About: Variants in common diseases

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scientific article published in Nature

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) im Februar 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published in Nature (en) наукова стаття, опублікована в Nature в лютому 2007 (uk)
publication date	wds:Q59066327-983E68C4-B72C-40B9-995E-7B360CD890A0
publication date	2007-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59066327-92F34A6D-2207-4D7B-AE43-F14096F7DFEE
language of work or name	English
exact match	wds:Q59066327-55DA41FF-47AE-438A-936E-689A38376027
exact match	https://scigraph.springernature.com/pub.10.1038/nature05568
cites work	wds:Q59066327-360CE9C2-BF78-45F4-8236-D73C36508EB5 wds:Q59066327-57D2504B-C543-4F41-AB4A-9A6AF8EC981A wds:Q59066327-6CA9FB7D-8FE3-42C6-9D9B-A1272843CC83 wds:Q59066327-7D5FA687-6E27-4EDA-A19A-279760AF3396 wds:Q59066327-894A2953-C174-4FD5-9C54-BF785D481577 wds:Q59066327-94AD52E1-4B5A-4EE8-90D6-3224CBF67813 wds:Q59066327-BBF0F03E-0B78-4392-8957-D1CC01DAC45C wds:Q59066327-C0581C18-C63C-44ED-85FA-1AB8F7923D6D wds:Q59066327-C68A9BF8-E0FF-4D28-BBE0-CF24877B34CE wds:Q59066327-D409FEAE-F1FD-44DC-8110-D6A79EC24D88 wds:Q59066327-E3684CB5-4DB9-4B55-AD25-934E66E851A4
cites work	Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies A genome-wide association study identifies IL23R as an inflammatory bowel disease gene A genome-wide association study identifies novel risk loci for type 2 diabetes A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 Complement factor H polymorphism in age-related macular degeneration A haplotype map of the human genome HTRA1 promoter polymorphism in wet age-related macular degeneration High-resolution whole-genome association study of Parkinson disease. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction Genetics. Delivering new disease genes
author name string	wds:Q59066327-1899F249-E0E1-4F87-9CD7-88D0E68191C0 wds:Q59066327-EE0A6952-4836-4536-8A80-5750A8F4F387
author name string	Nelson B Freimer Chiara Sabatti
rdfs:label	Variants in common diseases (en) Variants in common diseases (nl)
skos:prefLabel	Variants in common diseases (en) Variants in common diseases (nl)
name	Variants in common diseases (en) Variants in common diseases (nl)
title	wds:Q59066327-4002282A-E449-438A-A917-07C1D3E0DE70
title	Human genetics: variants in common diseases (en)
page(s)	wds:Q59066327-BE9D1E10-84C7-4BEC-BF27-6236C88A7DAE
page(s)	828-830
instance of	wds:Q59066327-53DDCF81-AEE6-4A28-9F81-7B76859BF5FE
instance of	scholarly article
PubMed ID	wds:Q59066327-4163F9CB-B3FC-4376-AC96-21EED308ECED
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17293879
PubMed ID	17293879
published in	wds:Q59066327-75A14664-DCE2-4C0C-80F2-5F7268F0943A
published in	Nature
issue	wds:Q59066327-01D0DCCC-4FA0-45F0-B5EB-9C0865DA1717
volume	wds:Q59066327-26197116-96B1-4BE8-81C3-A34BA4FCAB72
issue	7130
volume	445
DOI	wds:Q59066327-4B295387-E2F9-4A8A-AAA4-F830E7813801
DOI	http://dx.doi.org/10.1038/NATURE05568
DOI	10.1038/NATURE05568
Dimensions Publication ID	wds:Q59066327-FA6D76AD-24AF-4F88-BF98-322688C7F4A8
Dimensions Publication ID	1016916589
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59066327
is cites work of	Atrial fibrillation: current knowledge and future directions in epidemiology and genomics From genetic privacy to open consent MeDALL (Mechanisms of the Development of ALLergy): an integrated approach from phenotypes to systems medicine. Prep1 deficiency induces protection from diabetes and increased insulin sensitivity through a p160-mediated mechanism. Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis SNP-based pathway enrichment analysis for genome-wide association studies Pathway-based approaches for analysis of genomewide association studies Evolutionary evidence of the effect of rare variants on disease etiology Replicating genotype-phenotype associations Human genetic variation recognizes functional elements in noncoding sequence Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder The role of host genetics in the susceptibility for HIV-associated neurocognitive disorders Pathway-based analysis tools for complex diseases: a review Eating disorders: the current status of molecular genetic research LincSNP: a database of linking disease-associated SNPs to human large intergenic non-coding RNAs A two-stage mixed-effects model approach for gene-set analyses in candidate gene studies. Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies Social networking and personal genomics: suggestions for optimizing the interaction Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study Increased Micronuclei Frequency in Oral and Lingual Epithelium of Treated Diabetes Mellitus Patients. Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study Comparative network stratification analysis for identifying functional interpretable network biomarkers Susceptibility genes in movement disorders The genetics of Alzheimer's disease in Brazil: 10 years of analysis in a unique population
is cites work of	wds:Q33470869-64FC7163-00D0-4904-AADE-E9BF7CA0DF4A wds:Q27015706-0F80B5C1-8DD1-40EA-B3B9-4DFC69E368B9 wds:Q36347919-92E1A448-27D1-478C-916C-78450DC308C4 wds:Q54943067-5F9B9A1E-D8E3-4C1C-A226-E0A75A4D1A73 wds:Q24550752-B7D7435C-857D-4FBF-9CC6-EE1650B42F84 wds:Q34051756-8ED9E197-FA68-4DD1-9393-E56EDE638B55 wds:Q36329398-A63D78FC-47AB-4A13-B892-1EC8982E3EF5 wds:Q40089801-B3111D23-E217-4FC9-8AB1-C864D5A2AA04 wds:Q33731374-D83188D8-635E-448E-BB6B-4133AD4315B6

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