Citation Impact
Citing Papers
Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families
1993 StandoutScience
Capturing Chromosome Conformation
2002 StandoutScience
The study of variation in the human genome
1991
Amplification of fgfr4 gene in human breast and gynecological cancers
1993
Finishing the euchromatic sequence of the human genome
2004 StandoutNature
Progress towards completing the human linkage map
1991
Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity
1991 StandoutNobel
Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome
1993 StandoutNatureNobel
Loss of heterozygosity for 10q loci in human gliomas
1992
Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
1992
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
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1999 Standout
The human Y chromosome shows a low level of DNA polymorphism
1990
Malignant astrocytic glioma: genetics, biology, and paths to treatment
2007 Standout
A genetic model for colorectal tumorigenesis
1990 Standout
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 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
Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents
1992 StandoutNobel
The Utility of DNA Typing in Forensic Work
1991 StandoutScience
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses
1990
No Linkage Between D2 Dopamine Receptor Gene Region and Schizophrenia
1991
Tumor suppressor genes
1991 Standout
EGF–ERBB signalling: towards the systems level
2006 Standout
Role of the retinoblastoma protein in the pathogenesis of human cancer.
1997 StandoutNobel
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li–Fraumeni syndrome
1990 StandoutNature
Classification and diagnostic prediction of cancers using gene expression profiling and artificial neural networks
2001 Standout
Why do human diversity levels vary at a megabase scale?
2005 StandoutNobel
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
The p53 tumour suppressor gene
1991 StandoutNature
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
A search for restriction fragment length polymorphism on the human Y chromosome
1989
Reduction to homozygosity is the predominant spontaneous mutational event in cultured human lymphoblastoid cells
1991
Generation and Analysis of 25 Mb of Genomic DNA from the Pufferfish Fugu rubripes by Sequence Scanning
1999 StandoutNobel
Molecular themes in oncogenesis
1991 StandoutNobel
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
1993 Standout
Genetic mapping of “Lubag” (X‐linked dystonia‐parkinsonism) in a filipino kindred to the pericentromeric region of the X chromosome
1991
MULTIPLE GENETIC ALTERATIONS IN DISTAL AND PROXIMAL COLORECTAL CANCER
1989
Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker
1991 StandoutNobel
Nuclear DNA polymorphism in a Mandenka population from Senegal: Comparison with eight other human populations
1995
Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis
1997 StandoutNobel
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
1997 Standout
Evidence for Gradients of Human Genetic Diversity Within and Among Continents
2004 StandoutNobel
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations
1991
Parameters of the human genome.
1991
p53 Mutations in Human Cancers
1991 StandoutScience
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
Exclusion of close linkage of Tourette's syndrome to D1 dopamine receptor
1993
An Increased Percentage of Long Amyloid β Protein Secreted by Familial Amyloid β Protein Precursor (βApp 717 ) Mutants
1994 StandoutScience
Allele Loss at the Retinoblastoma Locus in Human Ovarian Cancer
1991
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).
1990
Genes for epidermal growth factor receptor, transforming growth factor alpha, and epidermal growth factor and their expression in human gliomas in vivo.
1991
Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms
1990 StandoutScience
Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray
1995 StandoutScience
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
1993 Standout
Allelic Loss of Chromosome 17P in Urothelial Cancer: Strong Association with Invasive Phenotype
1992 StandoutNobel
Allelic loss at chromosome 3p characterizes clear cell phenotype of renal cell carcinoma.
1991 StandoutNobel
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.
1990
Comparative sequence analysis of the human and pufferfish Huntington's disease genes
1995 StandoutNobel
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993 Standout
Neural Science
2000 StandoutNobel
Sequence variation of the human Y chromosome
1995 StandoutNatureNobel
Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.
1990
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
1995 StandoutScience
Genetic Dissection of Complex Traits
1994 StandoutScience
Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease
1993 Standout
Detecting immigration by using multilocus genotypes
1997 Standout
Survey of human and rat microsatellites
1992
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.
1991
Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.
1990
Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
1991 Science
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
1991
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
1996 StandoutScience
Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer disease.
1993 Standout
Chromosome bands, their chromatin flavors, and their functional features.
1992
Dopamine Receptors: From Structure to Function
1998 Standout
Mechanisms of p53 loss in human sarcomas.
1990
Suppression of Human Colorectal Carcinoma Cell Growth by Wild-Type p53
1990 StandoutScience
Works of R.K. Track being referenced
Report of the committee on human gene mapping by recombinant DNA techniques (Part 1 of 6)
1988
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14)
1990
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643
1989