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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.

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Showing 14 citing articles:

New insights into oocyte cytoplasmic lattice-associated proteins
Carlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Trends in Genetics (2024) Vol. 40, Iss. 10, pp. 880-890
Closed Access | Times Cited: 5
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report
Zahra Anvar, Farnoosh Jafarpour, Bahia Namavar Jahromi, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 1
Open Access
The subcortical maternal complex safeguards mouse oocyte-to-embryo transition by preventing nuclear entry of SPIN1
Chengpeng Xu, Dandan Qin, Xukun Lu, et al.
Nature Structural & Molecular Biology (2025)
Closed Access
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Deborah Mackay, Gabriella Gazdagh, David Monk, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Larissa Bilo, Eguzkine Ochoa, Sunwoo Lee, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
Laura Pignata, Francesco Cecere, Fabio Acquaviva, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 4
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum
Ken Higashimoto, Feifei Sun, Eri Imagawa, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 6, pp. 590-594
Closed Access | Times Cited: 1
MicroRNA dysregulation in ataxia telangiectasia
Emilia Cirillo, Antonietta Tarallo, Elisabetta Toriello, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer
Francesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Cancers (2023) Vol. 15, Iss. 7, pp. 1944-1944
Open Access | Times Cited: 3
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum
Francesco Fioravanti Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Genes (2022) Vol. 13, Iss. 10, pp. 1875-1875
Open Access | Times Cited: 4
Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Tatsuki Urakawa, Hidenobu Soejima, Kaori Yamoto, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
Open Access
A case of mosaic deletion of paternally‐inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under‐expression as a cause of growth restriction
Ahmed Alhendi, Gabriella Gazdagh, Derek Lim, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 2, pp. 383-388
Closed Access | Times Cited: 1
Genetics and Epigenetics of Precocious Puberty
Е. А. Саженова, S. A. Vasilyev, Л. В. Рычкова, et al.
Генетика (2023) Vol. 59, Iss. 12, pp. 1360-1371
Closed Access | Times Cited: 1
Genetics and Epigenetics of Precocious Puberty
Е. А. Саженова, S. A. Vasilyev, Л. В. Рычкова, et al.
Russian Journal of Genetics (2023) Vol. 59, Iss. 12, pp. 1277-1287
Closed Access
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