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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:

Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms
Rie Seyama, Naomi Tsuchida, Y. Okada, et al.
Journal of Human Genetics (2021) Vol. 67, Iss. 3, pp. 157-164
Closed Access | Times Cited: 23

Showing 23 citing articles:

The TET-Sall4-BMP regulatory axis controls craniofacial cartilage development
Weigang Wang, Na Yang, Liangliang Wang, et al.
Cell Reports (2024) Vol. 43, Iss. 3, pp. 113873-113873
Open Access | Times Cited: 6
The value of genome-wide analysis in craniosynostosis
Alexandra Topa, Anna Rohlin, André Fehr, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 5
Biallelic structural variations withinFGF12detected by long-read sequencing in epilepsy
Sachiko Ohori, Akihiko Miyauchi, Hitoshi Osaka, et al.
Life Science Alliance (2023) Vol. 6, Iss. 8, pp. e202302025-e202302025
Open Access | Times Cited: 12
Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation
Marika Oksanen, Francesca Mastropasqua, Krystyna Mazan-Mamczarz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome
Shiomi Otsuji, Yosuke Nishio, Maki Tsujita, et al.
Journal of Medical Genetics (2022) Vol. 60, Iss. 4, pp. 359-367
Open Access | Times Cited: 18
De novo heterozygous variants in KIF5B cause kyphomelic dysplasia
Toshiyuki Itai, Zheng Wang, Gen Nishimura, et al.
Clinical Genetics (2022) Vol. 102, Iss. 1, pp. 3-11
Closed Access | Times Cited: 14
Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants
S. Watanabe, Ming Lei, Eiji Nakagawa, et al.
Brain and Development (2023) Vol. 45, Iss. 5, pp. 270-277
Open Access | Times Cited: 7
Epigenetic mechanisms of inner ear development
Vinodh Balendran, Kristina Ritter, Donna M. Martin
Hearing Research (2022) Vol. 426, pp. 108440-108440
Open Access | Times Cited: 8
Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism
Rie Seyama, Yuri Uchiyama, Yosuke Kaneshi, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 5, pp. 363-367
Closed Access | Times Cited: 4
A novel NONO variant that causes developmental delay and cardiac phenotypes
Toshiyuki Itai, Atsushi Sugie, Yohei Nitta, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association
Rie Seyama, Masashi Nishikawa, Yuri Uchiyama, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
A novel de novo TET3 loss-of-function variant in a Turkish boy presenting with neurodevelopmental delay and electrical status epilepticus during slow-wave sleep
Safiye Güneş Sağer, Ayberk Türkyılmaz, Hediye Pınar Günbey, et al.
Brain and Development (2022) Vol. 45, Iss. 2, pp. 140-145
Closed Access | Times Cited: 7
Long-read sequencing revealing intragenic deletions in exome-negative spastic paraplegias
Hiromi Fukuda, Takeshi Mizuguchi, Hiroshi Doi, et al.
Journal of Human Genetics (2023) Vol. 68, Iss. 10, pp. 689-697
Closed Access | Times Cited: 3
Advanced Omics Techniques for Understanding Cochlear Genome, Epigenome, and Transcriptome in Health and Disease
Annamaria Tisi, Sakthimala Palaniappan, Mauro Maccarrone
Biomolecules (2023) Vol. 13, Iss. 10, pp. 1534-1534
Open Access | Times Cited: 2
Pathogenic variants detected by RNA sequencing in Cornelia de Lange syndrome
Rie Seyama, Yuri Uchiyama, José Ricard Magliocco Ceroni, et al.
Genomics (2022) Vol. 114, Iss. 5, pp. 110468-110468
Open Access | Times Cited: 3
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy
Masamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 12, pp. 2453-2463
Open Access | Times Cited: 3
Tet controls axon guidance in early brain development through glutamatergic signaling
Hiep Tran, Le Le, Badri Nath Singh, et al.
iScience (2024) Vol. 27, Iss. 5, pp. 109634-109634
Open Access
Drosophila TET acts with PRC1 to activate gene expression independently of its catalytic activity
Guerric Gilbert, Yoan Renaud, Camille Teste, et al.
Science Advances (2024) Vol. 10, Iss. 18
Open Access
PROSER1 Modulates DNA Demethylation through Dual Mechanisms to Prevent Syndromic Developmental Malformations
Anna Fleming, Elena V. Knatko, Xiang Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A New De Novo Missense Variant of the TET3 Gene in a Patient with Epilepsy and Macrocephaly
Miryam Rosa Stella Foti, Maria Giovanna Tedesco, Davide Colavito, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9676-9676
Open Access
Alterations in DNA 5-hydroxymethylation Patterns in the Hippocampus of an Experimental Model of Refractory Epilepsy
Rudhab Bahabry, Rebecca M. Hauser, Richard G. Sánchez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8
Masamune Sakamoto, Toshihide Shiiki, Shuji Matsui, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 4, pp. 247-253
Closed Access | Times Cited: 2
Tet Controls Axon Guidance in Early Brain Development through Glutamatergic Signaling
Hiep Tran, Le Le, Badri Nath Singh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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