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:

Inhibition of Notch signaling rescues cardiovascular development in Kabuki Syndrome
María de los Ángeles Serrano, Bradley L. Demarest, Tarlynn Tone-Pah-Hote, et al.
PLoS Biology (2019) Vol. 17, Iss. 9, pp. e3000087-e3000087
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

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: 65

The role of chromatin-related epigenetic modulations in CAKUT
Lars König, Miriam Schmidts
Current topics in developmental biology/Current Topics in Developmental Biology (2025)
Closed Access | Times Cited: 1

Animal models of kabuki syndrome and their applicability to novel drug discovery
M. Mertens, Leen Khalife, Xiaoting Ma, et al.
Expert Opinion on Drug Discovery (2025)
Closed Access

Genetics of single ventricle congenital heart disease
Sarah U. Morton, Tina O. Findley
Elsevier eBooks (2025), pp. 13-28
Closed Access

Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases
Dorothée Schoemaker, Joseph F. Arboleda‐Velásquez
American Journal Of Pathology (2021) Vol. 191, Iss. 11, pp. 1856-1870
Open Access | Times Cited: 22

The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
Jun‐yi Zhu, Joyce van de Leemput, Zhe Han
Journal of Cardiovascular Development and Disease (2023) Vol. 10, Iss. 7, pp. 305-305
Open Access | Times Cited: 8

Epigenetic regulation of craniofacial development and disease
Lomeli C. Shull, Kristin Artinger
Birth Defects Research (2023) Vol. 116, Iss. 1
Closed Access | Times Cited: 8

KMT2D loss drives aggressive tumor phenotypes in cutaneous squamous cell carcinoma.
Cara Dauch, Sharon Shim, Matthew W. Cole, et al.
PubMed (2022) Vol. 12, Iss. 3, pp. 1309-1322
Closed Access | Times Cited: 13

The Zebrafish Cardiac Endothelial Cell—Roles in Development and Regeneration
Vanessa Lowe, Laura Wisniewski, Caroline Pellet‐Many
Journal of Cardiovascular Development and Disease (2021) Vol. 8, Iss. 5, pp. 49-49
Open Access | Times Cited: 17

The power of zebrafish models for understanding the co‐occurrence of craniofacial and limb disorders
Brittany T. Truong, Kristin Artinger
genesis (2021) Vol. 59, Iss. 1-2
Open Access | Times Cited: 16

SETting up the genome: KMT2D and KDM6A genomic function in the Kabuki syndrome craniofacial developmental disorder
Karl B. Shpargel, Gabrielle Quickstad
Birth Defects Research (2023) Vol. 115, Iss. 20, pp. 1885-1898
Open Access | Times Cited: 5

A molecular signature of well-differentiated oral squamous cell carcinoma reveals a resistance mechanism to metronomic chemotherapy and novel therapeutic candidates
Shinichiro Kina, Reika Kawabata‐Iwakawa, Shô Miyamoto, et al.
Journal of drug targeting (2021) Vol. 29, Iss. 10, pp. 1118-1127
Closed Access | Times Cited: 11

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

Epigenetic disorders: Lessons from the animals–animal models in chromatinopathies
Elisabetta Di Fede, Paolo Grazioli, Antonella Lettieri, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 7

Chromatin Regulator SPEN/SHARP in X Inactivation and Disease
Benedetto Daniele Giaimo, Teresa Robert-Finestra, Franz Oswald, et al.
Cancers (2021) Vol. 13, Iss. 7, pp. 1665-1665
Open Access | Times Cited: 9

Advances in Cardiac Development and Regeneration Using Zebrafish as a Model System for High-Throughput Research
Nicholas Francoeur, Rwik Sen
Journal of Developmental Biology (2021) Vol. 9, Iss. 4, pp. 40-40
Open Access | Times Cited: 9

Loss of Histone Methyltransferase KMT2D Attenuates Angiogenesis in the Ischemic Heart by Inhibiting the Transcriptional Activation of VEGF-A
Xiangmin Meng, Shu-Bao Liu, Tian Deng, et al.
Journal of Cardiovascular Translational Research (2023) Vol. 16, Iss. 5, pp. 1032-1049
Open Access | Times Cited: 3

Distinct Roles for COMPASS Core Subunits Set1, Trx, and Trr in the Epigenetic Regulation of Drosophila Heart Development
Jun‐yi Zhu, Hangnoh Lee, Xiaohu Huang, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17314-17314
Open Access | Times Cited: 2

Histone methyltransferase KMT2D contributes to the protection of myocardial ischemic injury
Shu-Bao Liu, Xiangmin Meng, Yumeng Li, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 4

Delta-like ligand 4 level in colorectal cancer is associated with tumor aggressiveness and clinical outcome
Zixi Zhang, Xiao Li, Xueli Yan, et al.
Cancer Biomarkers (2021) Vol. 33, Iss. 3, pp. 415-422
Closed Access | Times Cited: 5

The role of Kabuki Syndrome genes KMT2D and KDM6A in development: Analysis in Human sequencing data and compared to mice and zebrafish
Rwik Sen, Ezra Lencer, Elizabeth A. Geiger, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 4

Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome
Chung‐Lin Lee, Chih‐Kuang Chuang, Ming‐Ren Chen, et al.
Diagnostics (2024) Vol. 14, Iss. 8, pp. 846-846
Open Access

Distinct roles of COMPASS subunits to Drosophila heart development
Jun‐yi Zhu, Joyce van de Leemput, Zhe Han
Biology Open (2024) Vol. 13, Iss. 10
Open Access

Using Xenopus to analyze neurocristopathies like Kabuki syndrome
Janina Schwenty‐Lara, Silke Pauli, Annette Borchers
genesis (2020) Vol. 59, Iss. 1-2
Open Access | Times Cited: 3

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