Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

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

1996 • 2,983 citations

Allelotype of Colorectal Carcinomas

1989 • 1,333 citations

DNA methylation represses FMR-1 transcription in fragile X syndrome

1992 • 665 citations

PREMEIOTIC INSTABILITY OF REPEATED SEQUENCES IN NEUROSPORA CRASSA

1990 • 648 citations

GENETICS OF HUMAN CANCER

1986 • 565 citations

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritance

1995 • 514 citations

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1994 • 466 citations

Gametic Imprinting in Mammals

1995 • 444 citations

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1994 • 318 citations

GENOMIC IMPRINTING IN HEREDITARY GLOMUS TUMOURS: EVIDENCE FOR NEW GENETIC THEORY

1989 • 305 citations

CpNpG methylation in mammalian cells

1995 • 259 citations

Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis

1991 • 246 citations

Familial carotid body tumors: Case report and epidemiologic review

1980 • 238 citations

ANTICIPATION IN MYOTONIC DYSTROPHY: FACT OR FICTION?

1989 • 234 citations

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

1992 • 215 citations

Tumor Cell Growth Arrest Caused by Subchromosomal Transferable DNA Fragments from Chromosome 11

1993 • 177 citations

Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24.

1994 • 147 citations

A radiation hybrid map of 506 STS markers spanning human chromosome 11

1994 • 146 citations

Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3.

1995 • 143 citations

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

1995 • 137 citations

Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3.

1994 • 129 citations

Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer

1993 • 119 citations

Familial Paragangliomas of the Head and Neck

1994 • 113 citations

Carotid Body Tumors in Humans: Genetics and Epidemiology

1982 • 108 citations

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

1995 • 108 citations

Deletion of chromosome 11 and of 14q sequences in neuroblastoma

1993 • 98 citations

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q

1993 • 92 citations

Deletion mapping of chromosome II in carcinoma of the bladder

1995 • 85 citations

11q deletions in human colorectal carcinomas: Cytogenetics and restriction fragment length polymorphism analysis

1993 • 66 citations

Further Localization of the Gene for Hereditary Paragangliomas and Evidence for Linkage in Unrelated Families

1994 • 65 citations

Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL

1994 • 61 citations

A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma.

1995 • 61 citations

Hereditary Deficiencies of Clotting Factors VII and X Associated with Carotid-Body Tumors

1964 • 57 citations

Anticipation in myotonic dystrophy

1992 • 56 citations

Is there evidence for anticipation in autosomal-dominant polycystic kidney disease?

1994 • 56 citations

Statistical pitfalls in detecting age-of-onset anticipation

1995 • 55 citations

Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers

1993 • 52 citations

Allelic losses in human chromosome II in lung cancers

1995 • 50 citations

Localization of a Tumor Suppressor Gene in 11p15.5 Using the G401 Wilms' Tumor Assay

1996 • 47 citations

Parents do matter: genomic imprinting and parental sex effects in neurological disorders

1995 • 16 citations

Familial chemodectoma

1981 • 9 citations