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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:

ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits
Tom Hearn
Journal of Molecular Medicine (2018) Vol. 97, Iss. 1, pp. 1-17
Open Access | Times Cited: 90

Showing 26-50 of 90 citing articles:

Insulin-like Growth Factor 1 Signaling in Mammalian Hearing
Ángela García-Mato, Blanca Cervantes, Silvia Murillo‐Cuesta, et al.
Genes (2021) Vol. 12, Iss. 10, pp. 1553-1553
Open Access | Times Cited: 16
Syndromic ciliopathy: a taiwanese single-center study
Yu‐Wen Pan, Tsung-Ying Ou, Yen‐Yin Chou, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 2
Glucagon‐like peptide‐1 analogues in monogenic syndromic obesity: Real‐world data from a large cohort of Alström syndrome patients
Sadaf Ali, Shanat Baig, Subadra Wanninayake, et al.
Diabetes Obesity and Metabolism (2023) Vol. 26, Iss. 3, pp. 989-996
Open Access | Times Cited: 6
Whole-exome sequencing reveals genetic risks of early-onset sporadic dilated cardiomyopathy in the Chinese Han population
Lei Xiao, Dongyang Wu, Yang Sun, et al.
Science China Life Sciences (2021) Vol. 65, Iss. 4, pp. 770-780
Closed Access | Times Cited: 14
Comprehensive medical evaluation of pediatric bilateral sensorineural hearing loss
Suat Kılıç, Malek H. Bouzaher, Michael S. Cohen, et al.
Laryngoscope Investigative Otolaryngology (2021) Vol. 6, Iss. 5, pp. 1196-1207
Open Access | Times Cited: 14
Untargeted Metabolome- and Transcriptome-Wide Association Study Suggests Causal Genes Modulating Metabolite Concentrations in Urine
Reyhan Sönmez Flitman, Bita Khalili, Zoltán Kutalik, et al.
Journal of Proteome Research (2021) Vol. 20, Iss. 11, pp. 5103-5114
Open Access | Times Cited: 12
New variants of ALMS1 gene and familial Alström syndrome case series
Isabela Carvalho de Queiroz, Natália Carasek, Luiza Costa Villela Ferreira, et al.
Brazilian Journal of Otorhinolaryngology (2024) Vol. 90, Iss. 3, pp. 101402-101402
Open Access | Times Cited: 1
Alström Syndrome: A Review Focusing on Its Diverse Clinical Manifestations and Their Etiology as a Ciliopathy
Keiichi Hanaki, Tomoe Kinoshita, Masanobu Fujimoto, et al.
Yonago acta medica (2024) Vol. 67, Iss. 2, pp. 93-99
Open Access | Times Cited: 1
Alström Syndrom: A Clinical Case
O. V. Pervishko, Н. Г. Лупаш, Anna Ivanenko, et al.
Ural Medical Journal (2024) Vol. 23, Iss. 3, pp. 136-145
Closed Access | Times Cited: 1
Whole-exome sequencing revealed a novel mutation of the ALMS1 gene in a Chinese family with Alström syndrome: a case report
Ming Hu, Shuang Chen, Jinyuan Wu, et al.
BMC Pediatrics (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Characterisation of infantile cardiomyopathy in Alström syndrome using ALMS1 knockout induced pluripotent stem cell derived cardiomyocyte model
Leena Patel, Ashwin Roy, Jonathan Barlow, et al.
Molecular Genetics and Metabolism (2024) Vol. 143, Iss. 1-2, pp. 108575-108575
Open Access | Times Cited: 1
Alström syndrome—wide clinical variability within the same variant: a case report and literature review
Diana Jecan-Toader, Adrian P. Trifa, Bogdan Lucian, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access | Times Cited: 1
Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients
Naglaa M. Kamal, Ahmed N. Sahly, Babajan Banaganapalli, et al.
Saudi Journal of Biological Sciences (2019) Vol. 27, Iss. 1, pp. 271-278
Open Access | Times Cited: 11
Proteomic and Transcriptomic Landscapes of Alström and Bardet–Biedl Syndromes
Urszula Smyczyńska, Marcin Stańczak, Miljan Kuljanin, et al.
Genes (2022) Vol. 13, Iss. 12, pp. 2370-2370
Open Access | Times Cited: 7
Genetic variation in NOTCH1 is associated with overweight and obesity in Brazilian elderly
Estevão Carlos Silva Barcelos, Michel Satya Naslavsky, Izadora Silveira Fernandes, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families
Omar I. Saadah, Babajan Banaganapalli, Naglaa M. Kamal, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 9
Ocular evaluation and genetic test for an early Alström Syndrome diagnosis
Tyler Etheridge, Elizabeth Kellom, Rachel Sullivan, et al.
American Journal of Ophthalmology Case Reports (2020) Vol. 20, pp. 100873-100873
Open Access | Times Cited: 9
LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice
Li Yu, Lina Wang, Wufan Tao, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2021) Vol. 48, Iss. 5, pp. 384-395
Closed Access | Times Cited: 8
Energy expenditure deficits drive obesity in a mouse model of Alström syndrome
Erin J. Stephenson, Clint E. Kinney, Amanda S. Stayton, et al.
Obesity (2023) Vol. 31, Iss. 11, pp. 2786-2798
Open Access | Times Cited: 3
Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in ALMS1, Including a de novo Variation
Laura Mauring, Louise F. Porter, Valérie Pelletier, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 8
Whole-Genome Sequencing Identifies Novel Heterozygous Mutation in ALMS1 in Three Men With Both Peyronie's and Dupuytren's Disease
Alexandra Dullea, Iakov Efimenko, Fakiha Firdaus, et al.
Urology (2022) Vol. 166, pp. 76-78
Open Access | Times Cited: 5
Ocular findings and genetic test in Alström syndrome in childhood
You Wang, Li Huang, Limei Sun, et al.
Experimental Eye Research (2022) Vol. 225, pp. 109277-109277
Closed Access | Times Cited: 5
Discovery of ciliary G protein-coupled receptors regulating pancreatic islet insulin and glucagon secretion
Chien-Ting Wu, Keren I. Hilgendorf, Romina J. Bevacqua, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 7
Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome
Shahram Torkamandi, Somaye Rezaei, Reza Mirfakhraei, et al.
Gene (2019) Vol. 727, pp. 144228-144228
Closed Access | Times Cited: 6
A very early diagnosis of Alstrӧm syndrome by next generation sequencing
Leonardo Gatticchi, Ján Miertuš, Paolo Enrico Maltese, et al.
BMC Medical Genetics (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 6

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