Published in Hum Mol Genet on January 01, 1996
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. Proc Natl Acad Sci U S A (1998) 3.14
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history. PLoS Genet (2006) 2.80
HLA and infectious diseases. Clin Microbiol Rev (2009) 2.35
MHC haplotype matching for unrelated hematopoietic cell transplantation. PLoS Med (2007) 1.83
LOD wars: the affected-sib-pair paradigm strikes back! Am J Hum Genet (1997) 1.35
The regulatory role of DR4 in a spontaneous diabetes DQ8 transgenic model. J Clin Invest (2001) 1.11
Analysis of MHC class II DP, DQ and DR alleles in Crohn's disease. Gut (1998) 1.05
Susceptibility loci for lupus: a guiding light from murine models? J Clin Invest (1997) 0.83
Genetics of autoimmune diabetes mellitus. Wien Med Wochenschr (2008) 0.82
Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family. J Clin Invest (1998) 0.81
Molecular biology and genetics of allergy and asthma. Arch Dis Child (1998) 0.78
Immunology of IDDM. Diabetologia (1997) 0.76
From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era. Rev Diabet Stud (2012) 0.75
The effect of parental imprinting on the INS-IGF2 locus of Korean type I diabetic patients. Korean J Intern Med (2001) 0.75
Family cell lines available for research--an endangered resource? Am J Hum Genet (1997) 0.75
Model organisms illuminate human genetics and disease. Mol Med (1997) 0.75
New names for old disciplines. J Inherit Metab Dis (2002) 0.75
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands. Nature (1987) 7.88
Localization of cystic fibrosis locus to human chromosome 7cen-q22. Nature (1985) 7.77
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Am J Hum Genet (1986) 3.83
Integrating case-control and TDT studies. Ann Hum Genet (2005) 3.19
Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. Genomics (1987) 3.03
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
Mapping of mutation causing Friedreich's ataxia to human chromosome 9. Nature (1988) 2.96
Genetic influences on F cells and other hematologic variables: a twin heritability study. Blood (2000) 2.95
Linkage of the angiotensinogen gene to essential hypertension. N Engl J Med (1994) 2.80
Measured haplotype analysis of the angiotensin-I converting enzyme gene. Hum Mol Genet (1998) 2.53
Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic fibrosis. Nucleic Acids Res (1986) 2.34
Physical and genetic analysis of cosmids from the vicinity of the cystic fibrosis locus. Nucleic Acids Res (1987) 2.16
Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications. Lancet (1985) 2.14
Predisposing locus for Alzheimer's disease on chromosome 21. Lancet (1989) 1.99
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice. Proc Natl Acad Sci U S A (2001) 1.96
Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass. Eur Heart J (2002) 1.89
Indirect cystic fibrosis carrier detection. Lancet (1987) 1.76
Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Clin Exp Allergy (2013) 1.74
Genetic homogeneity at the Friedreich ataxia locus on chromosome 9. Am J Hum Genet (1989) 1.66
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes. Lancet (1986) 1.61
Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study. Am J Hum Genet (1988) 1.60
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2. Nature (1990) 1.57
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice. Nat Genet (1997) 1.51
Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. Am J Hum Genet (2001) 1.50
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease. J Intern Med (2014) 1.48
Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. Am J Hum Genet (1988) 1.48
The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12. Am J Hum Genet (1992) 1.45
Linkage of an X-chromosome cleft palate gene. Nature (1987) 1.42
Experience with new DNA markers for the diagnosis of cystic fibrosis. N Engl J Med (1988) 1.37
LOD wars: the affected-sib-pair paradigm strikes back! Am J Hum Genet (1997) 1.35
Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24. Nature (1991) 1.32
Homozygosity mapping: familiarity breeds debility. Nat Genet (1993) 1.29
Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23. Am J Hum Genet (1998) 1.28
An extension of the Maximum Lod Score method to X-linked loci. Ann Hum Genet (1995) 1.21
A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families. J Med Genet (2005) 1.16
Fine-mapping of an ancestral recombination breakpoint in DCP1. Nat Genet (1999) 1.13
Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. Am J Hum Genet (1990) 1.10
Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. Am J Hum Genet (1993) 1.08
Report of the committee on the genetic constitution of chromosomes 7 and 8. Cytogenet Cell Genet (1989) 1.06
