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:

Understanding the genetic mechanisms and cognitive impairments in Down syndrome: towards a holistic approach
Yara Abukhaled, Kenana Hatab, Mohammad Awadhalla, et al.
Journal of Neurology (2023) Vol. 271, Iss. 1, pp. 87-104
Open Access | Times Cited: 10

Showing 10 citing articles:

Trisomic rescue via allele-specific multiple chromosome cleavage using CRISPR-Cas9 in trisomy 21 cells
Ryotaro Hashizume, Sachiko Wakita, Hirofumi Sawada, et al.
PNAS Nexus (2025) Vol. 4, Iss. 2
Open Access

Characteristics of effective parenting for children with Down syndrome: a systematic review
Masoumeh Saki, Masoud Asadi, کیوان صالحی
International Journal of Developmental Disabilities (2025), pp. 1-12
Closed Access

Unraveling Down Syndrome: From Genetic Anomaly to Artificial Intelligence-Enhanced Diagnosis
Aabid Koul, Faisel Ahmad, Abida Bhat, et al.
Biomedicines (2023) Vol. 11, Iss. 12, pp. 3284-3284
Open Access | Times Cited: 10

A Comprehensive Review of the Relationship Between Oral Health and Down Syndrome
Javier Enrique Botero, Carolina Rodríguez‐Medina, Sandra Amaya, et al.
Current Oral Health Reports (2024) Vol. 11, Iss. 1, pp. 15-22
Open Access | Times Cited: 2

Decoding the genetic landscape of autism: A comprehensive review
Mohammed Al‐Beltagi, Nermin Kamal Saeed, Adel Salah Bediwy, et al.
World Journal of Clinical Pediatrics (2024) Vol. 13, Iss. 3
Open Access | Times Cited: 2

Early identification of birth defects can reduce secondary disabilities in newborn infants
Akhil Maheshwari, Mario Motta, Kei Lui
Newborn (2024) Vol. 2, Iss. 4, pp. iv-vii
Open Access

Astroglial Activation Is Exacerbated in a Down Syndrome Mouse Model
Zuolin Zhou, Yanhua Bi, Chunchun Zhi, et al.
Neuroscience (2024) Vol. 547, pp. 88-97
Closed Access

Genetic interactions and co-operating effects of non-HSA21 genes on the phenotypic variability in down syndrome
Bani Bandana Ganguly, Nitin N. Kadam
Gene Reports (2024), pp. 102106-102106
Closed Access

Genetic and Molecular Tools for the Clinical Diagnosis of Down Syndrome
Mónica Paulina Manzano Vela, Dennis Renato Manzano Vela, Ana Carola Flores Mancheno, et al.
Salud Ciencia y Tecnología (2024) Vol. 5, pp. 1027-1027
Closed Access

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