Pages that link to "Q30348346"
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The following pages link to Braxton D. Mitchell (Q30348346):
Displaying 50 items.
- WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk (Q21090209) (← links)
- NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium (Q21144997) (← links)
- Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study (Q24338412) (← links)
- Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification (Q24569664) (← links)
- Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish (Q24600310) (← links)
- New loci associated with kidney function and chronic kidney disease (Q24630646) (← links)
- Downregulated kynurenine 3-monooxygenase gene expression and enzyme activity in schizophrenia and genetic association with schizophrenia endophenotypes (Q24631189) (← links)
- Thrombomodulin Ala455Val Polymorphism and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study (Q24808950) (← links)
- Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants (Q27008212) (← links)
- A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 (Q28118289) (← links)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Q28270700) (← links)
- Arsenic exposure is associated with diminished insulin sensitivity in non-diabetic Amish adults (Q28387333) (← links)
- Calcified granulomatous disease: occupational associations and lack of familial aggregation (Q28397934) (← links)
- Prioritizing Approaches to Engage Community Members and Build Trust in Biobanks: A Survey of Attitudes and Opinions of Adults within Outpatient Practices at the University of Maryland (Q28606569) (← links)
- Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data (Q28650283) (← links)
- Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes (Q28658238) (← links)
- Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling (Q28658849) (← links)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (Q28659915) (← links)
- Discovery and refinement of loci associated with lipid levels (Q28661470) (← links)
- Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts (Q28709200) (← links)
- Assessment of gene-by-sex interaction effect on bone mineral density (Q28727687) (← links)
- A genome-wide association search for type 2 diabetes genes in African Americans (Q28740367) (← links)
- Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q (Q28752440) (← links)
- Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects (Q28754654) (← links)
- Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (Q29147442) (← links)
- Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies (Q29417025) (← links)
- Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (Q29417129) (← links)
- Genetic variation at 16q24.2 is associated with small vessel stroke (Q30275184) (← links)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (Q30277642) (← links)
- Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans (Q30279161) (← links)
- Association between smallpox vaccination and hepatitis C antibody positive serology in Pakistani volunteers. (Q30350220) (← links)
- Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2 (Q30354370) (← links)
- Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. (Q30356365) (← links)
- Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease (Q30370974) (← links)
- From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. (Q30374131) (← links)
- Effect of genetic variants associated with plasma homocysteine levels on stroke risk (Q30384553) (← links)
- Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. (Q30410768) (← links)
- 17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status (Q30412878) (← links)
- Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25. (Q30419542) (← links)
- Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke? (Q30420031) (← links)
- CUBN is a gene locus for albuminuria (Q30428102) (← links)
- Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels (Q30441439) (← links)
- Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN) (Q30458056) (← links)
- Evidence of missense mutations on the neuregulin 1 gene affecting function of prepulse inhibition (Q30458275) (← links)
- Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study. (Q30536711) (← links)
- Transcriptomics of cortical gray matter thickness decline during normal aging (Q30543926) (← links)
- The effect of phenotype variation on detection of linkage in the COGA data (Q30585359) (← links)
- Identifying influential individuals in linkage analysis: application to a quantitative trait locus detected in the COGA data (Q30585382) (← links)
- Using step-wise linear regression to detect "functional" sequence variants: application to simulated data. (Q30670312) (← links)
- Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip (Q30844245) (← links)