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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:

Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy
Hamide Betül Gerik Çelebi, Hilal AYDIN, Hilmi Bolat, et al.
Molecular Syndromology (2023) Vol. 14, Iss. 3, pp. 208-218
Open Access | Times Cited: 8

Showing 8 citing articles:

Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders
Hamide Betül Gerik Çelebi, Hilmi Bolat, Gül Ünsel‐Bolat
Developmental Neurobiology (2024) Vol. 84, Iss. 3, pp. 158-168
Open Access | Times Cited: 4
Novel mutations found in genes involved in global developmental delay and intellectual disability by whole-exome sequencing, homology modeling, and systems biology
Nafiseh Moeinifar, Zohreh Hojati
The World Journal of Biological Psychiatry (2025), pp. 1-16
Closed Access
TMEM63 mechanosensitive ion channels: Activation mechanisms, biological functions and human genetic disorders
Xin Chen, Na Wang, Jiawei Liu, et al.
Biochemical and Biophysical Research Communications (2023) Vol. 683, pp. 149111-149111
Closed Access | Times Cited: 8
Shifting the Focus of Molecular Syndromology from Individual Diagnoses to Outcome Analyses
Martin Poot
Molecular Syndromology (2023) Vol. 14, Iss. 4, pp. 267-269
Closed Access | Times Cited: 1
A novel heterozygous TMEM63A variant in a familial case with early onset nystagmus, severe hypomyelination, and a favorable adult prognosis
Shota Yoneno, Kaoru Yamamoto, Kenshiro Tabata, et al.
Journal of Human Genetics (2024) Vol. 69, Iss. 11, pp. 607-611
Closed Access
Exome sequencing in 90 children with developmental delay: a single-center experience
Oksana Boyarchuk, L.A. Volianska, Olena Smashna, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
Pelin Özyavuz Çubuk, Ece Keskin, Lamiya Mardan Hacızade, et al.
Kırıkkale Üniversitesi Tıp Fakültesi Dergisi (2024) Vol. 26, Iss. 3, pp. 300-307
Open Access
Association of <i>ABCA13</i> Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders
Hamide Betül Gerik Çelebi, Gül Ünsel‐Bolat, Hilmi Bolat
Molecular Syndromology (2023) Vol. 15, Iss. 1, pp. 22-29
Open Access
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