Emerson A. Lim
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
Emerson A. Lim has a total of 168 co-authors. Here are the top co-authors by number of shared publications:
- Dawn L. Hershman
Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY
54 shared publications - Kevin Kalinsky
Winship Cancer Institute at Emory University, Atlanta, USA
54 shared publications - Alfred I. Neugut
Columbia University
52 shared publications - Ana Tergas
Division of Gynecologic Oncology, Department of Surgery City of Hope Comprehensive Cancer Center Duarte California USA
52 shared publications - Andrea Califano
Department of Systems Biology, Columbia University, New York, USA
52 shared publications - Andrew B. Lassman
Division of Neuro-Oncology, Department of Neurology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY
52 shared publications
Latest Publications
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S5 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Comprehensive list of clinically relevant drugs screened in cell lines (not all were available at time of study). The list is divided into three sections, including one with FDA approved antineoplastics, one with experimental antineoplastics in clinical trials, and one with non-antineoplastics and tool compounds selectively screened when demonstrating an EC50 < 2μM.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S5 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Comprehensive list of clinically relevant drugs screened in cell lines (not all were available at time of study). The list is divided into three sections, including one with FDA approved antineoplastics, one with experimental antineoplastics in clinical trials, and one with non-antineoplastics and tool compounds selectively screened when demonstrating an EC50 < 2μM.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Supplementary Figures S1-S6 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Supplementary Figures S1-S6 and figure legends.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figures S1-S6 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Supplementary Figures S1-S6 and figure legends.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S3 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Detailed summary of drugs prioritized for testing in PDX models, based on rank of OncoTarget and OncoTreat predictions by –log10(Bonferroni p).
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S3 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Detailed summary of drugs prioritized for testing in PDX models, based on rank of OncoTarget and OncoTreat predictions by –log10(Bonferroni p).
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S1 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Summary of enrollment for the N of 1 trial to date, including numbers by cancer type, the attempt to develop a PDX, establishment of PDX, RNASeq/VIPER profiling of PDX when established, and completion of drug testing.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S1 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Summary of enrollment for the N of 1 trial to date, including numbers by cancer type, the attempt to develop a PDX, establishment of PDX, RNASeq/VIPER profiling of PDX when established, and completion of drug testing.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S4 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Curated list of proteins with high-affinity inhibitor drugs for OncoTarget analysis.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S4 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Curated list of proteins with high-affinity inhibitor drugs for OncoTarget analysis.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S6 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Detailed summary of therapeutic response at end-of-study time point, organized by study group—OncoTreat, OncoTarget, or Negative control—and then stratified by each individual drug arm. The study was underpowered for statistical analyses of therapeutic response in individual drug arms.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S6 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Detailed summary of therapeutic response at end-of-study time point, organized by study group—OncoTreat, OncoTarget, or Negative control—and then stratified by each individual drug arm. The study was underpowered for statistical analyses of therapeutic response in individual drug arms.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S2 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Prioritized drugs, prediction basis, and dosing schedule for PDX therapeutic study.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Prioritized drugs, prediction basis, and dosing schedule for PDX therapeutic study.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S8 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
List of available interactomes (gene regulatory networks) that have been generated from RNASeq datasets of patient tumor samples using the ARACNe algorithm.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S8 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
List of available interactomes (gene regulatory networks) that have been generated from RNASeq datasets of patient tumor samples using the ARACNe algorithm.
- Open Access
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Table S7 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Current list of cancer cell lines with available drug perturbation RNASeq profiles, which together comprise the PanACEA resource.
- 11 December 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S7 from A Transcriptome-Based Precision Oncology Platform for Patient–Therapy Alignment in a Diverse Set of Treatment-Resistant Malignancies
Current list of cancer cell lines with available drug perturbation RNASeq profiles, which together comprise the PanACEA resource.