Published in Hum Mol Genet on March 01, 1996
Sequence mapping by electronic PCR. Genome Res (1997) 9.13
A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci U S A (1996) 4.30
RHdb: the Radiation Hybrid database. Nucleic Acids Res (2001) 4.12
Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase. Genes Dev (1998) 2.51
Radiation hybrid mapping of the zebrafish genome. Proc Natl Acad Sci U S A (1999) 2.27
A web server for performing electronic PCR. Nucleic Acids Res (2004) 2.02
Association of a lysine-232/alanine polymorphism in a bovine gene encoding acyl-CoA:diacylglycerol acyltransferase (DGAT1) with variation at a quantitative trait locus for milk fat content. Proc Natl Acad Sci U S A (2002) 2.01
A fast and scalable radiation hybrid map construction and integration strategy. Genome Res (2000) 1.91
beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics. Proc Natl Acad Sci U S A (2000) 1.89
A second-generation genetic linkage map of the domestic dog, Canis familiaris. Genetics (1999) 1.85
Selective mapping: a strategy for optimizing the construction of high-density linkage maps. Genetics (2000) 1.80
A first-generation whole genome-radiation hybrid map spanning the mouse genome. Genome Res (1997) 1.73
Microsatellite variation and recombination rate in the human genome. Genetics (2000) 1.71
Extensive conservation of sex chromosome organization between cat and human revealed by parallel radiation hybrid mapping. Genome Res (1999) 1.64
Evolutionary relationships among Rel domains indicate functional diversification by recombination. Proc Natl Acad Sci U S A (2001) 1.45
Molecular linguistics: extracting information from gene and protein sequences. Proc Natl Acad Sci U S A (1997) 1.43
Production and characterization of maize chromosome 9 radiation hybrids derived from an oat-maize addition line. Genetics (2000) 1.42
A placenta-specific receptor for the fusogenic, endogenous retrovirus-derived, human syncytin-2. Proc Natl Acad Sci U S A (2008) 1.40
Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins. Proc Natl Acad Sci U S A (2009) 1.33
Human and mouse homologs of Schizosaccharomyces pombe rad1(+) and Saccharomyces cerevisiae RAD17: linkage to checkpoint control and mammalian meiosis. Genes Dev (1998) 1.31
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis. Proc Natl Acad Sci U S A (1999) 1.24
The Radiation Hybrid Database. Nucleic Acids Res (1998) 1.24
Automated construction of high-density comparative maps between rat, human, and mouse. Genome Res (2001) 1.24
Characterization of whole genome radiation hybrid mapping resources for non-mammalian vertebrates. Nucleic Acids Res (1998) 1.23
The comprehensive mouse radiation hybrid map densely cross-referenced to the recombination map: a tool to support the sequence assemblies. Genome Res (2003) 1.22
Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26. Genome Res (2001) 1.17
Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene. BMC Genet (2001) 1.15
Estimation of synteny conservation and genome compaction between pufferfish (Fugu) and human. Yeast (2000) 1.15
The first-generation whole-genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes. Genome Res (2003) 1.15
Construction and extensive characterization of a goat bacterial artificial chromosome library with threefold genome coverage. Mamm Genome (1998) 1.15
Prostate cancer aggressiveness locus on chromosome 7q32-q33 identified by linkage and allelic imbalance studies. Neoplasia (2002) 1.11
The Radiation Hybrid Database. Nucleic Acids Res (1997) 1.10
The Genexpress IMAGE knowledge base of the human brain transcriptome: a prototype integrated resource for functional and computational genomics. Genome Res (1999) 1.09
Studies on locus content mapping. Proc Natl Acad Sci U S A (1996) 1.08
A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes. Genome Res (2010) 1.07
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22). J Med Genet (2000) 1.07
Selected locus and multiple panel models for radiation hybrid mapping. Am J Hum Genet (1996) 1.06
Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project. Genome Res (2000) 1.01
High-resolution physical and transcript map of human chromosome 2p21 containing the sitosterolaemia locus. Eur J Hum Genet (2001) 1.01
Parallel radiation hybrid mapping: a powerful tool for high-resolution genomic comparison. Genome Res (1998) 0.99
Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication. Genome Res (1999) 0.97
Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences. Chromosome Res (1999) 0.96
Glycerol as a correlate of impaired glucose tolerance: dissection of a complex system by use of a simple genetic trait. Am J Hum Genet (2000) 0.96
High-resolution radiation hybrid map of wheat chromosome 1D. Genetics (2006) 0.96
Endosperm tolerance of paternal aneuploidy allows radiation hybrid mapping of the wheat D-genome and a measure of γ ray-induced chromosome breaks. PLoS One (2012) 0.93
