Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder
Fei Chen, Haiming Yuan, Wenyong Wu, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 181, Iss. 2, pp. 218-225
Closed Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Enhancer–promoter specificity in gene transcription: molecular mechanisms and disease associations
Meyer J. Friedman, Tobias Wagner, Haram Lee, et al.
Experimental & Molecular Medicine (2024) Vol. 56, Iss. 4, pp. 772-787
Open Access | Times Cited: 13
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum
Enrico D.H. Konrad, Niels Nardini, Almuth Caliebe, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 12, pp. 2723-2733
Open Access | Times Cited: 59
Genome analysis and knowledge-driven variant interpretation with TGex
Dvir Dahary, Yaron Golan, Yaron Mazor, et al.
BMC Medical Genomics (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 44
Clustered Protocadherins Emerge as Novel Susceptibility Loci for Mental Disorders
Zhilian Jia, Qiang Wu
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 36
On the dependent recognition of some long zinc finger proteins
Zheng Zuo, Timothy Billings, Michael Walker, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 11, pp. 5364-5376
Open Access | Times Cited: 11
CCCTC-binding Factor N-terminal Domain Regulates Clustered Protocadherin Gene Expression by Enhancing Cohesin Processivity
Yijun Zhang, Qiang Wu
Journal of Biological Chemistry (2025), pp. 108337-108337
Open Access
Expansion of the genotypic and phenotypic spectrum of CTCF‐related disorder guides clinical management: 43 new subjects and a comprehensive literature review
Hannah Gabriela Valverde de Morales, Hsiao‐Lin V. Wang, Kathryn B. Garber, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 3, pp. 718-729
Open Access | Times Cited: 16
An updated catalog of CTCF variants associated with neurodevelopmental disorder phenotypes
Emma Price, Liron M. Fedida, Elena M. Pugacheva, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 9
Implications of Dosage Deficiencies in CTCF and Cohesin on Genome Organization, Gene Expression, and Human Neurodevelopment
Christopher T. Cummings, M. Jordan Rowley
Genes (2022) Vol. 13, Iss. 4, pp. 583-583
Open Access | Times Cited: 13
Clinical variants paired with phenotype: A rich resource for brain gene curation
Maya Chopra, Juliann M. Savatt, Taylor I. Bingaman, et al.
Genetics in Medicine (2023) Vol. 26, Iss. 3, pp. 101035-101035
Open Access | Times Cited: 6
A study on genotypes and phenotypes of short stature caused by epigenetic modification gene variants
Huakun Shangguan, Jian Wang, Jinduan Lin, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 3, pp. 1403-1414
Closed Access | Times Cited: 2
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment
Jie Zhang, Gongcheng Hu, Yuli Lu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Customised next-generation sequencing multigene panel to screen a large cohort of individuals with chromatin-related disorder
Gabriella Maria Squeo, Bartolomeo Augello, Valentina Massa, et al.
Journal of Medical Genetics (2020) Vol. 57, Iss. 11, pp. 760-768
Closed Access | Times Cited: 17
To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders
Miya St John, Tanya Tripathi, Angela Morgan, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 152, pp. 105293-105293
Closed Access | Times Cited: 4
3D genome perspective on cell fate determination, organ regeneration, and diseases
Hongxin Zhong, Jie Zhang, Yuli Lu, et al.
Cell Proliferation (2023) Vol. 56, Iss. 5
Open Access | Times Cited: 2
Ubiquitous Chromatin Modifiers in Congenital Retinal Diseases: Implications for Disease Modeling and Regenerative Medicine
Brian W. Basinski, Daniel A. Balikov, Michael Aksu, et al.
Trends in Molecular Medicine (2021) Vol. 27, Iss. 4, pp. 365-378
Open Access | Times Cited: 5
CTCF in parvalbumin-expressing neurons regulates motor, anxiety and social behavior and neuronal identity
Liron Davis, Prudhvi Raj Rayi, Dmitriy Getselter, et al.
Molecular Brain (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 3
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment
Mingjie Zhang, Gongcheng Hu, Yuli Lu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Exploring Disrupted Gene Networks in Human 22q11.2 Microdeletion
Camila Cristina de Oliveira Alves, Ivan Rodrigo Wolf, Bruno Faulin Gamba, et al.
Deleted Journal (2024) Vol. 1, Iss. 3, pp. 112-121
Open Access
CTCF N-terminal Domain Regulates Clustered Protocadherin Gene Expression by Enhancing Cohesin Processivity
Yijun Zhang, Qiang Wu
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
CTCF Point Mutation at R567 Disrupts Mouse Heart Development via 3D Genome Rearrangement and Transcription Dysregulation
Huawei Ren, Hongxin Zhong, Jie Zhang, et al.
Cell Proliferation (2024)
Open Access
CTCF variant begets to short stature by down-regulation of IGF1
Hong Chen, Weiyu Li, Suping Zhang, et al.
Journal of Molecular Endocrinology (2023) Vol. 70, Iss. 4
Open Access | Times Cited: 1
Expanding the mutational and clinical spectrum of Chinese intellectual disability patients with two novel CTCF variants
Bo Tan, Sihan Liu, Xiaoshu Feng, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 1
Development of clinical genetics in Asia
Brian Hon‐Yin Chung, Brooke Willis, Poh San Lai
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2019) Vol. 181, Iss. 2, pp. 150-154
Closed Access | Times Cited: 2
Germline variant in Ctcf links mental retardation to Wilms tumor predisposition
Pablo Gargallo, Silvestre Oltra, M Tasso, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 11, pp. 1288-1291
Open Access | Times Cited: 1
Page 1 - Next Page

Scroll to top