A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.

PubWeight™: 0.83‹?›

🔗 View Article (PMC 1682045)

Published in Am J Hum Genet on May 01, 1993

Authors

C W Richard1, M Boehnke, D J Berg, J H Lichy, T C Meeker, E Hauser, R M Myers, D R Cox

Author Affiliations

1: Department of Psychiatry, University of California, San Francisco.

Articles cited by this

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. Anal Biochem (1984) 66.58

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science (1990) 10.72

Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proc Natl Acad Sci U S A (1989) 8.68

Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science (1990) 5.35

Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature (1991) 2.87

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet (1989) 2.56

Wee1(+)-like gene in human cells. Nature (1991) 2.41

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somat Cell Mol Genet (1989) 2.29

Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet (1991) 2.16

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet (1989) 1.99

Monoallelic expression of the human H19 gene. Nat Genet (1992) 1.96

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2. Nat Genet (1992) 1.84

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr (1983) 1.68

PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids. Genomics (1991) 1.58

A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients. Proc Natl Acad Sci U S A (1990) 1.47

Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1----p15.4. Genomics (1991) 1.43

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. Hum Genet (1984) 1.42

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol Cell Biol (1989) 1.36

Vector-Alu PCR: a rapid step in mapping cosmids and YACs. Nucleic Acids Res (1990) 1.19

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. Proc Natl Acad Sci U S A (1989) 1.14

Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases. Ann Genet (1985) 1.04

Identification of a human chromosome 11 gene which is differentially regulated in tumorigenic and nontumorigenic somatic cell hybrids of HeLa cells. Cell Growth Differ (1992) 1.00

A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci. Am J Hum Genet (1991) 0.96

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature. Cancer Genet Cytogenet (1992) 0.96

Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11. Nucleic Acids Res (1988) 0.96

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma. Hum Genet (1989) 0.93

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome. Jinrui Idengaku Zasshi (1986) 0.92

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Res (1990) 0.92

Mapping of 262 DNA markers into 24 intervals on human chromosome 11. Am J Hum Genet (1992) 0.89

A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics (1990) 0.85

A cosmid clone map derived from a small region of human chromosome 11. Genomics (1989) 0.84

Analysis of human chromosome 11 by somatic cell genetics: reexamination of derivatives of human-hamster cell line J1. Somat Cell Mol Genet (1987) 0.80

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region. Genomics (1990) 0.80

The hemopexin gene maps to the same location as the beta-globin gene cluster on human chromosome 11. Genomics (1988) 0.78

The placental ribonuclease inhibitor (RNH) gene is located on chromosome subband 11p15.5. Genomics (1990) 0.77

Mitotic deletions of 11p15.5 in two different tumors indicate that the CALCA locus is distal to the PTH locus. Cytogenet Cell Genet (1989) 0.76

Articles by these authors

Initial sequencing and analysis of the human genome. Nature (2001) 212.86

Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples. Br J Cancer (1977) 53.23

Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design. Br J Cancer (1976) 22.55

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science (2001) 15.54

A gene map of the human genome. Science (1996) 14.32

Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol (1988) 13.73

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes. Proc Natl Acad Sci U S A (1989) 13.66

A physical map of 30,000 human genes. Science (1998) 12.43

A physical map of the human genome. Nature (2001) 12.39

Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature (2001) 10.96

Detection and localization of single base changes by denaturing gradient gel electrophoresis. Methods Enzymol (1987) 10.90

An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing. Science (2001) 8.73

Human homolog of patched, a candidate gene for the basal cell nevus syndrome. Science (1996) 8.06

Construction and analysis of simian virus 40 origins defective in tumor antigen binding and DNA replication. Proc Natl Acad Sci U S A (1980) 7.04

Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16. Cytogenet Cell Genet (1985) 6.87

Positive and negative effects of widespread badger culling on tuberculosis in cattle. Nature (2005) 6.64

Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis. Nucleic Acids Res (1985) 6.52

Fine structure genetic analysis of a beta-globin promoter. Science (1986) 6.36

Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes. Science (1985) 6.35

Structure and variability of human chromosome ends. Mol Cell Biol (1990) 6.18

Detection of single base substitutions in total genomic DNA. Nature (1985) 5.99

Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science (1990) 5.35

How many polymorphic genes will it take to span the human genome? Am J Hum Genet (1982) 5.11

A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet (1999) 4.96

Loss of information due to ambiguous haplotyping of SNPs. Nat Genet (1999) 4.90

Impact of localized badger culling on tuberculosis incidence in British cattle. Nature (2003) 4.84

Adenovirus DNA replication in vitro: identification of a host factor that stimulates synthesis of the preterminal protein-dCMP complex. Proc Natl Acad Sci U S A (1982) 4.72

SV40 gene expression is modulated by the cooperative binding of T antigen to DNA. Cell (1981) 4.64

Improved inference of relationship for pairs of individuals. Am J Hum Genet (2000) 4.47

Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet (1989) 4.42

TB policy and the badger culling trials. Vet Rec (2006) 4.02

Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study. Diabetes Care (1998) 3.99

A general method for saturation mutagenesis of cloned DNA fragments. Science (1985) 3.94

Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet (1993) 3.76

Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods. Hum Hered (1983) 3.74

Primary structure and functional expression of the 5HT3 receptor, a serotonin-gated ion channel. Science (1991) 3.73

TB policy and the badger culling trials. Vet Rec (2006) 3.67

An STS-based radiation hybrid map of the human genome. Genome Res (1997) 3.57

Formation of a covalent complex between the 80,000-dalton adenovirus terminal protein and 5'-dCMP in vitro. Proc Natl Acad Sci U S A (1981) 3.55

High-throughput genotyping with single nucleotide polymorphisms. Genome Res (2001) 3.55

Methods for estimating the case fatality ratio for a novel, emerging infectious disease. Am J Epidemiol (2005) 3.40

Expression during embryogenesis of a mouse gene with sequence homology to the Drosophila engrailed gene. Cell (1985) 3.30

Bovine tuberculosis: towards a future control strategy. Vet Rec (2000) 3.27

A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet (2000) 3.22

Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies. Nat Genet (2001) 3.20

Extensions to pedigree analysis. IV. Covariance components models for multivariate traits. Am J Med Genet (1983) 3.10

Identifying marker typing incompatibilities in linkage analysis. Am J Hum Genet (1996) 3.06

Evolutionarily conserved sequences on human chromosome 21. Genome Res (2001) 2.95

Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis. Nucleic Acids Res (1985) 2.90

Estimating the power of a proposed linkage study: a practical computer simulation approach. Am J Hum Genet (1986) 2.84

T helper cell 1-type CD4+ T cells, but not B cells, mediate colitis in interleukin 10-deficient mice. J Exp Med (1996) 2.79

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1) Science (1996) 2.73

Comparative DNA sequence analysis of mouse and human protocadherin gene clusters. Genome Res (2001) 2.66

Separation of the adenovirus terminal protein precursor from its associated DNA polymerase: role of both proteins in the initiation of adenovirus DNA replication. Proc Natl Acad Sci U S A (1982) 2.65

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat Genet (1995) 2.63

Thottapalayam virus: a presumptive arbovirus isolated from a shrew in India. Indian J Med Res (1971) 2.52

Genetic counseling for families with inherited susceptibility to breast and ovarian cancer. JAMA (1993) 2.51

Characterization of a candidate bcl-1 gene. Mol Cell Biol (1991) 2.48

Adenovirus DNA replication in vitro: purification of the terminal protein in a functional form. Proc Natl Acad Sci U S A (1981) 2.43

Concurrent isolation from patient of two arboviruses, Chikungunya and dengue type 2. Science (1967) 2.38

Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression. Proc Natl Acad Sci U S A (2005) 2.38

Quality of life measures in health care. III: Resource allocation. BMJ (1992) 2.31

Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides. Nature (1983) 2.25

Analysis of the site in CD4 that binds to the HIV envelope glycoprotein. J Immunol (1990) 2.21

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH. Nat Med (1996) 2.19

Dysregulation of the fibroblast growth factor system in major depression. Proc Natl Acad Sci U S A (2004) 2.19

Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia. Science (1993) 2.17

Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet (1991) 2.16

Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree. Hum Genet (1992) 2.15

Exon trapping: a genetic screen to identify candidate transcribed sequences in cloned mammalian genomic DNA. Proc Natl Acad Sci U S A (1990) 2.15

Statistical methods for polyploid radiation hybrid mapping. Genome Res (1995) 2.15

Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type. J Neurogenet (1987) 2.12

Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice. Anat Embryol (Berl) (1999) 2.12

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet Epidemiol (1996) 2.06

Genetic linkage analysis of complex genetic traits by using affected sibling pairs. Biometrics (1998) 2.04

Impacts of widespread badger culling on cattle tuberculosis: concluding analyses from a large-scale field trial. Int J Infect Dis (2007) 2.03

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet (1989) 1.99

Clustering of extensive somatic mutations in the variable region of an immunoglobulin heavy chain gene from a human B cell lymphoma. Cell (1986) 1.92

Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc Natl Acad Sci U S A (1999) 1.91

A clinical trial of anti-idiotype therapy for B cell malignancy. Blood (1985) 1.91

Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease. Eur J Neurol (2011) 1.90

BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis. Am J Hum Genet (1993) 1.90

On class differentials in educational attainment. Proc Natl Acad Sci U S A (2005) 1.90

Ascertainment and goodness of fit of variance component models for pedigree data. Prog Clin Biol Res (1984) 1.89

A look at linkage disequilibrium. Nat Genet (2000) 1.87

Functional effects of the mouse weaver mutation on G protein-gated inwardly rectifying K+ channels. Neuron (1996) 1.85

Comparative chromosome mapping of a conserved homoeo box region in mouse and human. Nature (1985) 1.77