Published in Am J Hum Genet on November 01, 1982
Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A (1984) 48.41
Identification of more than 500 RFLPs by screening random genomic clones. Am J Hum Genet (1988) 3.01
Estimating the power of a proposed linkage study: a practical computer simulation approach. Am J Hum Genet (1986) 2.84
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. Am J Hum Genet (1984) 2.58
A confidence-set approach for finding tightly linked genomic regions. Am J Hum Genet (2001) 1.87
Construction of a map of the short arm of human chromosome 6. Proc Natl Acad Sci U S A (1986) 1.80
Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation. Am J Hum Genet (1987) 1.77
Enhancing genetic mapping of complex genomes through the design of highly-multiplexed SNP arrays: application to the large and unsequenced genomes of white spruce and black spruce. BMC Genomics (2008) 1.57
Complete switchgrass genetic maps reveal subgenome collinearity, preferential pairing and multilocus interactions. Genetics (2010) 1.54
Cytonuclear genic incompatibilities cause increased mortality in male F2 hybrids of Nasonia giraulti and N. vitripennis. Genetics (2008) 1.51
Dense genetic linkage maps of three Populus species (Populus deltoides, P. nigra and P. trichocarpa) based on AFLP and microsatellite markers. Genetics (2001) 1.49
A gene-rich linkage map in the dioecious species Actinidia chinensis (kiwifruit) reveals putative X/Y sex-determining chromosomes. BMC Genomics (2009) 1.30
Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders. Am J Hum Genet (1986) 1.18
A microsatellite-based consensus linkage map for species of Eucalyptus and a novel set of 230 microsatellite markers for the genus. BMC Plant Biol (2006) 1.16
A consensus linkage map for sugi (Cryptomeria japonica) from two pedigrees, based on microsatellites and expressed sequence tags. Genetics (2003) 1.15
Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred. Am J Hum Genet (1984) 1.14
Berry and phenology-related traits in grapevine (Vitis vinifera L.): from quantitative trait loci to underlying genes. BMC Plant Biol (2008) 1.06
An annotated genetic map of loblolly pine based on microsatellite and cDNA markers. BMC Genet (2011) 1.01
A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information. J Med Genet (1986) 0.98
Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine. BMC Genomics (2011) 0.97
A second generation genetic map of the bumblebee Bombus terrestris (Linnaeus, 1758) reveals slow genome and chromosome evolution in the Apidae. BMC Genomics (2011) 0.94
A high-density gene map of loblolly pine (Pinus taeda L.) based on exome sequence capture genotyping. G3 (Bethesda) (2014) 0.91
A genetic linkage map of the soybean cyst nematode Heterodera glycines. Mol Genet Genomics (2005) 0.90
Near-saturated and complete genetic linkage map of black spruce (Picea mariana). BMC Genomics (2010) 0.86
Construction of a genetic linkage map of the fungal pathogen of banana Mycosphaerella fijiensis, causal agent of black leaf streak disease. Curr Genet (2008) 0.81
Potential chromosomal introgression barriers revealed by linkage analysis in a hybrid of Pinus massoniana and P. hwangshanensis. BMC Plant Biol (2010) 0.81
A Picea abies linkage map based on SNP markers identifies QTLs for four aspects of resistance to Heterobasidion parviporum infection. PLoS One (2014) 0.80
Genetic Map Construction and Detection of Genetic Loci Underlying Segregation Distortion in an Intraspecific Cross of Populus deltoides. PLoS One (2015) 0.80
Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations. BMC Genomics (2015) 0.79
Preliminary study on linkage mapping based on microsatellite DNA and AFLP markers using homozygous clonal fish in ayu (Plecoglossus altivelis). Mar Biotechnol (NY) (2004) 0.75
Quantitative Trait Loci for Light Sensitivity, Body Weight, Body Size, and Morphological Eye Parameters in the Bumblebee, Bombus terrestris. PLoS One (2015) 0.75
Development of a molecular genetic linkage map for Colletotrichum lindemuthianum and segregation analysis of two avirulence genes. Curr Genet (2006) 0.75
Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet (1980) 75.25
Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation. Proc Natl Acad Sci U S A (1978) 16.54
DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man. Cell (1979) 15.74
A highly polymorphic locus in human DNA. Proc Natl Acad Sci U S A (1980) 10.27
Isolation and localization of DNA segments from specific human chromosomes. Proc Natl Acad Sci U S A (1980) 5.76
The prior probability of autosomal linkage. Ann Hum Genet (1975) 3.45
The mapping of human chromosomes. Annu Rev Genet (1971) 2.67
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
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
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
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
Loss of information due to ambiguous haplotyping of SNPs. Nat Genet (1999) 4.90
Computer programs for multilocus haplotyping of general pedigrees. Am J Hum Genet (1995) 4.51
Improved inference of relationship for pairs of individuals. Am J Hum Genet (2000) 4.47
Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet (1989) 4.42
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
Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study. Diabetes Care (1998) 3.99
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst (1997) 3.92
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature (1988) 3.82
Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet (1993) 3.76
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
The affected sib-pair method using identity by state relations. Am J Hum Genet (1986) 3.63
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
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet (2000) 3.22
Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies. Nat Genet (2001) 3.20
