Marjolijn C.J. Jongmans

Utrecht University — Netherlands

Medicine · Health Sciences

41h-index5.8kcitations159works3.52yr avg
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Research Topics

Genetic factors in colorectal cancer(22), Genomics and Rare Diseases(17), Renal and related cancers(17), Neuroblastoma Research and Treatments(17), Childhood Cancer Survivors' Quality of Life(15)

Publications158 total

BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
The American Journal of Human Genetics·2025· 1 citedOpen Access
A multi-dimensional approach to recognize genetic predisposition in children with acute lymphoblastic leukemia
EJC Paediatric Oncology·2025Open Access
Genetic evaluation of five patients with ROHHAD-NET using whole genome sequencing and optical genome mapping
Orphanet Journal of Rare Diseases·2025Open Access
Integrative immune subtyping of HNSCC reveals clinically relevant phenotypes and treatment-associated transitions
2025Open Access
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9
Human Genetics and Genomics Advances·2025· 1 citedOpen Access
Exploring germline variants in genes associated with inborn errors of immunity and inherited bone marrow failure syndromes in pediatric hematological malignancies
European Journal of Cancer·2025· 2 citedOpen Access
Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline <i>SMARCA4</i> Variant
Pediatric Blood & Cancer·2025· 2 citedOpen Access
Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants
Genetics in Medicine·2025Open Access
Analysis of <i>BRCA1</i> , <i>BRCA2</i> and <i>PALB2</i> related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
2025Open Access
Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency
Nature Communications·2025· 4 citedOpen Access
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
Cancer Letters·2025Open Access
Corrigendum to “Implementation of paediatric precision oncology into clinical practice: The individualized therapies for children with cancer program ‘iTHER’” [Eur J Cancer 175 (2022) 311–325]
European Journal of Cancer·2025· 1 citedOpen Access
Non-serous ovarian cancer in PTEN Hamartoma Tumor Syndrome: additional evidence for increased risk
Familial Cancer·2025· 2 citedOpen Access
The incidence and outcome of acute kidney injury during pediatric kidney tumor treatment—a national cohort study
Pediatric Nephrology·2025· 1 citedOpen Access
Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric <i>NF2</i>-, <i>SMARCB1</i>-, and <i>LZTR1</i>-Related Schwannomatosis
Clinical Cancer Research·2025· 5 citedOpen Access
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression
2025Open Access
Gain of Chromosome 17 is an Early Genetic Abnormality in Neuroblastoma with Ppm1d Emerging as a Strong Candidate Oncogene Driving Tumor Progression
SSRN Electronic Journal·2025Open Access
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes
Clinical Cancer Research·2024· 4 citedOpen Access
Clinical syndromes linked to biallelic germline variants in <i>MCM8</i> and <i>MCM9</i>
2024· 1 citedOpen Access
Abstract A012: Stratifying immune subtypes in real-world HNSCC cohort to identify those with better outcomes to standard treatment regimens
Cancer Immunology Research·2024
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Frequent Co-authors

Roland P. Kuiper(17), Nicoline Hoogerbrugge(15), Marjolijn J. L. Ligtenberg(8), Esmé Waanders(8), Ad Geurts van Kessel(7), Marry M. van den Heuvel‐Eibrink(7), Jayne Y. Hehir‐Kwa(6), Eveline J. Kamping(6), Peter M. Hoogerbrugge(6), Arjen R. Mensenkamp(6), Ineke van der Burgt(5), Illja J. Diets(5), Alexander Hoischen(4), Lies H. Hoefsloot(4), Rolph Pfundt(4), C. Noordam(4), Christian P. Kratz(4), Janna A. Hol(4), Robbert D.A. Weren(3), Richarda M. de Voer(3)