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:
Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone
Dongye He, Yanying Li, Wanling Yang, et al.
Clinica Chimica Acta (2021) Vol. 524, pp. 1-10
Closed Access | Times Cited: 6
Dongye He, Yanying Li, Wanling Yang, et al.
Clinica Chimica Acta (2021) Vol. 524, pp. 1-10
Closed Access | Times Cited: 6
Showing 6 citing articles:
Phenotypic and genotypic landscape of PROKR2 in neuroendocrine disorders
Julian Martinez-Mayer, María Inés Pérez‐Millán
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
Julian Martinez-Mayer, María Inés Pérez‐Millán
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 5
Clinical and genetic evaluation of children with short stature of unknown origin
Qianqian Zhao, Yanying Li, Qian Shao, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 4
Qianqian Zhao, Yanying Li, Qian Shao, et al.
BMC Medical Genomics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 4
Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency
Shuoshuo Wei, Mei Zhang, Yanying Li, et al.
Gene (2024) Vol. 907, pp. 148283-148283
Closed Access | Times Cited: 1
Shuoshuo Wei, Mei Zhang, Yanying Li, et al.
Gene (2024) Vol. 907, pp. 148283-148283
Closed Access | Times Cited: 1
Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome
Shuoshuo Wei, Yanying Li, Wanling Yang, et al.
Heliyon (2024) Vol. 10, Iss. 6, pp. e28082-e28082
Open Access | Times Cited: 1
Shuoshuo Wei, Yanying Li, Wanling Yang, et al.
Heliyon (2024) Vol. 10, Iss. 6, pp. e28082-e28082
Open Access | Times Cited: 1
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, et al.
Journal of Clinical Research in Pediatric Endocrinology (2023) Vol. 15, Iss. 4, pp. 338-347
Open Access | Times Cited: 3
Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, et al.
Journal of Clinical Research in Pediatric Endocrinology (2023) Vol. 15, Iss. 4, pp. 338-347
Open Access | Times Cited: 3
Paleoenvironmental characteristics and organic matter enrichment mechanisms of the upper Ordovician-lower Silurian organic-rich black shales in the Yangtze foreland basin, South China
Liang Zhao, Yong Li, Chengjie Zou, et al.
Frontiers in Earth Science (2023) Vol. 11
Open Access | Times Cited: 3
Liang Zhao, Yong Li, Chengjie Zou, et al.
Frontiers in Earth Science (2023) Vol. 11
Open Access | Times Cited: 3
