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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:

Concurrent hearing and genetic screening in a general newborn population
Ling Guo, Jiale Xiang, Lei Sun, et al.
Human Genetics (2020) Vol. 139, Iss. 4, pp. 521-530
Closed Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

Early hearing detection and intervention (EHDI) programmes for infants and young children in low-income and middle-income countries in Asia: a systematic review
Deepashree Joshi B, Vidya Ramkumar, Lekha S. Nair, et al.
BMJ Paediatrics Open (2023) Vol. 7, Iss. 1, pp. e001752-e001752
Open Access | Times Cited: 14
Future directions for screening and treatment in congenital hearing loss
Ryan K. Thorpe, Richard J. Smith
Precision Clinical Medicine (2020) Vol. 3, Iss. 3, pp. 175-186
Open Access | Times Cited: 28
Association Between Expanded Genomic Sequencing Combined With Hearing Screening and Detection of Hearing Loss Among Newborns in a Neonatal Intensive Care Unit
Yunqian Zhu, Liyuan Hu, Lin Yang, et al.
JAMA Network Open (2022) Vol. 5, Iss. 7, pp. e2220986-e2220986
Open Access | Times Cited: 19
Newborn Screening for Deafness/Hard of Hearing in the Genomic Era
Anne B.S. Giersch, Cynthia C. Morton
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 54-60
Closed Access
Impact of over 6 months of digital hearing aid usage on auditory working memory in acquired severe to profound hearing loss
Arun Kumar Yadav, Amra Ahsan, Vijay Kumar, et al.
Journal of Family Medicine and Primary Care (2025) Vol. 14, Iss. 1, pp. 101-106
Open Access
The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide
Jiao Zhang, Yin Wang, Chengbin Yan, et al.
Ear and Hearing (2022) Vol. 44, Iss. 1, pp. 232-241
Open Access | Times Cited: 14
Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China
Qingwen Zhu, Mu-Ting Li, Xun Zhuang, et al.
JAMA Network Open (2021) Vol. 4, Iss. 9, pp. e2125544-e2125544
Open Access | Times Cited: 16
Concurrent newborn hearing and genetic screening of common hearing loss variants with bloodspot-based targeted next generation sequencing in Jiangxi province
Haiyan Luo, Yan Yang, Xinrong Wang, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 11
Genetics of Childhood Hearing Loss
Calli O. Mitchell, Cynthia C. Morton
Otolaryngologic Clinics of North America (2021) Vol. 54, Iss. 6, pp. 1081-1092
Closed Access | Times Cited: 14
Etiology of Prelingual Hearing Loss in the Universal Newborn Hearing Screening Era: A Scoping Review
Ashley Satterfield‐Nash, Ayesha Umrigar, Tatiana M. Lanzieri
Otolaryngology (2020) Vol. 163, Iss. 4, pp. 662-670
Open Access | Times Cited: 14
Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow‐up
Kun Lin, Huang Jiexiang, Lin Hua, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 4
Coalition for Global Hearing Health Hearing Care Pathways Working Group: Guidelines for Clinical Guidance for Readiness and Development of Evidence-Based Early Hearing Detection and Intervention Programs
Christine Yoshinaga‐Itano, Gwen Carr, Adrian Davis, et al.
Ear and Hearing (2024) Vol. 45, Iss. 5, pp. 1071-1088
Open Access | Times Cited: 1
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screening
Chanjuan Hao, Xuyun Hu, Ruolan Guo, et al.
European Journal of Human Genetics (2024)
Closed Access | Times Cited: 1
Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach
Jing Wang, Jiale Xiang, Lisha Chen, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 9
Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China
Luhang Cai, Liu Ya, Yaping Xu, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 9
Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns
Jiale Xiang, Hongfu Zhang, Xiangzhong Sun, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 6
Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families
Jianyan Pan, Shanshan Ma, Yanling Teng, et al.
Clinica Chimica Acta (2022) Vol. 532, pp. 53-60
Closed Access | Times Cited: 6
[The critical thoughts on diagnosis and treatment of childhood hearing loss].
Qiuju Wang
PubMed (2023) Vol. 37, Iss. 3, pp. 161-168
Closed Access | Times Cited: 3
Next-generation sequencing improves precision medicine in hearing loss
Teresa Imízcoz, C. Prieto, Raquel Manrique‐Huarte, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss
Т Г Маркова, Н. Н. Алексеева, M.R. Lalayants, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 11, pp. 1843-1843
Open Access | Times Cited: 5
A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns
Haiyan Yang, Hongyu Luo, Zhang Gui-Wei, et al.
BMC Medical Genomics (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 7
Combined hearing screening and genetic screening of deafness among Hakka newborns in China
Xiangxing Zeng, Zhifang Liu, Jing Wang, et al.
International Journal of Pediatric Otorhinolaryngology (2020) Vol. 136, pp. 110120-110120
Closed Access | Times Cited: 6
Preoperative factors influencing the rate and speed of available communication ability in prelingual paediatric cochlear implantation recipients
Hui-ru Fan, Dan Li, S J Wang, et al.
Acta Oto-Laryngologica (2023) Vol. 143, Iss. 6, pp. 481-488
Closed Access | Times Cited: 2
The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing
Calli O. Mitchell, Greysha Rivera‐Cruz, Matthew Hoi Kin Chau, et al.
International Journal of Neonatal Screening (2022) Vol. 8, Iss. 2, pp. 36-36
Open Access | Times Cited: 3
[Genetics of pediatric hearing loss].
Jiao Zhang, Jing Guan, Qiuju Wang
PubMed (2023) Vol. 37, Iss. 3, pp. 181-185
Closed Access | Times Cited: 1
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