{"doi":"10.1056/nejmp058255","title":"Genomic Cartography — Presenting the HapMap","abstract":null,"journal":"New England Journal of Medicine","year":2005,"id":631910,"datarank":0.9272146195624098,"base_score":2.3978952727983707,"endowment":2.3978952727983707,"self_citation_contribution":0.3596842909197557,"citation_network_contribution":0.5675303286426542,"self_endowment_contribution":0.3596842909197557,"citer_contribution":0.5675303286426542,"corpus_percentile":null,"corpus_rank":null,"citation_count":10,"citer_count":10,"citers_with_citation_signal":8,"citers_with_endowment":8,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1637745,"name":"Elizabeth G. Phimister","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"Genomic Cartography — Presenting the HapMap","abstract":"Many studies are based on the premise that a sample is representative of the larger body from which it was drawn. An article being published in Nature today1 provides a guide for sampling the human genome in a way that will facilitate the quest for genes that influence susceptibility to disease.The article describes a map of haplotypes, colloquially called the HapMap. (A haplotype is a set of closely linked markers on a single chromosome that tend to be inherited as a group.) It is a logical follow-on from the human genome project and fulfills the need for a new . . .","is_dataset_classified":null,"base_score":2.3978952727983707,"endowment":2.3978952727983707,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"16251532","pmcid":null,"openalex_id":"https://openalex.org/W2018955152","authors":[],"funders":[],"total_grants":0,"fwci":0.8899,"citation_percentile":0.74352935,"influential_citations":0,"citation_trend":[{"year":2012,"count":1}],"oa_status":"closed","license":null,"oa_locations":[{"url":"http://www.nejm.org/doi/pdf/10.1056/NEJMp058255","host_type":"publisher"},{"url":"https://doi.org/10.1056/nejmp058255","host_type":"journal"},{"url":"https://pubmed.ncbi.nlm.nih.gov/16251532","host_type":"repository"},{"url":"http://hdl.handle.net/10822/507706","host_type":"repository"}],"fields_of_study":["Genetic Associations and Epidemiology","Genomic variations and chromosomal abnormalities","Genomics and Rare Diseases","Chromosome Mapping","Genetic Variation","Genome, Human","Haplotypes","Humans","Linkage Disequilibrium","Polymorphism, Single Nucleotide"],"mesh_terms":["Chromosome Mapping","Haplotypes","Humans","Genetic Variation","Linkage Disequilibrium","Genome, Human","Polymorphism, Single Nucleotide"],"keywords":["International HapMap Project","Human genome","Haplotype","Premise","Genome","Genetics","Computational biology","Genomics","Biology","Evolutionary biology","Gene","Genealogy","History","Genotype","Epistemology"],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-08-06T01:04:16.210900Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}