Citation Impact
Citing Papers
Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene
1998
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
1993 StandoutNature
Chromosome 5 allele loss at the glucocorticoid receptor locus in human colorectal carcinomas
1988
β-Catenin regulates expression of cyclin D1 in colon carcinoma cells
1999 StandoutNature
Are different events involved in the development of sporadic versus hereditary tumours? The possible importance of the microenvironment in hereditary cancer
1990
WAF1, a potential mediator of p53 tumor suppression
1993 Standout
Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells
1992 StandoutNobel
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
1998
Overview of natural history, pathology, molecular genetics and management of HNPCC (Lynch syndrome)
1996
Nicotinic acetylcholine receptor α7 subunit is an essential regulator of inflammation
2002 StandoutNature
The secretory phospholipase A2 gene is a candidate for the Mom1 locus, a major modifier of ApcMin-induced intestinal neoplasia
1995
Genetic instabilities in human cancers
1998 StandoutNature
A genetic model for colorectal tumorigenesis
1990 Standout
A comprehensive genetic map of the human genome based on 5,264 microsatellites
1996 StandoutNature
Proliferation, cell cycle and apoptosis in cancer
2001 StandoutNature
A primary genetic map of markers for human chromosome 10
1988
Expression cloning of a cDNA encoding a retinoblastoma-binding protein with E2F-like properties
1992 StandoutNobel
Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours
1996 StandoutNature
Colon cancer genetics
1992
Alleles of the APC gene: An attenuated form of familial polyposis
1993
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree
1988 Nature
The Hallmarks of Cancer
2000 Standout
Lessons from Hereditary Colorectal Cancer
1996 Standout
Molecular Diagnosis of Familial Adenomatous Polyposis
1993
A linkage map of mouse Chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation
1992
Tumor suppressor genes
1991 Standout
Attenuated familial adenomatous polyposis (AFAP) a phenotypically and genotypically distinctive variant of FAP
1995
Genetic epilepsy model derived from common inbred mouse strains.
1994
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10
1997 StandoutNobel
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
1998 Nature
Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22
1988
Colorectal carcinomas in mice lacking the catalytic subunit of PI(3)Kγ
2000 StandoutNatureNobel
Mutations in the p53 gene occur in diverse human tumour types
1989 StandoutNature
The p53 tumour suppressor gene
1991 StandoutNature
The Use and Interpretation of CommercialAPCGene Testing for Familial Adenomatous Polyposis
1997
Immunity, Inflammation, and Cancer
2010 Standout
Phenotypic variation in colorectal adenoma/cancer expression in two families. Hereditary flat adenoma syndrome
1990
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II)
1991
New functions for nicotinic acetylcholine receptors?
1998
Hereditary Colorectal Cancer
2003 Standout
Hereditary Gastrointestinal Polyposis and Nonpolyposis Syndromes
1994
A constitutively open potassium channel formed by KCNQ1 and KCNE3
2000 StandoutNature
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
1992 StandoutNature
The Fas Death Factor
1995 StandoutScience
β1-Adrenoceptor gene variations: a role in idiopathic dilated cardiomyopathy?
2000
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: An updated review
1993
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients
1993
Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer
1993
Localization of a susceptibility locus for schizophrenia on chromosome 5
1988 Nature
Seven-transmembrane-spanning receptors and heart function
2002 StandoutNatureNobel
Mismatch Repair Deficiency in Phenotypically Normal Human Cells
1995 StandoutScienceNobel
Genetic Alterations during Colorectal-Tumor Development
1988 Standout
Exclusion of linkage to 5qll–13 in families with schizophrenia and other psychiatric disorders
1989 Nature
Wnt signalling in stem cells and cancer
2005 StandoutNature
Genetic Analysis of an Inherited Predisposition to Colon Cancer in a Family with a Variable Number of Adenomatous Polyps
1990
Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
1993
Cyclin A and the retinoblastoma gene product complex with a common transcription factor
1991 StandoutNatureNobel
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
1999
Molecular Neurobiology and Genetics: Investigation of Neural Function and Dysfunction
1998
The genetics and natural history of hereditary colon cancer
1997
Hypermutability and mismatch repair deficiency in RER+ tumor cells
1993 StandoutNobel
Allelic Loss in Colorectal Carcinoma
1989
Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors
1992 StandoutScience
Loss of constitutional heterozygosity in colorectal tumors from patients with familial polyposis coli and those with nonpolyposis colorectal carcinoma.
1989
p53 Mutations in Human Cancers
1991 StandoutScience
Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 Loci
1994 Science
A human colon cancer cell capable of initiating tumour growth in immunodeficient mice
2006 StandoutNature
Inactivation of a Serotonin-Gated Ion Channel by a Polypeptide Toxin from Marine Snails
1998 StandoutScienceNobel
Cell Cycle Control and Cancer
1994 StandoutScienceNobel
Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms
1990 StandoutScience
Concerted Nonsyntenic Allelic Loss in Human Colorectal Carcinoma
1988 Science
A Potassium Channel Mutation in Neonatal Human Epilepsy
1998 Science
HUMAN TUMOR SUPPRESSOR GENES
1990
Neural Science
2000 StandoutNobel
Constitutive Transcriptional Activation by a β-Catenin-Tcf Complex in APC −/− Colon Carcinoma
1997 StandoutScience
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Genetic Dissection of Complex Traits
1994 StandoutScience
Chromosome 18 allele loss at the D18S6 locus in human colorectal carcinomas
1988
Tumor Rejection After Direct Costimulation of CD8 + T Cells by B7-Transfected Melanoma Cells
1993 StandoutScienceNobel
Cancer Genome Landscapes
2013 StandoutScience
Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
1989 StandoutScience
PTEN , a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate Cancer
1997 StandoutScience
Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC
1997 StandoutScience
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.
1989
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs.
1995 StandoutNobel
Biallelic inactivation of hMLH 1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers
1998 StandoutNobel
p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis.
1990
Integrating Genetic Approaches into the Discovery of Anticancer Drugs
1997 StandoutScienceNobel
Familial adenomatous polyposis
1997
Association of Human Papillomavirus Types 16 and 18 E6 Proteins with p53
1990 StandoutScience
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.
1988
Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas
1989 StandoutScience
Allelotype of Colorectal Carcinomas
1989 Science
Multiple Intestinal Neoplasia Caused by a Mutation in the Murine Homolog of the APC Gene
1992 Science
Dimer formation by an N-terminal coiled coil in the APC protein.
1993
Works of Dora Stauffer being referenced
Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22
1992
Genetic mapping of adrenergic receptor genes in humans
1995
Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q
1990
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1998
The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5
1987 Science
Benign familial neonatal convulsions linked to genetic markers on chromosome 20
1989 Nature
Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.
1992