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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:

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

Showing 19 citing articles:

Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis
Rhiannon Mellis, Kathryn Oprych, Elizabeth Scotchman, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 6, pp. 662-685
Open Access | Times Cited: 147
Should we offer prenatal exome sequencing for intrauterine growth restriction or short long bones? A systematic review and meta-analysis
Fionnuala Mone, Rhiannon Mellis, Heinz Gabriel, et al.
American Journal of Obstetrics and Gynecology (2022) Vol. 228, Iss. 4, pp. 409-417.e4
Open Access | Times Cited: 25
Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis
Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, et al.
Diagnostics (2022) Vol. 12, Iss. 3, pp. 575-575
Open Access | Times Cited: 24
Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study
Yanlin Huang, Chang Liu, Hongke Ding, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 14
Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation
Alexandra Emms, James Castleman, Stephanie Allen, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1517-1517
Open Access | Times Cited: 20
Sequential prenatal diagnosis of fetal skeletal dysplasia: A cohort study
M.-J. Jiang, Bin Zhang, Jing Wang, et al.
Acta Obstetricia Et Gynecologica Scandinavica (2025)
Open Access
Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review
K. Tse, Ilham Utama Surya, Rima Irwinda, et al.
Genes (2023) Vol. 14, Iss. 6, pp. 1203-1203
Open Access | Times Cited: 7
Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience
Anna Kucińska‐Chahwan, Maciej Geremek, Tomasz Roszkowski, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 724-724
Open Access | Times Cited: 10
Genetic testing and diagnostic strategies of fetal skeletal dysplasia: a preliminary study in Wuhan, China
Wanlu Liu, Jing Cao, Xinwei Shi, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort
Katri Rajala, Ellamaija Kasanen, Sanna Toiviainen‐Salo, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 12, pp. 1525-1537
Open Access | Times Cited: 6
Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort
Alanna Strong, Meckenzie Behr, Carina Lott, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 2
The Osteogenesis Imperfecta Type V Mutant BRIL/IFITM5 Promotes Transcriptional Activation of MEF2, NFATc, and NR4A in Osteoblasts
Vincent Maranda, Marie-Hélène Gaumond, Pierre Moffatt
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 4, pp. 2148-2148
Open Access | Times Cited: 3
Prenatal ultrasound findings and prenatal diagnosis of fetal skeletal dysplasia
Lili Li, Xiaofei Jin, Suna Liu, et al.
Journal of Clinical Ultrasound (2024) Vol. 52, Iss. 5, pp. 575-587
Closed Access
Incremental yield of prenatal exome sequencing in fetuses with skeletal system abnormalities: A systematic review and meta‐analysis
Yan Wang, Yuan Lv, Jia Yao, et al.
Acta Obstetricia Et Gynecologica Scandinavica (2024)
Open Access
Whole-Exome Sequencing Data Analysis
Chadi Saad
Elsevier eBooks (2024)
Closed Access
Clinical features and genetic analysis of a case series of skeletal ciliopathies in a prenatal setting
Ying Peng, Lin Zhou, Jing Chen, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Diagnostic yield of exome sequencing in fetuses with skeletal dysplasia: systematic review and meta-analysis
Siqi Wu, Hongkun Lai, Yingying Chen, et al.
Research Square (Research Square) (2023)
Open Access
Application of whole-exome sequencing technology in clarifying 269 cases of fetal skeletal system disorders
yijun ge, Huizhen Yuan, Baitao Zeng, et al.
Research Square (Research Square) (2023)
Open Access
Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports
Li Wang, Ruiqi Li, Jingfang Zhai, et al.
Medicine (2022) Vol. 101, Iss. 43, pp. e31321-e31321
Open Access
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