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:
Primary ovarian insufficiency in a female with phosphomannomutase-2 gene (<i>PMM2</i>) mutations for congenital disorder of glycosylation
Yohei Masunaga, M. Mochizuki, Machiko Kadoya, et al.
Endocrine Journal (2021) Vol. 68, Iss. 5, pp. 605-611
Open Access | Times Cited: 8
Yohei Masunaga, M. Mochizuki, Machiko Kadoya, et al.
Endocrine Journal (2021) Vol. 68, Iss. 5, pp. 605-611
Open Access | Times Cited: 8
Showing 8 citing articles:
Selected Genetic Factors Associated with Primary Ovarian Insufficiency
Meng-Chi Chen, Haotian Jiang, Chunping Zhang
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 5, pp. 4423-4423
Open Access | Times Cited: 32
Meng-Chi Chen, Haotian Jiang, Chunping Zhang
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 5, pp. 4423-4423
Open Access | Times Cited: 32
Primary ovarian insufficiency: update on clinical and genetic findings
Silvia Federici, Raffaella Rossetti, Silvia Moleri, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 6
Silvia Federici, Raffaella Rossetti, Silvia Moleri, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 6
A comprehensive update of genotype–phenotype correlations in PMM2-CDG: insights from molecular and structural analyses
Tiago Oliveira, Ricardo Ferraz, Luı́sa Azevedo, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Tiago Oliveira, Ricardo Ferraz, Luı́sa Azevedo, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Clinical and Molecular Features of Patients With Congenital Disorders of Glycosylation in Japan
Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada
JIMD Reports (2025) Vol. 66, Iss. 3
Open Access
Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada
JIMD Reports (2025) Vol. 66, Iss. 3
Open Access
Revisiting the immunopathology of congenital disorders of glycosylation: an updated review
Carlota Pascoal, Rita Francisco, Patrícia Mexia, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
Carlota Pascoal, Rita Francisco, Patrícia Mexia, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
Genetic insights into the complexity of premature ovarian insufficiency
Linhang Nie, Xiaojie Wang, Songyuan Wang, et al.
Reproductive Biology and Endocrinology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Linhang Nie, Xiaojie Wang, Songyuan Wang, et al.
Reproductive Biology and Endocrinology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa
Nobutaka Tachibana, Katsuhiro Hosono, Shuhei Nomura, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 359-359
Open Access | Times Cited: 9
Nobutaka Tachibana, Katsuhiro Hosono, Shuhei Nomura, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 359-359
Open Access | Times Cited: 9
Assessing the effects of PMM2 variants on protein stability
Dulce Quelhas, João Carneiro, Mónica Lopes‐Marques, et al.
Molecular Genetics and Metabolism (2021) Vol. 134, Iss. 4, pp. 344-352
Closed Access | Times Cited: 5
Dulce Quelhas, João Carneiro, Mónica Lopes‐Marques, et al.
Molecular Genetics and Metabolism (2021) Vol. 134, Iss. 4, pp. 344-352
Closed Access | Times Cited: 5
