OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model
Denise Haslinger, Regina Waltes, Afsheen Yousaf, et al.
Molecular Autism (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

Recent Advances in NAMPT Inhibitors: A Novel Immunotherapic Strategy
Ubaldina Galli, Giorgia Colombo, Cristina Travelli, et al.
Frontiers in Pharmacology (2020) Vol. 11
Open Access | Times Cited: 124

Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants
Siwei Zhang, Hanwen Zhang, Yifan Zhou, et al.
Science (2020) Vol. 369, Iss. 6503, pp. 561-565
Open Access | Times Cited: 96

Beyond Energy Metabolism: Exploiting the Additional Roles of NAMPT for Cancer Therapy
Christine M. Heske
Frontiers in Oncology (2020) Vol. 9
Open Access | Times Cited: 84

The Kynurenine Pathway and Cancer: Why Keep It Simple When You Can Make It Complicated
Roumaïssa Gouasmi, Carole Ferraro‐Peyret, Stéphane Nancey, et al.
Cancers (2022) Vol. 14, Iss. 11, pp. 2793-2793
Open Access | Times Cited: 53

Analyzing the Potential Biological Determinants of Autism Spectrum Disorder: From Neuroinflammation to the Kynurenine Pathway
Rosa Savino, Marco Carotenuto, Anna Nunzia Polito, et al.
Brain Sciences (2020) Vol. 10, Iss. 9, pp. 631-631
Open Access | Times Cited: 41

CNTN4 modulates neural elongation through interplay with APP
Rosemary A. Bamford, Amila Zuko, Madeline Eve, et al.
Open Biology (2024) Vol. 14, Iss. 5
Open Access | Times Cited: 5

Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma
Laura E. Egolf, Zalman Vaksman, Gonzalo López, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 3, pp. 658-668
Open Access | Times Cited: 41

SFARI genes and where to find them; modelling Autism Spectrum Disorder specific gene expression dysregulation with RNA-seq data
Magdalena Navarro Torres Arpi, T. Ian Simpson
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 21

Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder
Elaine T. Lim, Yingleong Chan, Pepper Dawes, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 20

Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children
Rana Fetit, David J. Price, Stephen M. Lawrie, et al.
Psychiatric Genetics (2020) Vol. 30, Iss. 5, pp. 136-140
Open Access | Times Cited: 31

16pdel lipid changes in iPSC-derived neurons and function of FAM57B in lipid metabolism and synaptogenesis
Danielle L. Tomasello, Jiyoon L. Kim, Yara Khodour, et al.
iScience (2021) Vol. 25, Iss. 1, pp. 103551-103551
Open Access | Times Cited: 23

The Effects of Maternal Interleukin-17A on Social Behavior, Cognitive Function, and Depression-Like Behavior in Mice with Altered Kynurenine Metabolites
Yuki Murakami, Yukio Imamura, Yoshiyuki Kasahara, et al.
International Journal of Tryptophan Research (2021) Vol. 14
Open Access | Times Cited: 22

CRISPRroots: on- and off-target assessment of RNA-seq data in CRISPR–Cas9 edited cells
Giulia I. Corsi, Veerendra P. Gadekar, Jan Gorodkin, et al.
Nucleic Acids Research (2021) Vol. 50, Iss. 4, pp. e20-e20
Open Access | Times Cited: 19

Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes
Roberta Leone, Cecilia Zuglian, Riccardo Brambilla, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 2

Comparative psychopharmacology of autism and psychotic-affective disorders suggests new targets for treatment
Bernard J. Crespi
Evolution Medicine and Public Health (2019) Vol. 2019, Iss. 1, pp. 149-168
Open Access | Times Cited: 19

16p11.2 deletion accelerates subpallial maturation and increases variability in human iPSC-derived ventral telencephalic organoids
Rana Fetit, Michela Ilaria Barbato, Thomas Theil, et al.
Development (2023) Vol. 150, Iss. 4
Open Access | