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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:

Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype–Phenotype Correlations
Cristina Peduto, Mariateresa Zanobio, Vincenzo Nigro, et al.
Cancers (2023) Vol. 15, Iss. 4, pp. 1217-1217
Open Access | Times Cited: 25

Showing 25 citing articles:

Neurofibromatosis 1 (von Recklinghausen Disease)
Yuichi Yoshida
The Keio Journal of Medicine (2023)
Open Access | Times Cited: 15
Neurofibromatosis Type 1: Optimizing Management with a Multidisciplinary Approach
Shaan Lalvani, Rebecca Brown
Journal of Multidisciplinary Healthcare (2024) Vol. Volume 17, pp. 1803-1817
Open Access | Times Cited: 4
Identification of the Determinants of Plexiform Neurofibroma Morbidity in Pediatric and Young Adult Neurofibromatosis Type 1 Patients: A Pilot Multivariate Approach
Biagio de Brons, Britt A. E. Dhaenens, Rick van Minkelen, et al.
Cancers (2025) Vol. 17, Iss. 1, pp. 123-123
Open Access
Neuroendocrine Tumors: Germline Genetics and Hereditary Syndromes
E Lauricella, Nada Chaoul, Gabriella D’Angelo, et al.
Current Treatment Options in Oncology (2025)
Closed Access
Management of selumetinib-associated toxicity in children with neurofibromatosis type 1 and plexiform neurofibromas
Yu. V. Dinikina, N. S. Dekhtyareva
Podderživaûŝaâ terapiâ v onkologii. (2025) Vol. 2, Iss. 1, pp. 30-43
Closed Access
Unveiling the complexity of neurofibromatosis type 1: Innovations in genetic understanding and clinical management. A narrative review
Aurora Jurca, S. Pop, Claudia Maria Jurca, et al.
Biomedical Papers (2025)
Open Access
Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder
Ioana Balinisteanu, Lavinia Caba, Andreea Florea, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 8, pp. 9093-9121
Open Access | Times Cited: 3
Role of long non-coding RNAs in neurofibromatosis and Schwannomatosis: pathogenesis and therapeutic potential
Md Sadique Hussain, Somya Sharma, Alka Kumari, et al.
Epigenomics (2024) Vol. 16, Iss. 23-24, pp. 1453-1464
Closed Access | Times Cited: 2
[Gene therapy strategies and prospects for neurofibromatosis type 1].
Tingting Zheng, Beiyao Zhu, Zhichao Wang, et al.
PubMed (2024) Vol. 38, Iss. 1, pp. 1-8
Closed Access | Times Cited: 1
The Importance of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants in NF1 Gene and CRX Gene. Case Report and Short Literature Review
Aurora Jurca, Codruţa Diana Petcheşi, Claudia Jurcă, et al.
(2024)
Open Access | Times Cited: 1
The Surprises of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants
Aurora Jurca, Codruţa Diana Petcheşi, Claudia Jurcă, et al.
(2024)
Open Access | Times Cited: 1
Drosophila Contributions towards Understanding Neurofibromatosis 1
Kalliopi Atsoniou, Eleni Giannopoulou, Eirini‐Maria Georganta, et al.
Cells (2024) Vol. 13, Iss. 8, pp. 721-721
Open Access | Times Cited: 1
The Surprises of Molecular Testing in Neurofibromatosis Type 1: Rare Association between Two Mutational Variants
Aurora Jurca, Codruţa Diana Petcheşi, Claudia Jurcă, et al.
Pharmacophore (2024) Vol. 15, Iss. 2, pp. 70-78
Open Access | Times Cited: 1
Revolutionizing genetic diagnostics: Innovative techniques for inherited disease detection
Shradha Devi Dwivedi, Sachin Yadav, Divya Sahu, et al.
Gene Reports (2024) Vol. 36, pp. 101963-101963
Closed Access | Times Cited: 1
Quality of Life in Children with Neurofibromatosis Type 1: Agreement between Parents and Patients, and the Role of Disease Severity and Visibility
Nicola Davide Cavallo, Paola Maietta, Silverio Perrotta, et al.
Children (2024) Vol. 11, Iss. 8, pp. 1033-1033
Open Access | Times Cited: 1
Germline Variants in Cancer Predisposition Genes in Pediatric Patients with Central Nervous System Tumors
Aleksa Jovanović, Nataša Tos̆ić, Irena Marjanović, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17387-17387
Open Access | Times Cited: 2
Germline Predisposition to Hematopoietic Malignancies: An Overview
Yogameenakshi Haribabu, Emma Bhote, Lucy A. Godley
Annual Review of Cancer Biology (2024) Vol. 8, Iss. 1, pp. 309-329
Open Access
Familial schwannomatosis carrying LZTR1 variant p.R340X with brain tumor: A case report
Masaki Ibe, Shinobu Tamura, Hideki Kosako, et al.
Molecular Genetics and Metabolism Reports (2024) Vol. 40, pp. 101107-101107
Open Access
A Comprehensive Overview of NF1 Mutations in Iranian Patients
Shahram Savad, Mohammad Hossein Modarressi, Sarang Younesi, et al.
NeuroMolecular Medicine (2024) Vol. 26, Iss. 1
Closed Access
Nephrotic syndrome in a child with neurofibromatosis type 1: A case report and literature review
Bingjie Cheng, Huihui Yang, Lin Huang, et al.
Nephrology (2024)
Closed Access
Social Communication in Ras Pathway Disorders: A Comprehensive Review from Genetics to Behavior in Neurofibromatosis Type 1 and Noonan Syndrome
Monica Siqueiros-Sanchez, Yaffa Serur, Chloe McGhee, et al.
Biological Psychiatry (2024)
Closed Access
Genetic heterogeneity and metabolic reprogramming in breast cancer
Yarkın Dolaş, Ayşe Buruş, Başak Çeltikçi
Acta Medica (2024) Vol. 55, Iss. 4, pp. 227-246
Open Access
Evaluation of Molecular and Clinical Findings in Children With Neurofibromatosis Type 1: Identification of 15 Novel Variants
Yaşar BİLDİRİCİ, Ayça Kocaağa, Cefa Nil Karademir-Arslan, et al.
Pediatric Neurology (2023) Vol. 149, pp. 69-74
Closed Access | Times Cited: 1
Endocrine morbidity in neurofibromatosis 1: a nationwide, register-based cohort study
Line Kenborg, Andreas Ebbehøj, Cecilie Ejerskov, et al.
European Journal of Endocrinology (2023) Vol. 189, Iss. 2, pp. 190-198
Closed Access
Rare giant renal artery aneurysm in neurofibromatosis type 1 patient: a case report
Ali Jawad, Zein Alabdin Hannouneh, Jameel Soqia, et al.
Annals of Medicine and Surgery (2023) Vol. 85, Iss. 11, pp. 5748-5751
Open Access
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