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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:

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
Flora Tassone, Dragana Protić, Emily G. Allen, et al.
Cells (2023) Vol. 12, Iss. 18, pp. 2330-2330
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

A holistic approach to fragile X syndrome integrated guidance for person‐centred care
Kirsten Johnson, Andrew C. Stanfield, Gaia Scerif, et al.
Journal of Applied Research in Intellectual Disabilities (2024) Vol. 37, Iss. 3
Open Access | Times Cited: 5
The impact of mitochondrial dysfunction on ovarian aging
Xiaoyue Zhang, Ling Zhang, Wenpei Xiang
Journal of Translational Medicine (2025) Vol. 23, Iss. 1
Open Access
Reduced Respiratory Sinus Arrhythmia in Infants with the FMR1 Premutation
A. Chase, Lisa R. Hamrick, Holley P. Arnold, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 5, pp. 2186-2186
Open Access
Modification of the RNA methylome in neurodevelopmental disorders
Adriana PerezGrovas‐Saltijeral, Joseph Stones, Oliver C Orji, et al.
Current Opinion in Genetics & Development (2025) Vol. 92, pp. 102330-102330
Open Access
Tissue-Specific Effects of the DNA Helicase FANCJ/BRIP1/BACH1 on Repeat Expansion in a Mouse Model of the Fragile X-Related Disorders
Diego Antonio Jimenez, Alexandra K. Walker, Karen Usdin, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2655-2655
Open Access
Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders
Eddy N. de Boer, Arjen J. Scheper, Dennis Hendriksen, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 7, pp. 2850-2850
Open Access
Premutation Females with preFXTAS
Valentina Liani, Carme Torrents, Elisa Rolleri, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2825-2825
Open Access
Ovarian Insufficiency: Clinical Spectrum and Management Challenges
Cynthia A. Stuenkel
Journal of Women s Health (2024) Vol. 33, Iss. 4, pp. 397-406
Closed Access | Times Cited: 3
Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome
Jamie L. Randol, Kyoungmi Kim, Matthew D. Ponzini, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 356-356
Open Access | Times Cited: 3
Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome
YeEun Tak, Andrea Schneider, Ellery Santos, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 331-331
Open Access | Times Cited: 2
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder
Agata Kucińska, Wanda Hawuła, Lena Rutkowska, et al.
Brain Sciences (2024) Vol. 14, Iss. 3, pp. 273-273
Open Access | Times Cited: 2
A Comprehensive Review of Fragile X Syndrome and Fragile X Premutation Associated Conditions in Africa
Chioma Ngozichukwu Pauline Mbachu, Ikechukwu Innocent Mbachu, Randi J. Hagerman
Genes (2024) Vol. 15, Iss. 6, pp. 683-683
Open Access | Times Cited: 2
Population-based FMR1 carrier screening among reproductive women
Quratul Ain, Ye Hyun Hwang, D. K.‐W. Yeung, et al.
Journal of Assisted Reproduction and Genetics (2024)
Open Access | Times Cited: 2
Social and physical predictors of mental health impact in adult women who have an FMR1 premutation
Claudine M. Kraan, Minh Bui, Alison D. Archibald, et al.
Genetics in Medicine Open (2023) Vol. 1, Iss. 1, pp. 100829-100829
Open Access | Times Cited: 4
PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene
T. Persico, Maria Lucrezia Tranquillo, Renato Seracchioli, et al.
Genes (2023) Vol. 15, Iss. 1, pp. 6-6
Open Access | Times Cited: 4
State of the Art and New Trends from the Second International StemNet Meeting
Ivana Ferrero, Filippo Piccinini, Pasquale Marrazzo, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2221-2221
Open Access | Times Cited: 1
Ovarian reserve in patients with FMR1 gene premutation and the role of fertility preservation
T. Le Poulennec, Sophie Dubreuil, Michaël Grynberg, et al.
Annales d Endocrinologie (2024) Vol. 85, Iss. 4, pp. 269-275
Closed Access | Times Cited: 1
Cognitive status correlates of subclinical action tremor in female carriers of FMR1 premutation
Danuta Z. Loesch, Anna Atkinson, Deborah A. Hall, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 1
Case Series: Vestibular Migraines in Fragile X Premutation Carriers
YeEun Tak, Flora Tassone, Randi J. Hagerman
Journal of Clinical Medicine (2024) Vol. 13, Iss. 2, pp. 504-504
Open Access
Potential Prodromal Digital Postural Sway Markers for Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Detected via Dual-Tasking and Sensory Manipulation
Emily Timm, Nicollette Purcell, Bichun Ouyang, et al.
Sensors (2024) Vol. 24, Iss. 8, pp. 2586-2586
Open Access
Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome
Tri Indah Winarni, Ye Hyun Hwang, Susan M. Rivera, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 15, pp. 8103-8103
Open Access
Novel Advances in Cell-Free Therapy for Premature Ovarian Failure (POF): A Comprehensive Review
Yahya Yahyavi, Niloufar Kheradi, Abbas Karimi, et al.
Advanced Pharmaceutical Bulletin (2024) Vol. 14, Iss. 3, pp. 543-557
Open Access
Psychiatric Manifestations in Early to Middle Stages of Fragile X-Associated Tremor-Ataxia Syndrome (FXTAS)
Mei Hung, James A. Bourgeois, Ellery Santos, et al.
Journal of Neuropsychiatry (2024)
Closed Access
Language use predicts symptoms of fragile X-associated tremor/ataxia syndrome in men and women with the FMR1 premutation
Nell Maltman, Audra Sterling, Ellery Santos, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
From dynamic FMR1 mutation to variable phenotypes: A case series from a large Tunisian family
Imen Ketata, Emna Ellouz
Neurology and Clinical Neuroscience (2024)
Open Access
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