Colorado PROFILES, The Colorado Clinical and Translational Sciences Institute (CCTSI)
Last Name

Contact Us
If you have any questions or feedback please contact us.


Search Results to Ethan Lange

This is a "connection" page, showing the details of why an item matched the keywords from your search.


One or more keywords matched the following items that are connected to Lange, Ethan

Item TypeName
Concept Gene Frequency
Academic Article Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Academic Article Comparison of genome-wide variation between Malawians and African ancestry HapMap populations.
Academic Article Transcription factor 7-like 2 (TCF7L2) polymorphism and context-specific risk of impaired fasting glucose in African American and Caucasian adults: the atherosclerosis risk in communities (ARIC) study.
Academic Article DISSCO: direct imputation of summary statistics allowing covariates.
Academic Article Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer.
Academic Article Genetic variation in adiponectin (ADIPOQ) and the type 1 receptor (ADIPOR1), obesity and prostate cancer in African Americans.
Academic Article Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort.
Academic Article Exploring the genetic basis of chronic periodontitis: a genome-wide association study.
Academic Article Polymorphisms in the VKORC1 gene are strongly associated with warfarin dosage requirements in patients receiving anticoagulation.
Academic Article Family-based samples can play an important role in genetic association studies.
Academic Article Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples.
Academic Article Germ-line mutations of the macrophage scavenger receptor 1 gene: association with prostate cancer risk in African-American men.
Academic Article Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Academic Article Rare coding variants and X-linked loci associated with age at menarche.
Academic Article Single-nucleotide polymorphisms in the C-reactive protein (CRP) gene promoter that affect transcription factor binding, alter transcriptional activity, and associate with differences in baseline serum CRP level.
Academic Article Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Academic Article Population-specific coding variant underlies genome-wide association with adiponectin level.
Academic Article Prioritized subset analysis: improving power in genome-wide association studies.
Academic Article Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study.
Academic Article Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.
Academic Article The androgen receptor CAG and GGN repeat polymorphisms and prostate cancer susceptibility in African-American men: results from the Flint Men's Health Study.
Academic Article Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
Academic Article HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).
Academic Article Power for genetic association studies with random allele frequencies and genotype distributions.
Academic Article NCAM1 and neurocognition in schizophrenia.
Academic Article Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.
Academic Article Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.
Academic Article Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study.
Academic Article REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Academic Article Rare and low-frequency coding variants alter human adult height.
Academic Article Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Academic Article Variant-specific inflation factors for assessing population stratification at the phenotypic variance level.

Search Criteria
  • Gene Frequency

Copyright © 2021 The Regents of the University of Colorado, a body corporate. All rights reserved. (Harvard PROFILES RNS software version: 2.11.1)