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:
De novo missense variants in FBXO11 alter its protein expression and subcellular localization
Anne Gregor, Tanja Meerbrei, Thorsten Gerstner, et al.
Human Molecular Genetics (2021) Vol. 31, Iss. 3, pp. 440-454
Open Access | Times Cited: 12
Anne Gregor, Tanja Meerbrei, Thorsten Gerstner, et al.
Human Molecular Genetics (2021) Vol. 31, Iss. 3, pp. 440-454
Open Access | Times Cited: 12
Showing 12 citing articles:
The miR-155-5p/FBXO11 axis inhibits the progression of gastric cancer via the mTOR pathway
Tao Yuan, Haiyan Liu, Fangfang Li, et al.
Translational Cancer Research (2025) Vol. 14, Iss. 2, pp. 1375-1387
Open Access
Tao Yuan, Haiyan Liu, Fangfang Li, et al.
Translational Cancer Research (2025) Vol. 14, Iss. 2, pp. 1375-1387
Open Access
Cullin-RING Ubiquitin Ligases in Neurodevelopment and Neurodevelopmental Disorders
Honoka Ashitomi, Tadashi Nakagawa, Makiko Nakagawa, et al.
Biomedicines (2025) Vol. 13, Iss. 4, pp. 810-810
Open Access
Honoka Ashitomi, Tadashi Nakagawa, Makiko Nakagawa, et al.
Biomedicines (2025) Vol. 13, Iss. 4, pp. 810-810
Open Access
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals
Elisabeth Bosch, Bernt Popp, Esther Güse, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 11, pp. 100950-100950
Open Access | Times Cited: 9
Elisabeth Bosch, Bernt Popp, Esther Güse, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 11, pp. 100950-100950
Open Access | Times Cited: 9
Identification of two novel autism genes, TRPC4 and SCFD2, in Qatar simplex families through exome sequencing
Vijay Gupta, Afif Ben‐Mahmoud, Bonsu Ku, et al.
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 7
Vijay Gupta, Afif Ben‐Mahmoud, Bonsu Ku, et al.
Frontiers in Psychiatry (2023) Vol. 14
Open Access | Times Cited: 7
De novo structure prediction of meteorin and meteorin-like protein for identification of domains, functional receptor binding regions, and their high-risk missense variants
S. Shiva Shankar, Reema Banarjee, Swaraj M. Jathar, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 9, pp. 4522-4536
Closed Access | Times Cited: 4
S. Shiva Shankar, Reema Banarjee, Swaraj M. Jathar, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 9, pp. 4522-4536
Closed Access | Times Cited: 4
Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders
Danijela Krgović, Mario Gorenjak, Nika Rihar, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 4
Danijela Krgović, Mario Gorenjak, Nika Rihar, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 4
New ocular findings in a patient with a novel pathogenic variant in the FBXO11 gene
Raquel Gouveia Silva, Juliette Dupont, Eduardo Silva, et al.
Journal of American Association for Pediatric Ophthalmology and Strabismus (2022) Vol. 26, Iss. 5, pp. 268-270
Open Access | Times Cited: 3
Raquel Gouveia Silva, Juliette Dupont, Eduardo Silva, et al.
Journal of American Association for Pediatric Ophthalmology and Strabismus (2022) Vol. 26, Iss. 5, pp. 268-270
Open Access | Times Cited: 3
FBXO11 variants are associated with intellectual disability and variable clinical manifestation in Chinese affected individuals
Xin Pan, Li Liu, Xu Zhang, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 8, pp. 391-400
Closed Access
Xin Pan, Li Liu, Xu Zhang, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 8, pp. 391-400
Closed Access
How many phenotypes for the FBXO11 related disease? Report on a new patient with a tricho-rhino-phalangeal like phenotype
André Mégarbané, Cybel Mehawej, Daniel Mahfoud, et al.
European Journal of Medical Genetics (2024) Vol. 69, pp. 104944-104944
Open Access
André Mégarbané, Cybel Mehawej, Daniel Mahfoud, et al.
European Journal of Medical Genetics (2024) Vol. 69, pp. 104944-104944
Open Access
Clinical and genetic characteristics of a case of Koolen-De Vries syndrome caused by KANSL1 gene mutation and literature review: A case report
Haozheng Zhang, Limei Yuan, Meili Fan, et al.
Medicine (2024) Vol. 103, Iss. 49, pp. e40923-e40923
Open Access
Haozheng Zhang, Limei Yuan, Meili Fan, et al.
Medicine (2024) Vol. 103, Iss. 49, pp. e40923-e40923
Open Access
Elucidating the clinical and molecular spectrum ofSMARCC2-associated NDD in a cohort of 65 affected individuals
Elisabeth Bosch, Bernt Popp, Esther Güse, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Elisabeth Bosch, Bernt Popp, Esther Güse, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
FBXO11 Variants are Associated with Intellectual Disability and Variable Clinical Manifestation in Chinese Patients
Xin Pan, Li Liu, Xu Zhang, et al.
Research Square (Research Square) (2023)
Open Access
Xin Pan, Li Liu, Xu Zhang, et al.
Research Square (Research Square) (2023)
Open Access
