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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:

Haploinsufficiency of <b><i>NKX2-1</i></b> in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction
Rathi Prasad, Adeline K. Nicholas, Nadia Schoenmakers, et al.
Hormone Research in Paediatrics (2019) Vol. 92, Iss. 5, pp. 340-344
Open Access | Times Cited: 10

Showing 10 citing articles:

Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders
Sebastián Vishnopolska, María F. Mercogliano, María Andrea Camilletti, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 106, Iss. 7, pp. 1956-1976
Open Access | Times Cited: 16
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
Hironori Bando, Shin Urai, Keitaro Kanie, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 10
Recent Advances and Applications of Human Lung Alveolar Organoids
Sun Kyung Kim, Eunho Sung, Kyungtae Lim
Molecules and Cells (2024), pp. 100140-100140
Open Access | Times Cited: 1
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Chenxi Yu, Bobo Xie, Zhengye Zhao, et al.
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 7
Insights from European Reference Network for Rare Neurological Disorders Study surveys on Diagnosis, Treatment, and Management of NKX2-1-Related Disorders
Laia Nou‐Fontanet, Quang Nguyen, Anne‐Catherine Bachoud‐Lévi, et al.
European Journal of Paediatric Neurology (2024) Vol. 51, pp. 110-117
Closed Access
Differential diagnosis of Huntington’s disease− neurological aspects of NKX2-1-related disorders
Julia Skwara, Maciej Nowicki, Lucia Sharif, et al.
Journal of Neural Transmission (2024) Vol. 131, Iss. 9, pp. 1013-1024
Open Access
Systematic review of thyroid function in NKX2-1-related disorders: Screening and diagnosis
Beatriz Carmona‐Hidalgo, Carmen Martín Gómez, Estefanía Herrera‐Ramos, et al.
PLoS ONE (2024) Vol. 19, Iss. 7, pp. e0303880-e0303880
Open Access
Systematic review of thyroid function in NKX2-1-related disorders: Treatment and follow-up
Beatriz Carmona‐Hidalgo, Estefanía Herrera‐Ramos, Rocío Rodríguez López, et al.
PLoS ONE (2024) Vol. 19, Iss. 10, pp. e0309064-e0309064
Open Access
Persisting embryonal infundibular recess in a case of TITF-1 gene mutation
Elizabeth O’Mahony, Jonathan R. Ellenbogen, Shivaram Avula
Neuroradiology (2022) Vol. 64, Iss. 5, pp. 1033-1035
Closed Access | Times Cited: 2
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH)
Mohammad Heidari, Seyed Ali Madani Manshadi, Ahmad Reza Eshghi, et al.
Physiology International (2022) Vol. 109, Iss. 2, pp. 261-277
Open Access | Times Cited: 1
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