Published in Nucleic Acids Res on July 25, 1990
A genetic map of the mouse suitable for typing intraspecific crosses. Genetics (1992) 8.53
iPS cells produce viable mice through tetraploid complementation. Nature (2009) 6.51
Slippage synthesis of simple sequence DNA. Nucleic Acids Res (1992) 5.18
A new set of BXD recombinant inbred lines from advanced intercross populations in mice. BMC Genet (2004) 3.74
The genetic structure of recombinant inbred mice: high-resolution consensus maps for complex trait analysis. Genome Biol (2001) 3.17
Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 mice. Mol Cell Biol (1995) 2.89
Isolation and characterization of novel microsatellite markers and their application for diversity assessment in cultivated groundnut (Arachis hypogaea). BMC Plant Biol (2008) 2.43
Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes. Am J Hum Genet (1992) 2.10
A first-generation whole genome-radiation hybrid map spanning the mouse genome. Genome Res (1997) 1.73
Sequence-specific DNA purification by triplex affinity capture. Proc Natl Acad Sci U S A (1992) 1.69
Rat gene mapping using PCR-analyzed microsatellites. Genetics (1992) 1.57
Identification of four chromosomal loci determining obesity in a multifactorial mouse model. J Clin Invest (1995) 1.49
Genetic factors in lipoprotein metabolism. Analysis of a genetic cross between inbred mouse strains NZB/BINJ and SM/J using a complete linkage map approach. J Clin Invest (1995) 1.39
Genetic analysis of the NZB contribution to lupus-like autoimmune disease in (NZB x NZW)F1 mice. Proc Natl Acad Sci U S A (1994) 1.35
Complex trait analysis of the mouse striatum: independent QTLs modulate volume and neuron number. BMC Neurosci (2001) 1.29
Localization of atherosclerosis susceptibility loci to chromosomes 4 and 6 using the Ldlr knockout mouse model. Proc Natl Acad Sci U S A (2001) 1.29
Dual T cell receptor alpha chain T cells in autoimmunity. J Exp Med (1995) 1.26
Melanoma x macrophage hybrids with enhanced metastatic potential. Clin Exp Metastasis (1998) 1.23
Locus controlling Bordetella pertussis-induced histamine sensitization (Bphs), an autoimmune disease-susceptibility gene, maps distal to T-cell receptor beta-chain gene on mouse chromosome 6. Proc Natl Acad Sci U S A (1993) 1.21
Linkage maps of microsatellite DNA markers for the Pacific oyster Crassostrea gigas. Genetics (2004) 1.21
The conversion of mouse skin squamous cell carcinomas to spindle cell carcinomas is a recessive event. J Cell Biol (1993) 1.18
IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa. Mamm Genome (1997) 1.17
Mapping genes in the mouse using single-strand conformation polymorphism analysis of recombinant inbred strains and interspecific crosses. Proc Natl Acad Sci U S A (1992) 1.16
The polar-lethal Ovum mutant gene maps to the distal portion of mouse chromosome 11. Genetics (1992) 1.16
Origins of mouse inbred strains deduced from whole-genome scanning by polymorphic microsatellite loci. Mamm Genome (2005) 1.12
Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome. Proc Natl Acad Sci U S A (1995) 1.12
Effect of genetic background on the contribution of New Zealand black loci to autoimmune lupus nephritis. Proc Natl Acad Sci U S A (1996) 1.11
Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome. Genetics (1996) 1.07
Identification of a new susceptibility locus for insulin-dependent diabetes mellitus by ancestral haplotype congenic mapping. J Clin Invest (1995) 1.06
Genetic linkage of IgG autoantibody production in relation to lupus nephritis in New Zealand hybrid mice. J Clin Invest (1996) 1.00
Apoptosis resistance of nonobese diabetic peripheral lymphocytes linked to the Idd5 diabetes susceptibility region. Proc Natl Acad Sci U S A (1997) 0.98
A new source of polymorphic DNA markers for sperm typing: analysis of microsatellite repeats in single cells. Am J Hum Genet (1992) 0.98
Coincidence of genetic loci for plasma cholesterol levels and obesity in a multifactorial mouse model. J Clin Invest (1993) 0.98
Tetranucleotide repeat polymorphism at the HPRT locus. Nucleic Acids Res (1991) 0.97
The shiverer mutation affects the persistence of Theiler's virus in the central nervous system. J Virol (1997) 0.96
A diabetes-associated T-cell autoantigen maps to a telomeric locus on mouse chromosome 6. Proc Natl Acad Sci U S A (1995) 0.95
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. Am J Pathol (1997) 0.90