The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. Am J Hum Genet (2001) 0.93
A comparative radiation hybrid map of bovine chromosome 18 and homologous chromosomes in human and mice. Proc Natl Acad Sci U S A (2002) 0.91
The genexpress IMAGE knowledge base of the human muscle transcriptome: a resource of structural, functional, and positional candidate genes for muscle physiology and pathologies. Genome Res (1999) 0.91
A resource of mapped human bacterial artificial chromosome clones. Genome Res (1999) 0.90
2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4. Ann Hum Genet (2000) 0.90
Design factors that influence PCR amplification success of cross-species primers among 1147 mammalian primer pairs. BMC Genomics (2006) 0.88
A radiation hybrid map of chicken Chromosome 4. Mamm Genome (2004) 0.88
A high-resolution radiation hybrid map of chicken chromosome 5 and comparison with human chromosomes. BMC Genomics (2004) 0.88
Cosmid-derived markers anchoring the bovine genetic map to the physical map. Mamm Genome (1997) 0.88
An integrated physical map for the short arm of human chromosome 5. Genome Res (1999) 0.87
Molecular cloning and functional expression of a novel human gene encoding two 41-43 kDa skeletal muscle internal membrane proteins. Biochem J (1998) 0.87
Expression of SMARCF1, a truncated form of SWI1, in neuroblastoma. Am J Pathol (2001) 0.87
RHdb: the radiation hybrid database. Nucleic Acids Res (2000) 0.86
Development of a deer mouse whole-genome radiation hybrid panel and comparative mapping of Mus chromosome 11 loci. Mamm Genome (2006) 0.86
Expression, purification and characterization of a human serine-dependent phospholipase A2 with high specificity for oxidized phospholipids and platelet activating factor. Biochem J (1998) 0.86
High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes. Mamm Genome (1997) 0.85
Systematic evaluation of map quality: human chromosome 22. Am J Hum Genet (2002) 0.85
The Cancer Genome Anatomy Project: EST sequencing and the genetics of cancer progression. Neoplasia (1999) 0.85
Radiation hybrid map of the porcine genome comprising 2035 EST loci. Mamm Genome (2006) 0.83
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q. Genome Res (1998) 0.81
A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1. Genome Res (1999) 0.81
Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon. J Med Genet (2000) 0.81
A high-resolution 15,000(Rad) radiation hybrid panel for the domestic cat. Cytogenet Genome Res (2012) 0.80
Radiation hybrid maps of Medaka chromosomes LG 12, 17, and 22. DNA Res (2007) 0.80
GenMapDB: a database of mapped human BAC clones. Nucleic Acids Res (2001) 0.79
Application of AFLP technology to radiation hybrid mapping. Chromosome Res (2004) 0.79
Improved assay-dependent searching of nucleic acid sequence databases. Nucleic Acids Res (2008) 0.78
Application of dissociation curve analysis to radiation hybrid panel marker scoring: generation of a map of river buffalo (B. bubalis) chromosome 20. BMC Genomics (2008) 0.78
A comprehensive view of human chromosome 1. Genome Res (1999) 0.77
Radiation hybrid mapping of the two highly homologous human-variant pMCHL genes by PCR-SSCP. Genome Res (1998) 0.77
Construction of a radiation hybrid panel and the first yellowtail (Seriola quinqueradiata) radiation hybrid map using a nanofluidic dynamic array. BMC Genomics (2014) 0.76
Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting. Proc Natl Acad Sci U S A (1997) 0.75
Construction of whole genome radiation hybrid panels and map of chromosome 5A of wheat using asymmetric somatic hybridization. PLoS One (2012) 0.75
The immunophilin FKBP4 (FKBP52/FKBP59) maps to the distal short arm of human chromosome 12. Mamm Genome (1998) 0.75
Initial sequencing and analysis of the human genome. Nature (2001) 212.86
The genome sequence of Drosophila melanogaster. Science (2000) 74.32
A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature (1996) 27.61
Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA. Eur J Biochem (1980) 26.55
An STS-based map of the human genome. Science (1995) 17.72
The 1993-94 Généthon human genetic linkage map. Nat Genet (1994) 17.64
A second-generation linkage map of the human genome. Nature (1992) 16.32
Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence. Nat Genet (2000) 14.51
A gene map of the human genome. Science (1996) 14.32
A physical map of 30,000 human genes. Science (1998) 12.43
A physical map of the human genome. Nature (2001) 12.39
The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression. Genomics (1996) 11.71
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature (1990) 10.97
Whole genome amplification from a single cell: implications for genetic analysis. Proc Natl Acad Sci U S A (1992) 9.15
The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403. Genome Res (2001) 8.63
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature (1996) 8.02
Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi. Nature (2001) 7.53
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. Nature (1994) 7.30
Genome sequence of the plant pathogen Ralstonia solanacearum. Nature (2002) 6.23
SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene. Mol Cell Biol (1997) 5.72
Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature (1996) 5.44
Checking anaesthetic equipment 2012: association of anaesthetists of Great Britain and Ireland. Anaesthesia (2012) 5.41
FIGO staging classifications and clinical practice guidelines in the management of gynecologic cancers. FIGO Committee on Gynecologic Oncology. Int J Gynaecol Obstet (2000) 5.33
Mechanisms of evolution in Rickettsia conorii and R. prowazekii. Science (2001) 5.32
An interspersed repeated sequence specific for human subtelomeric regions. EMBO J (1990) 5.30
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet (1999) 4.74
The class II molecules of the human and murine major histocompatibility complex. Cell (1984) 4.34
Transmission/disequilibrium tests for extended marker haplotypes. Am J Hum Genet (1999) 4.07
Cystic fibrosis: steady steps lead to the gene. Nature (1989) 3.90
Genomic exploration of the hemiascomycetous yeasts: 1. A set of yeast species for molecular evolution studies. FEBS Lett (2000) 3.71
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Lancet (1997) 3.68
Sequence variation of the human Y chromosome. Nature (1995) 3.59
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat Genet (2001) 3.50
Novel gene transcripts preferentially expressed in human muscles revealed by quantitative hybridization of a high density cDNA array. Genome Res (1996) 3.41
A first-generation physical map of the human genome. Nature (1993) 3.40
DNA binding activity of recombinant SRY from normal males and XY females. Science (1992) 3.32
SRY, like HMG1, recognizes sharp angles in DNA. EMBO J (1992) 3.29
Genetic evidence equating SRY and the testis-determining factor. Nature (1990) 3.22
A method for constructing radiation hybrid maps of whole genomes. Nat Genet (1994) 3.19
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene. Nat Genet (2001) 3.15
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. Proc Natl Acad Sci U S A (1998) 3.14
The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution. Proc Natl Acad Sci U S A (2006) 3.11
Nucleotide sequence of a cloned cDNA corresponding to secreted mu chain of mouse immunoglobulin. Gene (1980) 3.10
A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes. Nature (1986) 3.09
Report of the Committee on the Genetic Constitution of the X and Y Chromosomes. Cytogenet Cell Genet (1985) 3.07
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nat Genet (1995) 3.05
A monoclonal antibody to the human epidermal growth factor receptor. J Cell Biochem (1982) 3.04
A deletion map of the human Y chromosome based on DNA hybridization. Am J Hum Genet (1986) 3.03
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet (2003) 3.02
A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2. Development (1996) 3.02
DNA microarrays in drug discovery and development. Nat Genet (1999) 3.02
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22. Nat Genet (1996) 3.00
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group. Nat Genet (1996) 2.98
Two interferon mRNAs in human fibroblasts: in vitro translation and Escherichia coli cloning studies. Proc Natl Acad Sci U S A (1980) 2.88
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distance. Science (1985) 2.88
The chicken B locus is a minimal essential major histocompatibility complex. Nature (1999) 2.84
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. Hum Mol Genet (1994) 2.83
cDNA clone for the heavy chain of the human B cell alloantigen DC1: strong sequence homology to the HLA-DR heavy chain. Proc Natl Acad Sci U S A (1982) 2.80
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet (1993) 2.79
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome. Am J Hum Genet (2001) 2.72
A second locus for Marfan syndrome maps to chromosome 3p24.2-p25. Nat Genet (1994) 2.71
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet (1997) 2.68
Function of plastid mRNA 3' inverted repeats. RNA stabilization and gene-specific protein binding. J Biol Chem (1989) 2.64
Finding new genes faster than ever. Nat Genet (1993) 2.61
Fire on an intensive care unit caused by an oxygen cylinder. Anaesthesia (2012) 2.61
Mutant WD-repeat protein in triple-A syndrome. Nat Genet (2000) 2.54
A radiation hybrid map of the rat genome containing 5,255 markers. Nat Genet (1999) 2.54
Rapid sequence evolution of the mammalian sex-determining gene SRY. Nature (1993) 2.52
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet (1995) 2.52
[Primary structure of transfer RNA]. Biochimie (1972) 2.43
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat Genet (1993) 2.40
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Hum Mol Genet (2000) 2.40