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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:

7q11.23 deletion and duplication
Lucy R. Osborne, Carolyn Β. Mervis
Current Opinion in Genetics & Development (2021) Vol. 68, pp. 41-48
Closed Access | Times Cited: 19

Showing 19 citing articles:

Williams syndrome
Beth A. Kozel, Boaz Barak, Chong Ae Kim, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 178
The contribution of copy number variants to psychiatric symptoms and cognitive ability
Josephine Mollon, Laura Almasy, Sébastien Jacquemont, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 4, pp. 1480-1493
Open Access | Times Cited: 47
Neurodevelopmental impact of CNV models in ASD: Recent advances and future directions
Kota Tamada, Toru Takumi
Current Opinion in Neurobiology (2025) Vol. 92, pp. 103001-103001
Open Access
Elastogenesis in Focus: Navigating Elastic Fibers Synthesis for Advanced Dermal Biomaterial Formulation
Roman Krymchenko, Gizem Coşar Kutluoğlu, Noor van Hout, et al.
Advanced Healthcare Materials (2024) Vol. 13, Iss. 27
Open Access | Times Cited: 3
Altered White Matter and microRNA Expression in a Murine Model Related to Williams Syndrome Suggests That miR-34b/c Affects Brain Development via Ptpru and Dcx Modulation
Meitar Grad, Ariel Nir, Gilad Levy, et al.
Cells (2022) Vol. 11, Iss. 1, pp. 158-158
Open Access | Times Cited: 11
Chromosomal abnormalities related to fever of unknown origin in a Chinese pediatric cohort and literature review
Bijun Sun, Mi‐Jin Yang, Jia Hou, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 8
Neuropsychological Genotype–Phenotype in Patients with Williams Syndrome with Atypical Deletions: A Systematic Review
Carlos Alberto Serrano‐Juárez, Belén Prieto‐Corona, Mario Rodríguez-Camacho, et al.
Neuropsychology Review (2022) Vol. 33, Iss. 4, pp. 891-911
Closed Access | Times Cited: 8
Genetic syndromes, neuroconstuctivism and replicable research; challenges and future directions
Emily K. Farran, Gaia Scerif
Infant and Child Development (2022) Vol. 31, Iss. 1
Open Access | Times Cited: 8
Deletion of Gtf2i via Systemic Administration of AAV-PHP.eB Virus Increases Social Behavior in a Mouse Model of a Neurodevelopmental Disorder
Omer Ophir, Gilad Levy, Ela Bar, et al.
Biomedicines (2023) Vol. 11, Iss. 8, pp. 2273-2273
Open Access | Times Cited: 2
DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number
Emma Strong, Carolyn Β. Mervis, Elaine Tam, et al.
npj Genomic Medicine (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 2
Neuronal Gtf2i deletion alters mitochondrial and autophagic properties
Ariel Nir Sade, Gilad Levy, Sari Schokoroy Trangle, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 2
Translational Study of Copy Number Variations in Schizophrenia
Min-Chih Cheng, Wei‐Hsien Chien, Yu‐Shu Huang, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 457-457
Open Access | Times Cited: 4
Machine Learning Models identify Signature Genes as potential Biomarkers for Hypertrophic Cardiomyopathy from Williams Syndrome
Hongxiao Yu, Xiping Liu, Manfang Sun, et al.
Research Square (Research Square) (2024)
Open Access
Genetic advances in neurodevelopmental disorders
Shilin Gao, Chaoyi Shan, Rong Zhang, et al.
Medical Review (2024) Vol. 5, Iss. 2, pp. 139-151
Open Access
Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?
Xiaojin Luo, Hongyan Niu, Fei Zhou, et al.
BMC Pregnancy and Childbirth (2024) Vol. 24, Iss. 1
Open Access
CNVs and Human Well-being: Integrating Psychiatric, Physical, and Socioeconomic Perspectives
Itaru Kushima, Masahiro Nakatochi, Norio Ozaki
Biological Psychiatry (2024)
Closed Access
Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders
Jonathan Lukas Lühmann, Gunnar Schmidt, Bernd Auber, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 7, pp. 1849-1857
Open Access | Times Cited: 1
Extended application of BACs-on-Beads technique in prenatal diagnosis
Shiyu Sun, Zhonghua Zhang, Jing Zhao, et al.
Archives of Medical Science (2022) Vol. 19, Iss. 1, pp. 250-257
Open Access | Times Cited: 1
Patent Highlights February–March 2021
Hermann AM Mucke
Pharmaceutical Patent Analyst (2021) Vol. 10, Iss. 4, pp. 183-190
Closed Access
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