about
Germline BAP1 mutations predispose to malignant mesotheliomaA genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucoseFactors that impact susceptibility to fiber-induced health effectsThe population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequencesGenome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signalsGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityThe genetic architecture of type 2 diabetesMeta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasia.Mutations in ECEL1 cause distal arthrogryposis type 5DOmics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19.Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.TCIRG1-associated congenital neutropenia.PRIMUS: rapid reconstruction of pedigrees from genome-wide estimates of identity by descent.Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait.Genome-wide meta-analysis for severe diabetic retinopathy.Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes.Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.Secondary findings and carrier test frequencies in a large multiethnic sample.Insulin gene mutations as a cause of permanent neonatal diabetes.Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas.Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.PADRE: Pedigree-Aware Distant-Relationship EstimationTransancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.Genome-Wide Studies of Type 2 Diabetes and Lipid Traits in Hispanics.Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.PRIMUS: improving pedigree reconstruction using mitochondrial and Y haplotypes.Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos.Utilizing graph theory to select the largest set of unrelated individuals for genetic analysisIdentification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
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description
hulumtuese
@sq
medical researcher
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wetenschapper
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հետազոտող
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name
Jennifer E Below
@ast
Jennifer E Below
@es
Jennifer E Below
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Jennifer Elizabeth Below
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type
label
Jennifer E Below
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Jennifer E Below
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Jennifer E Below
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Jennifer Elizabeth Below
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altLabel
Jennifer Below
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prefLabel
Jennifer E Below
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Jennifer E Below
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Jennifer E Below
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Jennifer Elizabeth Below
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P106
P1153
22936976900
P21
P31
P496
0000-0002-6372-6402