
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:
Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype–phenotype association
Maria Chiara Pelleri, Chiara Locatelli, Teresa Mattina, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Maria Chiara Pelleri, Chiara Locatelli, Teresa Mattina, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Showing 10 citing articles:
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Francesco Nappi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1734-1734
Open Access | Times Cited: 6
Francesco Nappi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1734-1734
Open Access | Times Cited: 6
Prenatal diagnosis of a familial 21q22.3 microduplication encompassing part of Down syndrome critical region in a pregnancy associated with an asymptomatic mother carrier without Down syndrome phenotype
Chih‐Ping Chen
Taiwanese Journal of Obstetrics and Gynecology (2025) Vol. 64, Iss. 2, pp. 383-384
Open Access
Chih‐Ping Chen
Taiwanese Journal of Obstetrics and Gynecology (2025) Vol. 64, Iss. 2, pp. 383-384
Open Access
Calcineurin inhibition may prevent Alzheimer disease in people with Down syndrome
Jacob Dohl, Zoe Treadwell, Christopher M. Norris, et al.
Alzheimer s & Dementia (2025) Vol. 21, Iss. 3
Open Access
Jacob Dohl, Zoe Treadwell, Christopher M. Norris, et al.
Alzheimer s & Dementia (2025) Vol. 21, Iss. 3
Open Access
Role of cystathionine-β-synthase and hydrogen sulfide in down syndrome
Csaba Szabó
Neurotherapeutics (2025), pp. e00584-e00584
Open Access
Csaba Szabó
Neurotherapeutics (2025), pp. e00584-e00584
Open Access
Revisión sistemática de las complicaciones perinatales en el síndrome de Down y su abordaje genético
Sofía Valencia, Marcus Vallejo, Natalia Beltrán, et al.
Revista Salud Bosque (2025) Vol. 14, Iss. 2
Open Access
Sofía Valencia, Marcus Vallejo, Natalia Beltrán, et al.
Revista Salud Bosque (2025) Vol. 14, Iss. 2
Open Access
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Francesco Nappi
(2024)
Open Access | Times Cited: 3
Francesco Nappi
(2024)
Open Access | Times Cited: 3
Epigenetics of Down Syndrome
Akhil Maheshwari, Srijan Singh
Newborn (2024) Vol. 3, Iss. 4, pp. 263-280
Open Access | Times Cited: 2
Akhil Maheshwari, Srijan Singh
Newborn (2024) Vol. 3, Iss. 4, pp. 263-280
Open Access | Times Cited: 2
A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101863-101863
Open Access | Times Cited: 1
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101863-101863
Open Access | Times Cited: 1
Key Features of Children with Down Syndrome (Ds) Attending Hvp Gatagara Gikondo Specialized School (Hvp/Ggss): An Observational Descriptive Study
Mutabazi David, Umutesi Rusa Divine, Nteziryayo Jean Pierre, et al.
(2024)
Closed Access
Mutabazi David, Umutesi Rusa Divine, Nteziryayo Jean Pierre, et al.
(2024)
Closed Access
Many Term infants with Persistent Patency of the Ductus Arteriosus could be Trisomy 21 Mosaics
Akhil Maheshwari, Varun Sharma, Srijan Singh, et al.
Newborn (2024) Vol. 3, Iss. 1, pp. 61-64
Open Access
Akhil Maheshwari, Varun Sharma, Srijan Singh, et al.
Newborn (2024) Vol. 3, Iss. 1, pp. 61-64
Open Access
Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
Yang Yang, Hao Wang
Molecular Cytogenetics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Yang Yang, Hao Wang
Molecular Cytogenetics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 1