Extensions to pedigree analysis. IV. Covariance components models for multivariate traits. Am J Med Genet (1983) 3.10
Identifying marker typing incompatibilities in linkage analysis. Am J Hum Genet (1996) 3.06
Statistical analysis of single sodium channels. Effects of N-bromoacetamide. Biophys J (1984) 3.01
Estimating the power of a proposed linkage study: a practical computer simulation approach. Am J Hum Genet (1986) 2.84
Genetic counseling for families with inherited susceptibility to breast and ovarian cancer. JAMA (1993) 2.51
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
A single dominant gene can account for eye tracking dysfunctions and schizophrenia in offspring of discordant twins. Arch Gen Psychiatry (1988) 2.21
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
Statistical methods for polyploid radiation hybrid mapping. Genome Res (1995) 2.15
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type. J Neurogenet (1987) 2.12
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
Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet Epidemiol (1996) 2.06
Genetic linkage analysis of complex genetic traits by using affected sibling pairs. Biometrics (1998) 2.04
Application of a recombination model in calculating the variance of sib pair genetic identity. Ann Hum Genet (1979) 2.01
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet (1989) 1.99
Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc Natl Acad Sci U S A (1999) 1.91
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis. Am J Hum Genet (1993) 1.90
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis. Medicine (Baltimore) (1991) 1.89
Ascertainment and goodness of fit of variance component models for pedigree data. Prog Clin Biol Res (1984) 1.89
A look at linkage disequilibrium. Nat Genet (2000) 1.87
Nephritis caused by Streptococcus zooepidemicus (Lancefield group C). Lancet (1983) 1.86
Accurate and superaccurate gene mapping. Am J Hum Genet (1985) 1.85
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
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators. Hum Hered (1999) 1.76
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
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
Sensor-augmented pump therapy from the diagnosis of childhood type 1 diabetes: results of the Paediatric Onset Study (ONSET) after 12 months of treatment. Diabetologia (2010) 1.48
A theoretical study of some maximum likelihood algorithms for emission and transmission tomography. IEEE Trans Med Imaging (1987) 1.48
Preliminary ranking procedures for multilocus ordering. Genomics (1987) 1.45
Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq. Am J Hum Genet (1994) 1.44
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease. Science (1988) 1.44
Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11. Am J Hum Genet (1998) 1.40
The effects of conditioning on probands to correct for multiple ascertainment. Am J Hum Genet (1984) 1.40
Multilocus ordering strategies based on sperm typing. Ann Hum Genet (1990) 1.40
Two models for a maternal factor in the inheritance of Huntington disease. Am J Hum Genet (1983) 1.37
A goodness-of-fit test for the polygenic threshold model: application to pyloric stenosis. Am J Med Genet (1978) 1.37
Application of the lod method to the detection of linkage between a quantitative trait and a qualitative marker: a simulation experiment. Am J Hum Genet (1976) 1.37
Approximate confidence intervals for risk prediction in genetic counseling. Am J Hum Genet (1986) 1.31
Gamete-competition models. Am J Hum Genet (2000) 1.28
The frequency of C4B variants of complement in familial and sporadic Alzheimer disease. Alzheimer Dis Assoc Disord (1987) 1.27
A multilocus extension of the affected-pedigree-member method of linkage analysis. Am J Hum Genet (1992) 1.26
Trials, tribulations, and triumphs of the EM algorithm in pedigree analysis. IMA J Math Appl Med Biol (1989) 1.25
A primary linkage map of the human chromosome 11q22-23 region. Genomics (1990) 1.25
Experimental design and error detection for polyploid radiation hybrid mapping. Genome Res (1995) 1.24
A new class of organic nitrates: investigations on bioactivation, tolerance and cross-tolerance phenomena. Br J Pharmacol (2009) 1.24
The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease. Am J Hum Genet (1994) 1.23
Partial characterization of antigenic streptococcal plasma membrane components in acute glomerulonephritis. J Clin Invest (1970) 1.20
Effects of reproductive compensation and genetic drift on X-linked lethals. Am J Hum Genet (1978) 1.20
Ethanol stimulates formation of leukotriene C4 in rat gastric mucosa. Prostaglandins (1986) 1.19
Grouped-coordinate ascent algorithms for penalized-likelihood transmission image reconstruction. IEEE Trans Med Imaging (1997) 1.18
Penalized regression for genome-wide association screening of sequence data. Pac Symp Biocomput (2011) 1.17
The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences. Diabetes (2001) 1.17
Multipoint mapping calculations for sperm-typing data. Am J Hum Genet (1994) 1.16
Diagnosis of human cytomegalovirus-induced retinitis in human immunodeficiency virus type 1-infected subjects by using the polymerase chain reaction. J Clin Microbiol (1991) 1.16
Evidence for the in situ origin of poststreptococcal glomerulonephritis: glomerular localization of endostreptosin and the clinical significance of the subsequent antibody response. Clin Nephrol (1983) 1.16
Comments on lack of interference in the four strand model of crossing over. J Math Biol (1977) 1.15
Computational advances in maximum likelihood methods for molecular phylogeny. Genome Res (1998) 1.15
Cosegregation of open-angle glaucoma and the nail-patella syndrome. Am J Ophthalmol (1997) 1.14
Toxic effects of indocyanine green, infracyanine green, and trypan blue on the human retinal pigmented epithelium. Graefes Arch Clin Exp Ophthalmol (2005) 1.14