What is he best known for?
The fields of study he is best known for:
- Gene
- Enzyme
- Cell membrane
Graham Warren mainly focuses on Golgi apparatus, Cell biology, Golgi reassembly, Golgi disassembly and Endoplasmic reticulum.
His Golgi apparatus study combines topics in areas such as Molecular biology and Membrane protein.
His Cell biology research is multidisciplinary, incorporating elements of Vesicle and Lipid bilayer fusion.
His Golgi reassembly study combines topics from a wide range of disciplines, such as Plasma protein binding, Mitosis and ASK1.
The various areas that Graham Warren examines in his Golgi disassembly study include Vesicle docking, Golgi inheritance and MAP kinase kinase kinase.
His research in Endoplasmic reticulum intersects with topics in Shc Signaling Adaptor Proteins, Cytoplasm, Exocytosis, Baby hamster kidney cell and Cell membrane.
His most cited work include:
- Characterization of a cis-Golgi matrix protein, GM130 (682 citations)
- Implications of the SNARE hypothesis for intracellular membrane topology and dynamics (512 citations)
- The road taken: past and future foundations of membrane traffic. (401 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Cell biology, Golgi apparatus, Mitosis, Endoplasmic reticulum and Biochemistry.
His Cell biology research integrates issues from Vesicle, Trypanosoma brucei and Molecular biology.
Many of his studies involve connections with topics such as Cell plate and Golgi apparatus.
His Mitosis research includes themes of Cell, Cell division, Nocodazole, Membrane and Interphase.
Graham Warren combines subjects such as Cytoplasm, Glycoprotein, Protein biosynthesis, Receptor and Membrane protein with his study of Endoplasmic reticulum.
His biological study spans a wide range of topics, including Golgi inheritance and Telophase.
He most often published in these fields:
- Cell biology (75.71%)
- Golgi apparatus (69.49%)
- Mitosis (22.60%)
What were the highlights of his more recent work (between 2004-2018)?
- Cell biology (75.71%)
- Golgi apparatus (69.49%)
- Trypanosoma brucei (14.12%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Golgi apparatus, Trypanosoma brucei, COPI and Biochemistry.
Graham Warren has included themes like Vesicle, Cell cycle and Molecular biology in his Cell biology study.
His Golgi apparatus study contributes to a more complete understanding of Endoplasmic reticulum.
The COPI study which covers RAB1 that intersects with Lipid bilayer fusion, Tethering and Exocytosis.
His work on Cell function as part of general Biochemistry study is frequently linked to Dna double helix and Vitalism, bridging the gap between disciplines.
His work carried out in the field of Golgi reassembly brings together such families of science as Golgi cisterna and Golgi disassembly.
Between 2004 and 2018, his most popular works were:
- Golgin tethers define subpopulations of COPI vesicles. (162 citations)
- Journeys through the golgi - taking stock in a new era (141 citations)
- Mapping the functional domains of the Golgi stacking factor GRASP65. (123 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Cell membrane
His scientific interests lie mostly in Cell biology, Golgi apparatus, Trypanosoma brucei, COPI and Endoplasmic reticulum.
His Cell biology study combines topics in areas such as Molecular biology and Cell cycle.
Golgi apparatus and Cognitive science are two areas of study in which he engages in interdisciplinary research.
Graham Warren interconnects Vesicular-tubular cluster, Vesicle and Matrix in the investigation of issues within COPI.
His Endoplasmic reticulum research incorporates themes from Receptor and Tethering.
His research integrates issues of Golgi cisterna, Golgi disassembly and Golgi reassembly in his study of Mitosis.
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.
