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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:

Bardet-Biedl Syndrome: Current Perspectives and Clinical Outlook
Andrea Melluso, Floriana Secondulfo, Giovanna Capolongo, et al.
Therapeutics and Clinical Risk Management (2023) Vol. Volume 19, pp. 115-132
Open Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

Bardet‐Biedl syndrome: A focus on genetics, mechanisms and metabolic dysfunction
Jeremy Tomlinson
Diabetes Obesity and Metabolism (2024) Vol. 26, Iss. S2, pp. 13-24
Closed Access | Times Cited: 14
Syndromic Retinitis Pigmentosa: A Narrative Review
Márta Janáky, Gábor Braunitzer
Vision (2025) Vol. 9, Iss. 1, pp. 7-7
Open Access | Times Cited: 1
Three Different Primary Cancers, Including Breast, Esophagus, and Renal in a Single Patient: A Case Report
Amir Alinejad Khorram, Mohammad Soleimani, Ali Amani‐Beni, et al.
Clinical Case Reports (2025) Vol. 13, Iss. 2
Open Access
‘In the dark’: parents’ lifelong commitment to supporting children with Bardet-Biedl syndrome
Jeanette Ullmann Miller, Lena Fauske, Sólrún Sigurðardóttir, et al.
Health Psychology and Behavioral Medicine (2025) Vol. 13, Iss. 1
Open Access
Pharmaceutical inhibition of the Chk2 kinase mitigates cone photoreceptor degeneration in an iPSC model of Bardet-Biedl syndrome
A Barabino, Alisar Katbe, Roy Hanna, et al.
iScience (2025) Vol. 28, Iss. 4, pp. 112130-112130
Open Access
Hyperphagia in Bardet–Biedl syndrome: Pathophysiology, burden, and management
Philip L. Beales, Metin Cetiner, Andrea M. Haqq, et al.
Obesity Reviews (2025)
Open Access
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet–Biedl Syndrome
Mohammad Reza Seyedtaghia, Mohsen Habibi, Feyzollah Hashemi‐Gorji, et al.
Biochemical Genetics (2025)
Closed Access
Healthcare needs, care use and health status outcomes in adults with Bardet-Biedl syndrome: a cross-sectional study in Norway
Cecilie F. Rustad, Ragnheiður Bragadóttir, Hilde Nordgarden, et al.
BMJ Open (2025) Vol. 15, Iss. 4, pp. e095986-e095986
Open Access
The emerging functions of intraflagellar transport 52 in ciliary transport and ciliopathies
Prajna Udupa, Debasish Kumar Ghosh
Traffic (2024) Vol. 25, Iss. 1
Closed Access | Times Cited: 3
A Comprehensive Review of Syndromic Forms of Obesity: Genetic Etiology, Clinical Features and Molecular Diagnosis
Laura Machado Lara Carvalho, Alexander A.L. Jorge, Débora Romeo Bertola, et al.
Current Obesity Reports (2024) Vol. 13, Iss. 2, pp. 313-337
Closed Access | Times Cited: 3
Review of the phenotypes and genotypes of Bardet-Biedl syndrome from China
Zou Xin-Yi, Yang-Li Dai, Zeng Ling-Hui
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 8
A comprehensive review of genetic causes of obesity
Marcio José Concepción‐Zavaleta, Juan Eduardo Quiroz‐Aldave, María del Carmen Durand‐Vásquez, et al.
World Journal of Pediatrics (2023) Vol. 20, Iss. 1, pp. 26-39
Closed Access | Times Cited: 7
Single-Center Experience of Pediatric Cystic Kidney Disease and Literature Review
Sara Grlić, Viktorija Gregurović, Mislav Martinić, et al.
Children (2024) Vol. 11, Iss. 4, pp. 392-392
Open Access | Times Cited: 2
Retinitis pigmentosa with iris coloboma due to miR‐204 gene variant in a Chinese family
Lei Zhang, Zhu He‐Lin, Haiyan Wang, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 6
Open Access | Times Cited: 2
Ciliary localization of GPR75 promotes fat accumulation in mice
Marcelo Chávez, Anushweta Asthana, Peter K. Jackson
Journal of Clinical Investigation (2024) Vol. 134, Iss. 19
Open Access | Times Cited: 2
Treatment of hypothalamic obesity with GLP-1 analogs
Paul Dimitri, Christian L. Roth
Journal of the Endocrine Society (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 2
A diagnostic conundrum in Bardet–Biedl syndrome: when genetic diagnosis precedes clinical diagnosis
Nele Van Roy, H. Allen Sylvester, Dashty Husein, et al.
Endocrinology Diabetes and Metabolism Case Reports (2023) Vol. 2023, Iss. 4
Open Access | Times Cited: 4
Intraflagellar transport: A critical player in photoreceptor development and the pathogenesis of retinal degenerative diseases
Mohona Gupta, Gregory J. Pazour
Cytoskeleton (2023) Vol. 81, Iss. 11, pp. 556-568
Open Access | Times Cited: 4
Verbesserte Versorgungs-und Behandlungsoptionen für Patienten mit Hyperphagie-assoziierter Adipositas bei Bardet-Biedl-Syndrom
Metin Cetiner, Carsten Bergmann, Markus Bettendorf, et al.
Klinische Pädiatrie (2024) Vol. 236, Iss. 05, pp. 269-279
Open Access | Times Cited: 1
The characterization and comorbidities of heterozygous Bardet-Biedl syndrome carriers
Meng-Hua Li, I‐Chieh Chen, Hui‐Wen Yang, et al.
International Journal of Medical Sciences (2024) Vol. 21, Iss. 5, pp. 784-794
Open Access | Times Cited: 1
Renal Pathology of Ciliopathies
Thivya Sekar, Neil J. Sebire
Pediatric and Developmental Pathology (2024) Vol. 27, Iss. 5, pp. 411-425
Closed Access | Times Cited: 1
Inflammation and olfactory loss are associated with at least 139 medical conditions
Michael Leon, Emily T. Troscianko, Cynthia C. Woo
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 1
Familial osteochondrodysplastic and cardiomyopathic syndrome in Chianina cattle
Joana G. P. Jacinto, Tolulope Grace Ogundipe, Cinzia Benazzi, et al.
Journal of Veterinary Internal Medicine (2024) Vol. 38, Iss. 6, pp. 3346-3357
Open Access | Times Cited: 1
Molecular mechanisms of the obesity associated with Bardet‐Biedl syndrome: An update
Banghua Zhong, Ning Nie, Ming Dong
Obesity Reviews (2024)
Open Access | Times Cited: 1
The Role of the Ophthalmic Genetics Multidisciplinary Team in the Management of Inherited Retinal Degenerations—A Case-Based Review
Marcus P. Conway, Kirk Stephenson, Julia Zhu, et al.
Life (2024) Vol. 14, Iss. 1, pp. 107-107
Open Access
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