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:
Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature
Alejandro Parra, Rachel Rabin, John Pappas, et al.
Genes (2023) Vol. 14, Iss. 6, pp. 1179-1179
Open Access | Times Cited: 7
Alejandro Parra, Rachel Rabin, John Pappas, et al.
Genes (2023) Vol. 14, Iss. 6, pp. 1179-1179
Open Access | Times Cited: 7
Showing 7 citing articles:
Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 ‐Related Disorders to a Syndromic Multiple Tumor Phenotype
Marie Lucain, Antonio Vitobello, Bekim Sadiković, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Marie Lucain, Antonio Vitobello, Bekim Sadiković, et al.
American Journal of Medical Genetics Part A (2025)
Open Access
Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development
Bo Chen, Chenyang Zhang, Hallgeir Rui, et al.
Human Genetics (2025)
Closed Access
Bo Chen, Chenyang Zhang, Hallgeir Rui, et al.
Human Genetics (2025)
Closed Access
Molecular and clinical aspects of histone-related disorders
Mode Al Ojaimi, Bashar J. Banimortada, Abduljalil Alragheb, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Mode Al Ojaimi, Bashar J. Banimortada, Abduljalil Alragheb, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Chromatin modifiers in human disease: from functional roles to regulatory mechanisms
Yali Nie, Chao Song, Hong Huang, et al.
Molecular Biomedicine (2024) Vol. 5, Iss. 1
Open Access | Times Cited: 2
Yali Nie, Chao Song, Hong Huang, et al.
Molecular Biomedicine (2024) Vol. 5, Iss. 1
Open Access | Times Cited: 2
Cellular and molecular functions of SETD2 in the central nervous system
Benjamin Mitchell, Stefan Thor, Michael Piper
Journal of Cell Science (2023) Vol. 136, Iss. 21
Open Access | Times Cited: 2
Benjamin Mitchell, Stefan Thor, Michael Piper
Journal of Cell Science (2023) Vol. 136, Iss. 21
Open Access | Times Cited: 2
Epilepsy and overgrowth–intellectual disability syndromes: a patient organization perspective on collaborating to accelerate pathways to treatment
Kerry Grens, Kit M. Church, Eric Chater‐Diehl, et al.
Therapeutic Advances in Rare Disease (2024) Vol. 5
Open Access
Kerry Grens, Kit M. Church, Eric Chater‐Diehl, et al.
Therapeutic Advances in Rare Disease (2024) Vol. 5
Open Access
NGS Custom Panel Implementation in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary Hospital
Ana Karen Sandoval-Talamantes, Jair Tenorio, Fernando Santos‐Simarro, et al.
Genes (2023) Vol. 14, Iss. 11, pp. 2091-2091
Open Access
Ana Karen Sandoval-Talamantes, Jair Tenorio, Fernando Santos‐Simarro, et al.
Genes (2023) Vol. 14, Iss. 11, pp. 2091-2091
Open Access
