Citation Impact
Citing Papers
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
Latrophilins Function as Heterophilic Cell-adhesion Molecules by Binding to Teneurins
2013 StandoutNobel
Crystal Structure of the Second LNS/LG Domain from Neurexin 1α
2006 StandoutNobel
Binding of the G domains of laminin α1 and α2 chains and perlecan to heparin, sulfatides, α-dystroglycan and several extracellular matrix proteins
1999
Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton
1996
Cell mechanics and the cytoskeleton
2010 StandoutNature
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
2008
The nuclear pore complex is involved in nuclear transfer of plasmid DNA condensed with an oligolysine–RGD peptide containing nuclear localisation properties
2001
Enzymatic Self-Assembly of Nanostructures for Theranostics
2012
Identification of FLRT1, FLRT2, and FLRT3: A Novel Family of Transmembrane Leucine-Rich Repeat Proteins
1999
Abdominal obesity and metabolic syndrome
2006 StandoutNature
Causal assessment of occupational carrying and low back pain: results of a systematic review
2010
Form and function: The laminin family of heterotrimers
2000
Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens
1998 StandoutNobel
Non-viral gene delivery in skeletal muscle: a protein factory
2003
Cell production rates in human tissues and tumours and their significance. Part II: clinical data
2000
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin 2-Chain
1997
Lamins A and C but Not Lamin B1 Regulate Nuclear Mechanics
2006
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
Oculopharyngeal Muscular Dystrophy
1999
Laminins and human disease
2000
The metabolic syndrome
2010 Standout
Hallmarks of aging: An expanding universe
2023 Standout
The functions of the nuclear envelope in mediating the molecular crosstalk between the nucleus and the cytoplasm
2011
Glycosylation in Cellular Mechanisms of Health and Disease
2006 Standout
Nuclear lamins and laminopathies
2011
Distant metastasis occurs late during the genetic evolution of pancreatic cancer
2010 StandoutNature
Adipocytes as regulators of energy balance and glucose homeostasis
2006 StandoutNature
The muscular dystrophies
2002 Standout
Protein glycosylation in disease: new insights into the congenital muscular dystrophies
2003
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
2011 Standout
The in vivo performance of an enzyme-assisted self-assembled peptide/protein hydrogel
2011
Dmdmdx-βgeo: A new allele for the mouse dystrophin gene
1998
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Muscular dystrophies, the cytoskeleton and cell adhesion
2002
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping
2001
DNA Damage, Aging, and Cancer
2009 Standout
A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy
1998
The metabolic syndrome
2005 Standout
Extracellular matrix structure
2015 Standout
Development, maintenance and disruption of the blood-brain barrier
2013 Standout
Lipodystrophies: rare disorders causing metabolic syndrome
2004
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis
1996 Standout
Monogenic forms of insulin resistance: apertures that expose the common metabolic syndrome
2003
A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation
2006
Regulation of LNS Domain Function by Alternative Splicing: The Structure of the Ligand-Binding Domain of Neurexin Iβ
1999 StandoutNobel
Mechanisms linking obesity to insulin resistance and type 2 diabetes
2006 StandoutNature
Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage
1995
Mutations in the integrin α7 gene cause congenital myopathy
1998
Extracellular Matrix: Functions in the Nervous System
2010
85th ENMC International Workshop on Congenital Muscular Dystrophy 6th International CMD Workshop 1st Workshop of the Myo-Cluster Project ‘GENRE’27–28th October 2000, Naarden, The Netherlands
2002
Intermediate Filament Proteins and Their Associated Diseases
2004
A constitutively open potassium channel formed by KCNQ1 and KCNE3
2000 StandoutNature
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
Integrins: Redundant or Important Players in Skeletal Muscle?
2003
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1997
Causal assessment of occupational bending or twisting and low back pain: results of a systematic review
2009
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
2002 StandoutNature
What We Talk About When We Talk About Fat
2014 Standout
Molecular mechanisms of muscular dystrophies: old and new players
2006
Agrin Is a High-affinity Binding Protein of Dystroglycan in Non-muscle Tissue
1998
Molecular basis of muscular dystrophies
2000
Genetics of Type 2 diabetes
2005
Muscular dystrophies: genes to pathogenesis
2003
The Hallmarks of Aging
2013 Standout
National, Regional, and Global Trends in Infertility Prevalence Since 1990: A Systematic Analysis of 277 Health Surveys
2012 Standout
Biomarkers for epithelial-mesenchymal transitions
2009 Standout
Infertility around the globe: new thinking on gender, reproductive technologies and global movements in the 21st century
2015 Standout
Non-specific low back pain
2011 Standout
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
Lipodystrophy: lessons in lipid and energy metabolism
2006
DYSTROPHIN-ASSOCIATED PROTEINS AND THE MUSCULAR DYSTROPHIES
1997
Diagnosis and Management of the Metabolic Syndrome
2005 Standout
The mouse and human genes encoding the recognition component of the N-end rule pathway
1998 StandoutNobel
An α-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain
2003 StandoutNobel
Chlamydia trachomatis and oral contraceptive use: a quantitative review.
1992
Supramolecular Hydrogelators and Hydrogels: From Soft Matter to Molecular Biomaterials
2015 Standout
Muscular Dystrophies—Diseases of the Dystrophin-Glycoprotein Complex
1995 Science
Antitumor Antibiotics: Bleomycin, Enediynes, and Mitomycin
2005 Standout
Molecular Pathology of Laminopathies
2021
Nonviral Vectors for Gene Delivery
2008 Standout
A stoichiometric complex of neurexins and dystroglycan in brain
2001 StandoutNobel
Domains of laminin
1996
Calcium Ion in Skeletal Muscle: Its Crucial Role for Muscle Function, Plasticity, and Disease
2000
Lamin A Truncation in Hutchinson-Gilford Progeria
2003 Science
Lipodystrophies: Genetic and Acquired Body Fat Disorders
2011
Collagen IV is essential for basement membrane stability but dispensable for initiation of its assembly during early development
2004
The Nuclear Envelope and Human Disease
2004
Use of Dithiodiglycolic Acid as a Tether for Cationic Lipids Decreases the Cytotoxicity and Increases Transgene Expression of Plasmid DNA in Vitro
1999
Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation
2004
Netrin-G1: a Novel Glycosyl Phosphatidylinositol-Linked Mammalian Netrin That Is Functionally Divergent from Classical Netrins
2000 StandoutNobel
The Laminin α Chains: Expression, Developmental Transitions, and Chromosomal Locations of α1-5, Identification of Heterotrimeric Laminins 8–11, and Cloning of a Novel α3 Isoform
1997
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
2001 StandoutNobel
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice
2002 StandoutNobel
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Operating Characteristics of a Rank Correlation Test for Publication Bias
1994 Standout
Functional characteristics of dystrophic skeletal muscle: insights from animal models
2002
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
1995
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Computational design of a red fluorophore ligase for site-specific protein labeling in living cells
2014 StandoutNobel
Works of A. Leclerc being referenced
Cationic lipid-mediated gene transfer: Analysis of cellular uptake and nuclear import of plasmid DNA
1998
Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C
2002
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings
1998
Cellular uptake of cationic lipid/DNA complexes by cultured myoblasts and myotubes
1999
Infertility in Central Africa: Infection is the cause
1988
Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy
1997
Combined flow cytometry and immunohistochemistry analyses for the assessment of nasopharyngeal carcinoma cell kinetics by in vivo bromodeoxyuridine infusion
1997
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
1995
Biomechanical strains and low back disorders: quantifying the effects of the number of years of exposure on various types of pain
2007
Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
2004
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.
1997
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.
1998
Urogenital Chlamydia trachomatis in Gabon: an unrecognised epidemic.
1988
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
1995
Congenital muscular dystrophy with merosin deficiency.
1994
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.
1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].
1996