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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:

Kabuki Syndrome—Clinical Review with Molecular Aspects
Snir Boniel, Krystyna Szymańska, Robert Śmigiel, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 468-468
Open Access | Times Cited: 64

Showing 1-25 of 64 citing articles:

Chromatinopathies: insight in clinical aspects and underlying epigenetic changes
Ewelina Bukowska‐Olech, Aleksandra Majchrzak‐Celińska, Marta Przyborska, et al.
Journal of Applied Genetics (2024) Vol. 65, Iss. 2, pp. 287-301
Open Access | Times Cited: 4
Ketogenic diet modifies ribosomal protein dysregulation in KMT2D Kabuki syndrome
Erica S. Tsang, Velda X. Han, Chloe Flutter, et al.
EBioMedicine (2024) Vol. 104, pp. 105156-105156
Open Access | Times Cited: 4
MLL4 regulates postnatal palate growth and midpalatal suture development
Jung-Mi Lee, Hunmin Jung, Bruno de Paula Machado Pasqua, et al.
Frontiers in Cell and Developmental Biology (2025) Vol. 13
Open Access
Kabuki and CHARGE syndromes: overlapping symptoms and diagnostic challenges
Bruno Pellozo Cerqueira, Elenice Andrade Milhomem, Ana Cristina Carvalho de Matos, et al.
Einstein (São Paulo) (2025) Vol. 23
Open Access
KMT2D Regulates Tooth Enamel Development
Jang‐Ming Lee, Han‐Sung Jung, Qingfeng Tang, et al.
Journal of Dental Research (2025)
Closed Access
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes
Michael C. Sierant, Sheng Chih Jin, Kaya Bilgüvar, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 13
Open Access
Molecular and clinical aspects of histone-related disorders
Mode Al Ojaimi, Bashar J. Banimortada, Abduljalil Alragheb, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
Sex-biased and parental allele-specific gene regulation by KDM6A
Wenxiu Ma, He Fang, Nicolas Pease, et al.
Biology of Sex Differences (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 16
Histone–lysine N-methyltransferase 2 (KMT2) complexes – a new perspective
Elżbieta Poręba, Krzysztof Leśniewicz, Julia Durzyńska
Mutation Research/Reviews in Mutation Research (2022) Vol. 790, pp. 108443-108443
Open Access | Times Cited: 16
Epigenetics of cognition and behavior: insights from Mendelian disorders of epigenetic machinery
Rowena Ng, Allison Kalinousky, Jacqueline Harris
Journal of Neurodevelopmental Disorders (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Genome‐wide DNA methylation profiling confirms a case of low‐level mosaic Kabuki syndrome 1
Carolina Montaño, Jacquelyn Britton, Jacqueline Harris, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2217-2225
Open Access | Times Cited: 15
Biological and structural phenotypes associated with neurodevelopmental outcomes in congenital heart disease
Charlotte E. Verrall, Shrujna Patel, Leksi Travitz, et al.
Translational Pediatrics (2023) Vol. 12, Iss. 4, pp. 768-786
Open Access | Times Cited: 9
The role of lysine-specific demethylase 6A (KDM6A) in tumorigenesis and its therapeutic potentials in cancer therapy
Lijuan Chen, Xin-Yang Xu, Xiao-Dan Zhong, et al.
Bioorganic Chemistry (2023) Vol. 133, pp. 106409-106409
Closed Access | Times Cited: 8
Chromatin condensates tune nuclear mechano-sensing in Kabuki Syndrome by constraining cGAS activation
Sarah D’Annunzio, Lucia Santomaso, Daniela Michelatti, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Neurobehavioral phenotype of Kabuki syndrome: Anxiety is a common feature
Allison Kalinousky, Tyler Rapp, Hadia Hijazi, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 10
Premature thelarche: An Updated Review
Alexander K. C. Leung, Joseph M. Lam, Kam‐Lun Ellis Hon
Current Pediatric Reviews (2023) Vol. 20, Iss. 4, pp. 500-509
Closed Access | Times Cited: 6
Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease
Linda M. Reis, Hüban Atilla, Pekka Kannus, et al.
Genes (2023) Vol. 14, Iss. 1, pp. 216-216
Open Access | Times Cited: 5
Immune dysregulation in Kabuki syndrome: a case report of Evans syndrome and hypogammaglobulinemia
Lucia Leonardi, Alessia Testa, Mariavittoria Feleppa, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 5
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations
Raymond Belanger Deloge, Xiaonan Zhao, Pamela N. Luna, et al.
European Journal of Human Genetics (2022) Vol. 31, Iss. 3, pp. 296-303
Open Access | Times Cited: 8
Molecular insights of KMT2D and clinical aspects of Kabuki syndrome type 1
Carly S. Golden, Saylor Williams, María de los Ángeles Serrano
Birth Defects Research (2023) Vol. 115, Iss. 19, pp. 1809-1824
Closed Access | Times Cited: 4
Treatment of immune thrombocytopenia with hetrombopag olamine tablets in a Kabuki syndrome patient with new KMT2D mutations
Peng Peng, Ying Pan, Xueqing Maggie Lu, et al.
Platelets (2023) Vol. 34, Iss. 1
Open Access | Times Cited: 4
Mll4 regulates postnatal palate growth and midpalatal suture development
Jung-Mi Lee, Hunmin Jung, Bruno de Paula Machado Pasqua, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Kabuki Syndrome and Charcot-Marie-Tooth Disease Co-Occurrence: Unique Case with Novel Variant
Ahmet Kablan, Esma Ertürkmen Aru
Molecular Syndromology (2024), pp. 1-6
Closed Access | Times Cited: 1
Role of histone methyltransferase KMT2D in BMSC osteogenesis via AKT signaling
Zhichun Zhang, Yanyan Guo, Xuejun Gao, et al.
Regenerative Therapy (2024) Vol. 26, pp. 775-782
Open Access | Times Cited: 1
The FUT2 Variant c.461G>A (p.Trp154*) Is Associated With Differentially Expressed Genes and Nasopharyngeal Microbiota Shifts in Patients With Otitis Media
Christina L. Elling, Melissa A. Scholes, Sven‐Olrik Streubel, et al.
Frontiers in Cellular and Infection Microbiology (2022) Vol. 11
Open Access | Times Cited: 7
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