Estimating the frequency of nonpaternity in Switzerland.

PubWeight™: 1.16‹?› | Rank: Top 10%

🔗 View Article (PMID 7860087)

Published in Hum Hered on March 22, 1995

Authors

G Sasse1, H Müller, R Chakraborty, J Ott

Author Affiliations

1: Department of Research, Kantonsspital, University of Basel, Switzerland.

Articles by these authors

(truncated to the top 100)

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

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet (1974) 23.66

Statistical studies on protein polymorphism in natural populations. I. Distribution of single locus heterozygosity. Genetics (1977) 17.08

The rapid generation of oligonucleotide-directed mutations at high frequency using phosphorothioate-modified DNA. Nucleic Acids Res (1985) 12.11

Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res (2001) 9.41

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Hum Hered (1992) 8.71

VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. Genetics (1993) 8.22

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet (1996) 6.58

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics (1992) 6.40

A computer program for linkage analysis of general human pedigrees. Am J Hum Genet (1976) 6.01

Signatures of population expansion in microsatellite repeat data. Genetics (1998) 5.76

Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet (1985) 5.61

Kin selection, social structure, gene flow, and the evolution of chimpanzees. Science (1994) 5.08

The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods. Ann Hum Genet (1986) 5.02

Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genet Epidemiol (1993) 4.98

Crystal structure of the outer membrane active transporter FepA from Escherichia coli. Nat Struct Biol (1999) 4.86

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature (1989) 4.69

Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis. Ann Hum Genet (1977) 4.54

Exclusion of paternity: the current state of the art. Am J Hum Genet (1974) 4.43

Genetic distance and electrophoretic identity of proteins between taxa. J Mol Evol (1973) 4.19

Relationship estimation in affected sib pair analysis of late-onset diseases. Eur J Hum Genet (1997) 4.16

Linkage analysis and family classification under heterogeneity. Ann Hum Genet (1983) 3.76

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

Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. Am J Hum Genet (1999) 3.60

Infinite allele model with varying mutation rate. Proc Natl Acad Sci U S A (1976) 3.56

Individual admixture estimates: disease associations and individual risk of diabetes and gallbladder disease among Mexican-Americans in Starr County, Texas. Am J Phys Anthropol (1986) 3.52

CODIS STR loci data from 41 sample populations. J Forensic Sci (2001) 3.43

Maximum likelihood estimation by counting methods under polygenic and mixed models in human pedigrees. Am J Hum Genet (1979) 3.36

Identification of differentially expressed mRNA species by an improved display technique (DDRT-PCR). Nucleic Acids Res (1993) 3.26

Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. Am J Hum Genet (1995) 3.12

The p53MH algorithm and its application in detecting p53-responsive genes. Proc Natl Acad Sci U S A (2002) 3.11

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE. Am J Hum Genet (1991) 3.07

An adoption study of human obesity. N Engl J Med (1986) 3.07

A major Pseudomonas aeruginosa clone common to patients and aquatic habitats. Appl Environ Microbiol (1994) 3.02

A simple scheme for the analysis of HLA linkages in pedigrees. Ann Hum Genet (1978) 3.01

Apaf-1 is a transcriptional target for E2F and p53. Nat Cell Biol (2001) 2.96

CDC25A phosphatase is a target of E2F and is required for efficient E2F-induced S phase. Mol Cell Biol (1999) 2.84

Cyclin D1 protein expression and function in human breast cancer. Int J Cancer (1994) 2.81

Report of the committee on linkage and gene order. Cytogenet Cell Genet (1989) 2.76

Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet (1987) 2.73

Relationship of prevalence of non-insulin-dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas. Genet Epidemiol (1986) 2.71

Frequencies of complex diseases in hybrid populations. Am J Phys Anthropol (1986) 2.68

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet (2001) 2.68

Endoscopic mucosal resection of early cancer and high-grade dysplasia in Barrett's esophagus. Gastroenterology (2000) 2.66

A novel measure of genetic distance for highly polymorphic tandem repeat loci. Mol Biol Evol (1995) 2.65

Malignant ameloblastoma or ameloblastic carcinoma. Oral Surg Oral Med Oral Pathol (1984) 2.51

Linkage studies in a large kindred with familial hypercholesterolemia. Am J Hum Genet (1974) 2.49

Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis. Genet Epidemiol (1990) 2.47

Predisposition to familial osteoarthrosis linked to type II collagen gene. Lancet (1989) 2.43

Testing the neutral mutation hypothesis by distribution of single locus heterozygosity. Nature (1976) 2.37

A microsatellite genetic linkage map of human chromosome 18. Genomics (1993) 2.35

A genomewide screen for autism susceptibility loci. Am J Hum Genet (2001) 2.30

The Tim core complex defines the number of mitochondrial translocation contact sites and can hold arrested preproteins in the absence of matrix Hsp70-Tim44. EMBO J (1997) 2.28

Identification of a novel common genetic risk factor for lumbar disk disease. JAMA (2001) 2.28