Mouse chromosome 4. Mamm Genome (1992) 0.90
Genetic analysis of diabetes and insulitis in an interspecific cross of the nonobese diabetic mouse with Mus spretus. Proc Natl Acad Sci U S A (1993) 0.88
Mouse chromosome 11. Mamm Genome (1991) 0.88
Tandemly repeated pentanucleotides in DNA sequences of eucaryotes. Nucleic Acids Res (1994) 0.88
Mouse forward genetics in the study of the peripheral nervous system and human peripheral neuropathy. Neurochem Res (2008) 0.85
Mouse chromosome 8. Mamm Genome (1991) 0.85
Allelotyping of butadiene-induced lung and mammary adenocarcinomas of B6C3F1 mice: frequent losses of heterozygosity in regions homologous to human tumor-suppressor genes. Proc Natl Acad Sci U S A (1994) 0.84
Mouse chromosome 2. Mamm Genome (1992) 0.84
Potential of (GATA)n microsatellites from rice for inter- and intra-specific variability studies. BMC Evol Biol (2001) 0.83
Mouse chromosome 14. Mamm Genome (1992) 0.83
Mouse chromosome 9. Mamm Genome (1992) 0.82
Mouse chromosome 1. Mamm Genome (1992) 0.81
Repertoire of SSRs in the Castor Bean Genome and Their Utilization in Genetic Diversity Analysis in Jatropha curcas. Comp Funct Genomics (2011) 0.81
Representativeness of microsatellite distributions in genomes, as revealed by 454 GS-FLX titanium pyrosequencing. BMC Genomics (2010) 0.81
SSLPs to map genetic differences between the 129 inbred strains and closed-colony, random-bred CD-1 mice. Mamm Genome (1997) 0.80
Mouse chromosome 6. Mamm Genome (1992) 0.79
Mouse chromosome 17. Mamm Genome (1992) 0.78
A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7. Mamm Genome (1997) 0.78
Mouse map of paralogous genes. Mamm Genome (1991) 0.78
Mouse chromosome 5. Mamm Genome (1992) 0.77
Analysis of the sex ratio in preimplantation embryos from B6.K1 and B6.K2 Ped gene congenic mice. J Assist Reprod Genet (2006) 0.77
Mouse chromosome 9. Mamm Genome (1991) 0.77
Mouse females devoid of exposure to males during fetal development exhibit increased maternal behavior. Psychoneuroendocrinology (2011) 0.77
A new strategy useful for rapid identification of microsatellites from DNA libraries with large size inserts. Nucleic Acids Res (1992) 0.77
A format for databasing and comparison of AFLP fingerprint profiles. BMC Bioinformatics (2003) 0.77
Mouse chromosome 11. Mamm Genome (1992) 0.76
1 + 1 = 3: Development and validation of a SNP-based algorithm to identify genetic contributions from three distinct inbred mouse strains. J Biomol Tech (2012) 0.76
Mouse chromosome 15. Mamm Genome (1991) 0.76
Mouse X chromosome. Mamm Genome (1991) 0.76
Mouse chromosome 1. Mamm Genome (1991) 0.76
Mouse chromosome 12. Mamm Genome (1991) 0.76
Genetic mapping of the vascular endothelial growth factor (Vegf) gene to mouse chromosome 17. Mamm Genome (1997) 0.75
Trinucleotide repeat polymorphism at the CRYG1 locus. Nucleic Acids Res (1991) 0.75
The dynamic of the t-haplotype in wild populations of the house mouse Mus musculus domesticus in Israel. Mamm Genome (2007) 0.75
Mouse chromosome 14. Mamm Genome (1991) 0.75
Mouse chromosome 8. Mamm Genome (1992) 0.75
Mouse chromosome 2. Mamm Genome (1991) 0.75
Mouse X chromosome. Mamm Genome (1992) 0.75
Development of AFLP-derived STS markers for the selection of 5-methyltryptophan-resistant rice mutants. Plant Cell Rep (2004) 0.75
Mouse chromosome 5. Mamm Genome (1991) 0.75
Mouse chromosome 12. Mamm Genome (1992) 0.75
Mouse chromosome 15. Mamm Genome (1992) 0.75
Genotypes for 66 microsatellite markers in the AXB and BXA recombinant inbred mouse strains. Mamm Genome (1998) 0.75
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science (1988) 220.77
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet (1989) 62.23
Hypervariable 'minisatellite' regions in human DNA. Nature (1985) 31.03
Variable number of tandem repeat (VNTR) markers for human gene mapping. Science (1987) 25.71
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am J Hum Genet (1989) 12.57
Hypervariability of simple sequences as a general source for polymorphic DNA markers. Nucleic Acids Res (1989) 10.34
Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Res (1988) 8.33
A novel repeated element with Z-DNA-forming potential is widely found in evolutionarily diverse eukaryotic genomes. Proc Natl Acad Sci U S A (1982) 8.15
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet (1990) 4.54
The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. Proc Natl Acad Sci U S A (1990) 3.72
