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Suzanne George

Harvard University · US
Area of research
Pulmonary and Respiratory Medicine · Gastroenterology
Research interest
Research interests include Gastrointestinal Tumor Research and Treatment, Sarcoma Diagnosis and Treatment, Gastric Cancer Management and Outcomes, and Cancer Genomics and Diagnostics.
h-index
74
citations
21,096
works
624
NIH funding
primary concept
Medicine
email

Recent publications

Digitally engaging participants in cancer clinical trials: Design and pilot of the Alliance Participant Engagement Portal (PEP).
2026cited by 0position: contributordoi
Multi-Omic Landscape of Gastrointestinal Stromal Tumors in a Real-World Patient Cohort of 1,427 Cases.
2026cited by 0position: contributordoi
A Phase 2 Study of the Eribulin in Patients with Metastatic Angiosarcoma and Epithelioid Hemangioendothelioma (EHE).
2026cited by 0position: contributordoi
Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable KDR Variants, Recurrent MED12 Mutations, and a High Burden of Germline POT1 Alterations.
2025cited by 6position: contributordoi
Navigating Ongoing Challenges in GI Stromal Tumors.
2025cited by 1position: contributordoi
Challenges in Automating Extraction of Real-World Radiographic Images and Adverse Events: Lessons From the ICAREdata Initiative.
2025cited by 1position: contributordoi
Updated Overall Survival and Long-Term Safety With Ripretinib Versus Sunitinib in Patients With GI Stromal Tumor: Final Overall Survival Analysis From INTRIGUE.
2025cited by 1position: contributordoi
Supplementary Figure S5 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Table S2 from Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable <i>KDR</i> Variants, Recurrent <i>MED12</i> Mutations, and a High Burden of Germline <i>POT1</i> Alterations
2025cited by 0position: contributordoi
Supplementary Figure S1 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S10 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Data from Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable <i>KDR</i> Variants, Recurrent <i>MED12</i> Mutations, and a High Burden of Germline <i>POT1</i> Alterations
2025cited by 0position: contributordoi
Supplementary Table S5 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S3 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Table S3 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Table S4 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Table S1 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S11 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
supplementary table TS1 from National Cancer Institute Combination Therapy Platform Trial with Molecular Analysis for Therapy Choice (ComboMATCH)
2025cited by 0position: contributordoi
Supplementary Table S1 from Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable <i>KDR</i> Variants, Recurrent <i>MED12</i> Mutations, and a High Burden of Germline <i>POT1</i> Alterations
2025cited by 0position: contributordoi
Supplementary Figure S8 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S1 from A Phase I, Multicenter, Open-Label, First-in-Human Study of DS-6157a in Patients with Advanced Gastrointestinal Stromal Tumor
2025cited by 0position: contributordoi
Supplementary Figure S6 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S4 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Table S2 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S3 from Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable <i>KDR</i> Variants, Recurrent <i>MED12</i> Mutations, and a High Burden of Germline <i>POT1</i> Alterations
2025cited by 0position: contributordoi
Supplementary Figure S7 from Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma
2025cited by 0position: contributordoi
Supplementary Figure S2 from A Phase I, Multicenter, Open-Label, First-in-Human Study of DS-6157a in Patients with Advanced Gastrointestinal Stromal Tumor
2025cited by 0position: contributordoi
Supplementary Figure S1 from Genomic Profiling of Cardiac Angiosarcoma Reveals Novel Targetable <i>KDR</i> Variants, Recurrent <i>MED12</i> Mutations, and a High Burden of Germline <i>POT1</i> Alterations
2025cited by 0position: contributordoi
Data from National Cancer Institute Combination Therapy Platform Trial with Molecular Analysis for Therapy Choice (ComboMATCH)
2025cited by 0position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

· 152 papers (2021–2026)Adrián Mariño-Enríquez · Dana-Farber Cancer Institute70 papers (2023–2025)Jonathan A. Fletcher · Borders General Hospital52 papers (2023–2025)Wen-Bin Ou · Zhejiang Sci-Tech University52 papers (2023–2025)Isabella Klooster · TE Laboratories (Ireland)52 papers (2023–2025)Meijun Z. Lundberg · Harvard University52 papers (2023–2025)Victor Mao · Harvard University51 papers (2023–2025)David E. Root · Broad Institute51 papers (2023–2025)Derrick L. Tao · Brigham and Women's Hospital51 papers (2023–2025)Doga C. Gulhan · Harvard University Press51 papers (2023–2025)Jan Philipp Novotny · Umeå University51 papers (2023–2025)Brittaney A. Leeper · Sidney Kimmel Cancer Center51 papers (2023–2025)Peter J. Park · Brearley School51 papers (2023–2025)Glenn S. Cowley · Broad Institute51 papers (2023–2025)Prafulla C. Gokhale · University of Georgia51 papers (2023–2025)Frank T. Zenke · Scripps Research Institute51 papers (2023–2025)Antuan Tran · Boston Medical Center51 papers (2023–2025)Karla V Ballman · Presbyterian Hospital51 papers (2023–2025)Joachim Albers · Merck (Germany)51 papers (2023–2025)Daniel F. Pilco‐Janeta · Universitat de Barcelona51 papers (2023–2025)