Citation Impact
Citing Papers
The C. elegans heterochronic gene lin-28 coordinates the timing of hypodermal and somatic gonadal programs for hermaphrodite reproductive system morphogenesis
2019 StandoutNobel
New York Science Journal
2015 Standout
A systematic review and meta-analysis of the effects of antibiotic consumption on antibiotic resistance
2014 Standout
Comparative efficacies of different antibiotic treatments to eradicate nontypeable Haemophilus influenzaeinfection
2008 StandoutNobel
The Fragile X Syndrome Protein FMRP Associates with BC1 RNA and Regulates the Translation of Specific mRNAs at Synapses
2003
The use of platensimycin and platencin to fight antibiotic resistance
2013
Quinolone-resistance mutations in the topoisomerase IV parC gene of Acinetobacter baumannii
1997
Molecular mechanisms of antibiotic resistance
2014 Standout
Partial characterization of a transposon containing the tet(A) determinant in a clinical isolate of Acinetobacter baumannii
2003
The association of nonsense codons with exon skipping
1998
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
On the Anglocentricities of current reading research and practice: The perils of overreliance on an "outlier" orthography.
2008 Standout
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Musical Training Influences Linguistic Abilities in 8-Year-Old Children: More Evidence for Brain Plasticity
2008 Standout
Utilization of fluoroquinolones andEscherichia coli resistance in urinary tract infection: inpatients and outpatients
2005
Cognitive functions correlate with white matter architecture in a normal pediatric population: A diffusion tensor MRI study
2005 Standout
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Intrinsic differences between authentic and cryptic 5' splice sites
2003
The spectrum of hearing loss due to mitochondrial DNA defects
2000
Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome
2002 Standout
BLAST Ring Image Generator (BRIG): simple prokaryote genome comparisons
2011 Standout
Hereditary deafness and phenotyping in humans
2002
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes
2008
An increasing threat in hospitals: multidrug-resistant Acinetobacter baumannii
2007 Standout
Mutational profiling of cancer candidate genes in glioblastoma, melanoma and pancreatic carcinoma reveals a snapshot of their genomic landscapes
2008
Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto‐oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal
2006
Mitochondrial DNA and disease
2005
Auxin: Regulation, Action, and Interaction
2005 Standout
Spatial and molecular cues for cell outgrowth during C. elegans uterine development
2014
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Antibacterial resistance worldwide: causes, challenges and responses
2004 Standout
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins
2000
Specific reading disability (dyslexia): what have we learned in the past four decades?
2004 Standout
Broca’s area: Nomenclature, anatomy, typology and asymmetry
2009 Standout
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping
2001
Sensorineural hearing loss in children
2005 Standout
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss
2005
The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder
1999
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Evolutionary origins of eukaryotic sodium/proton exchangers
2005
The neurological basis of developmental dyslexia: An overview and working hypothesis
2000
Canu: scalable and accurate long-read assembly via adaptive k -mer weighting and repeat separation
2017 Standout
The genetics of deafness
2003
Listening to silence and understanding nonsense: exonic mutations that affect splicing
2002 Standout
Metabolism of highly unsaturated n-3 and n-6 fatty acids
2000 Standout
Nanoscale organization of nicotinic acetylcholine receptors revealed by stimulated emission depletion microscopy
2006 StandoutNobel
Hybrid error correction and de novo assembly of single-molecule sequencing reads
2012
Genetic Factors in Aminoglycoside Toxicity
1999
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Review of antibiotic resistance in China and its environment
2017 Standout
Assembly of long, error-prone reads using repeat graphs
2019 Standout
Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data
2013 Standout
Molecular Cloning of cDNA Encoding Rat Very Long-chain Acyl-CoA Synthetase
1996
Sensors and regulators of intracellular pH
2009 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Anatomical correlates of dyslexia: frontal and cerebellar findings
2003
Molecular epidemiology of quinolone resistance in Acinetobacter spp.
