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:

Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands
Arijit Karmakar, Rishov Goswami, Tanusree Saha, et al.
BMC Medical Genetics (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 13

Showing 13 citing articles:

From aggression to autism: new perspectives on the behavioral sequelae of monoamine oxidase deficiency
Marco Bortolato, Gabriele Floris, Jean C. Shih
Journal of Neural Transmission (2018) Vol. 125, Iss. 11, pp. 1589-1599
Open Access | Times Cited: 56

ADHD co-morbidities: A review of implication of gene × environment effects with dopamine-related genes
Margus Kanarik, O. Grimm, Nina Roth Mota, et al.
Neuroscience & Biobehavioral Reviews (2022) Vol. 139, pp. 104757-104757
Closed Access | Times Cited: 22

Effect of MAOA rs1465108 polymorphism on susceptibility to substance/alcohol use disorder: a novel PCR-RFLP assay for the detection of MAOA rs1465108
Dilek Kaya-Akyüzlü, Selin Özkan-Kotiloğlu, Sariye Aybüke Yıldırım, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access | Times Cited: 2

miR‐522 facilitates the prosperities of endometrial carcinoma cells by directly binding to monoamine oxidase B
Hongchang Zhang, Yanyan Han, Xinmin Zhang, et al.
The Kaohsiung Journal of Medical Sciences (2019) Vol. 35, Iss. 10, pp. 598-606
Open Access | Times Cited: 19

Association of Monoamine Oxidase A (MAOA) Gene uVNTR and rs6323 Polymorphisms with Attention Deficit and Hyperactivity Disorder in Korean Children
In Wook Hwang, Myung Ho Lim, Ho‐Jang Kwon, et al.
Medicina (2018) Vol. 54, Iss. 3, pp. 32-32
Open Access | Times Cited: 11

“Jing-Ning Granules” Can Alleviate Attention Deficit Hyperactivity Disorder in Rats by Modulating Dopaminergic D2/D1-Like Receptor-Mediated Signaling Pathways
Jie Ding, Yiyun Ding, Jingjing Wu, et al.
Evidence-based Complementary and Alternative Medicine (2022) Vol. 2022, pp. 1-15
Open Access | Times Cited: 5

A three-pronged analysis confirms the association of the serotoninergic system with attention deficit hyperactivity disorder
Mahasweta Chatterjee, Sharmistha Saha, Swagata Sinha, et al.
World Journal of Pediatrics (2022) Vol. 18, Iss. 12, pp. 825-834
Closed Access | Times Cited: 4

Association of rs6323 with neuropsychiatric disorders: a mini-review
Arijit Karmakar
MGM Journal of Medical Sciences (2023) Vol. 10, Iss. 3, pp. 568-571
Open Access

A influência do gene MAOA em desordens mentais do indivíduo Autores
Elaine Viegas, Larissa Sousa Silva Bonasser, Gabriel Moura Alves Seixas, et al.
Revista de Divulgação Científica Sena Aires (2023), pp. 786-799
Open Access

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