Citation Impact
Citing Papers
Induced Pluripotent Stem Cells Generated from Patients with ALS Can Be Differentiated into Motor Neurons
2008 StandoutScience
Origins and Divergence of the Roma (Gypsies)
2001 Standout
Glutamate receptor ion channels
2005 Standout
A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene
2000
Glutamate Receptor Ion Channels: Structure, Regulation, and Function
2010 Standout
Multiple Regulatory Elements Control Transcription of the Peripheral Myelin Protein Zero Gene
1997
Siglecs and their roles in the immune system
2007 Standout
Packing of Myelin Protein Zero
1996
The Retinal Pigment Epithelium in Visual Function
2005 Standout
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease
2005
Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse
2009 Standout
Interleukin-17 Family Members and Inflammation
2004 Standout
Molecular Signature of CD8+ T Cell Exhaustion during Chronic Viral Infection
2007 Standout
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Pathological roles of MAPK signaling pathways in human diseases
2010 Standout
I-type lectins
2002
Mammalian phosphoinositide kinases and phosphatases
2009 StandoutNobel
Growth-suppressive effects of BPOZ and EGR2, two genes involved in the PTEN signaling pathway
2001
Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy
2000
Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in mice
2014
A Vast Repertoire of Dscam Binding Specificities Arises from Modular Interactions of Variable Ig Domains
2007 StandoutNobel
The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease
2015 Standout
Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis
2016
Many facets of the peripheral myelin protein PMP22 in myelination and disease
1998
Egr-2 and Egr-3 are negative regulators of T cell activation
2005
Neuregulin, a factor with many functions in the life of a Schwann cell
2000
ErbB2 Pathways in Heart and Neural Diseases
2003
Adipocytes as regulators of energy balance and glucose homeostasis
2006 StandoutNature
Design and development of polymers for gene delivery
2005 Standout
Phenotypic clustering in MPZ mutations
2004
Amyotrophic lateral sclerosis
2011 Standout
Myelin deficiencies in both the central and the peripheral nervous systems associated with aSOX10 mutation
1999
The transcription factor Sox10 is a key regulator of peripheral glial development
2001 Standout
A microRNA program in the C. elegans hypodermis couples to intestinal mTORC2/PQM-1 signaling to modulate fat transport
2016 StandoutNobel
Single-cell-based sensors and synchrotron FTIR spectroscopy: A hybrid system towards bacterial detection
2007 StandoutNobel
Pectins: structure, biosynthesis, and oligogalacturonide-related signaling
2001 Standout
Piezos thrive under pressure: mechanically activated ion channels in health and disease
2017 StandoutNobel
Metazoan MicroRNAs
2018 Standout
Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot–Marie–Tooth disease
2002
Hoxb1 neural crest preferentially form glia of the PNS
2003 StandoutNobel
Trastuzumab — Mechanism of Action and Use in Clinical Practice
2007 Standout
Molecular Genetics of Demyelination: New Wrinkles on an Old Membrane
1997
N-Acetylaspartate in the CNS: From neurodiagnostics to neurobiology
2007 Standout
Four structural risk factors identify most fibril-forming kappa light chains
2000
P-type lectins
2002
Transcriptional control of adipocyte formation
2006 Standout
Chromosome 21 and Down syndrome: from genomics to pathophysiology
2004 Standout
The transcriptional repressor Nab1 is a specific regulator of pathological cardiac hypertrophy
2005 Nobel
The Roles of Growth Factors in Tendon and Ligament Healing
2003 Standout
From Ionic Currents to Molecular Mechanisms
2000 Standout
Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma
2003
Structure/function relationships of axon-associated adhesion receptors of the immunoglobulin superfamily
1996
Antibodies to myelin protein zero (P0) protein as markers of auto-immune inner ear diseases
2007 StandoutNobel
Advances in Duchenne muscular dystrophy gene therapy
2003
A Novel Locus for Autosomal Recessive Peripheral Neuropathy in the EGR2 Region on 10q23
2000
Krox-20 patterns the hindbrain through both cell-autonomous and non cell-autonomous mechanisms
2001
Reversal of Hox1 Gene Subfunctionalization in the Mouse
2006 StandoutNobel
