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Florian Markowetz

University of Cambridge · GB
Area of research
Cancer Research · Molecular Biology
Research interest
Research interests include Cancer Genomics and Diagnostics, Ovarian cancer diagnosis and treatment, Gene expression and cancer classification, and Bioinformatics and Genomic Networks.
h-index
66
citations
35,451
works
365
NIH funding
primary concept
Biology
email

Recent publications

Deciphering selection patterns of somatic copy-number events
2026cited by 0position: contributordoi
WNT-driven chromosomal instability as a biomarker for PORCN inhibition
2026cited by 0position: contributordoi
A standardized framework for robust fragmentomic feature extraction from cell-free DNA sequencing data
Genome biology 2025cited by 17position: middledoi
Biomarker risk stratification with capsule sponge in the surveillance of Barrett's oesophagus: prospective evaluation of UK real-world implementation
The Lancet 2025cited by 16position: middledoi
Predicting resistance to chemotherapy using chromosomal instability signatures
Nature Genetics 2025cited by 14position: middledoi
Predicting resistance to chemotherapy using chromosomal instability signatures.
2025cited by 8position: contributordoi
Quantifying the tumour vasculature environment from CD-31 immunohistochemistry images of breast cancer using deep learning based semantic segmentation
Breast Cancer Research 2025cited by 7position: lastdoi
Clinical decision tree for optimizing endoscopic assessment of signet ring cell carcinoma in hereditary diffuse gastric cancer surveillance
Endoscopy 2025cited by 1position: middledoi
A Dirichlet-multinomial mixed model for determining differential abundance of mutational signatures
BMC Bioinformatics 2025cited by 0position: lastdoi
The tumor microenvironment of 14,837 breast cancers is associated with clinical outcome independently of genomic subtypes
Cell Reports Medicine 2025cited by 0position: middledoi
All models are wrong and yours are useless: making clinical prediction models impactful for patients
npj Precision Oncology 2024cited by 69position: firstdoi
All models are wrong and yours are useless: making clinical prediction models impactful for patients.
2024cited by 37position: contributordoi
Smoking-associated gene expression alterations in nasal epithelium reveal immune impairment linked to lung cancer risk
Genome Medicine 2024cited by 21position: middledoi
Genomic reproducibility in the bioinformatics era.
2024cited by 16position: contributordoi
scAbsolute: measuring single-cell ploidy and replication status
Genome biology 2024cited by 13position: lastdoi
scAbsolute: measuring single-cell ploidy and replication status.
2024cited by 11position: contributordoi
Crowd-sourced benchmarking of single-sample tumor subclonal reconstruction
Nature Biotechnology 2024cited by 9position: middledoi
A Dirichlet-multinomial mixed model for determining differential abundance of mutational signatures
2024cited by 0position: contributordoi
A Dirichlet-multinomial mixed model for determining differential abundance of mutational signatures
bioRxiv (Cold Spring Harbor Laboratory) 2024cited by 0position: lastdoi
A Dirichlet-multinomial mixed model for detecting differential abundance of mutational signatures
Research Square 2024cited by 0position: lastdoi
Integrated radiogenomics models predict response to neoadjuvant chemotherapy in high grade serous ovarian cancer
Nature Communications 2023cited by 65position: middledoi
The copy number and mutational landscape of recurrent ovarian high-grade serous carcinoma.
2023cited by 49position: contributordoi
Integrated radiogenomics models predict response to neoadjuvant chemotherapy in high grade serous ovarian cancer.
2023cited by 46position: contributordoi
High-grade serous ovarian carcinoma organoids as models of chromosomal instability
eLife 2023cited by 31position: middledoi
High-grade serous ovarian carcinoma organoids as models of chromosomal instability.
2023cited by 26position: contributordoi
SliDL: A toolbox for processing whole-slide images in deep learning
PLoS ONE 2023cited by 11position: lastdoi
Author Correction: The evolutionary history of 2,658 cancers
Nature 2023cited by 5position: middledoi
Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Nature Genetics 2023cited by 5position: middledoi
Author Correction: Patterns of somatic structural variation in human cancer genomes
Nature 2023cited by 4position: middledoi
Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Nature Genetics 2023cited by 4position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

· 66 papers (2019–2026)Geoff Macintyre · Centro Nacional de Investigaciones Científicas57 papers (2016–2026)James D. Brenton · University of Manchester49 papers (2020–2026) · 46 papers (2020–2026)Lena Morrill Gavarró · Cancer Research UK Cambridge Center43 papers (2020–2023)Philip S. Smith · Cancer Research UK Cambridge Center39 papers (2021–2023)Michelle Lockley · Genomics England38 papers (2021–2023)Iain A. McNeish · Imperial College London38 papers (2021–2023)Thomas Bradley · University of Cambridge38 papers (2021–2023)Hasan B. Mirza · Barts Health NHS Trust37 papers (2022–2023)Zhao Cheng · University of Cambridge36 papers (2021–2023)James D. Brenton · University of Cambridge19 papers (2014–2024)Mireia Crispin‐Ortuzar · University of Cambridge13 papers (2019–2023)Anna Piskorz · University of Cambridge12 papers (2015–2024)Lena Morrill Gavarró · Cancer Research UK Cambridge Center9 papers (2022–2025)Carlos Caldas · Concern Foundation8 papers (2012–2025)Xin Wang · Chinese University of Hong Kong7 papers (2012–2022)Carolin Margarethe Sauer · Cancer Research UK Cambridge Center7 papers (2021–2025)Ke Yuan · Shenzhen Maternity and Child Healthcare Hospital7 papers (2015–2023)Evis Sala · Università Cattolica del Sacro Cuore7 papers (2015–2022)