Whole-genome sequence-based analysis of high-density lipoprotein cholesterol

scientific article (publication date: August 2013)

Whole-genome sequence-based analysis of high-density lipoprotein cholesterol is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/NG.2671
P3181OpenCitations bibliographic resource ID4426311
P932PMC publication ID4030301
P698PubMed publication ID23770607
P5875ResearchGate publication ID262043731

P50authorJoshua C BisQ79326643
Christopher J O'DonnellQ89928448
Andrew D. JohnsonQ124721130
Eric BoerwinkleQ28050857
Gerardo HeissQ30004039
Bruce M. PsatyQ30429993
Donna MuznyQ32652849
L. Adrienne CupplesQ37638868
Jin YuQ55137366
Alanna MorrisonQ55856687
Richard A GibbsQ64856497
P2093author name stringKenneth Rice
Xiaoming Liu
Fuli Yu
Alexander Li
Chengsong Zhu
Arend Voorman
P2860cites workAnalysis of genetic inheritance in a family quartet by whole-genome sequencingQ22065898
Biological, clinical and population relevance of 95 loci for blood lipidsQ24622541
ORegAnno: an open-access community-driven resource for regulatory annotationQ24648942
PLINK: a tool set for whole-genome association and population-based linkage analysesQ24677407
ORegAnno: an open access database and curation system for literature-derived promoters, transcription factor binding sites and regulatory variationQ28290181
Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular riskQ28731522
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataQ29547161
Fast and accurate long-read alignment with Burrows-Wheeler transformQ29547193
Common SNPs explain a large proportion of the heritability for human heightQ29547221
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclassesQ29547647
NCBI Reference Sequences: current status, policy and new initiativesQ29614453
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathyQ30156928
Multiple splice defects in ABCA1 cause low HDL-C in a family with hypoalphalipoproteinemia and premature coronary diseaseQ33398695
Rare-variant association testing for sequencing data with the sequence kernel association testQ33954046
Novel N-terminal mutation of human apolipoprotein A-I reduces self-association and impairs LCAT activationQ34395097
Genome partitioning of genetic variation for complex traits using common SNPsQ34973837
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.Q37389540
Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindredsQ38314694
New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulationQ38315384
HDL cholesterol and other lipids in coronary heart disease. The cooperative lipoprotein phenotyping studyQ40057178
Low-coverage sequencing: implications for design of complex trait association studiesQ42596059
Human Gene Mutation Database: towards a comprehensive central mutation databaseQ57263756
P433issue8
P407language of work or nameEnglishQ1860
P921main subjectlipoproteinQ28350
whole genome sequencingQ2068526
HDL cholesterolQ67322514
P304page(s)899-901
P577publication date2013-08-01
P1433published inNature GeneticsQ976454
P1476titleWhole-genome sequence-based analysis of high-density lipoprotein cholesterol
P478volume45

Reverse relations

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