Published in Am J Hum Genet on September 01, 1994
High-resolution patterns of meiotic recombination across the human major histocompatibility complex. Am J Hum Genet (2002) 2.71
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping. Am J Hum Genet (2000) 1.74
Individual variation in recombination among human males. Am J Hum Genet (1996) 1.22
Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus. Am J Hum Genet (1996) 1.00
Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. Am J Hum Genet (1998) 0.89
Absence of age effect on meiotic recombination between human X and Y chromosomes. Am J Hum Genet (2002) 0.79
SPERMSEG: analysis of segregation distortion in single-sperm data. Am J Hum Genet (1999) 0.78
Constructing the parental linkage phase and the genetic map over distances <1 cM using pooled haploid DNA. Genetics (2005) 0.75
The behavior of meiosis in sperm. Am J Hum Genet (1994) 0.75
Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol (1988) 13.73
Amplification and analysis of DNA sequences in single human sperm and diploid cells. Nature (1988) 10.84
Whole genome amplification from a single cell: implications for genetic analysis. Proc Natl Acad Sci U S A (1992) 9.15
Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. Proc Natl Acad Sci U S A (1989) 3.50
Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: experimental design considerations. Am J Hum Genet (1989) 1.83
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics (1991) 1.69
Multilocus ordering strategies based on sperm typing. Ann Hum Genet (1990) 1.40
Trials, tribulations, and triumphs of the EM algorithm in pedigree analysis. IMA J Math Appl Med Biol (1989) 1.25
Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm. Am J Hum Genet (1993) 0.90
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science (1985) 95.08
Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet (1996) 17.95
Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees. Hum Hered (1975) 16.67
A gene map of the human genome. Science (1996) 14.32
Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol (1988) 13.73
The affected-pedigree-member method of linkage analysis. Am J Hum Genet (1988) 13.67
Amplification and analysis of DNA sequences in single human sperm and diploid cells. Nature (1988) 10.84
Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA. Nucleic Acids Res (1987) 10.38
Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes. Cell (1988) 10.29
Whole genome amplification from a single cell: implications for genetic analysis. Proc Natl Acad Sci U S A (1992) 9.15
Detection of human papilloma virus in paraffin-embedded tissue using the polymerase chain reaction. J Exp Med (1988) 9.10
A simple method for site-directed mutagenesis using the polymerase chain reaction. Nucleic Acids Res (1989) 6.78
A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human delta and beta globin genes. Nucleic Acids Res (1981) 6.70
EM reconstruction algorithms for emission and transmission tomography. J Comput Assist Tomogr (1984) 6.54
Statistical analysis of multilocus recombination. Biometrics (1983) 6.49
An alternative model of recombination and interference. Ann Hum Genet (1979) 6.26
Estimating kinetic constants from single channel data. Biophys J (1983) 6.14
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat Genet (1996) 6.06
Extensions to pedigree analysis. III. Variance components by the scoring method. Ann Hum Genet (1976) 5.86
A conditional inference framework for extending the transmission/disequilibrium test. Hum Hered (1998) 5.70
Heterogeneity of the ribosomal genes in mice and men. Cell (1977) 5.36
How many polymorphic genes will it take to span the human genome? Am J Hum Genet (1982) 5.11
A radiation hybrid map of the human genome. Hum Mol Genet (1996) 4.75
5' flanking region of immunoglobulin heavy chain constant region genes displays length heterogeneity in germlines of inbred mouse strains. Cell (1980) 4.62
Computer programs for multilocus haplotyping of general pedigrees. Am J Hum Genet (1995) 4.51
Use of population isolates for mapping complex traits. Nat Rev Genet (2000) 4.28
An algorithm for automatic genotype elimination. Am J Hum Genet (1987) 4.18
Metropolis sampling in pedigree analysis. Stat Methods Med Res (1993) 4.04
The polymerase chain reaction. Trends Genet (1989) 3.95
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst (1997) 3.92
Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes. Proc Natl Acad Sci U S A (1980) 3.92
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature (1988) 3.82
The role of early HIV infection in the spread of HIV through populations. J Acquir Immune Defic Syndr Hum Retrovirol (1997) 3.75
Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods. Hum Hered (1983) 3.74
Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR. Nucleic Acids Res (1992) 3.74
Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons. Neuron (1998) 3.72
The affected sib-pair method using identity by state relations. Am J Hum Genet (1986) 3.63
Detection of cytomegalovirus DNA in peripheral blood of patients infected with human immunodeficiency virus. J Infect Dis (1988) 3.52
Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. Proc Natl Acad Sci U S A (1989) 3.50
The prior probability of autosomal linkage. Ann Hum Genet (1975) 3.45
Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis. N Engl J Med (1987) 3.44
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell (1995) 3.34
