Frontiers in Genetics

Allelic diversity of the pharmacogene CYP2D6 in New Zealand Māori and Pacific peoples.  13. 2022

Editorial: Women in science: Genetics.  13. 2022

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

MiR-199b-5p Suppresses Tumor Angiogenesis Mediated by Vascular Endothelial Cells in Breast Cancer by Targeting ALK1.  10. 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

Epigenome-wide analyses identify two novel associations with recurrent stroke in the Vitamin Intervention for Stroke Prevention clinical trial.  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

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

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