About: Haplotype tagging for the identification of common disease genes

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About: Haplotype tagging for the identification of common disease genes Goto Sponge NotDistinct Permalink

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description	article (en) wetenschappelijk artikel (nl) مقالة علمية تنشرت ف 1 أكتوبر 2001 (ary) наукова стаття, опублікована в жовтні 2001 (uk) im Oktober 2001 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en octobre 2001 (fr)
publication date	wds:Q59200321-BFE4D1C9-67BF-4330-A34B-CD9695152985
publication date	2001-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59200321-EA12BC72-1338-433C-8A78-9B7968C53A52
language of work or name	English
exact match	wds:Q59200321-6F79BD92-4A14-4875-A4D2-488C329070C8
exact match	https://scigraph.springernature.com/pub.10.1038/ng1001-233
cites work	wds:Q59200321-08E5161A-B084-4F90-9AAA-3724F5FC2718 wds:Q59200321-160DCD46-DFEB-4E29-9CE0-7326B25F8BAF wds:Q59200321-16B3C4D4-8313-4E33-A4ED-FC1A13A02308 wds:Q59200321-181B5EDB-3A41-4880-B91E-36649314B639 wds:Q59200321-2069DA07-436D-4DB7-8FEB-896DFDA01973 wds:Q59200321-283EC370-B626-4E9D-9FBF-35191C9F7EB8 wds:Q59200321-2DCB2F3C-1280-4534-BC7F-86EB15830C56 wds:Q59200321-2FC49843-5385-4952-BC1D-D91B1EA2967D wds:Q59200321-2FDD9CCC-07B7-4B94-86C9-0B8A61129167 wds:Q59200321-318DE0BE-1457-4895-9CE9-F1BCC447B0F9 wds:Q59200321-318E9790-AC9E-41C4-B3CA-5B81FCE60A3C wds:Q59200321-325F33C3-3620-4BB2-941A-C41C7E6F58FA wds:Q59200321-363CB7A3-0170-4728-9D38-74C0F6B9FCA6 wds:Q59200321-4C924B55-4B45-468C-8244-93A1E960C152 wds:Q59200321-5C6AEAEE-5621-43A6-8BB9-C54907A43C70 wds:Q59200321-5FAF8F24-FD62-4C42-ABE8-995B145B64B7 wds:Q59200321-770EDBB5-7585-48CA-B158-2B9F3723D46E wds:Q59200321-95B05B4C-6542-4FB2-911D-EC85C13EA51D wds:Q59200321-9A388B69-45E2-4329-A569-3E9299D62A9B wds:Q59200321-9C0D4EDF-1FDF-41D4-A75F-3EB78169CFFD wds:Q59200321-9E02D191-08FE-4C60-BFCF-F8FF52D84C93 wds:Q59200321-A199D1DE-1C6B-404B-B585-FF9295363ECE wds:Q59200321-A403938C-268E-4206-9AD2-C1772F750008 wds:Q59200321-ABF824AA-F9C0-480D-AD7D-F61079B9E315 wds:Q59200321-ABFB4D0F-0F6F-44C7-9EBD-78AD18C4001B wds:Q59200321-B3C8E782-BB01-447B-A2E4-1710C7209F3A wds:Q59200321-BE1A5A54-DD01-425B-88F2-5A0FD7ABAE1E wds:Q59200321-C8AF8B0B-6CC4-410B-907F-F6311DACCFD3 wds:Q59200321-C8C67A22-03BD-499F-AA53-F2968BE072A6 wds:Q59200321-D1A97EC8-8790-48EC-B51C-B7891CC75CE4
cites work	A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease Evidence for variable selective pressures at MC1R Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase A comparison of linkage disequilibrium measures for fine-scale mapping Evolution of human and non-human primate CC chemokine receptor 5 gene and mRNA. Potential roles for haplotype and mRNA diversity, differential haplotype-specific transcriptional activity, and altered transcription factor binding to polymorphic nucle Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects Identification of susceptibility loci for insulin-dependent diabetes mellitus by trans-racial gene mapping. Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism Ancestral haplotypes reveal the role of the central MHC in the immunogenetics of IDDM Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease High-resolution haplotype structure in the human genome Linkage disequilibrium in the human genome SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease Single-nucleotide polymorphisms in the public domain: how useful are they? Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex Global patterns of linkage disequilibrium at the CD4 locus and modern human origins Linkage disequilibrium in humans: models and data Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation Sequence variation in the human angiotensin converting enzyme. Lactase haplotype diversity in the Old World A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR. The optimal measure of allelic association Complexity and power in case-control association studies Fine-mapping of an ancestral recombination breakpoint in DCP1
author name string	wds:Q59200321-11D70029-018D-4ED2-9964-572E124AA58A wds:Q59200321-2D92617F-9C36-40F8-AB85-19D7EE95929C wds:Q59200321-30DC85D7-6BB8-4EFE-A6DC-0D1456E73B2A wds:Q59200321-4B36743A-4A8B-4C83-A1CA-BF97F5944823 wds:Q59200321-5CBDA37B-AE54-49EE-9E4B-F2F65785DCF7 wds:Q59200321-668A13D6-9DFC-42EB-8C71-A144981E2C6A wds:Q59200321-6DEE9719-994E-45A9-A1DD-3BC823CCFF3D wds:Q59200321-73ECC295-AA7A-40B5-A7BD-7A31A12EE43E wds:Q59200321-7C0C29F0-162A-48BB-9B0D-08B961AEF835 wds:Q59200321-87B8B0BD-EE00-4953-A12B-365FC9B4BD4A wds:Q59200321-92BD7DE7-4687-43B8-9FC2-EF539C38DCED wds:Q59200321-9D96D5EC-2C3C-4090-A45D-753AA7E891C4 wds:Q59200321-A43A8AB3-5F43-41BD-8DF8-4AA29421BDCD wds:Q59200321-CEFECFEA-8E78-494B-836C-0778A88A5A9D wds:Q59200321-D6A13067-414B-4505-9A3D-46D5D1BBBD53 wds:Q59200321-D9448FAD-C5CB-49FF-830F-D519369AC878 wds:Q59200321-E3744477-EB82-4390-9EE7-4DA16834E910 wds:Q59200321-F7CE3928-3846-473A-AAF2-2A30AF0857F2
author name string	Tuomilehto J Todd JA Esposito L Ueda H Clayton DG Smith AN Johnson GC Hughes W Carr P

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