1998
Heavy use of prophylactic antibiotics in aquaculture: a growing problem for human and animal health and for the environment
2006 Standout
Evolution and Functions of Long Noncoding RNAs
2009 Standout
Very early detection of RET proto‐oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children
2002
Ambient pH gene regulation in fungi: making connections
2008
Cyclin D involvement demarcates a late transition in C. elegans embryogenesis
2005 StandoutNobel
Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads
2017 Standout
Mechanism of Quinolone Action and Resistance
2014 Standout
Mitochondrial deafness
2007
β-arrestin-mediated receptor trafficking and signal transduction
2011 StandoutNobel
Molecular and physiological characterization of fluoroquinolone resistance in relation to uropathogenicity among Escherichia coli isolates isolated from Wenyu River, China
2011
Multidrug efflux pumps: structure, function and regulation
2018 Standout
Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma
2015 Standout
Medullary Thyroid Cancer: Management Guidelines of the American Thyroid Association
2009 Standout
Acinetobacter baumannii : Emergence of a Successful Pathogen
2008 Standout
A new gene (DYX3) for dyslexia is located on chromosome 2.
1999
Increase in Quinolone Resistance in a Haemophilus influenzae Strain Isolated from a Patient with Recurrent Respiratory Infections Treated with Ofloxacin
1999
The Enzymes, Regulation, and Genetics of Bile Acid Synthesis
2003 Standout
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
2005 Standout
Massive Idiosyncratic Exon Skipping Corrects the Nonsense Mutation in Dystrophic Mouse Muscle and Produces Functional Revertant Fibers by Clonal Expansion
2000
Contributions of individual mechanisms to fluoroquinolone resistance in 36 Escherichia coli strains isolated from humans and animals
1996
Antibiotics and Bacterial Resistance in the 21st Century
2014 Standout
Temporal Interplay between Efflux Pumps and Target Mutations in Development of Antibiotic Resistance in Escherichia coli
2012
Pore-forming activity and structural autoinhibition of the gasdermin family
2016 StandoutNature
The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways
2015
High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain
1999
Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss
2002
LL5β
2005
Mutation in the gyrA gene of quinolone-resistant clinical isolates of Acinetobacter baumannii
1995
Genetic Characterization of Highly Fluoroquinolone-Resistant Clinical Escherichia coli Strains from China: Role of acrR Mutations
2001
Molecular Genetics of Hearing Loss
2001
Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3
2003
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
2003
Clinical Practice Guideline: Sudden Hearing Loss (Update)
2019 Standout
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections
2003
A Premature Termination Codon Interferes with the Nuclear Function of an Exon Splicing Enhancer in an Open Reading Frame-Dependent Manner
1999
Global Challenge of Multidrug-ResistantAcinetobacter baumannii
2007 Standout
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
2009 StandoutScience
Brain morphometry in reading-disabled twins
1999
Insights into the Environmental Resistance Gene Pool from the Genome Sequence of the Multidrug-Resistant Environmental Isolate Escherichia coli SMS-3-5
2008
Genetics of Sensory Mechanotransduction
2002 StandoutNobel
Works of Anna Barceló being referenced
Rare variants in the promoter of the fragile X syndrome gene (FMR1)
2000
Aberrantly spliced mRNAs of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene with a donor splice-site point mutation produce hereditary HL deficiency
1996
Genetic analysis of seven Mediterranean families with multiple endocrine neoplasia type 2A
1996
Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
1998
Identification of a new frameshift mutation (1801delAG) in the ALD gene
1994
Mutagenesis analysis of the yeast Nha1 Na+/H+ antiporter carboxy‐terminal tail reveals residues required for function in cell cycle
2003
Characterization of the Calcium-mediated Response to Alkaline Stress in Saccharomyces cerevisiae
2004
Neuron Navigator: A Human Gene Family with Homology to unc-53, a Cell Guidance Gene from Caenorhabditis elegans
2002
Association between double mutation in gyrA gene of ciprofloxacin-resistant clinical isolates of Escherichia coli and MICs
1994
A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
1997