Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Phenotypic and genotypic overlap between mosaic NF2 and schwannomatosis in patients with multiple non-intradermal schwannomas
Hildegard Kehrer‐Sawatzki, Lan Kluwe, Reinhard E. Friedrich, et al.
Human Genetics (2018) Vol. 137, Iss. 6-7, pp. 543-552
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation
Scott R. Plotkin, Ludwine Messiaen, Eric Legius, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 9, pp. 1967-1977
Open Access | Times Cited: 142
Mendelian inheritance revisited: dominance and recessiveness in medical genetics
Johannes Zschocke, Peter H. Byers, Andrew O.M. Wilkie
Nature Reviews Genetics (2023) Vol. 24, Iss. 7, pp. 442-463
Closed Access | Times Cited: 53
Current status and recommendations for imaging in neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis
Shivani Ahlawat, Jaishri O. Blakeley, Shannon Langmead, et al.
Skeletal Radiology (2019) Vol. 49, Iss. 2, pp. 199-219
Closed Access | Times Cited: 101
Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing
D. Gareth Evans, Claire Hartley, Philip Smith, et al.
Genetics in Medicine (2019) Vol. 22, Iss. 1, pp. 53-59
Open Access | Times Cited: 84
ERN GENTURIS clinical practice guidelines for the diagnosis, treatment, management and surveillance of people with schwannomatosis
D. Gareth Evans, S Mostaccioli, David Pang, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 7, pp. 812-817
Open Access | Times Cited: 25
Epigenomic, genomic, and transcriptomic landscape of schwannomatosis
Sheila Mansouri, Suganth Suppiah, Yasin Mamatjan, et al.
Acta Neuropathologica (2020) Vol. 141, Iss. 1, pp. 101-116
Open Access | Times Cited: 39
Rare multiple schwannomas of the left upper extremity: A case report
Huixia Chen, Xiguan Yao, Peigeng Wang, et al.
Oncology Letters (2025) Vol. 29, Iss. 4, pp. 1-6
Open Access
Hybrid granular cell tumor/perineurioma: a report of two rare cases with PIK3CA mutations
Ani Toklu, Gauri Panse, George Jour, et al.
Virchows Archiv (2025)
Closed Access
Non-NF2-related schwannomatosis and rhabdoid tumor predisposition syndrome
Scott R. Plotkin, D. Gareth Evans, Jay S. Loeffler, et al.
Oxford University Press eBooks (2025), pp. 339-344
Closed Access
Stereotactic radiosurgery for vestibular schwannomas in neurofibromatosis type 2 patients: a systematic review and meta-analysis
Umberto Tosi, Omri Maayan, Anjile An, et al.
Journal of Neuro-Oncology (2022) Vol. 156, Iss. 2, pp. 431-441
Closed Access | Times Cited: 17
Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features
Vera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 916-916
Open Access | Times Cited: 3
Stereotactic radiosurgery for vestibular schwannomas in neurofibromatosis type 2: a systematic review and meta-analysis
Bardia Hajikarimloo, Salem M. Tos, Mohammadamin Sabbagh Alvani, et al.
BMC Cancer (2025) Vol. 25, Iss. 1
Open Access
Neurofibromatosis type 2 and related disorders
Dorothy Halliday, Allyson Parry, D. Gareth Evans
Current Opinion in Oncology (2019) Vol. 31, Iss. 6, pp. 562-567
Open Access | Times Cited: 28
Management of Central and Peripheral Nervous System Tumors in Patients with Neurofibromatosis
Rebecca Brown
Current Oncology Reports (2023) Vol. 25, Iss. 12, pp. 1409-1417
Closed Access | Times Cited: 9
Historical Development of Diagnostic Criteria for NF2-related Schwannomatosis
Ryota Tamura, Masahiro Yo, Masahiro Toda
Neurologia medico-chirurgica (2024) Vol. 64, Iss. 8, pp. 299-308
Open Access | Times Cited: 2
Comparison of the frequency of loss‐of‐function LZTR1 variants between schwannomatosis patients and the general population
Fanxuan Deng, D. Gareth Evans, Miriam J. Smith
Human Mutation (2022) Vol. 43, Iss. 7, pp. 919-927
Open Access | Times Cited: 10
Sporadic vestibular schwannoma: a molecular testing summary
Katherine V. Sadler, Naomi L. Bowers, Claire Hartley, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 4, pp. 227-233
Closed Access | Times Cited: 16
From process to progress—2017 International Conference on Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis
Rosalie E. Ferner, Annette Bakker, Ype Elgersma, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 6, pp. 1098-1106
Open Access | Times Cited: 12
Updates on Revised Diagnostic Criteria and Targeted Therapies for Neurofibromatosis
Miguel Santiago-Cruz, Karan Dixit, Ssu-Wei Hsu, et al.
Advances in Oncology (2024) Vol. 4, Iss. 1, pp. 125-135
Closed Access | Times Cited: 1
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 11, pp. 101241-101241
Closed Access | Times Cited: 1
Understanding barriers to diagnosis in a rare, genetic disease: Delays and errors in diagnosing schwannomatosis
Vanessa L. Merker, Bronwyn Slobogean, Justin T. Jordan, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 9, pp. 2672-2683
Open Access | Times Cited: 5
Screening of potential novel candidate genes in schwannomatosis patients
Cristina Perez‐Becerril, Andrew Wallace, Hélene Schlecht, et al.
Human Mutation (2022) Vol. 43, Iss. 10, pp. 1368-1376
Open Access | Times Cited: 5
Age-related schwannomatosis with potential exosome-mediated contribution to prostate hyperplasia: a case report and mini-review
Bérengère Chignon‐Sicard, Véronique Hofman, D. Chevallier, et al.
Therapeutic Advances in Urology (2019) Vol. 11
Open Access | Times Cited: 6
Genetic testing to gain diagnostic clarity in neurofibromatosis type 2 and schwannomatosis
Rebecca Burns, Kristin B. Niendorf, Kathleen Steinberg, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 8, pp. 2413-2420
Closed Access | Times Cited: 4
Primary Cardiac Schwannoma: A Meta-Analysis of Individual Case Reports
Mohamed Rahouma, Massimo Baudo, Sherif Khairallah, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 10, pp. 3356-3356
Open Access | Times Cited: 2
Page 1 - Next Page

Scroll to top