What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Cell biology, Arabidopsis, Cell cycle, Genetics and Endoreduplication.
His research in Cell biology intersects with topics in Cyclin-dependent kinase, Botany, Control of chromosome duplication and Cell fate determination.
His Arabidopsis study frequently links to adjacent areas such as Trichome.
Trichome differentiation, Lateral inhibition and Root hair is closely connected to Trichome patterning in his research, which is encompassed under the umbrella topic of Trichome.
His work is dedicated to discovering how Cell cycle, Multicellular organism are connected with DNA damage and other disciplines.
The study of Genetics is intertwined with the study of Evolutionary dynamics in a number of ways.
His most cited work include:
- Genome sequencing and analysis of the model grass Brachypodium distachyon (1433 citations)
- Integrative epigenomic mapping defines four main chromatin states in Arabidopsis. (492 citations)
- TRIPTYCHON and CAPRICE mediate lateral inhibition during trichome and root hair patterning in Arabidopsis (414 citations)
What are the main themes of his work throughout his whole career to date?
Cell biology, Arabidopsis, Genetics, Cell cycle and Cyclin-dependent kinase are his primary areas of study.
His Cell biology research includes themes of Endoreduplication, Arabidopsis thaliana, Meiosis and Cell division.
Arp Schnittger has included themes like Cell fate determination and Trichome, Botany in his Arabidopsis study.
His work carried out in the field of Trichome brings together such families of science as Epidermis, Trichome patterning and Root hair.
In his work, DNA damage is strongly intertwined with DNA repair, which is a subfield of Cell cycle.
Arp Schnittger has researched Cyclin-dependent kinase in several fields, including Cyclin-dependent kinase 1, Anaphase-promoting complex, G2-M DNA damage checkpoint and Kinase activity.
He most often published in these fields:
- Cell biology (70.68%)
- Arabidopsis (57.14%)
- Genetics (38.35%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (70.68%)
- Meiosis (27.82%)
- Arabidopsis (57.14%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Cell biology, Meiosis, Arabidopsis, Arabidopsis thaliana and Homologous chromosome.
His Cell biology research is multidisciplinary, incorporating perspectives in Cyclin-dependent kinase 1, Cell cycle and Cell division, Cytokinesis.
His Cell cycle course of study focuses on Embryo and Leaf size, Transcriptome, Transcription factor and Endosperm.
Arp Schnittger works mostly in the field of Meiosis, limiting it down to topics relating to Live cell imaging and, in certain cases, Meiocyte.
His Arabidopsis study incorporates themes from HORMA domain, Homologous recombination and Green fluorescent protein.
In his research on the topic of Arabidopsis thaliana, Epigenetics, DNA demethylation, Gene and DNA methylation is strongly related with DNA.
Between 2018 and 2021, his most popular works were:
- Live cell imaging of meiosis in Arabidopsis thaliana (22 citations)
- Protein and metabolite composition of Arabidopsis stress granules. (22 citations)
- SWITCH 1/DYAD is a WINGS APART-LIKE antagonist that maintains sister chromatid cohesion in meiosis. (17 citations)
In his most recent research, the most cited papers focused on:
Arp Schnittger spends much of his time researching Cell biology, Arabidopsis, Meiosis, Prophase and Cohesin.
His Cell biology research incorporates elements of Arabidopsis thaliana, Mutant, Homologous chromosome and HORMA domain.
His Arabidopsis thaliana study integrates concerns from other disciplines, such as RAD51, DNA damage and DNA.
The various areas that Arp Schnittger examines in his Arabidopsis study include Proteome, Proteomics and Green fluorescent protein.
His Cohesin research includes elements of Phragmoplast, Live cell imaging, Sister chromatids and Meiocyte.
His Cyclin-dependent kinase 2 study combines topics in areas such as Cyclin-dependent kinase 1, Recombination and Kinase activity.
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