Candidate gene case-control association studies: advantages and potential pitfalls.
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Absence of association between angiotensin converting enzyme polymorphism and development of adult respiratory distress syndrome in patients with severe acute respiratory syndrome: a case control study.Role of tumour necrosis factor gene polymorphisms (-308 and -238) in breast cancer susceptibility and severityPolymorphisms of apolipoprotein E and aneurysmal subarachnoid haemorrhage: A meta-analysisGenetic associations in preterm birth: a primer of marker selection, study design, and data analysis.Host susceptibility to persistent hepatitis B virus infectionMHC-DQB1 Variation and Its Association with Resistance or Susceptibility to Cystic Echinococcosis in Chinese Merino SheepAssociation between polymorphisms in the coagulation factor VII gene and coronary heart disease risk in different ethnicities: a meta-analysisAssociation between polymorphisms in the adiponectin gene and cardiovascular disease: a meta-analysis.The hunt for new genes and polymorphisms that can control the response to drugs.Role of genetic polymorphisms in tumour angiogenesisLack of association of apolipoprotein E (Apo E) ε2/ε3/ε4 polymorphisms with primary open-angle glaucoma: a meta-analysis from 1916 cases and 1756 controlsHuman pharmacogenomic variations and their implications for antifungal efficacy.The Human Myotrophin Variant Attenuates MicroRNA-Let-7 Binding Ability but Not Risk of Left Ventricular Hypertrophy in Human Essential Hypertension.Assessing the quality of case-control association studies on the genetic basis of sepsis.Genetic differences on intracranial versus spinal cord ependymal tumors: a meta-analysis of genetic researches.Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: potential breast cancer risk alleles and their distribution across human populations.Genes or environment to determine alcoholic liver disease and non-alcoholic fatty liver disease.Introduction to genetics and childhood obesity: relevance to nursing practice.Candidate genes for cannabis use disorders: findings, challenges and directionsInfluence of CFH, HTRA1 and ARMS2 polymorphisms in the response to intravitreal ranibizumab treatment for wet age-related macular degeneration in a Spanish population.The role of vascular endothelial growth factor SNPs as predictive and prognostic markers for major solid tumors.Drug-induced liver injury: insights from genetic studies.Pharmacogenetics of drug-induced liver injury.Retroviral infections in sheep and goats: small ruminant lentiviruses and host interaction.Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.Genetic polymorphisms associated with overweight and obesity in uncontrolled Type 2 diabetes mellitus.Biology and therapeutic implications of VEGF-A splice isoforms and single-nucleotide polymorphisms in colorectal cancer.Genome-Wide Association Studies for Idiosyncratic Drug-Induced Hepatotoxicity: Looking Back-Looking Forward to Next-Generation Innovation.A Study of Single Nucleotide Polymorphisms of Tumour Necrosis Factor α-1031 And Tumour Necrosis Factor β+ 252 in Chronic RhinosinusitisSNPs in candidate genes MX dynamin-like GTPase and chemokine (C-C motif) receptor-5 are associated with ovine pulmonary adenocarcinoma progression in Latxa sheep.Quantification of population structure using correlated SNPs by shrinkage principal components.Backward genotype-trait association (BGTA)-based dissection of complex traits in case-control designs.Mitochondrial superoxide dismutase and glutathione peroxidase in idiosyncratic drug-induced liver injury.New variant identified in major susceptibility locus to tuberculosis on chromosomal region 8q12-q13 in Moroccan population: a case control study.Gamma-aminobutyric acid (GABA) receptors GABRA4, GABRE, and GABRQ gene polymorphisms and risk for migraine.Investigation of a peroxisome proliferator-activated receptor gamma haplotype effect on meat quality and carcass traits in pigs.Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome.VEGF A (rs699947 and rs833061) and VEGFR2 (rs2071559) gene polymorphisms are not associated with AMD susceptibility in a Spanish population.Genetic Approaches to the Study of Gene Variants and Their Impact on the Pathophysiology of Type 2 Diabetes.Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor.
P2860
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P2860
Candidate gene case-control association studies: advantages and potential pitfalls.
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Candidate gene case-control association studies: advantages and potential pitfalls.
@ast
Candidate gene case-control association studies: advantages and potential pitfalls.
@en
Candidate gene case-control association studies: advantages and potential pitfalls.
@nl
type
label
Candidate gene case-control association studies: advantages and potential pitfalls.
@ast
Candidate gene case-control association studies: advantages and potential pitfalls.
@en
Candidate gene case-control association studies: advantages and potential pitfalls.
@nl
prefLabel
Candidate gene case-control association studies: advantages and potential pitfalls.
@ast
Candidate gene case-control association studies: advantages and potential pitfalls.
@en
Candidate gene case-control association studies: advantages and potential pitfalls.
@nl
P2860
P1476
Candidate gene case-control association studies: advantages and potential pitfalls.
@en
P2093
P2860
P304
P356
10.1046/J.0306-5251.2001.01510.X
P407
P577
2001-11-01T00:00:00Z