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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:

Mosaic Disorders of the PI3K/PTEN/AKT/TSC/mTORC1 Signaling Pathway
Neera R. Nathan, Kim M. Keppler‐Noreuil, Leslie G. Biesecker, et al.
Dermatologic Clinics (2016) Vol. 35, Iss. 1, pp. 51-60
Open Access | Times Cited: 108

Showing 1-25 of 108 citing articles:

The PI3K Pathway in Human Disease
David A. Fruman, Honyin Chiu, Benjamin D. Hopkins, et al.
Cell (2017) Vol. 170, Iss. 4, pp. 605-635
Open Access | Times Cited: 2181
mTOR signaling pathway and mTOR inhibitors in cancer: progress and challenges
Zhilin Zou, Tao Tao, Hongmei Li, et al.
Cell & Bioscience (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 741
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, et al.
Journal of Clinical Investigation (2018) Vol. 128, Iss. 4, pp. 1496-1508
Open Access | Times Cited: 245
A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations
Guillaume Canaud, Adrienne M. Hammill, Denise M. Adams, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 106
The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions
Alice Man, Matteo Di Scipio, Shan Grewal, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 332-332
Open Access | Times Cited: 18
A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children
Emily Hansen‐Kiss, Sarah Beinkampen, Brent Adler, et al.
Journal of Medical Genetics (2017) Vol. 54, Iss. 7, pp. 471-478
Closed Access | Times Cited: 107
Macropinocytosis, mTORC1 and cellular growth control
Sei Yoshida, Regina Pacitto, Ken Inoki, et al.
Cellular and Molecular Life Sciences (2017) Vol. 75, Iss. 7, pp. 1227-1239
Open Access | Times Cited: 104
Vascular Anomalies
Denise M. Adams, Kiersten Ricci
Hematology/Oncology Clinics of North America (2019) Vol. 33, Iss. 3, pp. 455-470
Closed Access | Times Cited: 103
Overgrowth syndromes — clinical and molecular aspects and tumour risk
Frédéric Brioude, Annick Toutain, Éloïse Giabicani, et al.
Nature Reviews Endocrinology (2019) Vol. 15, Iss. 5, pp. 299-311
Closed Access | Times Cited: 88
Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data
Caroline F. Wright, Elena Prigmore, D. Rajan, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 80
PI3K/mTOR Pathway Inhibition: Opportunities in Oncology and Rare Genetic Diseases
Petra Hillmann, Doriano Fabbro
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 22, pp. 5792-5792
Open Access | Times Cited: 79
Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders
Francis Rossignol, Foudil Lamari, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access | Times Cited: 1
Genetics, genomics, and genotype–phenotype correlations of TSC: Insights for clinical practice
Angela Peron, Kit Sing Au, Hope Northrup
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2018) Vol. 178, Iss. 3, pp. 281-290
Open Access | Times Cited: 83
Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases
Roel W. Ten Broek, Astrid Eijkelenboom, C.J.M. van der Vleuten, et al.
Genes Chromosomes and Cancer (2019) Vol. 58, Iss. 8, pp. 541-550
Open Access | Times Cited: 63
PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature
William L. Macken, Marc Tischkowitz, Katherine Lachlan
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 181, Iss. 4, pp. 591-610
Closed Access | Times Cited: 62
Congenital Limb Overgrowth Syndromes Associated with Vascular Anomalies
Frederic J. Bertino, Kiery Braithwaite, C. Matthew Hawkins, et al.
Radiographics (2019) Vol. 39, Iss. 2, pp. 491-515
Closed Access | Times Cited: 58
Cross talk between autophagy and oncogenic signaling pathways and implications for cancer therapy
Sahib Zada, Jin Seok Hwang, Mahmoud Ahmed, et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2021) Vol. 1876, Iss. 1, pp. 188565-188565
Open Access | Times Cited: 52
Carbonic Anhydrase IX Inhibitors as Candidates for Combination Therapy of Solid Tumors
Stanislav Kalinin, Anna Malkova, Tatiana V. Sharonova, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13405-13405
Open Access | Times Cited: 48
Contemporary mTOR inhibitor scaffolds to diseases breakdown: A patent review (2015–2021)
Patrik Olekšák, Eugenie Nepovimová, Žofia Chrienová, et al.
European Journal of Medicinal Chemistry (2022) Vol. 238, pp. 114498-114498
Closed Access | Times Cited: 29
Targeted therapy of cancer stem cells: inhibition of mTOR in pre-clinical and clinical research
Boram Son, Wonhwa Lee, Hyeon-Jeong Kim, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 9
Open Access | Times Cited: 8
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype–Phenotype Correlations
Vanessa F. Schmidt, Friedrich Kapp, Constantin Goldann, et al.
Journal of the American Heart Association (2024) Vol. 13, Iss. 8
Open Access | Times Cited: 7
Update on classification and diagnosis of vascular malformations
Catherine McCuaïg
Current Opinion in Pediatrics (2017) Vol. 29, Iss. 4, pp. 448-454
Closed Access | Times Cited: 60
Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation
Brooke Sadler, Timothy Kuensting, Jennifer M. Strahle, et al.
Pediatric Neurology (2020) Vol. 106, pp. 32-37
Open Access | Times Cited: 49
PTEN somatic mutations contribute to spectrum of cerebral overgrowth
Daniel C. Koboldt, Katherine E. Miller, Anthony R. Miller, et al.
Brain (2021) Vol. 144, Iss. 10, pp. 2971-2978
Open Access | Times Cited: 33
The Klippel-Trénaunay Syndrome in 2022: Unravelling Its Genetic and Molecular Profile and Its Link to the Limb Overgrowth Syndromes
Patrick Harnarayan, Dave Harnanan
Vascular Health and Risk Management (2022) Vol. Volume 18, pp. 201-209
Open Access | Times Cited: 26
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