Citation Impact
Citing Papers
Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2
2003 StandoutScience
Cystic fibrosis carrier frequencies in populations of African origin.
1999
Small Interfering RNAs Mediate Sequence-Independent Gene Suppression and Induce Immune Activation by Signaling through Toll-Like Receptor 3
2004 StandoutNobel
The fragile X syndrome.
1998
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
1993
Nucleoside-modified VEGFC mRNA induces organ-specific lymphatic growth and reverses experimental lymphedema
2021 StandoutNobel
Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression
2006
Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.
1994
Ionotropic Glutamate Receptors & CNS Disorders
2008
RIM1α and Interacting Proteins Involved in Presynaptic Plasticity Mediate Prepulse Inhibition and Additional Behaviors Linked to Schizophrenia
2010 StandoutNobel
Functions of DNA methylation: islands, start sites, gene bodies and beyond
2012 Standout
Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome
1991
The Clinical Spectrum of Lymphatic Disease
2008
Mouse genetic models for prepulse inhibition: an early review
2002
A New Rett Syndrome Family Consistent with X-Linked Inheritance Expands the X Chromosome Exclusion Map
1997
Channel opening and gating mechanism in AMPA-subtype glutamate receptors
2017 StandoutNatureNobel
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Structural basis for triplet repeat disorders: a computational analysis
1999 StandoutNobel
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
2007 StandoutNobel
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment
2003
hEST2, the Putative Human Telomerase Catalytic Subunit Gene, Is Up-Regulated in Tumor Cells and during Immortalization
1997 Standout
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Infantile autism and urinary excretion of peptides and protein-associated peptide complexes
1988
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1999 Standout
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.
1993
Cancer drug resistance: an evolving paradigm
2013 Standout
Lymphangiogenesis: Molecular Mechanisms and Future Promise
2010 Standout
Genetic instabilities in human cancers
1998 StandoutNature
Methyl-CpG-binding protein 2 mutations in Rett syndrome
2000
Telomere end-replication problem and cell aging
1992 StandoutNobel
Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets
2009 Standout
Translational Control of Long-Lasting Synaptic Plasticity and Memory
2009
Prader–Willi syndrome and Angelman syndrome
2010
Persistent and transcriptionally-dependent increase in protein phosphorylation in long-term facilitation ofAplysia sensory neurons
1989 StandoutNatureNobel
Telomere dysfunction and the initiation of genome instability
2003 StandoutNobel
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Telomeres shorten during ageing of human fibroblasts
1990 StandoutNatureNobel
Autism: Towards an Integration of Clinical, Genetic, Neuropsychological, and Neurobiological Perspectives
1996 Standout
The Missing Diversity in Human Genetic Studies
2019 Standout
Social cognition skills among females with fragile X
1994
UBE3A/E6-AP mutations cause Angelman syndrome
1997
DNA Methylation and Its Basic Function
2012 Standout
A case of autism associated with partial tetrasomy 15
1995
pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest
1994 StandoutNature
RNA Cargoes Associating with FMRP Reveal Deficits in Cellular Functioning in Fmr1 Null Mice
2003
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Autism and Known Medical Conditions: Myth and Substance
1994
A phenotypic and molecular characterization of the fmr1‐tm1Cgr Fragile X mouse
2004
Altered anxiety‐related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome
2005
Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes
2017 StandoutNobel
Autism as a strongly genetic disorder: evidence from a British twin study
1995 Standout
Identification of Cyclobutane Pyrimidine Dimer-Responsive Genes Using UVB-Irradiated Human Keratinocytes Transfected with In Vitro-Synthesized Photolyase mRNA
2015 StandoutNobel
A Case‐Control Family History Study of Autism
1994
Psychiatric genetics: Research challenges and pathways forward
1994
Telomere length predicts replicative capacity of human fibroblasts.
1992 StandoutNobel
The marker (X) syndrome: a cytogenetic and genetic analysis
1984
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity.
1992 StandoutNobel
Selective killing of transformed cells by cyclin/cyclin-dependent kinase 2 antagonists
1999 StandoutNobel
Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryos.
