Caroline M. Nievergelt
University of California
101 papers found
Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel
FMR1, circadian genes and depression: suggestive associations or false discovery?
Loss of GSTM1, a NRF2 target, is associated with accelerated progression of hypertensive kidney disease in the African American Study of Kidney Disease (AASK)
Paraoxonase 1 (PON1) C/T-108 Association With Longitudinal Mean Arterial Blood Pressure
Neuropeptide Y (NPY)
Integrated Computational and Experimental Analysis of the Neuroendocrine Transcriptome in Genetic Hypertension Identifies Novel Control Points for the Cardiometabolic Syndrome
Autonomic and Hemodynamic Origins of Pre-Hypertension
Predictors of Risk and Resilience for Posttraumatic Stress Disorder Among Ground Combat Marines: Methods of the Marine Resiliency Study
A Survey of Genomic Studies Supports Association of Circadian Clock Genes with Bipolar Disorder Spectrum Illnesses and Lithium Response
Biomarkers of PTSD: Neuropeptides and immune signaling
Enrichment of Cis-Regulatory Gene Expression SNPs and Methylation Quantitative Trait Loci Among Bipolar Disorder Susceptibility Variants
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.
Single nucleotide polymorphisms and haplotypes in Native American populations
Functional genetic variation in the Rev-Erbαpathway and lithium response in the treatment of bipolar disorder
Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes
Delayed sleep phase syndrome is related to seasonal affective disorder
Polymorphisms in melatonin synthesis pathways: possible influences on depression
Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture
Naturally Occurring Genetic Variants in Human Chromogranin A (CHGA) Associated with Hypertension as well as Hypertensive Renal Disease
Matrix metalloproteinase haplotypes associated with coronary artery aneurysm formation in patients with Kawasaki disease
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