitute for potassium in activating the sodium pump in a crayfish sensory neuron
1987
A new inactivated tissue culture rabies vaccine for use in man Evaluation of PCEC-vaccine by laboratory tests
1984
Serum-Creatin-Kinase und Sulfhydril-Konzentration nach isch�mischer Arbeitsbelastung der Vorderarmmuskulatur bei Patienten und Konduktorinnen der progressiven Muskeldystrophie Duchenne
1971
The final state shape resonance of CO on an alkali modified transition metal surface
1986
[Biochemical, histological and clinical findings in carriers of Duchenne-type progressive muscular dystrophy].
1971
Zur Kenntnis der im alkalischen Gebiet optimal wirksamen Phosphomonoesterasen aus Oberhefe und Unterhefe
1951