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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:

8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature
Ilaria Catusi, Maria Garzo, Anna Paola Capra, et al.
Genes (2021) Vol. 12, Iss. 5, pp. 652-652
Open Access | Times Cited: 14

Showing 14 citing articles:

Genomic map of candidate human imprint control regions: the imprintome
Dereje D. Jima, David Skaar, Antonio Planchart, et al.
Epigenetics (2022) Vol. 17, Iss. 13, pp. 1920-1943
Open Access | Times Cited: 40
SAPAP Scaffold Proteins: From Synaptic Function to Neuropsychiatric Disorders
Yunxia Bai, Huimin Wang, Chunxia Li
Cells (2022) Vol. 11, Iss. 23, pp. 3815-3815
Open Access | Times Cited: 15
Altered odor perception in Dlgap2 mutant mice, a mouse model of autism spectrum disorder
Yu‐Fu Chen, Chih-Yu Tsao, Yuh-Tarng Chen, et al.
Behavioural Brain Research (2024), pp. 115365-115365
Closed Access | Times Cited: 2
Using multi-scale genomics to associate poorly annotated genes with rare diseases
Christina Canavati, Dana Sherill-Rofe, Lara Kamal, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
An asymptomatic male individual carrying a 5.72 Mb de novo deletion in 8p23.2‑p23.3: A case report
Christina Keramida, Ioannis Papoulidis, Efterpi Pappa, et al.
Experimental and Therapeutic Medicine (2024) Vol. 27, Iss. 6
Open Access | Times Cited: 1
m5C methylated lncRncr3–MeCP2 interaction restricts miR124a-initiated neurogenesis
J Zhang, Huili Li, Lee Niswander
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Altered synaptic protein expression, aberrant spine morphology, and impaired spatial memory inDlgap2mutant mice, a genetic model of autism spectrum disorder
Ming‐Yen Hsieh, Li‐Heng Tuan, Ho‐Ching Chang, et al.
Cerebral Cortex (2022) Vol. 33, Iss. 8, pp. 4779-4793
Closed Access | Times Cited: 7
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region
Serena Redaelli, Donatella Conconi, Elena Sala, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 6, pp. 3347-3347
Open Access | Times Cited: 6
Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity
Yu-Chin An, Chia‐Lin Tsai, Chih‐Sung Liang, et al.
Nature and Science of Sleep (2022) Vol. Volume 14, pp. 1075-1087
Open Access | Times Cited: 5
Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature
Giovanna Cantini Tolezano, Giovanna Civitate Bastos, Silvia Souza da Costa, et al.
Journal of Autism and Developmental Disorders (2022) Vol. 54, Iss. 3, pp. 1181-1212
Closed Access | Times Cited: 4
Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis
Chih‐Ping Chen, Fang-Yu Hung, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics and Gynecology (2023) Vol. 62, Iss. 1, pp. 128-131
Open Access | Times Cited: 1
A novel genotype-phenotype between persistent-cloaca-related VACTERL and mutations of 8p23 and 12q23.1
Yue Li, Peiqi Liu, Weilin Wang, et al.
Pediatric Research (2023) Vol. 95, Iss. 5, pp. 1246-1253
Closed Access | Times Cited: 1
Genetic Counseling Challenges: A Case Report of a 6-Year-Old Child with Developmental Delay and B-Acute Lymphoblastic Leukemia
Rekha Selvam, Kalpana Gowrishankar, Indhumathi Nagarathinam
Apollo Medicine (2023) Vol. 20, Iss. 2_suppl, pp. S66-S69
Open Access
Prenatal Diagnosis of 8p23 Deletion Syndrome by Single Nucleotide Polymorphism Microarray
Didem Kaymak, Verda Alpay, Zafer Başıbüyük, et al.
Journal of Fetal Medicine (2021) Vol. 08, Iss. 04, pp. 315-319
Open Access
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