Her primary scientific interests are in Internal medicine, Pathology, Endocrinology, Neuroscience and Genetics. Her Endocrinology study combines topics in areas such as Receptor and Muscarinic acetylcholine receptor. Her work in the fields of Neuroscience, such as Human brain, Cholinergic neuron, Nucleus basalis and Cholinergic, intersects with other areas such as In patient.
Her studies deal with areas such as Disease and Case-control study as well as Genetics. She usually deals with Gene expression and limits it to topics linked to Regulation of gene expression and Amygdala. Deborah C. Mash has researched Genetic variation in several fields, including Quantitative trait locus, Expression quantitative trait loci, Genetic variants, X chromosome and Genetic association.
Her primary areas of study are Internal medicine, Endocrinology, Neuroscience, Genetics and Dopamine. Her work on Human brain expands to the thematically related Internal medicine. Endocrinology connects with themes related to Receptor in her study.
Her study involves Locus, Gene, Single-nucleotide polymorphism, Genome-wide association study and Haplotype, a branch of Genetics. Deborah C. Mash interconnects Catecholamine and Pharmacology in the investigation of issues within Dopamine. Her Pharmacology research is multidisciplinary, incorporating perspectives in Agonist, Tabernanthe iboga, Addiction and Serotonin.
Her main research concerns Internal medicine, Genetics, Gene, Endocrinology and Computational biology. Her studies deal with areas such as Axon and Spinal cord as well as Internal medicine. Her Genetics research incorporates elements of Alzheimer's disease and Case-control study.
Her Endocrinology study combines topics in areas such as Motor neuron and Microglia. The various areas that Deborah C. Mash examines in her Computational biology study include DNA methylation, Reprogramming, Transcriptome, Genomics and Expression quantitative trait loci. Her studies in Gene expression integrate themes in fields like Regulation of gene expression and Cell type.
Deborah C. Mash focuses on Genetics, Gene, Genome-wide association study, Genetic association and Computational biology. The Genetics study combines topics in areas such as Internal medicine and Case-control study. Her research on Genetic association often connects related areas such as Genetic variation.
Her study in Computational biology is interdisciplinary in nature, drawing from both Cell, Regulation of gene expression and Gene expression. The concepts of her Regulation of gene expression study are interwoven with issues in Human genetic variation, Gene expression profiling, Quantitative trait locus, Biomedicine and Expression quantitative trait loci. In general Gene expression study, her work on RNA-Seq often relates to the realm of Immunofluorescence, thereby connecting several areas of interest.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The Genotype-Tissue Expression (GTEx) project
John Lonsdale;Jeffrey Thomas;Mike Salvatore;Rebecca Phillips.
Nature Genetics (2013)
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
Kristin G. Ardlie;David S. Deluca;Ayellet V. Segrè.
Dynamics of Hippocampal Neurogenesis in Adult Humans
Kirsty L. Spalding;Olaf Bergmann;Kanar Alkass;Samuel Bernard.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Adam C. Naj;Gyungah Jun;Gary W. Beecham;Li-San Wang.
Nature Genetics (2011)
The GTEx Consortium atlas of genetic regulatory effects across human tissues
F Aguet;AN Barbeira;R Bonazzola;A Brown.
Loss of M2 muscarine receptors in the cerebral cortex in Alzheimer's disease and experimental cholinergic denervation
Deborah C. Mash;Donna D. Flynn;Lincoln T. Potter.
Neurofibrillary tangles, amyloid, and memory in aging and mild cognitive impairment.
Angela L. Guillozet;Sandra Weintraub;Deborah C. Mash;M. Marsel Mesulam.
JAMA Neurology (2003)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.
Alvaro N. Barbeira;Scott P. Dickinson;Rodrigo Bonazzola;Jiamao Zheng.
Nature Communications (2018)
Genetic variation in human NPY expression affects stress response and emotion
Zhifeng Zhou;Guanshan Zhu;Guanshan Zhu;Ahmad R. Hariri;Mary Anne Enoch.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: