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Papers matching “DNA sequencing” 217

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Exhaustive circulating tumor DNA sequencing reveals the genomic landscape of Hodgkin lymphoma and facilitates ultrasensitive detection of minimal residual disease
2021 medRxiv preprint Medicine Lymphoma Diagnosis and Treatment Open access

Sophia Sobesky, Laman Mammadova, Melita Cirillo, Esther E.E. Drees, Julia Mattlener, Helge Dörr, +20 more

7

citations
Recommendations for reporting tissue and circulating tumour (ct)DNA next-generation sequencing results in non-small cell lung cancer
2024 British Journal of Cancer article Medicine Lung Cancer Treatments and Mutations Open access

Umberto Malapelle, Natasha B. Leighl, Alfredo Addeo, Dov Hershkovitz, Maximilian Johannes Hochmair, Ola Khorshid, +10 more

38

citations
Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing
2020 Journal of Thoracic Oncology article Medicine Lung Cancer Treatments and Mutations Open access

Danielle B. Cohen, Liesbeth M. Hondelink, Nienke Solleveld‐Westerink, Sandra M. Uljee, Dina Ruano, Anne‐Marie Cleton-Jansen, +12 more

126

citations
In-depth cell-free DNA sequencing reveals genomic landscape of Hodgkin’s lymphoma and facilitates ultrasensitive residual disease detection
2021 Med article Medicine Lymphoma Diagnosis and Treatment Open access

Sophia Sobesky, Laman Mammadova, Melita Cirillo, Esther E.E. Drees, Julia Mattlener, Helge Dörr, +20 more

74

citations
Longitudinal Monitoring of DNA Viral Loads in Transplant Patients Using Quantitative Metagenomic Next-Generation Sequencing
2022 Pathogens article Medicine Cytomegalovirus and herpesvirus research Open access cited by 2 patents

Ellen C. Carbo, Anne Russcher, Margriet E. M. Kraakman, Caroline S. van der Blij-de Brouwer, Igor A. Sidorov, Mariet C.W. Feltkamp, +3 more

11

citations
Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study
2022 Thrombosis Research article Medicine Glioma Diagnosis and Treatment Open access

Maaike Y. Kapteijn, Fleur H.J. Kaptein, Milou A.M. Stals, Eva E. Klaase, Inés García-Ortiz, Ronald van Eijk, +9 more

14

citations
Prognostic Markers of DNA Methylation and Next-Generation Sequencing in Progressive Glioblastoma from the EORTC-26101 Trial
2023 Clinical Cancer Research article Medicine Glioma Diagnosis and Treatment Open access

Tobias Keßler, Daniel Schrimpf, Laura Doerner, Ling Hai, Leon D. Kaulen, Jakob Ito, +13 more

27

citations
P05.01.B PROGNOSTIC MARKERS OF DNA METHYLATION AND NGS SEQUENCING IN PROGRESSIVE GLIOBLASTOMA FROM THE EORTC-26101 TRIAL
2023 Neuro-Oncology conference-abstract Medicine Glioma Diagnosis and Treatment Open access

Tobias Keßler, Daniel Schrimpf, Laura Doerner, Leon D. Kaulen, Jakob Ito, Martin J. van den Bent, +12 more

0

citations
Longitudinal monitoring of DNA viral loads in transplant patients using quantitative metagenomic next-generation sequencing
2021 medRxiv preprint Medicine Cytomegalovirus and herpesvirus research Open access

Ellen C. Carbo, Anne Russcher, Margriet E. M. Kraakman, Caroline S. van der Blij-de Brouwer, Igor A. Sidorov, Mariet C.W. Feltkamp, +3 more

1

citations
Comprehensive genetic analysis by targeted sequencing identifies risk factors and predicts patient outcome in Mantle Cell Lymphoma: results from the EU-MCL network trials
2024 Leukemia article Medicine Lymphoma Diagnosis and Treatment Open access

Mouhamad Khouja, Linmiao Jiang, Karol Pál, Martin Schwarz, Stefan Alig, Nikos Darzentas, +6 more

23

citations
Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients
2021 Familial Cancer article Medicine Genetic factors in colorectal cancer Open access

Fadwa A. Elsayed, Carli M.J. Tops, Maartje Nielsen, Hans M. Morreau, Frederik Jan Hes, Tom van Wezel

4

citations
Cell-free DNA genomic and fragmentomic features for early outcome prediction in large B cell lymphoma
2026 Cell Reports Medicine article Medicine Lymphoma Diagnosis and Treatment Open access

Steven Wang, Parisa Mapar, Norbert Moldován, Ymke van der Pol, Aram Safrastyan, Erik D. van Werkhoven, +29 more

