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:

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation
Eva-Cristiana Gavril, Roxana Popescu, Irina Nucă, et al.
Genes (2022) Vol. 13, Iss. 11, pp. 2083-2083
Open Access | Times Cited: 9

Showing 9 citing articles:

Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8317-8317
Open Access | Times Cited: 17
22q11.21 Deletions: A Review on the Interval Mediated by Low-Copy Repeats C and D
Veronica Bertini, Francesca Cambi, Annalisa Legitimo, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 72-72
Open Access
Inherited or Immunological Thrombocytopenia: The Complex Nature of Platelet Disorders in 22q11.2 Deletion Syndrome
Bartosz Urbański, Zuzanna Urbańska, Katarzyna Bąbol‐Pokora, et al.
Seminars in Thrombosis and Hemostasis (2025)
Closed Access
When Should We Raise Clinical Suspicion of DiGeorge Syndrome: Two Case Reports from a Tertiary Hospital in Indonesia
Joni Indah Sari, Nydia Rena Benita Sihombing, Nani Maharani, et al.
OBM Genetics (2025) Vol. 09, Iss. 01, pp. 1-16
Open Access
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Cinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
(2023)
Open Access | Times Cited: 7
Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study
Qing Lu, Laipeng Luo, Baitao Zeng, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review
Eva-Cristiana Gavril, Irina Nucă, Monica-Cristina Pânzaru, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 465-465
Open Access | Times Cited: 5
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
Homozygous 22q11.2 distal type II microdeletion is associated with syndromic neurodevelopmental delay
Somaya Salah, Hiba Jaber, Ayala Frumkin, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 10, pp. 2623-2630
Open Access
Page 1

Scroll to top