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:
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1605-1625
Closed Access | Times Cited: 4
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1605-1625
Closed Access | Times Cited: 4
Showing 4 citing articles:
Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome
Zoë J. Frazier, Seyda Kilic, Hailey Osika, et al.
Clinical Genetics (2025)
Closed Access | Times Cited: 2
Zoë J. Frazier, Seyda Kilic, Hailey Osika, et al.
Clinical Genetics (2025)
Closed Access | Times Cited: 2
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes
Dmitrijs Rots, Sanaa Choufani, Víctor Faúndes, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1626-1642
Closed Access | Times Cited: 5
Dmitrijs Rots, Sanaa Choufani, Víctor Faúndes, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1626-1642
Closed Access | Times Cited: 5
Highlighting cardiovascular manifestations of kleefstra syndrome: literature review and clinical insights
Haotai Xie, Pengkang He, Qinhui Sheng, et al.
BMC Cardiovascular Disorders (2025) Vol. 25, Iss. 1
Open Access
Haotai Xie, Pengkang He, Qinhui Sheng, et al.
BMC Cardiovascular Disorders (2025) Vol. 25, Iss. 1
Open Access
A Novel Frameshift Variant and a Partial EHMT1 Microdeletion in Kleefstra Syndrome 1 Patients Resulting in Variable Phenotypic Severity and Literature Review
Maria Tzetis, Anastasios Mitrakos, Ιωάννα Παπαθανασίου, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 521-521
Open Access
Maria Tzetis, Anastasios Mitrakos, Ιωάννα Παπαθανασίου, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 521-521
Open Access
Development of a Patient and Caregiver-Centered Pediatric Disease Concept Model for Kleefstra Syndrome
Kristen Connors, Nikkola Carmichael, Terry Jo Bichell, et al.
(2025) Vol. 12
Closed Access
Kristen Connors, Nikkola Carmichael, Terry Jo Bichell, et al.
(2025) Vol. 12
Closed Access
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome
Laura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Molecular Neurobiology (2024)
Closed Access
Laura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Molecular Neurobiology (2024)
Closed Access
