Back to search

Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers

Data up to Jan 2025

Published1999
Citations428
References36

Total Citations Per Year

Abstract

References (36)

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1996 • 2,983 citations

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

1998 • 1,472 citations

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

1978 • 1,287 citations

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.

1999 • 814 citations

Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

1996 • 777 citations

Multiple Primary Cancers in Families With Li-Fraumeni Syndrome

1998 • 548 citations

Binding and Stimulation of HIV-1 Integrase by a Human Homolog of Yeast Transcription Factor SNF5

1994 • 523 citations

Hereditary cancer: Two hits revisited

1996 • 497 citations

Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System: A Highly Malignant Tumor of Infancy and Childhood Frequently Mistaken for Medulloblastoma

1998 • 432 citations

Tumors associated with p53 germline mutations: a synopsis of 91 families.

1997 • 409 citations

Li-Fraumeni syndrome – a molecular and clinical review

1997 • 362 citations

An Analysis of 42 Cases Studied with Immunohistochemistry or Electron Microscopy

1994 • 324 citations

Spectrum of hSNF5IINI1 Somatic Mutations in Human Cancer and Genotype-Phenotype Correlations

1999 • 308 citations

Malignant rhabdoid tumors: a clinicopathologic review and conceptual discussion.

1995 • 248 citations

The association of embryonal tumors originating in the kidney and in the brain. A report of seven cases

1984 • 225 citations

Parent-of-origin effects in multiple endocrine neoplasia type 2B.

1994 • 224 citations

Parental origin of mutations of the retinoblastoma gene

1989 • 216 citations

Paternal origin of new mutations in Von Recklinghausen neurofibromatosis

1990 • 204 citations

Preferential germline mutation of the paternal allele in retinoblastoma

1989 • 169 citations

A human protein with homology toSaccharomyces cerevisiaeSNF5 interacts with the potential helicase hbrm

1995 • 141 citations

Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene

1995 • 133 citations

Congenital Disseminated Malignant Rhabdoid Tumor

1999 • 119 citations

Narrowing the critical region for a rhabdoid tumor locus in 22q11

1996 • 111 citations

Paravertebral malignant rhabdoid tumor in infancyin vitro studies of a familial tumor

1983 • 110 citations

Loss of heterozygosity at chromosome regions 22q11–12 and 11p15.5 in renal rhabdoid tumors

1996 • 98 citations

Malignant rhabdoid tumor: A highly malignant childhood tumor with minimal karyotypic changes

1990 • 75 citations

Molecular analysis of a partial deletion of 22q in a central nervous system rhabdoid tumor

1992 • 72 citations

Transcriptional regulation: SWItching circuitry

1999 • 49 citations

Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22

1998 • 47 citations

Solitary Choroid Plexus Metastasis From a Renal Cell Carcinoma

1998 • 42 citations

Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system: Associated tumors with different histologic, cytogenetic, and molecular findings

1994 • 41 citations

Single Solitary Metastasis of the Slowly Progressive Type of Renal Cell Carcinoma to the Choroid Plexus —Case Report—

1997 • 27 citations

Familial Medulloblastoma

1998 • 14 citations

Identical twins with medulloblastoma occurring in infancy

1998 • 9 citations

Rhabdoid tumor of the kidney with primitive neuroectodermal tumor of the central nervous system

1998 • 5 citations

Deleted Work

1955 • 0 citations

Cited By (0)

Loading...
Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers (1999) – The American Journal of Human Genetics | Metascience Observatory Explorer