Citation Impact
Citing Papers
TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
2008 StandoutScience
A hexahistidine-Zn 2+ -dye label reveals STIM1 surface exposure
2007 StandoutNobel
Common molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis
2007
Induced Pluripotent Stem Cells Generated from Patients with ALS Can Be Differentiated into Motor Neurons
2008 StandoutScience
Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia
2006 StandoutScience
Three conformational snapshots of the hepatitis C virus NS3 helicase reveal a ratchet translocation mechanism
2009 StandoutNobel
Hallmarks of Cancer: The Next Generation
2011 Standout
The DNA-damage response in human biology and disease
2009 StandoutNature
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
2007
Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells
2003
Genetic studies of amyotrophic lateral sclerosis: Controversies and perspectives
2009
Structural organization of gap junction channels
2005
The Ubiquitin Proteasome System in Neurodegenerative Diseases
2003 StandoutNobel
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
2013
R loops: new modulators of genome dynamics and function
2015
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS
2008
The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders
2008 Standout
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
Mechanisms Underlying Inflammation in Neurodegeneration
2010 Standout
Newborn Hearing Screening — A Silent Revolution
2006 Standout
The role of autophagy in neurodegenerative disease
2013 Standout
The Nuclear-Retained Noncoding RNA MALAT1 Regulates Alternative Splicing by Modulating SR Splicing Factor Phosphorylation
2010 Standout
Role of platelet-derived growth factors in physiology and medicine
2008 Standout
The DNA Damage Response Kinases DNA-dependent Protein Kinase (DNA-PK) and Ataxia Telangiectasia Mutated (ATM) Are Stimulated by Bulky Adduct-containing DNA
2011 StandoutNobel
Emerging pathways for hereditary axonopathies
2005
The Long Unwinding Road of RNA Helicases
2007
ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors
2006
Translation matters: protein synthesis defects in inherited disease
2007
Amyotrophic lateral sclerosis
2011 Standout
An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex
2014 Standout
Gap junctions in the inner ear: Comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals
2003
Mechanistic Basis of 5′-3′ Translocation in SF1B Helicases
2009
Nitric Oxide and Peroxynitrite in Health and Disease
2007 Standout
The Involvement of DNA-Damage and -Repair Defects in Neurological Dysfunction
2008
Mitochondria: In Sickness and in Health
2012 Standout
Molecular and Genetic Properties of Tumors Associated with Local Immune Cytolytic Activity
2015 Standout
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Decoding ALS: from genes to mechanism
2016 StandoutNature
Protein solubility and folding monitored in vivo by structural complementation of a genetic marker protein
2001
Genetics, environmental factors and the emerging role of epigenetics in neurodegenerative diseases
2008
Multiple ATR-Chk1 Pathway Proteins Preferentially Associate with Checkpoint-Inducing DNA Substrates
2011 StandoutNobel
The DNA Damage Response: Making It Safe to Play with Knives
2010 Standout
Trinucleotide repeats and neurodegenerative disease
2004
Diagnostic investigation and multidisciplinary management in motor neuron disease
2005
Misregulated RNA processing in amyotrophic lateral sclerosis
2012
Design, Activity, and Structure of a Highly Specific Artificial Endonuclease
2002 StandoutNobel
Alzheimer's disease
2006 Standout
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors
2020 Standout
Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy
2003
Non-coding RNAs in human disease
2011 Standout
Electrical Coupling and Neuronal Synchronization in the Mammalian Brain
2004
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
2015 Standout
Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks
2006 Standout
A Cα Model for the Transmembrane α Helices of Gap Junction Intercellular Channels
2004
State of play in amyotrophic lateral sclerosis genetics
2013
Mitochondria: The Next (Neurode)Generation
2011
Chemistry of Class 1 CRISPR-Cas effectors: Binding, editing, and regulation
2020 StandoutNobel
NODDI: Practical in vivo neurite orientation dispersion and density imaging of the human brain
2012 Standout
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
2001
Physiological Roles of Mitochondrial Reactive Oxygen Species
2012 Standout
Engineering domain fusion chimeras from I-OnuI family LAGLIDADG homing endonucleases
2012 StandoutNobel
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
2006
Endogenous retrovirus-K promoter: a landing strip for inflammatory transcription factors?
2013
Glia cells in amyotrophic lateral sclerosis: New clues to understanding an old disease?
2007
Evidence for an Expansion-Based Temporal Shh Gradient in Specifying Vertebrate Digit Identities
2004 Standout
Pathways towards and away from Alzheimer's disease
2004 StandoutNature
Human Senataxin Resolves RNA/DNA Hybrids Formed at Transcriptional Pause Sites to Promote Xrn2-Dependent Termination
2011
RNA processing and its regulation: global insights into biological networks
2009
Molecular mechanisms of mTOR-mediated translational control
2009 Standout
DNA methylation and human disease
2005 Standout
Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders
2011 Standout
From angiogenesis to neuropathology
2005 Nature
The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes
2012 Standout
Toward high-resolution prediction and design of transmembrane helical protein structures
2007 StandoutNobel
Protein clearing pathways in ALS.
2011
EPIDEMIOLOGY OF NEURODEGENERATION
2003
Intracellular Transport, Assembly, and Degradation of Wild-Type and Disease-linked Mutant Gap Junction Proteins
2000
Fast structural responses of gap junction membrane domains to AB5 toxins
2013 StandoutNobel
Aggregation-Induced Emission: Together We Shine, United We Soar!
2015 Standout
Microglia Function in the Central Nervous System During Health and Neurodegeneration
2017 Standout
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome
2011
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
A Targeted Bypass Screen Identifies Ynl187p, Prp42p, Snu71p, and Cbp80p for Stable U1 snRNP/Pre-mRNA Interaction
2009 StandoutNobel
Clinical presentation and diagnosis of Amyotrophic Lateral Sclerosis
2007
Excitotoxicity and Amyotrophic Lateral Sclerosis
2005
UNRAVELING THE MECHANISMS INVOLVED IN MOTOR NEURON DEGENERATION IN ALS
2004
miRNA malfunction causes spinal motor neuron disease
2010
Evolutionary Comparison of the Mechanism of DNA Cleavage with Respect to Immune Diversity and Genomic Instability
2012 StandoutNobel
Quality control in the endoplasmic reticulum
2003 Standout
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
2006 Nobel
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
Works of Annette Abel being referenced
Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V
2003
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34
2000
X‐linked Charcot‐Marie‐Tooth Disease and Connexin32
1999
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)
2004
Studies in Transgenic Mice Indicate a Loss of Connexin32 Function in X-Linked Charcot-Marie-Tooth Disease
1999
The Role of the Gap Junction Protein Connexin32 in the Pathogenesis of X‐Linked Charcot‐Marie‐Tooth Disease
2007
Androgen receptor mutation in Kennedy'sdisease
1999