Confidence limits for estimates of gene linkage based on analysis of recombinant inbred strains. J Hered (1986) 3.68
Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region. Proc Natl Acad Sci U S A (1989) 2.92
Statistical considerations for linkage analysis using recombinant inbred strains and backcrosses. Proc Natl Acad Sci U S A (1986) 2.60
A linkage map of endogenous murine leukemia proviruses. Genetics (1990) 2.60
Report of the committee on the genetic constitution of chromosome 17. Cytogenet Cell Genet (1989) 2.59
Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction. Nucleic Acids Res (1989) 2.48
Mouse DNA 'fingerprints': analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains. Nucleic Acids Res (1987) 2.47
Incomplete primer extension during in vitro DNA amplification catalyzed by Taq polymerase; exploitation for DNA sequencing. Nucleic Acids Res (1989) 2.21
A novel type of aberrant recombination in immunoglobulin genes and its implications for V-J joining mechanism. Nature (1983) 2.11
Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region. EMBO J (1989) 1.97
The isolation of high molecular weight DNA from whole organisms or large tissue masses. Anal Biochem (1978) 1.81
A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human. Genetics (1989) 1.65
Genetic identification of endogenous polytropic proviruses by using recombinant inbred mice. J Virol (1989) 1.56
Molecular cloning and analysis of DNA complementary to three mouse Mr = 68,000 heat shock protein mRNAs. J Biol Chem (1986) 1.42
Multilocus molecular mapping of the mouse X chromosome. Genomics (1988) 1.23
A cellular enhancer of retrovirus gene expression in embryonal carcinoma cells. Proc Natl Acad Sci U S A (1987) 1.18
Clustering of cytokine genes on mouse chromosome 11. J Exp Med (1990) 1.15
Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene. Nucleic Acids Res (1989) 1.07
An interspecific backcross linkage map of the proximal half of mouse chromosome 14. Genomics (1990) 1.02
A preferred region for integration of Friend murine leukemia virus in hematopoietic neoplasms is closely linked to the Int-2 oncogene. J Virol (1986) 0.98
Prognosis in HIV-1 infection predicted by the quantity of virus in plasma. Science (1996) 18.38
Plasma viral load and CD4+ lymphocytes as prognostic markers of HIV-1 infection. Ann Intern Med (1997) 16.44
Haplotype tagging for the identification of common disease genes. Nat Genet (2001) 11.27
Quantitation of HIV-1 RNA in plasma predicts outcome after seroconversion. Ann Intern Med (1995) 6.90
Maternal viral load, zidovudine treatment, and the risk of transmission of human immunodeficiency virus type 1 from mother to infant. Pediatric AIDS Clinical Trials Group Protocol 076 Study Group. N Engl J Med (1996) 4.44
Genetic analysis of autoimmune type 1 diabetes mellitus in mice. Nature (1991) 4.27
The genetically isolated populations of Finland and sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes. Nat Genet (2000) 3.92
Genetic analysis of autoimmune disease. Cell (1996) 3.87
Genetic control of autoimmune diabetes in the NOD mouse. Annu Rev Immunol (1995) 3.71
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. Nat Genet (1997) 3.62
Analysis of 17 autoimmune disease-associated variants in type 1 diabetes identifies 6q23/TNFAIP3 as a susceptibility locus. Genes Immun (2008) 3.48
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry. Hum Mol Genet (1996) 3.37
Rapid and precise quantification of HIV-1 RNA in plasma using a branched DNA signal amplification assay. J Acquir Immune Defic Syndr Hum Retrovirol (1995) 3.23
Towards fully automated genome-wide polymorphism screening. Nat Genet (1995) 3.13
Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. Am J Hum Genet (1995) 3.02
A search for type 1 diabetes susceptibility genes in families from the United Kingdom. Nat Genet (1998) 2.85
Type 1 diabetes in mice is linked to the interleukin-1 receptor and Lsh/Ity/Bcg genes on chromosome 1. Nature (1991) 2.84
Vaccination trials in rhesus monkeys with a minor, invariant, Plasmodium knowlesi 66 kD merozoite antigen. Parasite Immunol (1988) 2.79
CD226 Gly307Ser association with multiple autoimmune diseases. Genes Immun (2008) 2.76
Hopping hotspots: global shifts in marine biodiversity. Science (2008) 2.68
Genes encoding ligands for deletion of V beta 11 T cells cosegregate with mammary tumour virus genomes. Nature (1991) 2.65
