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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
Tim Ripperger, Stefan Bielack, Arndt Borkhardt, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 1017-1037
Closed Access | Times Cited: 244

Showing 1-25 of 244 citing articles:

Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma
Kari G. Rabe, Bin Zhu, Roelof Koster, et al.
JAMA Oncology (2020) Vol. 6, Iss. 5, pp. 724-724
Open Access | Times Cited: 195
A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era
Stefan M. Pfister, Miguel Reyes‐Múgica, John K. C. Chan, et al.
Cancer Discovery (2021) Vol. 12, Iss. 2, pp. 331-355
Open Access | Times Cited: 137
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology
Dominik Sturm, David Capper, Felipe Andreiuolo, et al.
Nature Medicine (2023) Vol. 29, Iss. 4, pp. 917-926
Open Access | Times Cited: 78
Molecular characteristics and therapeutic vulnerabilities across paediatric solid tumours
David Jones, Ana Banito, Thomas G. P. Grünewald, et al.
Nature reviews. Cancer (2019) Vol. 19, Iss. 8, pp. 420-438
Closed Access | Times Cited: 130
Primary intracranial spindle cell sarcoma with rhabdomyosarcoma-like features share a highly distinct methylation profile and DICER1 mutations
Christian Koelsche, Martin Mynarek, Daniel Schrimpf, et al.
Acta Neuropathologica (2018) Vol. 136, Iss. 2, pp. 327-337
Open Access | Times Cited: 127
Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient
Harriet Druker, Kristin Zelley, Rose B. McGee, et al.
Clinical Cancer Research (2017) Vol. 23, Iss. 13, pp. e91-e97
Closed Access | Times Cited: 124
Predisposition to cancer in children and adolescents
Christian P. Kratz, Marjolijn C.J. Jongmans, Hélène Cavé, et al.
The Lancet Child & Adolescent Health (2021) Vol. 5, Iss. 2, pp. 142-154
Closed Access | Times Cited: 92
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes
Anna Byrjalsen, Thomas van Overeem Hansen, Ulrik Kristoffer Stoltze, et al.
PLoS Genetics (2020) Vol. 16, Iss. 12, pp. e1009231-e1009231
Open Access | Times Cited: 90
Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing
Scott Newman, Joy Nakitandwe, Chimene Kesserwan, et al.
Cancer Discovery (2021) Vol. 11, Iss. 12, pp. 3008-3027
Open Access | Times Cited: 84
Inherited bone marrow failure in the pediatric patient
Inderjeet Dokal, Hemanth Tummala, Tom Vulliamy
Blood (2022) Vol. 140, Iss. 6, pp. 556-570
Open Access | Times Cited: 49
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers
Arne Jahn, Andreas Rump, Thomas J. Widmann, et al.
Annals of Oncology (2022) Vol. 33, Iss. 11, pp. 1186-1199
Open Access | Times Cited: 43
Next Generation Sequencing and Pediatric Brain Tumors: Detection of Cancer Predisposition Syndromes in Patients and Their Families
Kerstin Grund, Dominik Sturm, Christian Sutter, et al.
OBM Genetics (2017) Vol. 1, Iss. 4, pp. 1-1
Open Access | Times Cited: 82
Factors influencing risk‐based care of the childhood cancer survivor in the 21st century
Stephanie B. Dixon, Kari Bjornard, Nicole M. Alberts, et al.
CA A Cancer Journal for Clinicians (2018) Vol. 68, Iss. 2, pp. 133-152
Open Access | Times Cited: 66
Primary Immunodeficiency and Cancer Predisposition Revisited: Embedding Two Closely Related Concepts Into an Integrative Conceptual Framework
Oskar A. Haas
Frontiers in Immunology (2019) Vol. 9
Open Access | Times Cited: 62
Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma
Matthias Begemann, Sebastian M. Waszak, Giles Robinson, et al.
Journal of Clinical Oncology (2019) Vol. 38, Iss. 1, pp. 43-50
Open Access | Times Cited: 62
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors
Sara Akhavanfard, Roshan Padmanabhan, Lamis Yehia, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 56
The acquisition of molecular drivers in pediatric therapy-related myeloid neoplasms
Jason R. Schwartz, Jing Ma, Jennifer L. Kamens, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 54
Genetic Predisposition to Solid Pediatric Cancers
Mario Capasso, Annalaura Montella, Matilde Tirelli, et al.
Frontiers in Oncology (2020) Vol. 10
Open Access | Times Cited: 52
Cancer Progress and Priorities: Childhood Cancer
Philip J. Lupo, Logan G. Spector
Cancer Epidemiology Biomarkers & Prevention (2020) Vol. 29, Iss. 6, pp. 1081-1094
Open Access | Times Cited: 51
Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer
Rabea Wagener, Julia Taeubner, Carolin Walter, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 8, pp. 1301-1311
Open Access | Times Cited: 47
European guideline for imaging in paediatric and adolescent rhabdomyosarcoma — joint statement by the European Paediatric Soft Tissue Sarcoma Study Group, the Cooperative Weichteilsarkom Studiengruppe and the Oncology Task Force of the European Society of Paediatric Radiology
Roelof van Ewijk, Reineke A. Schoot, Monika Sparber‐Sauer, et al.
Pediatric Radiology (2021) Vol. 51, Iss. 10, pp. 1940-1951
Open Access | Times Cited: 46
Epidemiology, genetics and treatment of multiple myeloma and precursor diseases
Kari Hemminki, Asta Försti, Richard S. Houlston, et al.
International Journal of Cancer (2021) Vol. 149, Iss. 12, pp. 1980-1996
Open Access | Times Cited: 46
Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer
Christian P. Kratz, Dmitrii Smirnov, Robert Autry, et al.
JNCI Journal of the National Cancer Institute (2022) Vol. 114, Iss. 11, pp. 1523-1532
Open Access | Times Cited: 31
Joint EANM/SIOPE/RAPNO practice guidelines/SNMMI procedure standards for imaging of paediatric gliomas using PET with radiolabelled amino acids and [18F]FDG: version 1.0
Arnoldo Piccardo, Nathalie L. Albert, Lise Borgwardt, et al.
European Journal of Nuclear Medicine and Molecular Imaging (2022) Vol. 49, Iss. 11, pp. 3852-3869
Open Access | Times Cited: 29
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer
Illja J. Diets, Esmé Waanders, Marjolijn J. L. Ligtenberg, et al.
Clinical Cancer Research (2018) Vol. 24, Iss. 7, pp. 1594-1603
Open Access | Times Cited: 58
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