Kyle R. Jackson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Kyle R. Jackson has a total of 268 co-authors. Here are the top co-authors by number of shared publications:
- Dorry Lidor Segev
Department of Surgery New York University New York New York USA
29 shared publications Allan B. Massie
Department of Surgery Johns Hopkins University School of Medicine Baltimore MD USA
17 shared publications- Allan B. Massie
Department of Surgery, New York University Langone Transplant Institute, New York, USA
11 shared publications - Jacqueline Garonzik-Wang
Department of Surgery, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama, USA; Comprehensive Transplant Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA
10 shared publications Niraj Desai
Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD
10 shared publications- Courtenay M. Holscher
Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD
9 shared publications
Latest Publications
- 16 September 2026
- Published by Wolters Kluwer Health in Liver Transplantation
Why the SRTR metric “Survival on the Waitlist” is still useful in the age of short liver transplant waiting times
Was not provided for this article.
- 16 September 2026
- Published by Wolters Kluwer Health in Liver Transplantation
Why the SRTR metric “Survival on the Waitlist” is still useful in the age of short liver transplant waiting times
Was not provided for this article.
- Open Access
- 30 May 2026
- Published by American Geophysical Union (AGU) in GeoHealth
- Vol. 10 (6)
Pediatric Risk Mapping From Co‐Exposure to Extreme Temperatures and Air Pollutants
Exposure to extreme temperatures and fine particulate matter is hazardous to human health, especially among children. With growing evidence on the impact of these environmental hazards on child health—including increased risks of respiratory illnesses, heat‐related illnesses, and developmental challenges—there is a substantial need to identify high‐risk areas for potential adverse pediatric health outcomes. In this study, we developed pediatric vulnerability indices at the census tract scale across the contiguous United States (CONUS) using five dimensionality reduction methods, including unsupervised machine learning and deep learning approaches. We integrated these indices with data on extreme temperature (2012–2024), PM 2.5 , and black carbon exposures from 2010 to 2020, enabling spatial analysis of environmental hazards and pediatric vulnerability. Among the five methods tested, principal component analysis (PCA) was selected for its balanced representation of 12 vulnerability factors, which explained 23% of the variance in the data. We observed that co‐exposure to extreme temperature and air pollutant exposures were highest in the West, Southwest, and certain parts of the South and Northeast. Approximately 36% of the CONUS showed statistically significant hotspots of co‐exposures to higher temperatures and air pollutants, concentrated in the West, Northwest, and Southwest. High‐risk areas for pediatric vulnerability and co‐exposure to environmental hazards were identified in both urban and rural communities, including indigenous lands and agricultural regions. These findings can aid policymakers and public health officials as a preliminary resource in developing heat action plans and allocating cooling centers to protect children living in the most affected communities.
- 30 May 2026
- Published by American Geophysical Union (AGU) in GeoHealth
- Vol. 10 (6)
Open AccessPediatric Risk Mapping From Co‐Exposure to Extreme Temperatures and Air Pollutants
Exposure to extreme temperatures and fine particulate matter is hazardous to human health, especially among children. With growing evidence on the impact of these environmental hazards on child health—including increased risks of respiratory illnesses, heat‐related illnesses, and developmental challenges—there is a substantial need to identify high‐risk areas for potential adverse pediatric health outcomes. In this study, we developed pediatric vulnerability indices at the census tract scale across the contiguous United States (CONUS) using five dimensionality reduction methods, including unsupervised machine learning and deep learning approaches. We integrated these indices with data on extreme temperature (2012–2024), PM 2.5 , and black carbon exposures from 2010 to 2020, enabling spatial analysis of environmental hazards and pediatric vulnerability. Among the five methods tested, principal component analysis (PCA) was selected for its balanced representation of 12 vulnerability factors, which explained 23% of the variance in the data. We observed that co‐exposure to extreme temperature and air pollutant exposures were highest in the West, Southwest, and certain parts of the South and Northeast. Approximately 36% of the CONUS showed statistically significant hotspots of co‐exposures to higher temperatures and air pollutants, concentrated in the West, Northwest, and Southwest. High‐risk areas for pediatric vulnerability and co‐exposure to environmental hazards were identified in both urban and rural communities, including indigenous lands and agricultural regions. These findings can aid policymakers and public health officials as a preliminary resource in developing heat action plans and allocating cooling centers to protect children living in the most affected communities.