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet (2000) 3.22
Human nucleolus organizers on nonhomologous chromosomes can share the same ribosomal gene variants. Proc Natl Acad Sci U S A (1981) 3.21
Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res (1990) 3.13
Extensions to pedigree analysis. IV. Covariance components models for multivariate traits. Am J Med Genet (1983) 3.10
Statistical analysis of single sodium channels. Effects of N-bromoacetamide. Biophys J (1984) 3.01
The evolutionarily conserved repetitive sequence d(TG.AC)n promotes reciprocal exchange and generates unusual recombinant tetrads during yeast meiosis. Mol Cell Biol (1986) 2.86
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. Proc Natl Acad Sci U S A (1992) 2.83
Distribution of ribosomal gene length variants among mouse chromosomes. Proc Natl Acad Sci U S A (1982) 2.66
Species-specific rDNA transcription is due to promoter-specific binding factors. Mol Cell Biol (1984) 2.51
A multiple-tubes approach for accurate genotyping of very small DNA samples by using PCR: statistical considerations. Am J Hum Genet (1992) 2.42
EM algorithms without missing data. Stat Methods Med Res (1997) 2.39
The calcium scare--what would Austin Bradford Hill have thought? Osteoporos Int (2011) 2.35
Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction. Proc Natl Acad Sci U S A (1990) 2.33
Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair. Nat Genet (1998) 2.32
Permanence and the dynamics of biological systems. Math Biosci (1992) 2.28
A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins. Arch Gen Psychiatry (1988) 2.21
Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci. Proc Natl Acad Sci U S A (1985) 2.19
Using PCR in preimplantation genetic disease diagnosis. Hum Reprod (1991) 2.18
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain. Nat Genet (1992) 2.16
Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet (1991) 2.16
Fast computation of genetic likelihoods on human pedigree data. Hum Hered (1992) 2.15
New HLA-DPB1 alleles generated by interallelic gene conversion detected by analysis of sperm. Nat Genet (1995) 2.14
Hydroxylated quantum dots as luminescent probes for in situ hybridization. J Am Chem Soc (2001) 2.12
Identification of the in vivo and in vitro origin of transcription in human rDNA. Nucleic Acids Res (1982) 2.11
NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees. Am J Med Genet (1998) 2.09
Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium. Am J Hum Genet (1995) 2.07
Analysis of DNA sequences in forty-year-old paraffin-embedded thin-tissue sections: a bridge between molecular biology and classical histology. Cancer Res (1988) 2.06
Genetic analysis using the polymerase chain reaction. Annu Rev Genet (1992) 2.06
Application of a recombination model in calculating the variance of sib pair genetic identity. Ann Hum Genet (1979) 2.01
Bacteriophage T7 lysozyme is an N-acetylmuramyl-L-alanine amidase. J Biol Chem (1973) 1.92
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis. Medicine (Baltimore) (1991) 1.89
Structure and organization of the highly repeated and interspersed 1.3 kb EcoRI-Bg1II sequence family in mice. Nucleic Acids Res (1980) 1.89
Ascertainment and goodness of fit of variance component models for pedigree data. Prog Clin Biol Res (1984) 1.89
Nephritis caused by Streptococcus zooepidemicus (Lancefield group C). Lancet (1983) 1.86
Accurate and superaccurate gene mapping. Am J Hum Genet (1985) 1.85
Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: experimental design considerations. Am J Hum Genet (1989) 1.83
Triplet repeats form secondary structures that escape DNA repair in yeast. Proc Natl Acad Sci U S A (1999) 1.83
Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm. Proc Natl Acad Sci U S A (2006) 1.80
Stimulation of human leukocyte thromboplastic activity by endotoxin. Proc Soc Exp Biol Med (1971) 1.79
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
The genetic behaviour of a cloned mouse ribosomal DNA segment mimics mouse ribosomal gene evolution. J Mol Biol (1979) 1.75
Mouse rDNA nontranscribed spacer sequences are found flanking immunoglobulin CH genes and elsewhere throughout the genome. Cell (1980) 1.74
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping. Am J Hum Genet (2000) 1.74
A first-generation whole genome-radiation hybrid map spanning the mouse genome. Genome Res (1997) 1.73
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. Am J Hum Genet (2001) 1.72
Ethylene detection in fruit supply chains. Philos Trans A Math Phys Eng Sci (2014) 1.72
Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium. Am J Med Genet (1998) 1.72
Routine immunohistology in renal diseases. Ann Intern Med (1966) 1.69
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics (1991) 1.69
The genetic transmission of schizophrenia: application of Mendelian latent structure analysis to eye tracking dysfunctions in schizophrenia and affective disorder. J Psychiatr Res (1986) 1.65
Nup50, a nucleoplasmically oriented nucleoporin with a role in nuclear protein export. Mol Cell Biol (2000) 1.64
Characterization of mouse ribosomal gene fragments purified by molecular cloning. Gene (1979) 1.64
Recombination hot spot in the human beta-globin gene cluster: meiotic recombination of human DNA fragments in Saccharomyces cerevisiae. Mol Cell Biol (1985) 1.63
Spontaneous closure of the human fetal ductus arteriosus--A cause of fetal congestive heart failure. Am J Obstet Gynecol (1996) 1.61