Citation Impact
Citing Papers
A Decade of Molecular Studies of Fragile X Syndrome
2002
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure.
1996
Proteomics Analysis Identifies Phosphorylation-dependent α-Synuclein Protein Interactions
2008
Activating Smoothened mutations in sporadic basal-cell carcinoma
1998 StandoutNature
Loss of methylation activates Xist in somatic but not in embryonic cells.
1995
lincRNAs: Genomics, Evolution, and Mechanisms
2013 Standout
Acquired chromosome rearrangements in human lymphocytes: effect of aging
1988
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
2006 StandoutNature
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
1992 Standout
Modular regulatory principles of large non-coding RNAs
2012 StandoutNature
Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome
1990
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.
1993
Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
2009 StandoutNature
An alternative pathway for yeast telomere maintenance rescues est1− senescence
1993 StandoutNobel
X Chromosome Inactivation Is Mediated by Xist RNA Stabilization
1997
The search for the mouse X-chromosome inactivation centre
1990
X-chromosome inactivation: molecular mechanisms and genetic consequences
1994
Functional Classification and Experimental Dissection of Long Noncoding RNAs
2018 Standout
The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers
1996 Standout
A ceRNA Hypothesis: The Rosetta Stone of a Hidden RNA Language?
2011 Standout
Genes Expressed in Neurons of Adult Male Drosophila
1997 StandoutNobel
Down syndrome: Toward a molecular definition of the phenotype
2005
Telomeres shorten during ageing of human fibroblasts
1990 StandoutNatureNobel
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16
1991
Oxidative and other DNA damages as the basis of aging: a review
1992
X-inactivation profile reveals extensive variability in X-linked gene expression in females
2005 StandoutNature
Amplification of a gene encoding a p53-associated protein in human sarcomas
1992 StandoutNature
Down's syndrome: The effects of prenatal diagnosis and demographic factors in a region of the eastern part of Germany
2000
T-cell antigen receptor genes and T-cell recognition
1988 StandoutNature
A Ligand‐Library Approach to the Highly Efficient Rhodium/Phosphoramidite‐Catalyzed Asymmetric Arylation of N,N‐Dimethylsulfamoyl‐Protected Aldimines
2006 StandoutNobel
The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
1992
The Noncoding RNA Revolution—Trashing Old Rules to Forge New Ones
2014 Standout
Histone acetylation in chromatin structure and transcription
1997 StandoutNature
Down's syndrome
2003 Standout
Systematic Mutagenesis of α-Synuclein Reveals Distinct Sequence Requirements for Physiological and Pathological Activities
2012 StandoutNobel
Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome
1991 Nature
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
1998 StandoutNature
Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes
1988
Evolution and Functions of Long Noncoding RNAs
2009 Standout
Physical linkage of the fragile site FRA11B and a Jacobsen Syndrome chromosome deletion breakpoint in 11q23. 3
1994
lincRNAs act in the circuitry controlling pluripotency and differentiation
2011 StandoutNature
Controlled Microwave Heating in Modern Organic Synthesis
2004 Standout
The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression
1993
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
1991 Nature
Limited diversity of γδ antigen receptor genes of thy-1+ dendritic epidermal cells
1988 StandoutNobel
Localization of the X inactivation centre on the human X chromosome in Xq13
1991 Nature
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation
1994 Nature
Palladium‐Catalyzed CN and CO Coupling–A Practical Guide from an Industrial Vantage Point†
2004
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
A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14q
1994 StandoutNobel
Clustering of aberrations to specific chromosomes in human neoplasms
2009
The T cell antigen receptor complex expressed on normal peripheral blood CD4-, CD8- T lymphocytes. A CD3-associated disulfide-linked gamma chain heterodimer.
1987 StandoutNobel
T-cell gamma gene is allelically but not isotypically excluded and is not required in known functional T-cell subsets.
1987 StandoutNobel
Population incidence and segregation ratios in the Martin‐Bell syndrome
1986
Fertility in patients with X chromosome deletions
1982
Rb-Mediated Heterochromatin Formation and Silencing of E2F Target Genes during Cellular Senescence
2003 Standout
The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry
2007 Standout
Polymorphisms of a human variable heavy chain gene show linkage with constant heavy chain genes.
1984 StandoutNobel
Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
1982 Nature
Functional Coherence of the Human Y Chromosome
1997 StandoutScience
An Alternative Pathway for Meiotic Chromosome Segregation in Yeast
1986 StandoutScienceNobel
Lack of telomere shortening during senescence inParamecium.
1994 StandoutNobel
The Clonal Evolution of Tumor Cell Populations
1976 StandoutScience
Reactivation of the Paternal X Chromosome in Early Mouse Embryos
2004 StandoutScienceNobel
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
1981
Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
1985 StandoutNature
Human γ-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7
1985 Nature
Recombination of exogenous interleukin 2 receptor gene flanked by immunoglobulin recombination signal sequences in a pre-B cell line and transgenic mice.
1991 StandoutNobel
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Genomic organization of mouse J kappa recombination signal binding protein (RBP-J kappa) gene.
1992 StandoutNobel
Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.
1983
Constitutive Fragile Sites and Cancer
1984 Science
Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain γ1 immunoglobulin locus
1982
Translating the Histone Code
2001 StandoutScience
Kontrolliertes Erhitzen mit Mikrowellen in der modernen organischen Synthese
2004
Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
2016 Standout
TRISOMY IN MAN
1984
Determination of the Number of Conserved Chromosomal Segments Between Species
2001
Identification of an Amplified, Highly Expressed Gene in a Human Glioma
1987 Science
Structural Dynamics of Eukaryotic Chromosome Evolution
2003 StandoutScience
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
1996 StandoutScience
Complete sequence of the bithorax complex of Drosophila.
1995 StandoutNobel
Muscular dystrophy in girls with X;autosome translocations.
1986
Immunological Memory and Protective Immunity: Understanding Their Relation
1996 StandoutScience
A DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation
2006 StandoutNobel
The Molecular Genetics of the T-Cell Antigen Receptor and T-Cell Antigen Recognition
1986
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Works of F Giraud being referenced
Distribution of spontaneous chromosome breaks in man
1979
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12.
1977
Maternal age and origin of non-disjunction in trisomy 21.
1980
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach
1981
Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns
1981
Constitutional chromosomal breakage
1976
Structural anomalies of the X chromosome and inactivation center
1981
Attitudes towards Down's syndrome: follow up of a cohort of 280 cases.
1995
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects
1976
X-Autosome translocations: Cytogenetic characteristics and their consequences
1982
A dynamic study in two new cases of X chromosome translocations
1978
An efficient route from coumarins to highly functionalized N-phenyl-2-quinolinones via Buchwald–Hartwig amination
2003