0

citations
Genomic profiling of post-transplant lymphoproliferative disorders using cell-free DNA
2023 Journal of Hematology & Oncology article Medicine Viral-associated cancers and disorders Open access

Nick Veltmaat, Yujie Zhong, Filipe Montes de Jesus, Geok Wee Tan, Johanna A.A. Bult, Martijn M. Terpstra, +13 more

15

citations
Effect of DNA methylation on inhibitor development in people with hemophilia A treated with FVIII concentrates
2025 Research and Practice in Thrombosis and Haemostasis article Medicine Hemophilia Treatment and Research Open access

Shermarke Hassan, Andrea Cairo, Roberta Palla, Flora Peyvandi, Maria Elisa Mancuso, Frits Richard Rosendaal

2

citations
Identifying aging and Alzheimer’s disease associated somatic mutations in excitatory neurons from the human frontal cortex using whole genome sequencing and single cell RNA sequencing data
2022 medRxiv preprint Medicine Alzheimer's disease research and treatments Open access

Meng Zhang, Gerard A. Bouland, Henne H. Holstege, Marcel J. T. Reinders

2

citations
Single cell RNA sequence analysis of human bone marrow samples reveals new targets for isolation of skeletal stem cells using DNA-coated gold nanoparticles
2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Medicine Mesenchymal stem cell research Open access

Elloise Matthews, Stuart Lanham, Maria Eleni Kyriazi, Konstantina Alexaki, Afaf Helmy El-Sagheer, Tom Brown, +5 more

3

citations
The Role of Age-Related Clonal Hematopoiesis in Genetic Sequencing Studies
2020 The American Journal of Human Genetics article Medicine Acute Myeloid Leukemia Research Open access cited by 1 patent

Henne H. Holstege, Marc Hulsman, Sven J. van der Lee, Erik B. van den Akker

7

citations
Nanopore Sequencing-Based High-Resolution Karyotyping Compared to Conventional Karyotyping in Patients with Acute Myeloid Leukemia
2022 Blood article Medicine Acute Myeloid Leukemia Research

Martina Margrit Crysandt, Pia Krüger, Steffen Koschmieder, Ingo Kurth, Tim H. Brümmendorf, Florian Kraft, +1 more

0

citations
Identification of clinically-relevant genetic alterations in uveal melanoma using RNA sequencing
2023 medRxiv preprint Medicine Ocular Oncology and Treatments Open access

Rogier J. Nell, Marco Versluis, Davy Cats, Hailiang Mei, Robert M. Verdijk, Wilma G. M. Kroes, +3 more

2

citations
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
2023 The Lancet Neurology article Medicine Epilepsy research and treatment Open access

Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, Fadil Boodhoo, Sarah Buts, Natalie Jane Chandler, +32 more

81

citations
Identification of diagnostic and prognostic genetic alterations in uveal melanoma using RNA sequencing
2025 Scientific Reports article Medicine Ocular Oncology and Treatments Open access

Rogier J. Nell, Mieke Versluis, Davy Cats, Hailiang Mei, Robert M. Verdijk, Wilma G. M. Kroes, +3 more

4

citations
Development of an amplicon nanopore sequencing strategy for detection of mutations conferring intermediate resistance to vancomycin in Staphylococcus aureus strains
2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Medicine Antimicrobial Resistance in Staphylococcus Open access

Abraham G Moller, Robert A. Petit, Michelle H. Davis, Timothy D. Read

0

citations
Cell-Free DNA as a Diagnostic and Prognostic Biomarker in Pediatric Rhabdomyosarcoma
2023 JCO Precision Oncology article Medicine Sarcoma Diagnosis and Treatment Open access

Nathalie S.M. Lak, Lieke M. J. van Zogchel, Lily Zappeij‐Kannegieter, Ahmad Javadi, Ruben Van Paemel, Charlotte Vandeputte, +12 more

25

citations
The Evolving Role of Next-Generation Sequencing in Screening and Diagnosis of Hemoglobinopathies
2021 Frontiers in Physiology article Medicine Hemoglobinopathies and Related Disorders Open access

Ahlem Achour, Tamara T. Koopmann, Frank F. Baas, Cornelis L. Harteveld

50

citations
mRNA Sequencing to Identify Aberrant Splicing in X-linked Alport Syndrome
2026 Kidney International Reports article Medicine Renal Diseases and Glomerulopathies Open access

Dipti Rao, Bartholomeus T. van den Berge, Anneke T. Vulto‐van Silfhout, Ilse M. Rood, Joanna A.E. van Wijk, Arend Bökenkamp, +8 more

1

citations