Frontiers in Genetics

Journal

Publication Venue For

  • PAGER Web APP: An Interactive, Online Gene Set and Network Interpretation Tool for Functional Genomics.  13. 2022
  • Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies.  12. 2021
  • Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population.  12. 2021
  • Identification of Prognostic Markers in Cholangiocarcinoma Using Altered DNA Methylation and Gene Expression Profiles.  11. 2020
  • Combining PARP and DNA-PK Inhibitors With Irradiation Inhibits HPV-Negative Head and Neck Cancer Squamous Carcinoma Growth.  11. 2020
  • Differential DNA Methylation Encodes Proliferation and Senescence Programs in Human Adipose-Derived Mesenchymal Stem Cells.  11. 2020
  • The Epigenetic Connection Between the Gut Microbiome in Obesity and Diabetes.  10. 2020
  • An exome-wide sequencing study of the GOLDN cohort reveals novel associations of coding variants and fasting plasma lipids.  10. 2019
  • Erratum: Functional urate-associated genetic variants influence expression of lincRNAs LINC01229 and MAFTRr (Frontiers in Genetics (2019) 9 (733) DOI: 10.3389/fgene.2018.00733).  10. 2019
  • Functional urate-associated genetic variants influence expression of lincRNAs LINC01229 and MAFTRR.  10. 2019
  • Programmable base editing of the sheep genome revealed no genome-wide off-target mutations.  10. 2019
  • Fgf10 Signaling in Lung Development, Homeostasis, Disease, and Repair After Injury.  9. 2018
  • Gene-expression analysis identifies IGFBP2 dysregulation in dental pulp cells from Human Cleidocranial dysplasia.  9. 2018
  • Multiplexed Nanopore Sequencing of HLA-B Locus in Māori and Pacific Island Samples.  9. 2018
  • Evidence for loss in identity, de-differentiation, and trans-differentiation of islet β-cells in type 2 diabetes.  8. 2017
  • SRBreak: A read-depth and split-read framework to identify breakpoints of different events inside simple copy-number variable regions.  7. 2016
  • Regulation of the telomerase reverse transcriptase subunit through epigenetic mechanisms.  7. 2016
  • EM adaptive LASSO-a multilocus modeling strategy for detecting SNPs associated with zero-inflated count phenotypes.  7. 2016
  • Estimation of cell-type composition including T and B cell subtypes for whole blood methylation microarray data.  7. 2016
  • Association of SLC2A9 genotype with phenotypic variability of serum urate in pre-menopausal women.  6. 2015
  • Integrated genomic and BMI analysis for type 2 diabetes risk assessment.  5. 2015
  • Lipid changes due to fenofibrate treatment are not associated with changes in DNA methylation patterns in the GOLDN study.  6. 2015
  • PCSK9 variation and association with blood pressure in African Americans: Preliminary findings from the HyperGEN and REGARDS studies.  6. 2015
  • A bioinformatics workflow for detecting signatures of selection in genomic data.  5. 2014
  • A hidden markov model for haplotype inference for present-absent data of clustered genes using identified haplotypes and haplotype patterns.  5. 2014
  • Lupus risk variants in the PXK locus alter B-cell receptor internalization.  5. 2014
  • The CNVrd2 package: Measurement of copy number at complex loci using high-throughput sequencing data.  5. 2014
  • Genetic associations with 25-hydroxyvitamin D deficiency in HIV-1-infected youth: Fine-mapping for the GC/DBP gene that encodes the vitamin D-binding protein.  4. 2013
  • G protein-linked signaling pathways in bipolar and major depressive disorders.  4. 2013
  • Heritability of pulmonary function estimated from pedigree and whole-genome markers.  4. 2013
  • Sarcopenia and piscines: The case for indeterminate-growing fish as unique genetic model organisms in aging and longevity research.  4. 2013
  • Fatty acid desaturase gene variants, cardiovascular risk factors, and myocardial infarction in the Costa Rica Study.  3. 2012
  • Measured, modeled, and causal conceptions of fitness.  3. 2012
  • More than insulator: Multiple roles of CTCF at the H19-Igf2 imprinted domain.  3. 2012
  • Statistics for next generation sequencing - Meeting report.  3. 2012
  • Submitted for your consideration: Potential advantages of a novel clinical trial design and initial patient reaction.  3. 2012
  • The utility of mitochondrial and Y chromosome phylogenetic data to improve correction for population stratification.  3. 2012
  • Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy.  3. 2012
  • Association of allelic variation in genes mediating aspects of energy homeostasis with weight gain during administration of antipsychotic drugs (CATIE study).  2. 2011
  • Capitalizing on admixture in genome-wide association studies: A two-stage testing procedure and application to height in African-Americans.  2. 2011
  • Epigenomics of ovarian cancer and its chemoprevention.  2. 2011
  • Grand challenges in statistical genetics/genomics methodology.  2. 2011
  • Validity and power of missing data imputation for extreme sampling and terminal measures designs in mediation analysis.  2. 2011
  • A Method to Assess Linkage Disequilibrium between CNVs and SNPs Inside Copy Number Variable Regions..  2:17. 2011
  • Electronic International Standard Serial Number (eissn)

  • 1664-8021