- Open Access
- 23 December 2023
- Published by Elsevier in American Journal of Transplantation
- Vol. 24 (4) , 606-618
A2/A2B to B deceased donor kidney transplantation in the Kidney Allocation System era
- 23 December 2023
- Published by Elsevier in American Journal of Transplantation
- Vol. 24 (4) , 606-618
Open AccessA2/A2B to B deceased donor kidney transplantation in the Kidney Allocation System era
- Open Access
- 23 September 2023
- Published by Elsevier in American Journal of Transplantation
- Vol. 23 (12) , 1980-1989
Characterizing the risk of human leukocyte antigen-incompatible living donor kidney transplantation in older recipients
- 23 September 2023
- Published by Elsevier in American Journal of Transplantation
- Vol. 23 (12) , 1980-1989
Open AccessCharacterizing the risk of human leukocyte antigen-incompatible living donor kidney transplantation in older recipients
- Open Access
- 30 December 2022
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (5) , 1838-1847
Liver transplantation in the United States during the COVID-19 pandemic: National and center-level responses
- 30 December 2022
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (5) , 1838-1847
Open AccessLiver transplantation in the United States during the COVID-19 pandemic: National and center-level responses
- Open Access
- 1 October 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (10) , 3305-3311
MELD is MELD is MELD? Transplant center–level variation in waitlist mortality for candidates with the same biological MELD
- 1 October 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (10) , 3305-3311
Open AccessMELD is MELD is MELD? Transplant center–level variation in waitlist mortality for candidates with the same biological MELD
- Open Access
- 31 August 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 22 (4) , 1031-1036
Rethinking incompatibility in kidney transplantation
- 31 August 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 22 (4) , 1031-1036
Open AccessRethinking incompatibility in kidney transplantation
- Open Access
- 27 February 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (4) , 1612-1621
Delayed graft function and acute rejection following HLA-incompatible living donor kidney transplantation
- 27 February 2021
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (4) , 1612-1621
Open AccessDelayed graft function and acute rejection following HLA-incompatible living donor kidney transplantation
- 1 February 2021
- Published by Wolters Kluwer Health in Transplantation
- Vol. 105 (2) , 436-442
Center-level Variation in HLA-incompatible Living Donor Kidney Transplantation Outcomes
Background.: Desensitization protocols for HLA-incompatible living donor kidney transplantation (ILDKT) vary across centers. The impact of these, as well as other practice variations, on ILDKT outcomes remains unknown. Methods.: We sought to quantify center-level variation in mortality and graft loss following ILDKT using a 25-center cohort of 1358 ILDKT recipients with linkage to Scientific Registry of Transplant Recipients for accurate outcome ascertainment. We used multilevel Cox regression with shared frailty to determine the variation in post-ILDKT outcomes attributable to between-center differences and to identify any center-level characteristics associated with improved post-ILDKT outcomes. Results.: After adjusting for patient-level characteristics, only 6 centers (24%) had lower mortality and 1 (4%) had higher mortality than average. Similarly, only 5 centers (20%) had higher graft loss and 2 had lower graft loss than average. Only 4.7% of the differences in mortality (P < 0.01) and 4.4% of the differences in graft loss (P < 0.01) were attributable to between-center variation. These translated to a median hazard ratio of 1.36 for mortality and 1.34 of graft loss for similar candidates at different centers. Post-ILDKT outcomes were not associated with the following center-level characteristics: ILDKT volume and transplanting a higher proportion of highly sensitized, prior transplant, preemptive, or minority candidates. Conclusions.: Unlike most aspects of transplantation in which center-level variation and volume impact outcomes, we did not find substantial evidence for this in ILDKT. Our findings support the continued practice of ILDKT across these diverse centers.
- 1 February 2021
- Published by Wolters Kluwer Health in Transplantation
- Vol. 105 (2) , 436-442
Center-level Variation in HLA-incompatible Living Donor Kidney Transplantation Outcomes
Background.: Desensitization protocols for HLA-incompatible living donor kidney transplantation (ILDKT) vary across centers. The impact of these, as well as other practice variations, on ILDKT outcomes remains unknown. Methods.: We sought to quantify center-level variation in mortality and graft loss following ILDKT using a 25-center cohort of 1358 ILDKT recipients with linkage to Scientific Registry of Transplant Recipients for accurate outcome ascertainment. We used multilevel Cox regression with shared frailty to determine the variation in post-ILDKT outcomes attributable to between-center differences and to identify any center-level characteristics associated with improved post-ILDKT outcomes. Results.: After adjusting for patient-level characteristics, only 6 centers (24%) had lower mortality and 1 (4%) had higher mortality than average. Similarly, only 5 centers (20%) had higher graft loss and 2 had lower graft loss than average. Only 4.7% of the differences in mortality (P < 0.01) and 4.4% of the differences in graft loss (P < 0.01) were attributable to between-center variation. These translated to a median hazard ratio of 1.36 for mortality and 1.34 of graft loss for similar candidates at different centers. Post-ILDKT outcomes were not associated with the following center-level characteristics: ILDKT volume and transplanting a higher proportion of highly sensitized, prior transplant, preemptive, or minority candidates. Conclusions.: Unlike most aspects of transplantation in which center-level variation and volume impact outcomes, we did not find substantial evidence for this in ILDKT. Our findings support the continued practice of ILDKT across these diverse centers.
- Open Access
- 19 September 2020
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (4) , 1564-1575
Quantifying infection risks in incompatible living donor kidney transplant recipients
- 19 September 2020
- Published by Elsevier in American Journal of Transplantation
- Vol. 21 (4) , 1564-1575
Open AccessQuantifying infection risks in incompatible living donor kidney transplant recipients