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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:

SLC2A3single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder
S. Merker, Andreas Reif, Georg Ziegler, et al.
Journal of Child Psychology and Psychiatry (2017) Vol. 58, Iss. 7, pp. 798-809
Closed Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Genetics of ADHD: What Should the Clinician Know?
O. Grimm, Thorsten M. Kranz, Andreas Reif
Current Psychiatry Reports (2020) Vol. 22, Iss. 4
Open Access | Times Cited: 68
Identification and experimental validation of ferroptosis-related gene SLC2A3 is involved in rheumatoid arthritis
Jing Xiang, Haiqing Chen, Zhiping Lin, et al.
European Journal of Pharmacology (2023) Vol. 943, pp. 175568-175568
Closed Access | Times Cited: 20
Glucose transporter 3 in neuronal glucose metabolism: Health and diseases
Wuxue Peng, Changhong Tan, Lijuan Mo, et al.
Metabolism (2021) Vol. 123, pp. 154869-154869
Closed Access | Times Cited: 40
Neurodevelopment Is Dependent on Maternal Diet: Placenta and Brain Glucose Transporters GLUT1 and GLUT3
Tomoko Daida, Bo‐Chul Shin, Carlos Cepeda, et al.
Nutrients (2024) Vol. 16, Iss. 14, pp. 2363-2363
Open Access | Times Cited: 6
Cellular effects and clinical implications of SLC2A3 copy number variation
Georg Ziegler, P.Z. Álmos, Rhiannon V. McNeill, et al.
Journal of Cellular Physiology (2020) Vol. 235, Iss. 12, pp. 9021-9036
Open Access | Times Cited: 36
Neural Deletion of Glucose Transporter Isoform 3 Creates Distinct Postnatal and Adult Neurobehavioral Phenotypes
Bo‐Chul Shin, Carlos Cepeda, Ana María Estrada‐Sánchez, et al.
Journal of Neuroscience (2018) Vol. 38, Iss. 44, pp. 9579-9599
Open Access | Times Cited: 23
Recent developments in the genetics of attention‐deficit hyperactivity disorder
O. Grimm, Sarah Kittel‐Schneider, Andreas Reif
Psychiatry and Clinical Neurosciences (2018) Vol. 72, Iss. 9, pp. 654-672
Open Access | Times Cited: 22
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing
Jordi Corominas, Marieke Klein, Tetyana Zayats, et al.
Molecular Psychiatry (2018) Vol. 25, Iss. 9, pp. 2047-2057
Open Access | Times Cited: 19
Novel approach to evaluate central autonomic regulation in attention deficit/hyperactivity disorder (ADHD)
Nikola Sekaninova, Michal Mestanik, Andrea Mestanikova, et al.
Physiological Research (2019), pp. 531-545
Open Access | Times Cited: 18
Morinda officinalis oligosaccharides ameliorate depressive‐like behaviors in poststroke rats through upregulating GLUT3 to improve synaptic activity
Jiayi Zhu, Qiwei Peng, Yi Xu, et al.
The FASEB Journal (2020) Vol. 34, Iss. 10, pp. 13376-13395
Closed Access | Times Cited: 15
A Common CDH13 Variant Is Associated with Low Agreeableness and Neural Responses to Working Memory Tasks in ADHD
Georg Ziegler, Ann‐Christine Ehlis, Heike Weber, et al.
Genes (2021) Vol. 12, Iss. 9, pp. 1356-1356
Open Access | Times Cited: 13
KCNJ6 variants modulate reward‐related brain processes and impact executive functions in attention‐deficit/hyperactivity disorder
Georg Ziegler, Christoph Röser, Tobias Renner, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2019) Vol. 183, Iss. 5, pp. 247-257
Closed Access | Times Cited: 14
Possible immune regulation mechanisms for the progression of chronic thromboembolic pulmonary hypertension
Ran Miao, Xingbei Dong, Juanni Gong, et al.
Thrombosis Research (2020) Vol. 198, pp. 122-131
Closed Access | Times Cited: 11
Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3
Charline Jansch, Katharina Günther, Jonas Waider, et al.
Stem Cell Research (2018) Vol. 28, pp. 136-140
Open Access | Times Cited: 11
SLC2A3 rs12842 polymorphism and risk for Alzheimer’s disease
Stylianos Arseniou, Vasileios Siokas, Athina‐Maria Aloizou, et al.
Neurological Research (2020) Vol. 42, Iss. 10, pp. 853-861
Closed Access | Times Cited: 10
Genetics and epigenetics of attention deficit hyperactivity disorder
Р. Н. Мустафин, Р. Ф. Еникеева, Sergey Malykh, et al.
S S Korsakov Journal of Neurology and Psychiatry (2018) Vol. 118, Iss. 9, pp. 106-106
Open Access | Times Cited: 9
Transcript Analysis of Zebrafish GLUT3 Genes, slc2a3a and slc2a3b, Define Overlapping as Well as Distinct Expression Domains in the Zebrafish (Danio rerio) Central Nervous System
Carina G. Lechermeier, Frederic Zimmer, Teresa M. Lüffe, et al.
Frontiers in Molecular Neuroscience (2019) Vol. 12
Open Access | Times Cited: 7
Temporomandibular Disorders Slow Down the Regeneration Process of Masticatory Muscles: Transcriptomic Analysis
Cinzia Sindona, Michele Runci Anastasi, Luigi Chiricosta, et al.
Medicina (2021) Vol. 57, Iss. 4, pp. 354-354
Open Access | Times Cited: 7
SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population
Lijing Ma, Jiaxin Xu, Qisheng Tang, et al.
Journal of Clinical Laboratory Analysis (2022) Vol. 36, Iss. 6
Open Access | Times Cited: 5
Functional analysis of a triplet deletion in the gene encoding the sodium glucose transporter 3, a potential risk factor for ADHD
Nadine Schäfer, Maximilian Friedrich, Morten Egevang Jørgensen, et al.
PLoS ONE (2018) Vol. 13, Iss. 10, pp. e0205109-e0205109
Open Access | Times Cited: 6
Influence of genetic copy number variants of the human GLUT3 glucose transporter gene SLC2A3 on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study
Kim R. Simpfendorfer, Wentian Li, Andrew Shih, et al.
Molecular Genetics and Metabolism Reports (2019) Vol. 19, pp. 100470-100470
Open Access | Times Cited: 6
The conundrums of human development - implications for the study of child and adolescent disorder
Alice M. Gregory
Journal of Child Psychology and Psychiatry (2017) Vol. 58, Iss. 7, pp. 749-752
Open Access | Times Cited: 3
Deciphering the role of siRNA in anxiety and depression
Rajeshwari Bale, Gaurav Doshi
European Journal of Pharmacology (2024) Vol. 981, pp. 176868-176868
Closed Access
Adult glut3 homozygous null mice survive to demonstrate neural excitability and altered neurobehavioral responses reminiscent of neurodevelopmental disorders
Bo‐Chul Shin, Carlos Cepeda, Mason Eghbali, et al.
Experimental Neurology (2021) Vol. 338, pp. 113603-113603
Open Access | Times Cited: 3
Genetische Grundlagen der Aufmerksamkeitsdefizit-/Hyperaktivitätsstörung
O. Grimm, Thorsten M. Kranz, Andreas Reif
Nervenheilkunde (2019) Vol. 38, Iss. 09, pp. 618-624
Closed Access
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