Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q - Wikidata - thesis-toulmin - TriplyDB

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

http://www.wikidata.org/entity/Q33905086

about

Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse The role of large pedigrees in an era of high-throughput sequencing A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.WWOX gene is associated with HDL cholesterol and triglyceride levels.Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels Genetic causes of high and low serum HDL-cholesterol.Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol.Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects Genetic loci for blood lipid levels identified by linkage and association analyses in Caribbean Hispanics.A male-specific quantitative trait locus on 1p21 controlling human stature.Genetically defined hyperlipidemia.Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels.Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family A pleiotropic QTL on 2p influences serum Lp-PLA2 activity and LDL cholesterol concentration in a baboon model for the genetics of atherosclerosis risk factors.Unraveling the complex genetics of familial combined hyperlipidemia.FOXC2 controls Ang-2 expression and modulates angiogenesis, vascular patterning, remodeling, and functions in adipose tissue.WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels Linkage of type 2 diabetes on chromosome 9p24 in Mexican Americans: additional evidence from the Veterans Administration Genetic Epidemiology Study (VAGES).Atherosclerosis and transit of HDL through the lymphatic vasculature.Genetics and coronary heart disease.Unifying ideas for non-parametric linkage analysis.Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia.Determinants of low HDL levels in familial combined hyperlipidemia.Genome-wide linkage scan reveals multiple susceptibility loci influencing lipid and lipoprotein levels in the Quebec Family Study.Quantitative trait loci that determine lipoprotein cholesterol levels in an intercross of 129S1/SvImJ and CAST/Ei inbred mice.Genetic contributors to lipoprotein cholesterol levels in an intercross of 129S1/SvImJ and RIIIS/J inbred mice.Association of two CETP polymorphisms with HDL levels in the Chinese obese population.Hypertriglyceridemia is associated with prebeta-HDL concentrations in subjects with familial low HDL.The FOXC2 C-512T polymorphism is associated with obesity and dyslipidemia.Interaction between obesity-susceptibility loci in chromosome regions 2p25-p24 and 13q13-q21.

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P2860

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

http://www.wikidata.org/entity/Q33905086

description

2003 nî lūn-bûn

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2003 թուականի Մարտին հրատարակուած գիտական յօդուած

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2003 թվականի մարտին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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prefLabel

Combined analysis of genome sc ...... cholesterol on chromosome 16q

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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American Journal of Human Genetics

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Combined analysis of genome sc ...... cholesterol on chromosome 16q

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P2093

Aino Soro

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Ali Kuraishy

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Heidi E Lilja

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Hooman Allayee

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Ilpo Nuotio

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Kelly L Krass

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Marja-Riitta Taskinen

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Päivi Pajukanta

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Rebecca Mar

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Rita M Cantor

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P2860

Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

How many diseases does it take to map a gene with SNPs?

Disease gene mapping in isolated human populations: the example of Finland

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

Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig

The structure of haplotype blocks in the human genome

Strategies for multilocus linkage analysis in humans

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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10.1086/374177

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4

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72

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Leena Peltonen-Palotie

Jerome I Rotter

Aldons Jake Lusis

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10855428

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12638083

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susceptibility locus

HDL cholesterol

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1180353

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