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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 Profiles and Genetic Spectra of 814 Chinese Children With Short Stature
Xin Li, Ruen Yao, Guoying Chang, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 107, Iss. 4, pp. 972-985
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature
Ledjona Toni, Lukáš Plachý, Petra Dušátková, et al.
Hormone Research in Paediatrics (2023) Vol. 97, Iss. 1, pp. 40-52
Open Access | Times Cited: 15
Molecular diagnosis is an important indicator for response to growth hormone therapy in children with short stature
Qianqian Zhao, Mei Zhang, Yanying Li, et al.
Clinica Chimica Acta (2024) Vol. 554, pp. 117779-117779
Open Access | Times Cited: 5
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Short Stature
Qing Li, Zefu Chen, Jie Wang, et al.
JAMA Pediatrics (2023) Vol. 177, Iss. 11, pp. 1149-1149
Closed Access | Times Cited: 10
Association of IGF1R Polymorphisms with Idiopathic Short Stature in Children: A Meta-Analysis
Ahmad Hemmatyar, Maryam Vafapour, Hanieh Talebi, et al.
Research Square (Research Square) (2025)
Open Access
Identification and functional analysis of NPR2 truncating mutations in two Chinese families with short stature
Shuoshuo Wei, Rong Li, Dongye He, et al.
BMC Pediatrics (2025) Vol. 25, Iss. 1
Open Access
A polygenic score for height identifies an unmeasured genetic predisposition among pediatric patients with idiopathic short stature
John P. Shelley, Mingjian Shi, Josh F. Peterson, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience
Su Jin Kim, Eunyoung Joo, Jisun Park, et al.
Annals of Pediatric Endocrinology & Metabolism (2024) Vol. 29, Iss. 1, pp. 38-45
Open Access | Times Cited: 2
A study on genotypes and phenotypes of short stature caused by epigenetic modification gene variants
Huakun Shangguan, Jian Wang, Jinduan Lin, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 3, pp. 1403-1414
Closed Access | Times Cited: 2
Approach to the Patient With Short Stature: Genetic Testing
Reena Perchard, Philip Murray, Peter Clayton
The Journal of Clinical Endocrinology & Metabolism (2022) Vol. 108, Iss. 4, pp. 1007-1017
Closed Access | Times Cited: 10
Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature
Nathalia Liberatoscioli Menezes De Andrade, Mariana Ferreira de Assis Funari, Alexsandra C. Malaquias, et al.
Endocrine Connections (2022) Vol. 11, Iss. 12
Open Access | Times Cited: 9
Long-acting PEGylated growth hormone in children with idiopathic short stature
Xiaoping Luo, Sha Zhao, Yu Yang, et al.
European Journal of Endocrinology (2022) Vol. 187, Iss. 5, pp. 709-718
Open Access | Times Cited: 7
Adult height in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countrywide REPAR database
Ledjona Toni, Aneta Kodytková, Lukáš Plachý, et al.
Česko-slovenská pediatrie (2024) Vol. 78, Iss. Suppl.3, pp. 22-29
Open Access | Times Cited: 1
Genetic findings in short Turkish children born to consanguineous parents
Sjoerd D. Joustra, Emregül Işık, Jan M. Wit, et al.
Hormone Research in Paediatrics (2024), pp. 1-11
Open Access | Times Cited: 1
Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search
Dongye He, Mei Zhang, Yanying Li, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 1
Molecular diagnosis of patients with syndromic short stature identified by trio whole-exome sequencing
Huihui Sun, Geng Zhang, Na Li, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 1
Assessment of Nutritional Status in the Diagnostic Evaluation of the Child with Growth Failure
Hester Vlaardingerbroek, Sjoerd D. Joustra, Wilma Oostdijk, et al.
Hormone Research in Paediatrics (2023) Vol. 97, Iss. 1, pp. 11-21
Open Access | Times Cited: 3
Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders
Raíssa Rezende, Nathalia Liberatoscioli Menezes De Andrade, Naiara Castelo Branco Dantas, et al.
The Journal of Pediatrics (2023) Vol. 265, pp. 113841-113841
Closed Access | Times Cited: 3
Case Report: The success of face analysis technology in extremely rare genetic diseases in Korea: Tatton–Brown–Rahman syndrome and Say–Barber –Biesecker–Young–Simpson variant of ohdo syndrome
Sunha Park, Jae-Won Kim, Taeyoung Song, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
Long-acting PEGylated growth hormone in children with idiopathic short stature: time to reconsider our diagnostic and treatment policy?
Jan M. Wit, Sjoerd D. Joustra
European Journal of Endocrinology (2023) Vol. 188, Iss. 1, pp. R1-R4
Open Access | Times Cited: 2
Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children
Paolo Cavarzere, Angelo Pietrobelli, Alberto Gandini, et al.
Journal of Endocrinological Investigation (2023) Vol. 47, Iss. 5, pp. 1237-1250
Closed Access | Times Cited: 1
A novel 11 base pair deletion in KMT2C resulting in Kleefstra syndrome 2
Whitney Whitford, Juliet Taylor, Ian Hayes, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 1
Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel PLCB4 Splicing Variant and 5-Year Follow-up
Yunting Lin, Ye Zhang, Jian Ma, et al.
The Cleft Palate-Craniofacial Journal (2024)
Closed Access
Clinical profiles and molecular genetic analyses of 98 Chinese children with short statures
Danfeng Fang, Xing Li, Zhigang Zhang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
A polygenic score for height identifies an unmeasured genetic predisposition among pediatric patients with idiopathic short stature
John P. Shelley, Mingjian Shi, Josh F. Peterson, et al.
Research Square (Research Square) (2024)
Open Access
Identification and functional analysis of NPR2 truncating mutations in two Chinese families with Short Stature
Shuoshuo Wei, Rong Li, Dongye He, et al.
Research Square (Research Square) (2024)
Open Access
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