Marjolijn C.J. Jongmans

Also affiliated with Heidelberg University, University Hospital Heidelberg, University Medical Center Utrecht, Princess Máxima Center, Wilhelmina Children's Hospital

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Mutational Landscape and Patterns of Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia”.

Mutational Landscape and Patterns of Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia

Blood Cancer Discovery(2020)10.1158/0008-5472.bcd-19-0041

N/A

3.9DataRank · unranked

152 citations

Zhaohui Gu, Stephanie M. Dobson, Željko Antić, Jeremy Chase Crawford, Xiaotu Ma +38 more

TINF2 is a haploinsufficient tumor suppressor that limits telomere length

eLife(2020)10.7554/elife.61235

N/A

0DataRank · unranked

58 citations

Arjen R. Mensenkamp, Kaori Takai, Maaike Haadsma, Liesbeth Spruijt, Richarda M. de Voer +7 more

Mutational Landscape and Patterns of Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia

Blood Cancer Discovery(2020)10.1158/2643-3249.bcd-19-0041

N/A

0DataRank · unranked

10 citations

Zhaohui Gu, Stephanie M. Dobson, Željko Antić, Jeremy Chase Crawford, Xiaotu Ma +38 more

De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies

medRxiv(2021)10.1101/2021.12.07.21266342

N/A

0DataRank · unranked

3 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +67 more

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

Science Translational Medicine(2023)10.1126/scitranslmed.abo3189

N/A

0DataRank · unranked

36 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +69 more

Germline pathogenic SMARCA4 variants in neuroblastoma

Journal of Medical Genetics(2023)10.1136/jmg-2022-108854

N/A

0DataRank · unranked

19 citations

Kim E. Nichols, Marjolijn C.J. Jongmans, Nienke van Engelen, Ronald R. de Krijger, Jennifer Herrera-Mullar +10 more

Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1611

N/A

0DataRank · unranked

30 citations

Anirban Das, Sarah Scollon, Sarah G. Mitchell, Mary‐Louise C. Greer, Marielle E. Yohe +22 more

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)10.1158/1078-0432.ccr-24-2171

N/A

0DataRank · unranked

9 citations

Sun Young Kim, Sarah G. Mitchell, Marjolijn C.J. Jongmans, Jonathan D. Wasserman, Melissa R. Perrino +14 more

Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2 -, SMARCB1 -, and LZTR1 -Related Schwannomatosis

Clinical Cancer Research(2025)10.1158/1078-0432.ccr-24-3278

N/A

0DataRank · unranked

8 citations

Marjolijn C.J. Jongmans, Gail E. Tomlinson, Mary‐Louise C. Greer, Sarah Scollon, Sarah G. Mitchell +18 more

Wilms tumor characteristics in children with heterozygous germline DIS3L2 variants

Genetics in Medicine(2025)10.1016/j.gim.2025.101478

N/A

0DataRank · unranked

2 citations

Taryn D. Treger, Jenny Wegert, Janna A. Hol, Jessica Le Gall, Eveliina Jakkula +20 more