Application of branched DNA signal amplification to monitor human immunodeficiency virus type 1 burden in human plasma. J Infect Dis (1994) 2.60
Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design. Ann Hum Genet (2002) 2.51
Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood. Nat Genet (1998) 2.49
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins. Hum Mol Genet (2001) 2.43
Unbiased application of the transmission/disequilibrium test to multilocus haplotypes. Am J Hum Genet (2000) 2.22
Strategies in complex disease mapping. Curr Opin Genet Dev (2000) 2.20
Aspartic acid at position 57 of the HLA-DQ beta chain protects against type I diabetes: a family study. Proc Natl Acad Sci U S A (1988) 2.19
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene. Am J Hum Genet (1999) 2.17
Beta 2-microglobulin-deficient NOD mice do not develop insulitis or diabetes. Diabetes (1994) 2.16
The MHC haplotype project: a resource for HLA-linked association studies. Tissue Antigens (2002) 2.16
Cost-effective analysis of candidate genes using htSNPs: a staged approach. Genes Immun (2004) 2.07
Microsatellites for linkage analysis of genetic traits. Trends Genet (1992) 2.05
Cloning of a novel member of the low-density lipoprotein receptor family. Gene (1998) 1.97
Confirmation of HLA class II independent type 1 diabetes associations in the major histocompatibility complex including HLA-B and HLA-A. Diabetes Obes Metab (2009) 1.94
Isolation and characterization of LRP6, a novel member of the low density lipoprotein receptor gene family. Biochem Biophys Res Commun (1998) 1.93
No association of multiple type 2 diabetes loci with type 1 diabetes. Diabetologia (2009) 1.92
Allelic variation in the DR subregion of the human major histocompatibility complex. Proc Natl Acad Sci U S A (1987) 1.92
Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome. Lancet (1997) 1.91
Reduced heat resistance of mutant spores after cloning and mutagenesis of the Bacillus subtilis gene encoding penicillin-binding protein 5. J Bacteriol (1986) 1.83
Additional microsatellite markers for mouse genome mapping. Mamm Genome (1991) 1.79
Cloning and expression in Escherichia coli of the insecticidal delta-endotoxin gene of Bacillus thuringiensis var. israelensis. FEBS Lett (1984) 1.77
Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography, chromosome recombination frequency and selection. Hum Mol Genet (2000) 1.76
Bacillus thuringiensis var. israelensis delta-endotoxin. Cloning and expression of the toxin in sporogenic and asporogenic strains of Bacillus subtilis. J Mol Biol (1986) 1.74
An RGD-oligolysine peptide: a prototype construct for integrin-mediated gene delivery. Hum Gene Ther (1998) 1.73
Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation. Genome Res (2000) 1.71
The generation of a library of PCR-analyzed microsatellite variants for genetic mapping of the mouse genome. Genomics (1991) 1.61
New genetic loci that control susceptibility and symptoms of experimental allergic encephalomyelitis in inbred mice. J Immunol (1998) 1.58
The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1. Diabetes (2001) 1.58
Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3-q14.1. Genes Immun (2009) 1.53
Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test. Ann Hum Genet (2000) 1.53
Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease. Genes Immun (2004) 1.53
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients. Nat Genet (1998) 1.50
Resistance alleles at two non-major histocompatibility complex-linked insulin-dependent diabetes loci on chromosome 3, Idd3 and Idd10, protect nonobese diabetic mice from diabetes. J Exp Med (1994) 1.49
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families. Am J Hum Genet (2001) 1.49
Analysis of the type 2 diabetes gene, TCF7L2, in 13,795 type 1 diabetes cases and control subjects. Diabetologia (2006) 1.46
I-E-independent deletion of V beta 17a+ T cells by Mtv-3 from the nonobese diabetic mouse. J Immunol (1992) 1.46
Human type 1 diabetes and the insulin gene: principles of mapping polygenes. Annu Rev Genet (1996) 1.46
NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans. Diabetes (2000) 1.46
Direct and quantitative detection of HIV-1 RNA in human plasma with a branched DNA signal amplification assay. AIDS (1993) 1.42
Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families. Genes Immun (2009) 1.42
