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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:

Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study
Yihui Zhu, Charles E. Mordaunt, Dag H. Yasui, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 16, pp. 2659-2674
Open Access | Times Cited: 73

Showing 26-50 of 73 citing articles:

Altered DNA methylation in a severe subtype of idiopathic autism: Evidence for sex differences in affected metabolic pathways
Valerie W. Hu, Yi Hong, Minyi Xu, et al.
Autism (2020) Vol. 25, Iss. 4, pp. 887-910
Closed Access | Times Cited: 17
Prenatal vitamin intake in first month of pregnancy and DNA methylation in cord blood and placenta in two prospective cohorts
John Dou, Lauren Y. M. Middleton, Yihui Zhu, et al.
Epigenetics & Chromatin (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 11
The genetics of autism and steroid-related traits in prenatal and postnatal life
Alex Tsompanidis, Varun Warrier, Simon Baron‐Cohen
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 6
Epigenome-Wide Associations of Placental DNA Methylation and Behavioral and Emotional Difficulties in Children at 3 Years of Age
Aurélie Nakamura, Lucile Broséus, Jörg Tost, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11772-11772
Open Access | Times Cited: 6
A New Era for Epigenetic Epidemiology
Chathura Gunasekara, Robert A. Waterland
Epigenomics (2019) Vol. 11, Iss. 15, pp. 1647-1649
Open Access | Times Cited: 17
Expression Changes in Epigenetic Gene Pathways Associated With One‐Carbon Nutritional Metabolites in Maternal Blood From Pregnancies Resulting in Autism and Non‐Typical Neurodevelopment
Yihui Zhu, Charles E. Mordaunt, Blythe Durbin‐Johnson, et al.
Autism Research (2020) Vol. 14, Iss. 1, pp. 11-28
Open Access | Times Cited: 15
The Promise of DNA Methylation in Understanding Multigenerational Factors in Autism Spectrum Disorders
Julia S. Mouat, Janine M. LaSalle
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 9
Association between acetaminophen metabolites and CYP2E1 DNA methylation level in neonate cord blood in the Boston Birth Cohort
Yijun Li, Xiumei Hong, Liming Liang, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Metastable epialleles in humans
Maria Derakhshan, Noah J. Kessler, Garrett Hellenthal, et al.
Trends in Genetics (2023) Vol. 40, Iss. 1, pp. 52-68
Open Access | Times Cited: 5
Cataloging Recent Advances in Epigenetic Alterations in Major Mental Disorders and Autism
Hamid M. Abdolmaleky, Jin‐Rong Zhou, Sam Thiagalingam
Epigenomics (2021) Vol. 13, Iss. 15, pp. 1231-1245
Open Access | Times Cited: 12
Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo
Maria Derakhshan, Noah J. Kessler, Miho Ishida, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 12, pp. 6735-6752
Open Access | Times Cited: 9
Prenatal epigenetic factors are predisposing for neurodevelopmental disorders—Considering placenta as a model
Srividhya Durbagula, Aruna Korlimarla, Gayatri Ravikumar, et al.
Birth Defects Research (2022) Vol. 114, Iss. 20, pp. 1324-1342
Closed Access | Times Cited: 8
Intrauterine developmental origin, programming mechanism, and prevention strategy of fetal‐originated hypercholesterolemia
Kexin Liu, Ze Chen, Wen Hu, et al.
Obesity Reviews (2023) Vol. 25, Iss. 3
Open Access | Times Cited: 4
Exploratory focused pharmacogenetic testing reveals novel markers associated with risperidone pharmacokinetics in Saudi children with autism
Sireen Abdul Rahim Shilbayeh, Iman Sharaf Adeen, Ezzeldeen Ghanem, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 1
A systematic review of maternal exposures and the risk of autism spectrum disorders in their infants
Shae Jansen, Kyle Baugh, James B. Adams, et al.
North American Proceedings in Gynecology & Obstetrics (2024) Vol. 3, Iss. 2
Open Access | Times Cited: 1
Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes
Charles E. Mordaunt, Julia M. Jianu, Benjamin I. Laufer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 10
Artificial intelligence and placental DNA methylation: newborn prediction and molecular mechanisms of autism in preterm children
Ray Bahado‐Singh, Sangeetha Vishweswaraiah, Buket Aydas, et al.
The Journal of Maternal-Fetal & Neonatal Medicine (2021) Vol. 35, Iss. 25, pp. 8150-8159
Closed Access | Times Cited: 9
Comethyl: a network-based methylome approach to investigate the multivariate nature of health and disease
Charles E. Mordaunt, Julia S. Mouat, Rebecca J. Schmidt, et al.
Briefings in Bioinformatics (2021) Vol. 23, Iss. 2
Open Access | Times Cited: 9
Defective placentation syndromes and autism spectrum disorder in the offspring: population-based cohort and sibling-controlled studies
Eduardo Villamor, Ezra Susser, Sven Cnattingius
European Journal of Epidemiology (2022) Vol. 37, Iss. 8, pp. 827-836
Open Access | Times Cited: 5
Elevated exposures to persistent endocrine disrupting compounds impact the sperm methylome in regions associated with autism spectrum disorder
Angela G. Maggio, Henry T. Shu, Benjamin I. Laufer, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
Multi-omic brain and behavioral correlates of cell-free fetal DNA methylation in macaque maternal obesity models
Benjamin I. Laufer, Yu Hasegawa, Zhichao Zhang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Altered DNA methylation of CYP2E1 gene in schizophrenia patients with tardive dyskinesia
Ping Zhang, Yanli Li, Kesheng Wang, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 5
The epigenetic regulation of synaptic genes contributes to the etiology of autism
Annamária Srančíková, Zuzana Bačová, Ján Bakoš
Reviews in the Neurosciences (2021) Vol. 32, Iss. 7, pp. 791-802
Closed Access | Times Cited: 5
Genome-Wide DNA Methylation Profiles of Neurodevelopmental Disorder Genes in Mouse Placenta and Fetal Brain Following Prenatal Exposure to Polychlorinated Biphenyls
Benjamin I. Laufer, Kari Neier, Anthony E. Valenzuela, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 5
The diagnostic potential of the epigenome in autism spectrum disorders
Fabio Coppedè
Epigenomics (2021) Vol. 13, Iss. 20, pp. 1587-1590
Closed Access | Times Cited: 5

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