Mitochondrial protein import: biochemical and genetic evidence for interaction of matrix hsp70 and the inner membrane protein MIM44. J Cell Biol (1994) 2.28

Lysosomal (vacuolar) proteinases of yeast are essential catalysts for protein degradation, differentiation, and cell survival. J Biol Chem (1989) 2.25

Alopecia universalis associated with a mutation in the human hairless gene. Science (1998) 2.23

Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. Arch Ophthalmol (1998) 2.19

A chi-square test to distinguish allelic association from other causes of phenotypic association between two loci. Genet Epidemiol (1985) 2.15

CD8(+) lymphocytes respond to different HIV epitopes in seronegative and infected subjects. J Clin Invest (2001) 2.15

Evaluation of 13 short tandem repeat loci for use in personal identification applications. Am J Hum Genet (1994) 2.15

E2F-6: a novel member of the E2F family is an inhibitor of E2F-dependent transcription. Oncogene (1998) 2.12

DNA tumor virus oncoproteins and retinoblastoma gene mutations share the ability to relieve the cell's requirement for cyclin D1 function in G1. J Cell Biol (1994) 2.11

Risk calculations under heterogeneity. Am J Hum Genet (1989) 2.07

Estimation of race admixture--a new method. Am J Phys Anthropol (1975) 2.06

Selecting SNPs in two-stage analysis of disease association data: a model-free approach. Ann Hum Genet (2000) 2.05

Genetic susceptibility to heroin addiction: a candidate gene association study. Genes Brain Behav (2008) 2.00

In vivo biosynthesis of the vacuolar proteinases A and B in the yeast Saccharomyces cerevisiae. J Biol Chem (1982) 1.98

Measures of variation at DNA repeat loci under a general stepwise mutation model. Theor Popul Biol (1996) 1.97

Sec8p and Sec15p are components of a plasma membrane-associated 19.5S particle that may function downstream of Sec4p to control exocytosis. J Cell Biol (1992) 1.96

Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Hum Genet (2000) 1.95

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet (1991) 1.93

Inbreeding and risk of late onset complex disease. J Med Genet (2003) 1.92

Equine connective tissue tumors contain unintegrated bovine papilloma virus DNA. J Virol (1980) 1.90

Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7. Am J Hum Genet (1991) 1.89

Linkage analysis with misclassification at one locus. Clin Genet (1977) 1.89

Detection of nonrandom association of alleles from the distribution of the number of heterozygous loci in a sample. Genetics (1984) 1.88

True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms. Hum Hered (1999) 1.88

Tests of gene order from three-locus linkage data. Ann Hum Genet (1987) 1.87

Sec2 protein contains a coiled-coil domain essential for vesicular transport and a dispensable carboxy terminal domain. J Cell Biol (1990) 1.86

An allele of COL9A2 associated with intervertebral disc disease. Science (1999) 1.85

Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am J Hum Genet (1993) 1.84

Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA). J Forensic Sci (1998) 1.80

Polynesian origins: insights from the Y chromosome. Proc Natl Acad Sci U S A (2000) 1.79

Phaeohyphomycosis caused by Phaeoacremonium inflatipes. J Clin Microbiol (1998) 1.78

Antibodies to high molecular weight polypeptides of desmosomes: specific localization of a class of junctional proteins in cells and tissue. Differentiation (1981) 1.77

Dynamics of repeat polymorphisms under a forward-backward mutation model: within- and between-population variability at microsatellite loci. Genetics (1996) 1.77

Maturation of vacuolar (lysosomal) enzymes in yeast: proteinase yscA and proteinase yscB are catalysts of the processing and activation event of carboxypeptidase yscY. EMBO J (1987) 1.76

GT repeats are associated with recombination on human chromosome 22. Genome Res (2000) 1.75

Scan statistics to scan markers for susceptibility genes. Proc Natl Acad Sci U S A (2000) 1.73

Family cell lines available for research. Am J Hum Genet (1990) 1.72

Risk factors for postoperative bleeding after thyroid surgery. Br J Surg (2012) 1.72

Preprotein translocase of the outer mitochondrial membrane: molecular dissection and assembly of the general import pore complex. Mol Cell Biol (1998) 1.71

Anaerobic benzene oxidation coupled to nitrate reduction in pure culture by two strains of Dechloromonas. Nature (2001) 1.71

Goodness-of-fit tests for locus order in three-point mapping. Genet Epidemiol (1987) 1.71

Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. Am J Hum Genet (1982) 1.69

A power analysis of microsatellite-based statistics for inferring past population growth. Mol Biol Evol (2000) 1.69

Abnormal patterns of D-type cyclin expression and G1 regulation in human head and neck cancer. Cancer Res (1995) 1.68

Epidemiology and factor analysis of obesity, type II diabetes, hypertension, and dyslipidemia (syndrome X) on the Island of Kosrae, Federated States of Micronesia. Hum Hered (2001) 1.67