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Michael von Bergwelt‐Baildon

Helmholtz Association of German Research Centres · DE
🔎 Find collaborators in Oncology · Immunology →
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Area of research
Oncology · Immunology
Research interest
Research interests include CAR-T cell therapy research, Cancer Immunotherapy and Biomarkers, Immunotherapy and Immune Responses, and Immune Cell Function and Interaction.
h-index
57
citations
13,735
works
556
NIH funding
primary concept
Medicine
email

Recent publications

Prognostic significance of immune reconstitution following CD19 CAR T‐cell therapy for relapsed/refractory B‐cell lymphoma
HemaSphere 2025cited by 19position: middledoi
Advances in the critical care management for patients with hematological malignancies
Blood Reviews 2025cited by 11position: middledoi
Dissection of single-cell landscapes for the development of chimeric antigen receptor T cells in Hodgkin lymphoma
Blood 2025cited by 9position: middledoi
Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation.
2025cited by 8position: contributordoi
Effective eradication of acute myeloid leukemia stem cells with FLT3-directed antibody-drug conjugates
Leukemia 2025cited by 7position: middledoi
ARID1A mutations protect follicular lymphoma from FAS-dependent immune surveillance by reducing RUNX3/ETS1-driven FAS-expression
Cell Death and Differentiation 2025cited by 6position: middledoi
Treatment gaps and survival outcomes of hepatocellular carcinoma: insights from a nationwide, claims-based study
Therapeutic Advances in Medical Oncology 2025cited by 3position: middledoi
Gastrointestinal toxicity of gemtuzumab ozogamicin: real-life data from the AMLCG, SAL, and CELL study groups
Blood Advances 2025cited by 3position: middledoi
Gastrointestinal toxicity of gemtuzumab ozogamicin: real-life data from the AMLCG, SAL, and CELL study groups.
2025cited by 3position: contributordoi
Navigating rare cancer care: Patient-reported insights into patient journeys, time to diagnosis, decision-making and care coordination from a national cross-sectional study in Germany
European Journal of Cancer 2025cited by 2position: lastdoi
Clinical features, course, and risk factors of infection-associated secondary hemophagocytic lymphohistiocytosis.
2025cited by 2position: contributordoi
Infections during AML induction chemotherapy in a contemporary cohort without fluoroquinolone prophylaxis
Infection 2025cited by 1position: middledoi
Maintenance treatment with trofosfamide in patients with advanced soft tissue sarcoma – a retrospective single-centre analysis
Acta Oncologica 2025cited by 1position: middledoi
Precision Oncology in Rare Endocrine and Neuroendocrine Neoplasms: Experiences and Challenges of the CCCMunichLMU Molecular Tumor Board
Targeted Oncology 2025cited by 1position: middledoi
Supplementary Figure S5 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
A platform of robust patient-derived leukemia models covering subgroups for which no cell lines exist
2025cited by 0position: contributordoi
Supplementary Figure S11 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figure S2 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Table S1 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Tables from Influence of Adipose Tissue Distribution, Sarcopenia, and Nutritional Status on Clinical Outcomes After CD19 CAR T-cell Therapy
2025cited by 0position: contributordoi
Supplementary Figure S9 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figure S8 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Table S2 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figure S1 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figures from Influence of Adipose Tissue Distribution, Sarcopenia, and Nutritional Status on Clinical Outcomes After CD19 CAR T-cell Therapy
2025cited by 0position: contributordoi
Supplementary Figure S6 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figure S4 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Figure S10 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Supplementary Table S3 from Tertiary Lymphoid Structures in Pancreatic Cancer are Structurally Homologous, Share Gene Expression Patterns and B-cell Clones with Secondary Lymphoid Organs, but Show Increased T-cell Activation
2025cited by 0position: contributordoi
Data from Influence of Adipose Tissue Distribution, Sarcopenia, and Nutritional Status on Clinical Outcomes After CD19 CAR T-cell Therapy
2025cited by 0position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

Marion Subklewe · Cancer Research Center45 papers (2019–2025)Sebastian Theurich · Gene Therapy Laboratory28 papers (2014–2025)Veit Bücklein · Cancer Research Center25 papers (2019–2025) · 25 papers (2021–2025) · 22 papers (2023–2025)Kai Rejeski · Cornell University21 papers (2021–2025)Viktoria Blumenberg · Harvard University21 papers (2021–2025) · 19 papers (2023–2025) · 19 papers (2023–2025) · 18 papers (2023–2025)Paul Trinkner · 18 papers (2023–2025)Khushali Jhaveri · Moffitt Cancer Center18 papers (2023–2025)Philipp Karschnia · University Hospital Heidelberg18 papers (2023–2025)Christian Schmidt · 18 papers (2023–2025)Lian Liu · 18 papers (2023–2025)Sophie Günther · 18 papers (2023–2025)Michael Jain · Moffitt Cancer Center18 papers (2023–2025) · 18 papers (2023–2025)David M. Cordas dos Santos · Massachusetts Institute of Technology18 papers (2023–2025) · 18 papers (2023–2025)
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