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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:

Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome
Ying Peng, Jialun Pang, Jiancheng Hu, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 8
Open Access | Times Cited: 10

Showing 10 citing articles:

Genetic Background of Fetal Growth Restriction
Beata Nowakowska, Katarzyna Pankiewicz, Urszula Nowacka, et al.
International Journal of Molecular Sciences (2021) Vol. 23, Iss. 1, pp. 36-36
Open Access | Times Cited: 29
Whole Exome Sequencing Analysis in Fetal Skeletal Dysplasia Detected by Ultrasonography: An Analysis of 38 Cases
Ying Peng, Shuting Yang, Xiaoliang Huang, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 19
Cognitive–Behavioral Profile in Pediatric Patients with Syndrome 5p-; Genotype–Phenotype Correlationships
Cristina Bel‐Fenellós, Chantal Biencinto, Belén Sáenz-Rico de Santiago, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1628-1628
Open Access | Times Cited: 5
Deep Phenotyping and Genetic Characterization of a Cohort of 70 Individuals With 5p Minus Syndrome
Julián Nevado, Cristina Bel‐Fenellós, Ana Karen Sandoval-Talamantes, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 12
Understanding the Genetic and Non-Genetic Interconnections in the Aetiology of Syndromic Congenital Heart Disease: An Updated Review: Part 2
Jyoti Maddhesiya, Bhagyalaxmi Mohapatra
Current Cardiology Reports (2024) Vol. 26, Iss. 3, pp. 167-178
Closed Access | Times Cited: 1
Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family
Ying Peng, Shuting Yang, Hui Xi, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 3
Open Access | Times Cited: 4
Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review
Kuntharee Traisrisilp, Yuri Yanase, Srimeunwai Ake‐sittipaisarn, et al.
Diagnostics (2022) Vol. 12, Iss. 2, pp. 421-421
Open Access | Times Cited: 2
Highly precise breakpoint detection of chromosome balanced translocation in chronic myelogenous leukaemia: Case series
Chuanchun Yang, Xiaoli Cui, Lei Xu, et al.
Journal of Cellular and Molecular Medicine (2022) Vol. 26, Iss. 17, pp. 4721-4726
Open Access | Times Cited: 2
Copy Number Variation Analysis of 5p Deletion Provides Accurate Prenatal Diagnosis and Reveals Candidate Pathogenic Genes
Guoming Chu, Pingping Li, Juan Wen, et al.
Frontiers in Medicine (2022) Vol. 9
Open Access | Times Cited: 1
Highly precise breakpoint detection of chromosome balanced translocation in a Chronic Myelogenous Leukemia patient
Chuanchun Yang, Xiaoli Cui, Lei Xu, et al.
Research Square (Research Square) (2021)
Open Access
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