What is she best known for?
The fields of study she is best known for:
- Gene
- Internal medicine
- Immune system
Her primary areas of study are Immunology, Chemokine, Inflammation, Monocyte and Cell biology.
Her Immunology study integrates concerns from other disciplines, such as Stroke, Endothelium and Homeostasis.
Her Chemokine research is multidisciplinary, incorporating perspectives in Macrophage migration inhibitory factor and Cytokine.
Her Inflammation research includes elements of LDL receptor, Antigenic protein, DNA and Pathology.
She interconnects CCR2 and Neointimal hyperplasia in the investigation of issues within Monocyte.
In the subject of general Cell biology, her work in Cell adhesion molecule is often linked to TREM2, thereby combining diverse domains of study.
Her most cited work include:
- JAM-1 is a ligand of the beta(2) integrin LFA-1 involved in transendothelial migration of leukocytes. (546 citations)
- Platelet Microparticles: A Transcellular Delivery System for RANTES Promoting Monocyte Recruitment on Endothelium (288 citations)
- Auto-Antigenic Protein-DNA Complexes Stimulate Plasmacytoid Dendritic Cells to Promote Atherosclerosis (218 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of investigation include Immunology, Inflammation, Cell biology, Pathology and Chemokine.
Her Immunology study combines topics in areas such as Endothelium and Disease.
Her Inflammation study incorporates themes from Neovascularization and Cytokine.
Her study in Cell biology is interdisciplinary in nature, drawing from both Endothelial stem cell, Cell and Molecular biology.
Her Chemokine research integrates issues from Blood vessel and Chemotaxis.
The Monocyte study combines topics in areas such as CCR2 and Neointimal hyperplasia.
She most often published in these fields:
- Immunology (41.45%)
- Inflammation (31.58%)
- Cell biology (23.03%)
What were the highlights of her more recent work (between 2016-2021)?
- Inflammation (31.58%)
- Pathology (21.71%)
- Cell (5.92%)
In recent papers she was focusing on the following fields of study:
Her primary scientific interests are in Inflammation, Pathology, Cell, Cell biology and Immune system.
Her Inflammation research incorporates elements of Receptor, Cardiac metabolism and Bioinformatics.
Her research in Cell intersects with topics in Transcriptome, Gene expression, Mass cytometry, LDL receptor and Apolipoprotein E.
Her Cell biology research is multidisciplinary, relying on both Apoptosis, CD98, Fibrous cap, Cation homeostasis and CD19.
Her Immune system study necessitates a more in-depth grasp of Immunology.
Her Immunology study combines topics from a wide range of disciplines, such as Transcription factor and Infarction.
Between 2016 and 2021, her most popular works were:
- Single-Cell RNA-Seq Reveals the Transcriptional Landscape and Heterogeneity of Aortic Macrophages in Murine Atherosclerosis (192 citations)
- Atlas of the Immune Cell Repertoire in Mouse Atherosclerosis Defined by Single-Cell RNA-Sequencing and Mass Cytometry (152 citations)
- Macrophages in vascular inflammation and atherosclerosis (70 citations)
In her most recent research, the most cited papers focused on:
- Gene
- Internal medicine
- Immune system
The scientist’s investigation covers issues in Inflammation, Pathology, Immune system, Cancer research and Receptor.
Alma Zernecke studies Chemokine, a branch of Inflammation.
Her work deals with themes such as Phenotype, Tissue healing, Myocardial infarction and Ischemic stroke, which intersect with Pathology.
Her Immune system study is associated with Immunology.
When carried out as part of a general Immunology research project, her work on Macrophage inflammatory protein is frequently linked to work in Molecular medicine, therefore connecting diverse disciplines of study.
The Neovascularization research she does as part of her general Cancer research study is frequently linked to other disciplines of science, such as Intrinsic resistance, therefore creating a link between diverse domains of science.
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