The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial
1999
Adipocyte differentiation from the inside out
2006 Standout
Protein Tyrosine Phosphatases in the Human Genome
2004 Standout
Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene
1999
No evidence of auditory dysfunction in guinea pigs immunized with myelin P0 protein
2001
The transcription factor Egr-1: a potential drug in wound healing and tissue repair
2001
A Rheostat Model for a Rapid and Reversible Form of Imprinting-Dependent Evolution
2002
Regulation of cardiac hypertrophy by intracellular signalling pathways
2006 Standout
Piezo2 senses airway stretch and mediates lung inflation-induced apnoea
2016 StandoutNatureNobel
Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome
1999
Down syndrome
2020 Standout
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
2006
Central Sensitization: A Generator of Pain Hypersensitivity by Central Neural Plasticity
2009 Standout
Krox20 stimulates adipogenesis via C/EBPβ-dependent and -independent mechanisms
2005
Crystal Structure of the Extracellular Domain from P0, the Major Structural Protein of Peripheral Nerve Myelin
1996
Amyotrophic Lateral Sclerosis
2001 Standout
Charcot‐Marie‐Tooth disease and related neuropathies: Mutation distribution and genotype‐phenotype correlation
2001
Molecular Mechanisms of Amyloidosis
2003 Standout
The peripheral myelin protein 22 and epithelial membrane protein family
2000
Functional studies and distribution define a family of transmembrane AMPA receptor regulatory proteins
2003
MOLECULAR MECHANISMS FOR GENOMIC DISORDERS
2002
Roles of N-Linked Glycans in the Endoplasmic Reticulum
2004 Standout
Applications of the Morris water maze in the study of learning and memory
2001 Standout
Pathogen Recognition and Inflammatory Signaling in Innate Immune Defenses
2009 Standout
CD4+CD25−LAG3+regulatory T cells controlled by the transcription factor Egr-2
2009 StandoutNobel
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
2002 StandoutScience
MAB-10/NAB acts with LIN-29/EGR to regulate terminal differentiation and the transition from larva to adult in C. elegans
2011 Nobel
The Enzymes, Regulation, and Genetics of Bile Acid Synthesis
2003 Standout
Molecular Basis of Genetic Heterogeneity: Role of the Clinical Neurologist
1998
ADHESION MOLECULES AND INHERITED DISEASES OF THE HUMAN NERVOUS SYSTEM
1998
IL-17 Family Cytokines and the Expanding Diversity of Effector T Cell Lineages
2007 Standout
Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3 , as potential susceptibility candidates in schizophrenia
2007 Nobel
Neural Science
2000 StandoutNobel
Biology of Oligodendrocyte and Myelin in the Mammalian Central Nervous System
2001 Standout
A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.
2004
THE MOLECULAR STRUCTURE OF CELL ADHESION MOLECULES
1997
A Dual Role oferbB2in Myelination and in Expansion of the Schwann Cell Precursor Pool
2000
Trans-Acting Epigenetic Effects of Chromosomal Aneuploidies: Lessons From Down Syndrome and Mouse Models
2016
Claudins and the Modulation of Tight Junction Permeability
2013 Standout
p38 Mitogen-Activated Protein Kinase-Dependent and -Independent Signaling of mRNA Stability of AU-Rich Element-Containing Transcripts
2003
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: A developmental ?neural crest syndrome? related to a SOX10 mutation
2000
Works of Laura E. Warner being referenced
Absence ofPMP22 coding region mutations in CMT1A duplication patients: Further evidence supporting gene dosage as a mechanism for charcot-marie-tooth disease type 1A
1996
Multiplede novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case
1997
Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelinopathies
1999
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
1998
Molecular Mechanisms for CMT1A Duplication and HNPP Deletion
1999
Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
1996
Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease
1996
Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophy
2002
Hereditary Peripheral Neuropathies: Clinical Forms, Genetics, and Molecular Mechanisms
1999
Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype
1999
Absence of PMP22 coding region mutations in CMT1A duplication patients: Further evidence supporting gene dosage as a mechanism for charcot‐marie‐tooth disease type 1A
1996