What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Phosphorylation, Signal transduction, Proteomics, Biochemistry and Cell biology.
As part of his studies on Phosphorylation, he often connects relevant areas like Kinase.
The concepts of his Signal transduction study are interwoven with issues in Receptor, Epidermal growth factor receptor, Cancer research and Cell growth.
Forest M. White has included themes like Proteome, Proteogenomics and Phosphoproteomics in his Proteomics study.
Forest M. White combines subjects such as Epitope and Molecular biology with his study of Biochemistry.
As a part of the same scientific family, Forest M. White mostly works in the field of Cell biology, focusing on Epidermal growth factor and, on occasion, Neuregulin, LNCaP, Forskolin and Androgen receptor.
His most cited work include:
- Phosphoproteome analysis by mass spectrometry and its application to Saccharomyces cerevisiae (1406 citations)
- Proteogenomic characterization of human colon and rectal cancer (831 citations)
- Time-resolved Mass Spectrometry of Tyrosine Phosphorylation Sites in the Epidermal Growth Factor Receptor Signaling Network Reveals Dynamic Modules (495 citations)
What are the main themes of his work throughout his whole career to date?
Forest M. White mainly investigates Cell biology, Phosphorylation, Signal transduction, Cancer research and Computational biology.
His Cell biology research is multidisciplinary, incorporating perspectives in Downregulation and upregulation and Immunology.
His Phosphorylation study is associated with Biochemistry.
His Signal transduction study integrates concerns from other disciplines, such as Phosphorylation sites, Receptor, Epidermal growth factor and Bioinformatics.
His Cancer research study combines topics in areas such as Cancer, Epidermal growth factor receptor, Cell growth, Mutation and Tyrosine kinase.
His Computational biology study which covers Proteomics that intersects with Phosphoproteomics and Mass spectrometry.
He most often published in these fields:
- Cell biology (26.50%)
- Phosphorylation (26.50%)
- Signal transduction (24.50%)
What were the highlights of his more recent work (between 2018-2021)?
- Cancer research (22.50%)
- Cell biology (26.50%)
- Phosphoproteomics (14.50%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Cancer research, Cell biology, Phosphoproteomics, Phosphorylation and Tyrosine phosphorylation.
His Cancer research study combines topics from a wide range of disciplines, such as Cancer, Colorectal cancer, Antigen, Kinase and Tumor antigen.
His biological study spans a wide range of topics, including MHC class I, Interferon gamma, Antigen presentation and Immunotherapy.
His Phosphoproteomics research is multidisciplinary, incorporating elements of Proteogenomics, Proteomics and Microglia.
His Phosphorylation research includes elements of PLK1, Zinc finger, Chromatin, Gene and Signal transduction.
His study looks at the intersection of Tyrosine phosphorylation and topics like Computational biology with Precision medicine and Targeted mass spectrometry.
Between 2018 and 2021, his most popular works were:
- Proteogenomic Analysis of Human Colon Cancer Reveals New Therapeutic Opportunities. (142 citations)
- Systemic analysis of tyrosine kinase signaling reveals a common adaptive response program in a HER2-positive breast cancer (21 citations)
- Localized metabolomic gradients in patient-derived xenograft models of glioblastoma (16 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Cancer research, Proteomics, Immune system, Antigen and Phosphoproteomics.
His Cancer research research integrates issues from Metabolism, Fatty acid metabolism, Tyrosine kinase and Protein kinase A.
His Proteomics study incorporates themes from Proteogenomics and Immunotherapy.
His Phosphoproteomics study deals with Tyrosine intersecting with Cell biology.
The Cell biology study combines topics in areas such as Zinc finger, Mutant and PLK1.
In the subject of general Major histocompatibility complex, his work in MHC class I is often linked to Repertoire, thereby combining diverse domains of study.
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