The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137. Immunity (2000) 1.40
IDDM2/insulin VNTR modifies risk conferred by IDDM1/HLA for development of Type 1 diabetes and associated autoimmunity. Diabetologia (2003) 1.37
HLA class II typing of whole genome amplified mouth swab DNA. Tissue Antigens (2000) 1.37
Segregation of the polypeptide translocation apparatus to regions of the endoplasmic reticulum containing ribophorins and ribosomes. I. Functional tests on rat liver microsomal subfractions. J Cell Biol (1984) 1.36
Transmission ratio distortion at the INS-IGF2 VNTR. Nat Genet (1999) 1.34
Congenic mapping of the type 1 diabetes locus, Idd3, to a 780-kb region of mouse chromosome 3: identification of a candidate segment of ancestral DNA by haplotype mapping. Genome Res (2000) 1.34
Serial studies of numbers of circulating T and B lymphocytes in children with acute lymphoblastic leukaemia. Arch Dis Child (1977) 1.34
Alteration in the penicillin-binding profile of Bacillus megaterium during sporulation. Nature (1982) 1.32
Determinants of the quantity of hepatitis C virus RNA. J Infect Dis (2000) 1.32
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group. Nat Genet (1997) 1.31
Analysis of the obesity gene FTO in 14,803 type 1 diabetes cases and controls. Diabetologia (2007) 1.29
A newly characterized HLA DQ beta allele associated with pemphigus vulgaris. Science (1988) 1.28
Localization of two insulin-dependent diabetes (Idd) genes to the Idd10 region on mouse chromosome 3. Mamm Genome (1998) 1.27
Calciphylaxis in a patient with normal renal function: response to treatment with sodium thiosulfate. Clin Exp Dermatol (2008) 1.24
c-fos and c-myc gene activation, ionic signals, and DNA synthesis in thymocytes. J Biol Chem (1986) 1.24
Cell binding and internalization by filamentous phage displaying a cyclic Arg-Gly-Asp-containing peptide. J Biol Chem (1994) 1.23
Differential glycosylation of interleukin 2, the molecular basis for the NOD Idd3 type 1 diabetes gene? Cytokine (2000) 1.23
Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application to nonobese diabetic (NOD) mouse and human insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet (1993) 1.22
The British Diabetic Association--Warren repository. Autoimmunity (1990) 1.22
Follow-up of 1715 SNPs from the Wellcome Trust Case Control Consortium genome-wide association study in type I diabetes families. Genes Immun (2009) 1.22
An extension of the Maximum Lod Score method to X-linked loci. Ann Hum Genet (1995) 1.21
Locus controlling Bordetella pertussis-induced histamine sensitization (Bphs), an autoimmune disease-susceptibility gene, maps distal to T-cell receptor beta-chain gene on mouse chromosome 6. Proc Natl Acad Sci U S A (1993) 1.21
Expression of the type I diabetes-associated gene LRP5 in macrophages, vitamin A system cells, and the Islets of Langerhans suggests multiple potential roles in diabetes. J Histochem Cytochem (2000) 1.20
Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and -DRB1. Genes Immun (2003) 1.19
Analysis of the CD3 gene region and type 1 diabetes: application of fluorescence-based technology to linkage disequilibrium mapping. Hum Mol Genet (1995) 1.19
The molecular basis of HLA-disease association. Adv Hum Genet (1989) 1.18
Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21. Hum Mol Genet (2000) 1.17
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases. Diabetes (2001) 1.17
A type 1 diabetes subgroup with a female bias is characterised by failure in tolerance to thyroid peroxidase at an early age and a strong association with the cytotoxic T-lymphocyte-associated antigen-4 gene. Diabetologia (2007) 1.17
Congenic mapping of the insulin-dependent diabetes (Idd) gene, Idd10, localizes two genes mediating the Idd10 effect and eliminates the candidate Fcgr1. J Immunol (1997) 1.17
Lipid-mediated enhancement of transfection by a nonviral integrin-targeting vector. Hum Gene Ther (1998) 1.16
Continuous subcutaneous analgesics and antiemetics in domiciliary terminal care. Lancet (1981) 1.15
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases. Hum Mol Genet (2000) 1.15
The sporulation-specific penicillin-binding protein 5a from Bacillus subtilis is a DD-carboxypeptidase in vitro. Biochem J (1985) 1.13
Mapping of the IDDM locus Idd3 to a 0.35-cM interval containing the interleukin-2 gene. Diabetes (1997) 1.13