1976
Aneuploidy correlated 100% with chemical transformation of Chinese hamster cells
1997
Extinction of the HPV18 upstream regulatory region in cervical carcinoma cells after fusion with non-tumorigenic human keratinocytes under non-selective conditions.
1991 StandoutNobel
Human cell transformation by simian virus 40—A review
1981
Fragile X and autism: A multicenter survey
1986
Population incidence and segregation ratios in the Martin‐Bell syndrome
1986
The future of cloning
1999 StandoutNatureNobel
Cell Cycle Control and Cancer
1994 StandoutScienceNobel
Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
1997 Standout
Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line.
1988 Standout
Genetic Influences in Autism
1990
Relative Difficulties in Transforming Human and Animal Cells in Vitro
1983
Proposed Mechanism of Inheritance and Expression of the Human Fragile-X Syndrome of Mental Retardation
1987
Fmr1 knockout mice: A model to study fragile X mental retardation
1994
Mechanisms Underlying Ubiquitination
2001 Standout
X-CHROMOSOME INACTIVATION IN MAMMALS
1997
Mechanisms of human cell neoplastic transformation: X-ray-induced abnormal clone formation in long-term cultures of human diploid fibroblasts.
1985
The ubiquitin-proteasome pathway: on protein death and cell life
1998 StandoutNobel
Two-dimensional gel electrophoresis of proteins
1987
A Broader Phenotype of Autism: The Clinical Spectrum in Twins
1996
Oncogene v-src transforms and establishes embryonic rodent fibroblasts but not diploid human fibroblasts.
1988 StandoutNobel
Characterization of RAD9 of Saccharomyces cerevisiae and evidence that its function acts posttranslationally in cell cycle arrest after DNA damage.
1990 StandoutNobel
Serotonin receptor 1A knockout: An animal model of anxiety-related disorder
1998
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
Serotonin receptor knockouts: A moody subject
1998 StandoutNobel
Requirement of Hippocampal Neurogenesis for the Behavioral Effects of Antidepressants
2003 StandoutScience
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands.
1992 Standout
Explaining the high mutation rates of cancer cells to drug and multidrug resistance by chromosome reassortments that are catalyzed by aneuploidy
2000
THE UBIQUITIN SYSTEM
1998 StandoutNobel
Chromosomes and Neoplasia
1979
Plakoglobin Suppresses Epithelial Proliferation and Hair Growth in Vivo
2000 StandoutNobel
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Works of T. Webb being referenced
The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
1981
Prevalence of, and risk factors for, physical ill‐health in people with Prader‐Willi syndrome: a population‐based study
2002
Prevalence of fragile X syndrome
1996
Prevalence of the Fragile X Anomaly amongst Autistic Twins and Singletons
1993
Maternal origin of deletion 15q11–13 in 25/25 cases of Angelman syndrome
1992
Alterations in replication timing of X‐chromosome bands in Rett syndrome
1995
Neither uniparental disomy nor skewed X‐inactivation explains Rett syndrome
1993
Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome
2004
Familial Prader‐Willi syndrome: case report and a literature review
2000
Further evidence for dominant inheritance at the chromosome 15q11‐13 locus in familial angelman syndrome
1992
Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel).
1991
X‐inactivation in girls with Rett syndrome
1992
A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS
2002
Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence.
1985
Cytogenetically marked clones in human fibroblasts cultured from normal subjects
1976
Fragile X syndrome is less common than previously estimated.
1997
The transformation by simian virus 40 of cells from patients with mucopolysaccharidosis and from normal controls.
1976
A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.
1985
Chromosome complement and SV40 transformation of cells from patients susceptible to malignant disease
1977
The chromosome analysis and susceptibility to transformation by Simian Virus 40 of fibroblasts from ataxia-telangiectasia.
1977
Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13.
1992
Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy?
1985
Mapping viral integration sites in somatic cell hybrids
1976
Studies on the relationship between concanavalin A and SV40-transformed human fibroblasts
1976
Detection of Proteins in Human Amniotic Fluid Using Two-Dimensional Gel Electrophoresis
1981
Fragile X in families multiplex for autism and related phenotypes
1992
The frequency of the fragile X chromosome among schoolchildren in Coventry.
1986