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Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.

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Molecular Population Genetics of the Northern Elephant Seal Mirounga angustirostris

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Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.

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Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function

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The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3

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Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)

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Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

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Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.

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Association mapping identifies quantitative trait loci (QTL) for digestibility in rice straw

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Integration of association statistics over genomic regions using Bayesian adaptive regression splines

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Discovery of Cancer Susceptibility Genes: Study Designs, Analytic Approaches, and Trends in Technology

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Are moment bounds on the recombination fraction between a marker and a disease locus too good to be true? Allelic association mapping revisited for simple genetic diseases in the Finnish population.

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Genomewide Markers for Controlling Background Variation in Association Mapping

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Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

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The power of the transmission disequilibrium test (TDT) with both case–parent and control–parent trios

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Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium

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Finding similarities and differences among genomes

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Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions

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Issues and Strategies in the Genetic Analysis of Alcoholism and Related Addictive Behaviors

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Microsatellite, restriction fragment-length polymorphism, and sequence-specific oligonucleotide typing of the tumor necrosis factor region comparisons of the 4AOHW cell panel

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Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.Preprint

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Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population

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Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus

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Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis.

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Assignment of the Locus for a New Lethal Neonatal Metabolic Syndrome to 2q33-37

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Polymorphic microsatellites and Wilson disease (WD).

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Robust LOD scores for variance component-based linkage analysis

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Giant axonal neuropathy locus refinement to a < 590 kb critical interval

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Gene for a tissue-specific transcriptional activator (EBF or Olf-1), expressed in early B lymphocytes, adipocytes, and olfactory neurons, is located on human Chromosome 5, band q34, and proximal mouse Chromosome 11

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Mutational analysis of the human mitochondrial genome branches into the realm of bacterial genetics.

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Selected Methodological Issues in Meiotic Mapping of Obesity Genes in Humans: Issues of Power and Efficiency

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Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22

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Analysis of Genetic Linkage Data for Mendelian Traits

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Global Genetic Analysis

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A General Statistical Framework for Unifying Interval and Linkage Disequilibrium Mapping

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Relationship between case-control studies and the transmission/disequilibrium test

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Multipoint Linkage-Disequilibrium–Mapping Approach Based on the Case-Parent Trio Design

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Lung cancer risk in families of nonsmoking probands: Heterogeneity by age at diagnosis

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Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome

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Founder mutations among the Dutch*

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Human Microsatellites: Mutation and Evolution

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Genetic homogeneity of cartilage-hair hypoplasia

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Sulfate Transport in Chondrodysplasia,a

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Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity

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Classical Twin Design in Modern Pharmacogenomics Studies

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Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae

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POPSIM: a general population simulation program.

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The comparative patterns of linkade disequilibrium in European populations and its implication for genetic association studies

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A chronology of fine-scale gene mapping by linkage disequilibrium

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Multilocus genomics of outcrossing plant populations

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Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function

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Joint Tests of Linkage and Association for Quantitative Traits

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Localization of a Gene for Molybdenum Cofactor Deficiency, on the Short Arm of Chromosome 6, by Homozygosity Mapping

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Repetitive DNA sequences: Some considerations for simple sequence repeats

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Molecular Epidemiology of Hereditary Nonpolyposis Colorectal Cancer in Finland

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Novel association suggests multiple independent QTLs within chromosome 5q21–33 region control variation in total humans IgE levels

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Linkage to Gaucher Mutations in the Ashkenazi Population: Effect of Drift on Decay of Linkage Disequilibrium and Evidence for Heterozygote Selection

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Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11

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Founder variants and population genomes—Toward precision medicine

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Genetic Mapping in Forest Trees: Markers, Linkage Analysis and Genomics

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Quantitative genetics, genomics and the future of plant breeding.

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The Quest for Genes Causing Complex Traits in Ocular Medicine

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Prospects for Association-Based Fine Mapping of a Susceptibility Gene for a Complex Disease

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The human genome project: a historical perspective

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PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confirm the assignment to the EPM1 locus

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Structure of Linkage Disequilibrium in Humans: Genome Factors and Population StratificationPreprint

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NFκB1: a common biomarker linking Alzheimer's and Parkinson's disease pathology

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Basic molecular genetics for epidemiologists

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On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case–control samples

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Cartilage Disorders: The importance of being sulphated

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Assessing candidate genes as risk factors for mental disorders: the value of population-based epidemiological studies

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A comparison between methods for linkage disequilibrium fine mapping of quantitative trait loci

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Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families

Kotze, M. J., de Villiers, J. N. P., Groenewald, J. Z., Rooney, R. N., Loubser, O., Thiart, R., Oosthuizen, C. J., Niekerk, M. M. V., Groenewald, I. M., Retief, A. E., et al. (1998) · Molecular and Cellular Probes · doi:10.1006/mcpr.1998.0188 · Cited by 13

Theoretical strategies for high-resolution mapping of complex genetic disorders in humans

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Monoamine oxidases and alcoholism. II. Studies in alcoholic families

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Genome scanning methods

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Allelic association is increased by correlation of effective family size

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Association Mapping: A New Paradigm for Dissection of Complex Traits in Crops

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Estimating the number of founder lineages from haplotypes of closely linked SNPs

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Association Analysis and Its Application in Plant Genetic Research

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Specific mutations in the HEXA gene among Iraqi Jewish Tay-Sachs disease carriers: dating of founder ancestor

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Refinement of the DFNA41 locus and candidate genes analysis

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Bivariate familial correlation analysis of quantitative traits by use of estimating equations: Application to a familial analysis of the insulin resistance syndrome

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Drug-Targeted Genomes: Mutability of Ion Channels and GPCRs

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Identify LD blocks based on hierarchical spatial data

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Linkage disequilibrium interval mapping of quantitative trait loci

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Infantile Onset Spinocerebellar Ataxia Represents an Allelic Disease Distinct from Other Hereditary Ataxias

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Modeling Linkage Disequilibrium Between a Polymorphic Marker Locus and a Locus Affecting Complex Dichotomous Traits in Natural Populations

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A semiparametric test to detect associations between quantitative traits and candidate genes in structured populations

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Mapping of the variegate porphyria (VP) gene: Contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32

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Estimating Linkage Disequilibrium Between a Polymorphic Marker Locus and a Trait Locus in Natural Populations

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Linkage disequilibrium under polysomic inheritance

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Advanced glossary on genetic epidemiology

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Linkage disequilibrium mapping in isolated populations: The example of Finland revisited

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The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

Varilo, T. (2002) · Human Molecular Genetics · doi:10.1093/hmg/12.1.51 · Cited by 8

A comparison of genetic map distance and linkage disequilibrium between 15 polymorphic dinucleotide repeat loci in two populations

Urbanek, M., Goldman, D. A., & Long, J. C. (1994) · The American Journal of Human Genetics

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

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