Published in Heredity (Edinb) on February 01, 1977
Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A (1984) 48.41
A maximum likelihood map of chromosome 1. Am J Hum Genet (1979) 4.34
A high-density consensus map of barley linking DArT markers to SSR, RFLP and STS loci and agricultural traits. BMC Genomics (2006) 3.18
Constructing large-scale genetic maps using an evolutionary strategy algorithm. Genetics (2003) 1.73
Multipoint gene mapping using seriation. I. General methods. Am J Hum Genet (1987) 1.61
Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms. Proc Natl Acad Sci U S A (1990) 1.38
Empirical power of three preliminary methods for ordering loci. Am J Hum Genet (1988) 0.87
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet (1985) 87.59
Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A (1984) 48.41
Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet (1984) 28.51
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. Genomics (1990) 13.23
Construction of human linkage maps: likelihood calculations for multilocus linkage analysis. Genet Epidemiol (1986) 8.95
A closely linked genetic marker for cystic fibrosis. Nature (1985) 7.85
Resolution of linkage for irregular phenotype systems. Hum Hered (1981) 6.99
Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19. Cytogenet Cell Genet (1985) 6.88
Molecular basis of human hypertension: role of angiotensinogen. Cell (1992) 6.07
A unified model for complex segregation analysis. Am J Hum Genet (1983) 5.67
Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet (1985) 5.61
Complex segregation analysis with pointers. Hum Hered (1981) 5.59
A maximum likelihood map of chromosome 1. Am J Hum Genet (1979) 4.34
A primary genetic map of markers of human chromosome 10. Genomics (1988) 4.23
A primary genetic map of chromosome 13q. Am J Hum Genet (1986) 4.01
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Am J Hum Genet (1986) 3.83
A mapped set of DNA markers for human chromosome 17. Genomics (1988) 3.55
A chimaeric 11 beta-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature (1992) 3.40
Efficient computations in multilocus linkage analysis. Am J Hum Genet (1988) 3.39
Elements of a paracrine tubular renin-angiotensin system along the entire nephron. Hypertension (1999) 3.33
Genotyping and sequence analysis of apolipoprotein E isoforms. Genomics (1988) 3.20
Isolation and mapping of a polymorphic DNA sequence (pTHH22) on chromosome 9 [D9S12]. Nucleic Acids Res (1988) 3.17
A mapped set of genetic markers for human chromosome 9. Genomics (1988) 2.80
Combined linkage and segregation analysis using regressive models. Am J Hum Genet (1988) 2.33
Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps. N Engl J Med (1990) 2.32
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro. J Clin Invest (1997) 2.23
A detailed genetic map of the long arm of chromosome 11. Genomics (1990) 2.11
The CEPH consortium linkage map of human chromosome 1. Genomics (1991) 2.09
Robustness and power of the unified model in the analysis of quantitative measurements. Am J Hum Genet (1986) 1.98
Tests of gene order from three-locus linkage data. Ann Hum Genet (1987) 1.87
Characterization of eight VNTR loci by agarose gel electrophoresis. Genomics (1989) 1.74
Angiotensin-converting enzyme gene polymorphism is associated with myocardial infarction but not with development of coronary stenosis. Circulation (1995) 1.73
Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. Genomics (1987) 1.70
A systematic study of HLA class II-beta DNA restriction fragments in insulin-dependent diabetes mellitus. Proc Natl Acad Sci U S A (1985) 1.69
Tightly linked markers for the neurofibromatosis type 1 gene. Genomics (1987) 1.68
Missense mutation (Gly----Glu188) of human lipoprotein lipase imparting functional deficiency. J Biol Chem (1990) 1.57
Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44). Nucleic Acids Res (1987) 1.51
Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30). Nucleic Acids Res (1987) 1.48
Isolation and mapping of a polymorphic DNA sequence (pEFD145) on chromosome 3 [D3S32]. Nucleic Acids Res (1988) 1.47
Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30]. Nucleic Acids Res (1988) 1.44
Genetic counseling in sex linkage. Birth Defects Orig Artic Ser (1979) 1.43
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. Genomics (1989) 1.40
Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature (1989) 1.40
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. Genomics (1990) 1.38
Detection of linkage between a quantitative trait and a marker locus by the lod score method: sample size and sampling considerations. Ann Hum Genet (1988) 1.35
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension. Nat Genet (1992) 1.34
Genetic epidemiology of Lesch-Nyhan disease. Am J Hum Genet (1977) 1.33
Lipoprotein lipase. Molecular model based on the pancreatic lipase x-ray structure: consequences for heparin binding and catalysis. J Biol Chem (1994) 1.33
Clusters of HLA class II beta restriction fragments describe allelic series. Proc Natl Acad Sci U S A (1984) 1.32
