scholarly article | Q13442814 |
P819 | ADS bibcode | 2000PNAS...97....2O |
P356 | DOI | 10.1073/PNAS.97.1.2 |
P932 | PMC publication ID | 33508 |
P698 | PubMed publication ID | 10618359 |
P5875 | ResearchGate publication ID | 51363881 |
P2093 | author name string | Ott J | |
P2860 | cites work | The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping | Q24321747 |
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis | Q24322669 | ||
Gene mapping in isolated populations: new roles for old friends? | Q28146139 | ||
Identification of the cystic fibrosis gene: genetic analysis | Q29614402 | ||
Linkage disequilibrium in Huntington's disease: an improved localisation for the gene | Q33593370 | ||
Allelic association between marker loci | Q35006287 | ||
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes | Q35250515 | ||
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval | Q35642894 | ||
Mapping a disease locus by allelic association | Q35887837 | ||
Genetic epidemiology of single-nucleotide polymorphisms. | Q36783218 | ||
Linkage disequilibrium as a gene-mapping tool. | Q42951153 | ||
Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3. | Q45291152 | ||
Positional cloning of disease genes: advantages of genetic isolates | Q47697449 | ||
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland | Q55671005 | ||
Limb Girdle Muscular Dystrophy Type 2A (CAPN3): Mapping Using Allelic Association | Q57398259 | ||
Human genetics: the molecular challenge | Q68759889 | ||
Demographic history and linkage disequilibrium in human populations | Q73941561 | ||
Prospects for whole-genome linkage disequilibrium mapping of common disease genes | Q77883184 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | linkage disequilibrium | Q2064311 |
P304 | page(s) | 2-3 | |
P577 | publication date | 2000-01-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Predicting the range of linkage disequilibrium | |
P478 | volume | 97 |
Q39224910 | 2015 Curt Stern Award |
Q42696196 | A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs |
Q31059859 | A new method for detecting human recombination hotspots and its applications to the HapMap ENCODE data |
Q48557029 | Ancestral origins of the prion protein gene D178N mutation in the Basque Country |
Q34186026 | Association study designs for complex diseases |
Q48905215 | Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples |
Q30625643 | Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease |
Q36828742 | Genetic variants in the cocaine- and amphetamine-regulated transcript gene (CARTPT) and cocaine dependence |
Q53975421 | Genome-wide search for markers associated with bovine spongiform encephalopathy. |
Q24799062 | Haplotype analysis of the PPARgamma Pro12Ala and C1431T variants reveals opposing associations with body weight. |
Q22337263 | How many diseases does it take to map a gene with SNPs? |
Q46657347 | Influence of the C161T but not Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-gamma on colorectal cancer in an Indian population. |
Q28190352 | Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex |
Q34511206 | Linkage disequilibrium: what history has to tell us. |
Q57306883 | Linkage mapping of a novel susceptibility locus for Behçet's disease to chromosome 6p22-23 |
Q34281207 | Lithium-related genetics of bipolar disorder |
Q34972782 | Mechanisms regulating the expression, self-maintenance, and signaling-function of the bradykinin B2 and B1 receptors. |
Q34566566 | Of replications and refutations: the status of Alzheimer's disease genetic research |
Q33906823 | Pharmacogenetics and the practice of medicine |
Q57242592 | Power of QTL detection using association tests with family controls |
Q55030378 | Probing the role of PPARγ in the regulation of late-onset Alzheimer's disease-associated genes. |
Q63804719 | Signatures of selection? Patterns of microsatellite diversity on a chromosome containing a selected locus |
Q34142054 | Statistical approaches to gene mapping |
Q39787855 | The problems of using the transmission/disequilibrium test to infer tight linkage |
Q63432864 | The value of isolated populations |
Q34043662 | Worldwide genetic analysis of the CFTR region |
Search more.