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Translational Medicine / 转化医学Pediatric Oncology

Stefan Pfister

斯特凡·普菲斯特

MD

🏢German Cancer Research Center (DKFZ) / Heidelberg University Hospital(德国癌症研究中心/海德堡大学医院)🌐Germany

Division Head, Pediatric Neurooncology儿童神经肿瘤科部门主任

72
h-index
3
Key Papers
5
Awards
3
Key Contributions

👥Biography 个人简介

Stefan Pfister is a preeminent pediatric neuro-oncologist at DKFZ Heidelberg who revolutionized brain tumor classification through DNA methylation profiling, co-led landmark medulloblastoma subgroup genomics studies, and founded the Heidelberg Brain Tumor Reference Center serving global diagnostics.

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🧪Research Fields 研究领域

Pediatric Brain Tumor Genomics儿童脑肿瘤基因组学
Medulloblastoma Subgroups髓母细胞瘤分子亚型
DNA Methylation ClassificationDNA甲基化分类
Epigenomics表观基因组学

🎓Key Contributions 主要贡献

DNA Methylation Brain Tumor Classification

Co-developed the DKFZ DNA methylation classifier for CNS tumors, a paradigm-shifting tool now used worldwide to precisely classify over 150 brain tumor entities from a single assay.

Medulloblastoma Genomics

Co-led international genomic studies defining medulloblastoma's four molecular subgroups (WNT, SHH, Group 3, Group 4) and their distinct driver mutations and clinical outcomes.

Pediatric Glioma Epigenomics

Identified recurrent histone H3 mutations (H3K27M, H3G34R/V) in pediatric high-grade gliomas, establishing new tumor entities with distinct biological and clinical properties.

Representative Works 代表性著作

[1]

DNA methylation-based classification of central nervous system tumours

Nature (2018)

Landmark study introducing genome-wide DNA methylation profiling as the gold standard for objective CNS tumor classification.

[2]

Subgroup-specific structural variation across 1,000 medulloblastoma genomes

Nature (2022)

Comprehensive structural genomic analysis of 1,000 medulloblastomas revealing subgroup-specific vulnerabilities and therapeutic targets.

[3]

K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

Acta Neuropathologica (2012)

Identified H3.3 K27M as a hallmark mutation in DIPG with prognostic significance.

🏆Awards & Recognition 奖项与荣誉

🏆Gottfried Wilhelm Leibniz Prize (DFG)
🏆German Cancer Award
🏆ISNO Distinguished Service Award
🏆ERC Advanced Grant
🏆Heinz Nixdorf Foundation Award

📄Data Sources 数据来源

Last updated: 2026-01-15 | All information from publicly available academic sources

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