Citation Impact
Citing Papers
Finishing the euchromatic sequence of the human genome
2004 StandoutNature
Mismatch repair, genetic stability and tumour avoidance
1995 StandoutNobel
High-Resolution Analysis of DNA Copy Number Using Oligonucleotide Microarrays
2004
MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations
1987 Standout
The development of human linkage analysis
1986
Male development of chromosomally female mice transgenic for Sry
1991 StandoutNature
Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma
2005 StandoutNature
Hematologic and Cytogenetic Responses to Imatinib Mesylate in Chronic Myelogenous Leukemia
2002 Standout
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man
1989
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
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome
2000
Molecular basis of human hypertension: Role of angiotensinogen
1992 Standout
Efficacy and Safety of a Specific Inhibitor of the BCR-ABL Tyrosine Kinase in Chronic Myeloid Leukemia
2001 Standout
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
Dasatinib in Imatinib-Resistant Philadelphia Chromosome–Positive Leukemias
2006 Standout
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
2004
Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosome
1992
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
1993 Standout
Tau in physiology and pathology
2015 Standout
Differential Roles for Sox15 and Sox2 in Transcriptional Control in Mouse Embryonic Stem Cells
2005 StandoutNobel
Conservation, Variability and the Modeling of Active Protein Kinases
2007 StandoutNobel
Molecular determinants of glucocorticoid sensitivity and resistance in acute lymphoblastic leukemia
2003
A human XY female with a frame shift mutation in the candidate testis-determining gene SRY
1990 Nature
Angelman syndrome: a review of clinical and genetic aspects
1999
Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease
1989 Standout
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
1994 Standout
Tumour heterogeneity and cancer cell plasticity
2013 StandoutNature
A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes
1990 StandoutNature
Activity of a Specific Inhibitor of the BCR-ABL Tyrosine Kinase in the Blast Crisis of Chronic Myeloid Leukemia and Acute Lymphoblastic Leukemia with the Philadelphia Chromosome
2001 Standout
Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia
2013 Standout
Importance of quantitative genetic variations in the etiology of hypertension
2000 StandoutNobel
Cell cycle, CDKs and cancer: a changing paradigm
2009 Standout
The Origin and Functions of Multiple Human Glucocorticoid Receptor Isoforms
2004
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
1990 StandoutNature
From head to toes: the multiple facets of Sox proteins
1999 Standout
If it goes up, must it come down? Chronic stress and the hypothalamic-pituitary-adrenocortical axis in humans.
2007 Standout
Chronic Myeloid Leukemia
1999
Corticosteroid Receptor Genetic Polymorphisms and Stress Responsivity
2005
The ced-8 Gene Controls the Timing of Programmed Cell Deaths in C. elegans
2000 StandoutNobel
Hypermutability and mismatch repair deficiency in RER+ tumor cells
1993 StandoutNobel
DNA profiling by arrayCGH in acute myeloid leukemia and myelodysplastic syndromes
2007
Mouse and hamster mutants as models for Waardenburg syndromes in humans.
1990
The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective
2000 StandoutScience
Parameters of the human genome.
1991
Construction and characterization of genomic libraries from specific human chromosomes.
1982
Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females
1987
Human Breast Cancer: Correlation of Relapse and Survival with Amplification of the HER-2/neuOncogene
1987 StandoutScience
Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis
1987
Primary structure and expression of a functional human glucocorticoid receptor cDNA
1985 StandoutNature
Multiple dispersed spontaneous mutations: a novel pathway of mutation in a malignant human cell line.
1991
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary
1990
Down syndrome phenotypes: the consequences of chromosomal imbalance.
1994 Standout
Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.
1991
The Human Y Chromosome: A 43-Interval Map Based on Naturally Occurring Deletions
1992 Science
Antibody fragments from a ‘single pot’ phage display library as immunochemical reagents.
1994 StandoutNobel
Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2
1986
Functional Coherence of the Human Y Chromosome
1997 StandoutScience
Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray
1995 StandoutScience
Carbohydrate Sulfotransferases of the GalNAc/Gal/GlcNAc6ST Family
2002 StandoutNobel
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
1993
Sox10, a Novel Transcriptional Modulator in Glial Cells
1998 Standout
Comparative sequence analysis of the human and pufferfish Huntington's disease genes
1995 StandoutNobel
Dinucleotide repeat polymorphism in the human angiotensinogen gene
1991
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993 Standout
Genetic identification of HSD-1, a conserved steroidogenic enzyme that directs larval development inCaenorhabditis elegans
2008 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
Identification of a Second Pseudoautosomal Region Near the Xq and Yq Telomeres
1992 Science
Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs
2005 Standout
XY female mice resulting from a heritable mutation in the primary testis determining gene, Tdy
1990
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
1986 Standout
Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.
1993
A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells
1996
Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau.
1988 StandoutNobel
Structural Mechanism for STI-571 Inhibition of Abelson Tyrosine Kinase
2000 StandoutScience
High incidence of XXY and XYY males among the offspring of female chimeras from embryonic stem cells.
1995 StandoutNobel
DNA Binding Activity of Recombinant SRY from Normal Males and XY Females
1992 Science
A small deletion of 16q23.1→16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348−, P5432+)] in a boy with iris coloboma and minor anomalies
1997
Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells.
1987 StandoutNobel
Overview of Steroidogenic Enzymes in the Pathway from Cholesterol to Active Steroid Hormones
2004
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
Long-range restriction map around the Duchenne muscular dystrophy gene
1986 Nature
Localization of a novel v-erbB-related gene, c-erbB-2, on human chromosome 17 and its amplification in a gastric cancer cell line.
1986
The Connectivity Map: Using Gene-Expression Signatures to Connect Small Molecules, Genes, and Disease
2006 StandoutScience
High-Resolution Chromosome Sorting and DNA Spot-Blot Analysis Assign McArdle's Syndrome to Chromosome 11
1984 Science
Normal and abnormal interchanges between the human X and Y chromosomes
1987
Works of E. Boyd being referenced
Regional chromosomal assignment of the Kell blood group locus (KEL) to chromosome 7q33-q35 by fluorescence in situ hybridization: evidence for the polypeptide nature of antigenic variation
1993
The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndromes
2001
Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry
1989
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?
1988
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1
1990
Regional chromosomal assignment of human 3-beta-hydroxy-5-ene steroid dehydrogenase to 1p13.1 by non-isotopic in situ hybridisation
1991
Identification of variant translocations in chronic myeloid leukemia by fluorescence in situ hybridization
1997
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31
1989
Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes
1987
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination
1990
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome
1989
Assignment of the human angiotensin gene to chromosome 1q42–q43 by nonisotopic in situ hybridization
1990
Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X- chromosome and autosomal sequences
1986
High-resolution analysis of human peripheral lymphocyte chromosomes by flow cytometry.
1981
A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.
1998
Determination of the DNA content of human chromosomes by flow cytometry
1986
Analysis of the origin of Turner's syndrome using polymorphic DNA probes.
1991
Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry
1986
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
1989
A comparison of in situ hybridization techniques for gene localization
1977
Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.
1987