D-Index & Metrics Best Publications
Chris A. Kaiser

Chris A. Kaiser

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 51 Citations 14,706 63 World Ranking 9888 National Ranking 4367

Research.com Recognitions

Awards & Achievements

2010 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Amino acid

Chris A. Kaiser mainly investigates Biochemistry, Endoplasmic reticulum, ER oxidoreductin, Protein disulfide-isomerase and Cell biology. Biochemistry is a component of his Conserved sequence, Saccharomyces cerevisiae and Yeast studies. In his work, Amino acid permease and Regulation of gene expression is strongly intertwined with Amino acid, which is a subfield of Saccharomyces cerevisiae.

The Endoplasmic reticulum study combines topics in areas such as Electron transport chain, Glutathione, Thiol and Dithiol. His ER oxidoreductin research includes elements of RoGFP, Glutaredoxin and Mutant. His research in Protein disulfide-isomerase intersects with topics in Periplasmic space and Protein folding.

His most cited work include:

  • The genetic landscape of a cell. (1828 citations)
  • Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway (585 citations)
  • Formation and transfer of disulphide bonds in living cells. (551 citations)

What are the main themes of his work throughout his whole career to date?

Chris A. Kaiser focuses on Biochemistry, Endoplasmic reticulum, Cell biology, Saccharomyces cerevisiae and Protein disulfide-isomerase. His work on Biochemistry deals in particular with Amino acid, Amino acid permease, Yeast, Transport protein and Mutant. Chris A. Kaiser is involved in the study of Endoplasmic reticulum that focuses on ER oxidoreductin in particular.

The study incorporates disciplines such as Vesicle and Secretion in addition to Cell biology. His Saccharomyces cerevisiae research incorporates themes from Invertase and Peptide sequence. His Protein disulfide-isomerase research is multidisciplinary, relying on both Oxidoreductase, Cysteine, Thiol and Stereochemistry.

He most often published in these fields:

  • Biochemistry (56.58%)
  • Endoplasmic reticulum (39.47%)
  • Cell biology (38.16%)

What were the highlights of his more recent work (between 2010-2018)?

  • Cell biology (38.16%)
  • Genetics (10.53%)
  • Endoplasmic reticulum (39.47%)

In recent papers he was focusing on the following fields of study:

Chris A. Kaiser mostly deals with Cell biology, Genetics, Endoplasmic reticulum, Biochemistry and Small molecule. His Gene, Synthetic lethality, Karyotype and Gene duplication study, which is part of a larger body of work in Genetics, is frequently linked to Genome instability, bridging the gap between disciplines. Biophysics, Glutathione, Protein disulfide-isomerase, Thiol and Glutathione disulfide is closely connected to Oxidative phosphorylation in his research, which is encompassed under the umbrella topic of Endoplasmic reticulum.

His Yeast, Saccharomyces cerevisiae and Transport protein study in the realm of Biochemistry connects with subjects such as Vacuole. The various areas that Chris A. Kaiser examines in his Saccharomyces cerevisiae study include Amino acid, Protein catabolism, Amino acid permease, Mutant and Cell membrane. Chris A. Kaiser works mostly in the field of Small molecule, limiting it down to concerns involving Computational biology and, occasionally, In vivo and Small Molecule Libraries.

Between 2010 and 2018, his most popular works were:

  • Mapping the Cellular Response to Small Molecules Using Chemogenomic Fitness Signatures (168 citations)
  • Redox signaling via the molecular chaperone BiP protects cells against endoplasmic reticulum-derived oxidative stress (64 citations)
  • Balanced Ero1 activation and inactivation establishes ER redox homeostasis (55 citations)

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.

Best Publications

The genetic landscape of a cell.

Michael Costanzo;Anastasia Baryshnikova;Jeremy Bellay;Yungil Kim.
Science (2010)

2362 Citations

Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway

Chris A. Kaiser;Randy Schekman.
Cell (1990)

917 Citations

Formation and transfer of disulphide bonds in living cells.

Carolyn S. Sevier;Chris A. Kaiser.
Nature Reviews Molecular Cell Biology (2002)

773 Citations

Nitrogen regulation in Saccharomyces cerevisiae.

Boris Magasanik;Chris A Kaiser.
Gene (2002)

757 Citations

The ERO1 gene of yeast is required for oxidation of protein dithiols in the endoplasmic reticulum

Alison R Frand;Chris A Kaiser.
Molecular Cell (1998)

651 Citations

Exploration of essential gene functions via titratable promoter alleles

Sanie Mnaimneh;Armaity P Davierwala;Jennifer Haynes;Jason Moffat.
Cell (2004)

651 Citations

Ero1p oxidizes protein disulfide isomerase in a pathway for disulfide bond formation in the endoplasmic reticulum.

Alison R Frand;Chris A Kaiser.
Molecular Cell (1999)

498 Citations

Many random sequences functionally replace the secretion signal sequence of yeast invertase.

Chris A. Kaiser;Daphne Preuss;Paula Grisafi;David Botstein.
Science (1987)

482 Citations

Pathways for protein disulphide bond formation.

Alison R Frand;John W Cuozzo;Chris A Kaiser.
Trends in Cell Biology (2000)

426 Citations

Competition between glutathione and protein thiols for disulphide-bond formation.

John W. Cuozzo;Chris A. Kaiser.
Nature Cell Biology (1999)

379 Citations

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