Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies.
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Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosisHeritability of performance deficit accumulation during acute sleep deprivation in twinsAssociation of estrogen receptor gene polymorphisms with human precocious puberty: a systematic review and meta-analysisThe role of TLR4 896 A>G and 1196 C>T in susceptibility to infections: a review and meta-analysis of genetic association studiesAssociation of plasminogen activator inhibitor-type 1 (-675 4G/5G) polymorphism with pre-eclampsia: systematic reviewAssociation of BAK1 single nucleotide polymorphism with a risk for dengue hemorrhagic feverThe FNTB promoter polymorphism rs11623866 as a potential predictive biomarker for lonafarnib treatment of ovarian cancer patients.Association between SLCO1B1 -521T>C and -388A>G polymorphisms and risk of statin-induced adverse drug reactions: A meta-analysisComparison of lactase persistence polymorphism in ancient and present-day Hungarian populationsAssociations of DNMT3B -149C>T and -2437T>A polymorphisms and lung cancer risk in Chinese populationInfluence of hepatitis C virus and IL28B genotypes on liver stiffnessEffect of smoking on physical and cognitive capability in later life: a multicohort study using observational and genetic approachesITPA Polymorphisms Are Associated with Hematological Side Effects during Antiviral Therapy for Chronic HCV InfectionGRM7 variants associated with age-related hearing loss based on auditory perception.Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.Additional selection for insecticide resistance in urban malaria vectors: DDT resistance in Anopheles arabiensis from Bobo-Dioulasso, Burkina FasoGenotyping, Platelet Activation, and Cardiovascular Outcome in Patients after Percutaneous Coronary Intervention: Two Pieces of the Puzzle of Clopidogrel Resistance.Genetic Variations and mRNA Expression of NRF2 in Parkinson's Disease.FCGR2A and FCGR3A polymorphisms and clinical outcome in metastatic colorectal cancer patients treated with first-line 5-fluorouracil/folinic acid and oxaliplatin +/- cetuximab.Intima-media thickness of the descending aorta in patients with bicuspid aortic valve.Genetic variation in the adiponectin receptor 2 (ADIPOR2) gene is associated with coronary artery disease and increased ADIPOR2 expression in peripheral monocytesAssociations between the SS variant of 5-HTTLPR and PTSD among adults with histories of childhood emotional abuse: results from two African American independent samples.Genetic risk factors for major bleeding in patients treated with warfarin in a community setting.Adcyap1r1 genotype, posttraumatic stress disorder, and depression among women exposed to childhood maltreatment.Identification of novel variants of metadherin in breast cancerCOMT Associations with Disordered Gambling and Drinking Measures.Evaluating the clinical relevance of codon 594 (g>a) polymorphism of estrogen receptor alpha in knee osteoarthritis.Functional prostacyclin synthase promoter polymorphisms. Impact in pulmonary arterial hypertension.A single nucleotide polymorphism in the stromal cell-derived factor 1 gene is associated with coronary heart disease in Chinese patients.Renin gene polymorphisms in bangladeshi hypertensive populationRapid evolution of BRCA1 and BRCA2 in humans and other primates.Kawasaki disease patients homozygous for the rs12252-C variant of interferon-induced transmembrane protein-3 are significantly more likely to develop coronary artery lesions.Genotype and ancestry modulate brain's DAT availability in healthy humans.MTNR1B Genetic Variability Is Associated with Gestational Diabetes in Czech Women.Association of the rs1424954 polymorphism of the ACVR2A gene with the risk of pre-eclampsia is not replicated in a Finnish study population.Tumor necrosis factor-alpha and polycystic ovarian syndrome: a clinical, biochemical, and molecular genetic studyAssociation of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study.ERCC1 single nucleotide polymorphism C8092A, but not its expression is associated with survival of esophageal squamous cell carcinoma patients from Fujian province, China.Polymorphisms of NRF2 and NRF2 target genes in urinary bladder cancer patients.Genetic variation I148M in patatin-like phospholipase 3 gene and risk of non-alcoholic fatty liver disease among Filipinos.
P2860
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P2860
Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Hardy-Weinberg equilibrium tes ...... ndelian randomization studies.
@en
type
label
Hardy-Weinberg equilibrium tes ...... ndelian randomization studies.
@en
prefLabel
Hardy-Weinberg equilibrium tes ...... ndelian randomization studies.
@en
P2860
P356
P1476
Hardy-Weinberg equilibrium tes ...... ndelian randomization studies.
@en
P2093
Ian N M Day
Santiago Rodriguez
P2860
P304
P356
10.1093/AJE/KWN359
P407
P50
P577
2009-01-06T00:00:00Z