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes. Prenat Diagn (1987) 1.05
Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes. Atherosclerosis (2008) 1.04
Prenatal diagnosis of Friedreich ataxia. Am J Med Genet (1989) 1.03
Linkage of the angiotensinogen gene locus to human essential hypertension in African Caribbeans. J Clin Invest (1995) 1.02
Twenty-five loci form a continuous linkage map of markers for human chromosome 7. Genomics (1989) 1.01
Genetic homogeneity of cystic fibrosis. Nucleic Acids Res (1986) 1.01
Resolving an apparent paradox concerning the role of TGFA in CL/P. Am J Hum Genet (1993) 1.00
Genetic differences between cystic fibrosis with and without meconium ileus. Lancet (1988) 1.00
Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions. Am J Hum Genet (1991) 0.98
Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7. Hum Genet (1987) 0.97
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. J Med Genet (1986) 0.96
An estimation of the number of susceptibility loci for isolated cleft palate. J Craniofac Genet Dev Biol (1994) 0.96
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci. Am J Hum Genet (1995) 0.95
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus. J Med Genet (1992) 0.95
Epistasis between type 2 diabetes susceptibility Loci on chromosomes 1q21-25 and 10q23-26 in northern Europeans. Ann Hum Genet (2006) 0.95
Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage. Hum Genet (1990) 0.92
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities. J Med Genet (1994) 0.91
Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia. Arterioscler Thromb (1994) 0.89
Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study. Clin Endocrinol (Oxf) (2007) 0.87
Mutational mechanisms for generating microsatellite allele-frequency distributions: an analysis of 4,558 markers. Am J Hum Genet (1998) 0.86
Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11. Am J Hum Genet (1986) 0.85
A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis. Genomics (1990) 0.85
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4. Am J Hum Genet (1986) 0.85
Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region. Genomics (1997) 0.82
Further data on linkage between cystic fibrosis and 7C22 (D7S16) Am J Hum Genet (1987) 0.81
Linkage between the cystic fibrosis locus and markers on chromosome 7q. Cytogenet Cell Genet (1986) 0.81
Gene targeting for somatic cell manipulation: rapid analysis of reduced chromosome hybrids by Alu-PCR fingerprinting and chromosome painting. Hum Mol Genet (1992) 0.81
Genetics of Alzheimer's disease. Adv Neurol (1990) 0.81
Chorea-acanthocytosis: genetic linkage to chromosome 9q21. Am J Hum Genet (1997) 0.81
The gene CYP3 encoding P450pcn1 (nifedipine oxidase) is tightly linked to the gene COL1A2 encoding collagen type 1 alpha on 7q21-q22.1. Am J Hum Genet (1988) 0.79
Absence of linkage of the epithelial sodium channel to hypertension in black Caribbeans. Am J Hypertens (1998) 0.79
Exclusion of the Friedreich ataxia gene from chromosome 19. Hum Genet (1987) 0.78
Angiotensinogen in human essential hypertension. Hypertension (1996) 0.78
Report of the committee on the genetic constitution of chromosomes 7 and 8. Cytogenet Cell Genet (1988) 0.78
Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus. Hum Mol Genet (1994) 0.77
Cystic fibrosis carrier detection using a linked gene probe. J Med Genet (1986) 0.76
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis. Am J Hum Genet (1987) 0.75
Inheritance of chronic inflammatory bowel disease. BMJ (1993) 0.75
Absence of genetic linkage between polymorphisms of the insulin receptor gene and essential hypertension. J Hum Hypertens (1995) 0.75
DNA markers for the cystic fibrosis locus. Prog Clin Biol Res (1987) 0.75
A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers. Cytogenet Cell Genet (1987) 0.75
Cystic fibrosis. Nature (1989) 0.75
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defects. Clin Genet (1994) 0.75
The cystic fibrosis locus. Enzyme (1987) 0.75
Isolation of a polymorphic genomic clone from chromosome 7. Physical and genetic linkage studies to markers around the cystic fibrosis locus. Hum Genet (1987) 0.75
The application of molecular genetics to the study of the basic defect causing cystic fibrosis. Prog Clin Biol Res (1987) 0.75
Prenatal diagnosis of cystic fibrosis using linked DNA probes. Prenat Diagn (1988) 0.75
Molecular genetics and the basic defect causing cystic fibrosis. Cold Spring Harb Symp Quant Biol (1986) 0.75
Report of the committee on the genetic constitution of chromosome 7. Cytogenet Cell Genet (1990) 0.75
Cystic fibrosis linkage exclusion data. Cytogenet Cell Genet (1986) 0.75
Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertion. Hum Genet (1990) 0.75