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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:

Pathogenesis of POLR1C-dependent Type 3 Treacher Collins Syndrome revealed by a zebrafish model
Marco Lau, Ernest Man Lok Kwong, Keng Po Lai, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2016) Vol. 1862, Iss. 6, pp. 1147-1158
Closed Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

Ribosomal proteins and human diseases: molecular mechanisms and targeted therapy
Jian Kang, Natalie Brajanovski, Keefe T. Chan, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 254
Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders
Eliezer Calo, Bo Gu, Margot E. Bowen, et al.
Nature (2018) Vol. 554, Iss. 7690, pp. 112-117
Open Access | Times Cited: 148
Perfluorohexanesulfonic acid (PFHxS) induces oxidative stress and causes developmental toxicities in zebrafish embryos
Zulvikar Syambani Ulhaq, William Ka Fai Tse
Journal of Hazardous Materials (2023) Vol. 457, pp. 131722-131722
Closed Access | Times Cited: 38
The role of p53 in developmental syndromes
Margot E. Bowen, Laura D. Attardi
Journal of Molecular Cell Biology (2019) Vol. 11, Iss. 3, pp. 200-211
Open Access | Times Cited: 67
Zebrafish models of orofacial clefts
Kaylia Duncan, Kusumika Mukherjee, Robert A. Cornell, et al.
Developmental Dynamics (2017) Vol. 246, Iss. 11, pp. 897-914
Open Access | Times Cited: 50
Transcriptome Profiling Identifies Ribosome Biogenesis as a Target of Alcohol Teratogenicity and Vulnerability during Early Embryogenesis
Mark E. Berres, Ana Garic, George R. Flentke, et al.
PLoS ONE (2017) Vol. 12, Iss. 1, pp. e0169351-e0169351
Open Access | Times Cited: 46
The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Małgorzata Grzanka, Agnieszka Piekiełko‐Witkowska
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 5, pp. 2482-2482
Open Access | Times Cited: 32
Deciphering the pathogenesis of retinopathy associated with carnitine palmitoyltransferase I deficiency in zebrafish model
Zulvikar Syambani Ulhaq, Yukiko Ogino, William Ka Fai Tse
Biochemical and Biophysical Research Communications (2023) Vol. 664, pp. 100-107
Closed Access | Times Cited: 11
ctdsp2 Knockout Induces Zebrafish Craniofacial Dysplasia via p53 Signaling Activation
Xin Xia, Wenjie Song, Fuyu Zhang, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 3, pp. 1297-1297
Open Access
Rare syndromes of the head and face: mandibulofacial and acrofacial dysostoses
Karla Terrazas, Jill Dixon, Paul A. Trainor, et al.
Wiley Interdisciplinary Reviews Developmental Biology (2017) Vol. 6, Iss. 3
Open Access | Times Cited: 39
Developmental toxicity of the common UV filter, benophenone-2, in zebrafish embryos
Henry C.H. Fong, Jeff Cheuk Hin Ho, Angela Cheung, et al.
Chemosphere (2016) Vol. 164, pp. 413-420
Closed Access | Times Cited: 38
Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
Mauro S. Porcel de Peralta, Valeria S. Mouguelar, María Antonella Sdrigotti, et al.
Cell Death and Disease (2016) Vol. 7, Iss. 10, pp. e2397-e2397
Open Access | Times Cited: 36
Counterclockwise Craniofacial Distraction Osteogenesis for Tracheostomy-Dependent Children with Treacher Collins Syndrome
Richard A. Hopper, Hitesh Kapadia, Srinivas M. Susarla, et al.
Plastic & Reconstructive Surgery (2018) Vol. 142, Iss. 2, pp. 447-457
Closed Access | Times Cited: 35
Zebrafish Models for Human Skeletal Disorders
Manuel Marí‐Beffa, Ana B. Mesa-Román, Iván Durán
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 26
FGF8 rescues motor deficits in zebrafish model of limb-girdle muscular dystrophy R18
Zulvikar Syambani Ulhaq, Yukiko Ogino, William Ka Fai Tse
Biochemical and Biophysical Research Communications (2023) Vol. 652, pp. 76-83
Open Access | Times Cited: 10
Transcriptomic analysis reveals mitochondrial dysfunction in the pathogenesis of Nager syndrome in sf3b4-depleted zebrafish
Zulvikar Syambani Ulhaq, William Ka Fai Tse
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 4, pp. 167128-167128
Closed Access | Times Cited: 3
Functional and Genetic Analyses Unveil the Implication of CDC27 in Hemifacial Microsomia
Wenjie Song, Xin Xia, Yue Fan, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4707-4707
Open Access | Times Cited: 3
Bioinformatics analysis of candidate genes involved in ethanol-induced microtia pathogenesis based on a human genome database: GeneCards
Yangyang Lin, Zhensheng Hu
International Journal of Pediatric Otorhinolaryngology (2021) Vol. 142, pp. 110595-110595
Closed Access | Times Cited: 20
Treacher Collins syndrome: New insights from animal models
William Ka Fai Tse
The International Journal of Biochemistry & Cell Biology (2016) Vol. 81, pp. 44-47
Closed Access | Times Cited: 21
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
Susan M. Motch Perrine, Meng Wu, Greg Holmes, et al.
Journal of Developmental Biology (2020) Vol. 8, Iss. 4, pp. 30-30
Open Access | Times Cited: 19
Transcriptomic Analysis in Marine Medaka Gill Reveals That the Hypo-Osmotic Stress Could Alter the Immune Response via the IL17 Signaling Pathway
Rong Li, Jiaqi Liu, Chi Tim Leung, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12417-12417
Open Access | Times Cited: 11
A common cellular response to broad splicing perturbations is characterized by metabolic transcript downregulation driven by the Mdm2–p53 axis
Jade E. Varineau, Eliezer Calo
Disease Models & Mechanisms (2024) Vol. 17, Iss. 2
Open Access | Times Cited: 2
Alcohol exposure suppresses ribosome biogenesis and causes nucleolar stress in cranial neural crest cells
George R. Flentke, Thomas E. Wilkie, Josh Baulch, et al.
PLoS ONE (2024) Vol. 19, Iss. 6, pp. e0304557-e0304557
Open Access | Times Cited: 2
Proteasomal inhibition attenuates craniofacial malformations in a zebrafish model of Treacher Collins Syndrome
Mauco Gil Rosas, Agustín Lorenzatti, Mauro S. Porcel de Peralta, et al.
Biochemical Pharmacology (2019) Vol. 163, pp. 362-370
Closed Access | Times Cited: 19
Autosomal recessive Treacher Collins syndrome due to POLR1C mutations: Report of a new family and review of the literature
Leïla Ghesh, Marie Vincent, Anne‐Sophie Delemazure, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 7, pp. 1390-1394
Closed Access | Times Cited: 19
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