Genetic linkage between lipoprotein(a) phenotype and a DNA polymorphism in the plasminogen gene. Genomics (1988) 1.31
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene. Nucleic Acids Res (1990) 1.29
Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy. Circulation (1992) 1.29
Isolation and mapping of a polymorphic DNA sequence pHHH202 on chromosome 17 [D17S33]. Nucleic Acids Res (1988) 1.27
An extended genetic linkage map of markers for human chromosome 10. Genomics (1988) 1.26
Linkage studies in spinocerebellar ataxia (SCA). Am J Med Genet (1980) 1.25
Etiological heterogeneity in X-linked spastic paraplegia. Am J Hum Genet (1987) 1.25
Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension. JAMA (1988) 1.25
Frequent recombination is observed in the distal end of the long arm of chromosome 14. Genomics (1989) 1.24
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). Am J Hum Genet (1990) 1.24
Haplotypes of angiotensinogen in essential hypertension. Am J Hum Genet (1997) 1.23
Bioassay of kinship in a South American Indian population. Am J Hum Genet (1973) 1.22
A primary map of ten DNA markers and two serological markers for human chromosome 19. Genomics (1988) 1.22
Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15). Nucleic Acids Res (1987) 1.22
Renin and kallikrein in connecting tubule of mouse. Kidney Int (2003) 1.22
Sets of linked genetic markers for human chromosomes. Annu Rev Genet (1988) 1.20
Genetic regulation of plasma and red blood cell magnesium concentration in man. II. Segregation analysis. Am J Hum Genet (1983) 1.19
A mutation of angiotensinogen in a patient with preeclampsia leads to altered kinetics of the renin-angiotensin system. J Biol Chem (1995) 1.19
Angiotensinogen as a risk factor for essential hypertension in Japan. J Clin Invest (1994) 1.18
Isolation and mapping of a polymorphic DNA sequence pMLJ14 on chromosome 14 [D14S13]. Nucleic Acids Res (1988) 1.18
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22). Nucleic Acids Res (1983) 1.17
Blunted renal vascular response to angiotensin II is associated with a common variant of the angiotensinogen gene and obesity. J Hypertens (1996) 1.16
Linkage disequilibrium between DNA markers at the low-density lipoprotein receptor gene. Genet Epidemiol (1990) 1.15
A BglII RFLP at the lipoprotein lipase gene. Nucleic Acids Res (1989) 1.14
Construction of human genetic linkage maps: I. Progress and perspectives. Cold Spring Harb Symp Quant Biol (1986) 1.10
Isolation and mapping of a polymorphic DNA sequence pHBI18P2 on chromosome 11 [D11S147]. Nucleic Acids Res (1988) 1.10
Twelve loci form a continuous linkage map for human chromosome 18. Genomics (1988) 1.07
A primary map of 24 loci on human chromosome 16. Genomics (1990) 1.07
DNA polymorphism of HLA class I and class II regions. Immunol Rev (1985) 1.06
Genetic regulation of plasma and red blood cell magnesium concentrations in man. I. Univariate and bivariate path analyses. Am J Hum Genet (1982) 1.05
A mapped set of DNA markers for human chromosome 15. Genomics (1988) 1.04
Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84]. Nucleic Acids Res (1988) 1.02
Construction of human genetic linkage maps: II. Methodological issues. Cold Spring Harb Symp Quant Biol (1986) 1.02
An extended genetic linkage map and an "index" map for human chromosome 17. Genomics (1993) 1.01
Complex segregation analysis of hyperlipidemia in a Seattle sample. Hum Hered (1982) 1.01
Path analysis under generalized assortative mating. II. American I.Q. Genet Res (1982) 1.01
Twenty-five loci form a continuous linkage map of markers for human chromosome 7. Genomics (1989) 1.01
Immunoglobulin E revisited. Am J Hum Genet (1980) 1.01
Recurrence risks in complex inheritance with special regard to pyloric stenosis. J Med Genet (1977) 1.00
Isolation and mapping of a polymorphic DNA sequence (pYNZ32) on chromosome 4p [D4S125]. Nucleic Acids Res (1988) 1.00
Guidelines of the National Heart, Lung, and Blood Institute Working Group on Blood Drawing, Processing, and Storage for Genetic Studies. Am J Epidemiol (1996) 0.99
Isolation and mapping of a polymorphic DNA sequence pEFD126.3 on chromosome 9q (D9S7). Nucleic Acids Res (1987) 0.99
Topology of kinship in Micronesia. Am J Hum Genet (1973) 0.98
Cellular catabolism of normal very low density lipoproteins via the low density lipoprotein receptor-related protein/alpha 2-macroglobulin receptor is induced by the C-terminal domain of lipoprotein lipase. J Biol Chem (1994) 0.98
Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia. Am J Cardiol (1989) 0.98
Chromosome mapping with DNA markers. Sci Am (1988) 0.98
Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene. Am J Hum Genet (1990) 0.97
Angiotensinogen T235 expression is elevated in decidual spiral arteries. J Clin Invest (1997) 0.97
Angiotensinogen Thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first-trimester decidua. Am J Obstet Gynecol (1999) 0.97
Kinship and inbreeding on Namu Atoll (Marshall Islands). Hum Biol (1972) 0.96
Isolation and mapping of a polymorphic DNA sequence (pEKMDA2-I) on chromosome 16 [D16S83]. Nucleic Acids Res (1988) 0.96