Automated Author Profile

Hall, Alex

Current S-Index

23.3

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

1.6

Average Dataset Index per dataset

Total Datasets

15

Total datasets for this author

Average FAIR Score

60.5%

Average FAIR Score per dataset

Total Citations

6

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

A Facile Synthesis of Bulk LiPON in Solution for Solid-State Electrolyte

No description available

Authors

  • Gomez, Osma ;
  • Antar, Adam ;
  • Hall, Alex ;
  • Tapia-Aracayo, Leopoldo ;
  • Seo, Joshua ;
  • Kim, Nam ;
  • Sun, Zihan ;
  • Lim, Ryan ;
  • Chen, Fu ;
  • Li, Yue ;
  • Cumings, John ;
  • Rubloff, Gary ;
  • Lee, Sang Bok ;
  • Stewart, David ;
  • Wang, Yang
0 Citations0 Mentions77% FAIR1.9 Dataset Index
10.13016/uzs5-zinyJanuary 2025

Additional file 3: of The Vitamin C, Thiamine and Steroids in Sepsis (VICTAS) Protocol: a prospective, multi-center, double-blind, adaptive sample size, randomized, placebo-controlled, clinical trial

World Health Organization Trial Registration Data. (XLSX 10 kb)

Authors

  • Hager, David ;
  • Hooper, Michael ;
  • Bernard, Gordon ;
  • Busse, Laurence ;
  • E. Ely ;
  • Fowler, Alpha ;
  • Gaieski, David ;
  • Hall, Alex ;
  • Hinson, Jeremiah ;
  • Jackson, James ;
  • Gabor Kelen ;
  • Levine, Mark ;
  • Lindsell, Christopher ;
  • Malone, Richard ;
  • McGlothlin, Anna ;
  • Rothman, Richard ;
  • Viele, Kert ;
  • Wright, David ;
  • Sevransky, Jonathan ;
  • Martin, Greg
1 Citation0 Mentions15% FAIR0.7 Dataset Index
10.6084/m9.figshare.7961279.v1January 2019

Additional file 3: of The Vitamin C, Thiamine and Steroids in Sepsis (VICTAS) Protocol: a prospective, multi-center, double-blind, adaptive sample size, randomized, placebo-controlled, clinical trial

World Health Organization Trial Registration Data. (XLSX 10 kb)

Authors

  • Hager, David ;
  • Hooper, Michael ;
  • Bernard, Gordon ;
  • Busse, Laurence ;
  • E. Ely ;
  • Fowler, Alpha ;
  • Gaieski, David ;
  • Hall, Alex ;
  • Hinson, Jeremiah ;
  • Jackson, James ;
  • Gabor Kelen ;
  • Levine, Mark ;
  • Lindsell, Christopher ;
  • Malone, Richard ;
  • McGlothlin, Anna ;
  • Rothman, Richard ;
  • Viele, Kert ;
  • Wright, David ;
  • Sevransky, Jonathan ;
  • Martin, Greg
1 Citation0 Mentions15% FAIR0.7 Dataset Index
10.6084/m9.figshare.7961279January 2019

Gradient_experiment

No description available

Authors

  • Arias-Sánchez, Flor Inés ;
  • Allen, Richard ;
  • Hall, Alex
0 Citations0 Mentions77% FAIR1.9 Dataset Index
10.5061/dryad.60h3r/3January 2017

AB-Phage_experiment

No description available

Authors

  • Arias-Sánchez, Flor Inés ;
  • Allen, Richard ;
  • Hall, Alex
0 Citations0 Mentions77% FAIR1.9 Dataset Index
10.5061/dryad.60h3r/1January 2017

FluctuationTest

No description available

Authors

  • Arias-Sánchez, Flor Inés ;
  • Allen, Richard ;
  • Hall, Alex
0 Citations0 Mentions77% FAIR1.9 Dataset Index
10.5061/dryad.60h3r/2January 2017

Data from: Effects of antibiotic resistance alleles on bacterial evolutionary responses to viral parasites (Version: 2)

Antibiotic resistance has wide-ranging effects on bacterial phenotypes and evolution. However, the influence of antibiotic resistance on bacterial responses to parasitic viruses remains unclear, despite the ubiquity of such viruses in nature and current interest in therapeutic applications. We experimentally investigated this by exposing various Escherichia coli genotypes, including eight antibiotic-resistant genotypes and a mutator, to different viruses (lytic bacteriophages). Across 960 populations, we measured changes in population density and sensitivity to viruses, and tested whether variation among bacterial genotypes was explained by their relative growth in the absence of parasites, or mutation rate towards phage resistance measured by fluctuation tests for each phage. We found that antibiotic resistance had relatively weak effects on adaptation to phages, although some antibiotic-resistance alleles impeded the evolution of resistance to phages via growth costs. By contrast, a mutator allele, often found in antibiotic-resistant lineages in pathogenic populations, had a relatively large positive effect on phage-resistance evolution and population density under parasitism. This suggests costs of antibiotic resistance may modify the outcome of phage therapy against pathogenic populations previously exposed to antibiotics, but the effects of any co-occurring mutator alleles are likely to be stronger.

Authors

  • Arias-Sánchez, Flor I. ;
  • Hall, Alex
1 Citation0 Mentions77% FAIR2.0 Dataset Index
10.5061/dryad.90qb7April 2016

FEMSME_data.zip

No description available

Authors

  • Hall, Alex
0 Citations0 Mentions15% FAIR0.4 Dataset Index
10.5905/ethz-1007-68January 2016

Arias_Hall_BiolLett_2016_data

No description available

Authors

  • Arias-Sánchez, Flor I. ;
  • Hall, Alex
0 Citations0 Mentions77% FAIR1.7 Dataset Index
10.5061/dryad.90qb7.3/1.3January 2016

Arias_Hall_BiolLett_2016_data

No description available

Authors

  • Arias-Sánchez, Flor I. ;
  • Hall, Alex
0 Citations0 Mentions77% FAIR1.7 Dataset Index
10.5061/dryad.90qb7/1January 2016