About: High-resolution haplotype structure in the human genome

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description	article (en) ലേഖനം (ml) wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2001 (uk) im Oktober 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56002085-8F24CEBC-85A2-4683-9CE0-CFE75ACE4C60
publication date	2001-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56002085-541263F2-272A-490B-B4BC-BEA7973D6159
language of work or name	English
exact match	wds:Q56002085-F950543F-135A-47A8-A7CA-6BBDB4148EEE
exact match	https://scigraph.springernature.com/pub.10.1038/ng1001-229
cites work	wds:Q56002085-0A6C33CC-27E5-4CE6-879D-CF2D5452EFC7 wds:Q56002085-18278ADD-C10D-4F89-8D04-A7A4A9206909 wds:Q56002085-23177B80-9346-46C6-BE25-3A67FA5AD230 wds:Q56002085-288A295A-9581-4697-975A-DBD415978D0E wds:Q56002085-2B581F93-37DE-47C1-BE01-C9C367103103 wds:Q56002085-30826FE2-F0E5-4598-971A-7C8C6FCEB624 wds:Q56002085-358C0247-8704-4582-855D-A26D6E70525F wds:Q56002085-5EAEE55C-E6AD-495E-B15E-AE41E8944CCC wds:Q56002085-6CF6205E-5E05-4BFA-9122-E65E200AA390 wds:Q56002085-6E4DF3E7-178A-4317-9CDB-6949EBECE5C5 wds:Q56002085-88949BD9-B588-4CE1-AE2F-464E2D180C82 wds:Q56002085-90C4E6ED-59B2-42C2-A738-2E8199EF4632 wds:Q56002085-B55190CB-C2A4-4671-B269-D7EAEE2FDE2A wds:Q56002085-B9FC3BCE-C59A-4A8D-8347-75065DE0F384 wds:Q56002085-D5429D6D-21F8-4293-A714-8A897B91E299 wds:Q56002085-E410DFE7-D99A-4D36-AED9-B5E1D207BFA0
cites work	Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness Initial sequencing and analysis of the human genome Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms Linkage disequilibrium and homozygosity of chromosome segments in finite populations Linkage disequilibrium in the human genome Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex Haplotype tagging for the identification of common disease genes Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot Recombinational and mutational hotspots within the human lipoprotein lipase gene New polymorphisms in the IL-10 promoter region Identification of new single-nucleotide polymorphisms in the thrombin receptor gene and their effects on coronary artery diseases in Koreans Allele associations reveal four prominent haplotypes at the human interleukin-6 (IL-6) locus
author name string	wds:Q56002085-0A49BE5B-F583-4F45-A7D1-34DDAB615CDA
author name string	Thomas J. Hudson
rdfs:label	High-resolution haplotype structure in the human genome (en) High-resolution haplotype structure in the human genome (nl)
skos:prefLabel	High-resolution haplotype structure in the human genome (en) High-resolution haplotype structure in the human genome (nl)
name	High-resolution haplotype structure in the human genome (en) High-resolution haplotype structure in the human genome (nl)
author	wds:Q56002085-4211DDE1-B5E3-4F52-A1C9-EF407D6BBA40 wds:Q56002085-62096EC7-0436-4AA7-8508-6197A80A2040 wds:Q56002085-C3DFEDF4-016B-4E25-8887-98CFE67B4B71 wds:Q56002085-F521AD48-C023-4A16-A12F-DF5C4A97B5FC
author	Mark Joseph Daly Eric Lander John D. Rioux Stephen F Schaffner
title	wds:Q56002085-EC1CC71C-FB3C-4AA3-B562-6F8D128FDB97
title	High-resolution haplotype structure in the human genome (en)
page(s)	wds:Q56002085-2D38C62E-9115-42F6-AA32-018B18EAE513
page(s)	229-232
instance of	wds:Q56002085-39E3DBC3-F6AD-43BF-975A-5989DEF54E16
instance of	scholarly article
PubMed ID	wds:Q56002085-DC79E7A6-1C74-4AA2-B3CB-D1BF73D62B3F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11586305
PubMed ID	11586305
published in	wds:Q56002085-B09FE6A6-993C-4C9C-8B5F-ACD647019501
published in	Nature Genetics
issue	wds:Q56002085-A85F3192-DB8F-4D51-B35E-378B75A6920B
volume	wds:Q56002085-7802F81C-3819-4F7B-AE69-FC2C6C0D92B9
issue	2
volume	29
DOI	wds:Q56002085-8BF44C12-64E7-43C1-B4D1-91FDAC213FEB
DOI	http://dx.doi.org/10.1038/NG1001-229
DOI	10.1038/NG1001-229
ResearchGate publication ID	wds:Q56002085-17390564-2870-4256-8AAE-2E6826A516CB
ResearchGate publication ID	11763944
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56002085
is cites work of	Using haplotype blocks to map human complex trait loci The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations Methods for high-density admixture mapping of disease genes The mosaic that is our genome Integrating ethics and science in the International HapMap Project Beyond race: towards a whole-genome perspective on human populations and genetic variation Are medical and nonmedical uses of large-scale genomic markers conflating genetics and 'race'? Linkage disequilibrium: what history has to tell us. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes Autism: in search of susceptibility genes Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint The future of association studies: gene-based analysis and replication The road to genome-wide association studies Linkage disequilibrium decay and haplotype block structure in the pig. Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution. Colorectal cancer as a complex disease: defining at-risk subjects in the general population - a preventive strategy Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study

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