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Katrin Heider
Katrin Heider
Research Associate, University of Cambridge
Adresse e-mail validée de cruk.cam.ac.uk
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Enhanced detection of circulating tumor DNA by fragment size analysis
F Mouliere, D Chandrananda, AM Piskorz, EK Moore, J Morris, ...
Science translational medicine 10 (466), eaat4921, 2018
8172018
Residual ctDNA after treatment predicts early relapse in patients with early-stage non-small cell lung cancer
D Gale, K Heider, A Ruiz-Valdepenas, S Hackinger, M Perry, G Marsico, ...
Annals of Oncology 33 (5), 500-510, 2022
1422022
ctDNA monitoring using patient-specific sequencing and integration of variant reads
JCM Wan, K Heider, D Gale, S Murphy, E Fisher, F Mouliere, ...
Science translational medicine 12 (548), eaaz8084, 2020
1412020
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
CG Smith, T Moser, F Mouliere, J Field-Rayner, M Eldridge, AL Riediger, ...
Genome medicine 12, 1-17, 2020
852020
Fragmentation patterns and personalized sequencing of cell‐free DNA in urine and plasma of glioma patients
F Mouliere, CG Smith, K Heider, J Su, Y van der Pol, M Thompson, ...
EMBO Molecular Medicine 13 (8), e12881, 2021
742021
Characteristics, origin, and potential for cancer diagnostics of ultrashort plasma cell-free DNA
I Hudecova, CG Smith, R Hänsel-Hertsch, CS Chilamakuri, JA Morris, ...
Genome Research 32 (2), 215-227, 2022
422022
Detection of ctDNA from dried blood spots after DNA size selection
K Heider, JCM Wan, J Hall, J Belic, S Boyle, I Hudecova, D Gale, ...
Clinical Chemistry 66 (5), 697-705, 2020
392020
Selecting short DNA fragments in plasma improves detection of circulating tumour DNA
F Mouliere, AM Piskorz, D Chandrananda, E Moore, J Morris, CG Smith, ...
BioRxiv, 134437, 2017
332017
Enhanced detection of circulating tumor DNA by fragment size analysis. Sci Transl Med. 2018; 10 (466): eaat4921
F Mouliere, D Chandrananda, AM Piskorz, EK Moore, J Morris, ...
23
Enhanced detection of circulating tumor DNA by fragment size analysis. Sci Transl Med. 2018; 10
F Mouliere, D Chandrananda, AM Piskorz, EK Moore, J Morris, ...
12
Residual ctDNA after treatment predicts early relapse in patients with early-stage NSCLC.
D Gale, K Heider, M Perry, G Marsico, A Ruiz-Valdepeñas, V Rundell, ...
Journal of Clinical Oncology 39 (15_suppl), 8517-8517, 2021
92021
Longitudinal monitoring of disease burden and response using ctDNA from dried blood spots in xenograft models
CM Sauer, K Heider, J Belic, SE Boyle, JA Hall, DL Couturier, A An, ...
EMBO Molecular Medicine 14 (8), e15729, 2022
52022
MA 11.02 circulating tumor DNA in early stage NSCLC: High sensitivity analysis in low burden disease. LUCID study update
A Ruiz-Valdepenas, K Heider, G Doughton, W Qian, C Massie, ...
Journal of Thoracic Oncology 12 (11), S1843-S1844, 2017
52017
Sensitive detection of ctDNA in early-stage non-small cell lung cancer patients with a personalized sequencing assay
K Heider, D Gale, A Ruiz-Valdepenas, G Marsico, G Sharma, M Perry, ...
Cancer 31, 34.4, 2020
42020
High-sensitivity monitoring of ctDNA by patient-specific sequencing panels and integration of variant reads
JCM Wan, K Heider, D Gale, S Murphy, E Fisher, J Morris, F Mouliere, ...
bioRxiv, 759399, 2019
42019
Detection of residual disease and recurrence in early-stage non-small cell lung cancer (NSCLC) patients using sensitive personalized ctDNA sequencing assays.
K Heider, DG Gale, G Marsico, A Ruiz-Valdepeñas, G Sharma, M Perry, ...
Journal of Clinical Oncology 38 (15_suppl), e15560-e15560, 2020
32020
Comparison of tumor‐informed and tumor‐naïve sequencing assays for ctDNA detection in breast cancer
A Santonja, WN Cooper, MD Eldridge, PAW Edwards, JA Morris, ...
EMBO molecular medicine, e16505, 2023
22023
ctDNA detection by personalised assays in early-stage NSCLC
K Heider, JCM Wan, D Gale, A Ruiz-Valdepenas, F Mouliere, J Morris, ...
MedRxiv, 2021.06. 01.21258171, 2021
22021
Individualised monitoring of patients with metastatic melanoma using plasma DNA
J Wan, S Murphy, D Gale, J Morris, FC Mouliere, F Marass, K Heider, ...
The Lancet 389, S99, 2017
12017
Improvements in variant detection
K Heider, J Wan, N Rosenfeld
US Patent App. 17/295,338, 2022
2022
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