A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study. - Wikidata - awgldk - TriplyDB

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

http://www.wikidata.org/entity/Q33910046

about

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17 A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking Molecular genetics of coronary artery disease Advances in the genetic basis of coronary artery disease Genetic causation of neointimal hyperplasia in hemodialysis vascular access dysfunction Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.GATA2 is associated with familial early-onset coronary artery disease.Genetic and functional association of FAM5C with myocardial infarction Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis Lack of MEF2A mutations in coronary artery disease.Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.The relationships between FAM5C SNP (rs10920501) variability and metabolic syndrome and inflammation in women with coronary heart disease Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.Identifying novel genes for atherosclerosis through mouse-human comparative genetics.A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5 Emerging clinical applications in cardiovascular pharmacogenomics.Association of the HLA-DRB1 gene with premature death, particularly from cardiovascular disease, in patients with rheumatoid arthritis and inflammatory polyarthritis.Genomic approaches to coronary artery disease Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.Genomics of heart failure.Transcription factor MEF2A mutations in patients with coronary artery disease.Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.Genetic and genomic insights into the molecular basis of atherosclerosis.Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse.Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies.Characterizing the phenotype of advanced pelvic organ prolapse.Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse.An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.Genetic susceptibility to myocardial infarction and coronary artery disease.Identification of atherosclerosis-modifying genes: pathogenic insights and therapeutic potential.Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease Unraveling the genetics of atherosclerosis: implications for diagnosis and treatment.Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.Genes, diet and public health.Molecular genetics of myocardial infarction Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.

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P2860

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

http://www.wikidata.org/entity/Q33910046

description

2004 nî lūn-bûn

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2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2004 թվականի հուլիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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American Journal of Human Genetics

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A genomewide scan for early-on ...... families: the GENECARD Study.

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Alan G Bartel

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Alan H Wiseman

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Allen D Roses

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Bernhard R Winkelmann

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Bonnie Pedersen

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Brendan McAdam

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Carol Haynes

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Charles A Dennis

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Christopher J H Jones

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David C Crossman

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P2860

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Atherosclerosis

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Comprehensive human genetic maps: individual and sex-specific variation in recombination

Estimation of allele frequencies with data on sibships.

Association mapping in structured populations

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.

Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24.

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

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Margaret A. Pericak-Vance

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William E. Kraus

Sheila E. Francis

Christopher B. Granger

Jonathan L Haines

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