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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:

Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder
Tom S. Koemans, Tjitske Kleefstra, Melissa C. Chubak, et al.
PLoS Genetics (2017) Vol. 13, Iss. 10, pp. e1006864-e1006864
Open Access | Times Cited: 135

Showing 1-25 of 135 citing articles:

COMPASS and SWI/SNF complexes in development and disease
Bercin Kutluk Cenik, Ali Shilatifard
Nature Reviews Genetics (2020) Vol. 22, Iss. 1, pp. 38-58
Closed Access | Times Cited: 196
Drosophila Histone Demethylase KDM5 Regulates Social Behavior through Immune Control and Gut Microbiota Maintenance
Kun Chen, Xiaoting Luan, Qisha Liu, et al.
Cell Host & Microbe (2019) Vol. 25, Iss. 4, pp. 537-552.e8
Open Access | Times Cited: 162
Histone H3 lysine K4 methylation and its role in learning and memory
Bridget E. Collins, Celeste B. Greer, Benjamin C. Coleman, et al.
Epigenetics & Chromatin (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 155
Regulation, functions and transmission of bivalent chromatin during mammalian development
Trisha A. Macrae, Julie Fothergill-Robinson, Miguel Ramalho‐Santos
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 1, pp. 6-26
Closed Access | Times Cited: 116
COMPASS Ascending: Emerging clues regarding the roles of MLL3/KMT2C and MLL2/KMT2D proteins in cancer
Richard Fagan, Andrew K. Dingwall
Cancer Letters (2019) Vol. 458, pp. 56-65
Open Access | Times Cited: 137
The chromatin basis of neurodevelopmental disorders: Rethinking dysfunction along the molecular and temporal axes
Michele Gabriele, Alejandro Tobon, Giuseppe D’Agostino, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2018) Vol. 84, pp. 306-327
Open Access | Times Cited: 90
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
Britt Mossink, Moritz Negwer, Dirk Schubert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2517-2563
Open Access | Times Cited: 80
A Multiplex Human Pluripotent Stem Cell Platform Defines Molecular and Functional Subclasses of Autism-Related Genes
Gustav Y. Cederquist, Jason Tchieu, Scott J. Callahan, et al.
Cell stem cell (2020) Vol. 27, Iss. 1, pp. 35-49.e6
Open Access | Times Cited: 73
Smith-Magenis Syndrome—Clinical Review, Biological Background and Related Disorders
Berardo Rinaldi, Roberta Villa, Alessandra Sironi, et al.
Genes (2022) Vol. 13, Iss. 2, pp. 335-335
Open Access | Times Cited: 43
Identification of clinically actionable variants from genome sequencing of families with congenital heart disease
Dimuthu Alankarage, Eddie Ip, Justin O. Szot, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 5, pp. 1111-1120
Open Access | Times Cited: 72
De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism
Takuya Hiraide, Mitsuko Nakashima, Kaori Yamoto, et al.
Human Genetics (2018) Vol. 137, Iss. 1, pp. 95-104
Closed Access | Times Cited: 71
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1210-1222
Open Access | Times Cited: 71
KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an emerging class of congenital regulopathies
William J. Lavery, Artem Barski, Susan Wiley, et al.
Clinical Epigenetics (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 68
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
Joost Kummeling, Diante E. Stremmelaar, Nicholas Raun, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 6, pp. 2013-2024
Open Access | Times Cited: 56
Whole exome sequencing reveals mutations in FAT1 tumor suppressor gene clinically impacting on peripheral T-cell lymphoma not otherwise specified
Maria Antonella Laginestra, Luciano Cascione, Giovanna Motta, et al.
Modern Pathology (2019) Vol. 33, Iss. 2, pp. 179-187
Open Access | Times Cited: 55
Allostery, and how to define and measure signal transduction
Ruth Nussinov, Chung‐Jung Tsai, Hyunbum Jang
Biophysical Chemistry (2022) Vol. 283, pp. 106766-106766
Open Access | Times Cited: 37
The Epigenetic Factor Landscape of Developing Neocortex Is Regulated by Transcription Factors Pax6→ Tbr2→ Tbr1
Gina E. Elsen, Francesco Bedogni, Rebecca D. Hodge, et al.
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 56
Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype
Monica Frega, Martijn Selten, Britt Mossink, et al.
Cell Reports (2020) Vol. 30, Iss. 1, pp. 173-186.e6
Open Access | Times Cited: 49
The phenomenal epigenome in neurodevelopmental disorders
Ummi Ciptasari, Hans van Bokhoven
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R42-R50
Open Access | Times Cited: 48
Linking genetics to epigenetics: The role of folate and folate‐related pathways in neurodevelopmental disorders
Carla Lintas
Clinical Genetics (2018) Vol. 95, Iss. 2, pp. 241-252
Closed Access | Times Cited: 47
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features
Elliot Stolerman, E. Nicolás Francisco, Jennifer L. Stallworth, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 7, pp. 1276-1286
Closed Access | Times Cited: 45
Intellectual disability and autism spectrum disorders ‘on the fly’: insights from Drosophila
Mireia Coll-Tané, Alina Krebbers, Anna Castells‐Nobau, et al.
Disease Models & Mechanisms (2019) Vol. 12, Iss. 5
Open Access | Times Cited: 45
Investigation of autism-related transcription factors underlying sex differences in the effects of bisphenol A on transcriptome profiles and synaptogenesis in the offspring hippocampus
Surangrat Thongkorn, Songphon Kanlayaprasit, Kasidit Kasitipradit, et al.
Biology of Sex Differences (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 15
Detection of Constitutional Structural Variants by Optical Genome Mapping
Ulrich Broeckel, M. Anwar Iqbal, Brynn Levy, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 3, pp. 213-226
Open Access | Times Cited: 5
Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes
Dmitrijs Rots, Sanaa Choufani, Víctor Faúndes, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 8, pp. 1626-1642
Closed Access | Times Cited: 5
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