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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:

The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration
Janina Schwenty‐Lara, Denise Nehl, Annette Borchers
Human Molecular Genetics (2019) Vol. 29, Iss. 2, pp. 305-319
Open Access | Times Cited: 47

Showing 1-25 of 47 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
Molecular Regulation of Palatogenesis and Clefting: An Integrative Analysis of Genetic, Epigenetic Networks, and Environmental Interactions
Hyuna Im, Yujeong Song, Jae Kyeom Kim, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 3, pp. 1382-1382
Open Access | Times Cited: 1
The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs
Andreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 17
The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology
Karl B. Shpargel, Cassidy L. Mangini, Guojia Xie, et al.
Development (2020)
Open Access | Times Cited: 41
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation
Ettore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2020) Vol. 46, Iss. 1
Open Access | Times Cited: 40
KMT2D regulates activation, localization, and integrin expression by T-cells
Sarah J. Potter, Li Zhang, Michael Kotliar, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 5
Role of epigenetics and miRNAs in orofacial clefts
Michael A. Garland, Bo Sun, Shuwen Zhang, et al.
Birth Defects Research (2020) Vol. 112, Iss. 19, pp. 1635-1659
Open Access | Times Cited: 34
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole‐exome sequencing
Takuya Hiraide, Kaori Yamoto, Yohei Masunaga, et al.
Clinical Genetics (2021) Vol. 100, Iss. 1, pp. 40-50
Closed Access | Times Cited: 31
The Mendelian disorders of chromatin machinery: Harnessing metabolic pathways and therapies for treatment
Sarah Donoghue, Jordan L. Wright, Anne K. Voss, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 1, pp. 108360-108360
Open Access | Times Cited: 4
Genetics Underlying the Interactions between Neural Crest Cells and Eye Development
Jochen Weigele, Brenda L. Bohnsack
Journal of Developmental Biology (2020) Vol. 8, Iss. 4, pp. 26-26
Open Access | Times Cited: 29
Study on the Role of Sema3F in the Nervous System
泽睿 杨
Advances in Clinical Medicine (2025) Vol. 15, Iss. 01, pp. 121-126
Open Access
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
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
-BET activity plays an essential role in control of stem cell attributes in Xenopus
Paul B Huber, Anjali Rao, Carole LaBonne
Development (2024) Vol. 151, Iss. 13
Open Access | Times Cited: 3
O-GlcNAc Transferase Congenital Disorder of Glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome
Johnathan M. Mayfield, Naomi L. Hitefield, Ignacy Czajewski, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107599-107599
Open Access | Times Cited: 3
Functions of histone modifications and histone modifiers in Schwann cells
Mert Duman, M. Martinez-Moreno, Claire Jacob, et al.
Glia (2020) Vol. 68, Iss. 8, pp. 1584-1595
Open Access | Times Cited: 23
Xenopus, an emerging model for studying pathologies of the neural crest
Laura Medina-Cuadra, Anne H. Monsoro‐Burq
Current topics in developmental biology/Current Topics in Developmental Biology (2021), pp. 313-348
Closed Access | Times Cited: 20
Neurobiology of puberty and its disorders
Selma F. Witchel, Tony M. Plant
Handbook of clinical neurology (2021), pp. 463-496
Closed Access | Times Cited: 20
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 deficiency leads to cellular developmental disorders and enhancer dysregulation in neural-crest-containing brain organoids
Ziyun Shan, Yingying Zhao, Xiuyu Chen, et al.
Science Bulletin (2024)
Closed Access | Times Cited: 2
Whole‐exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways
Elin Tønne, Bernt Johan Due‐Tønnessen, Magnus Dehli Vigeland, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 5, pp. 1464-1475
Open Access | Times Cited: 10
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
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
KMT2D haploinsufficiency in Kabuki syndrome disrupts neuronal function through transcriptional and chromatin rewiring independent of H3K4-monomethylation
Michele Gabriele, Alessandro Vitriolo, Sara Cuvertino, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 12
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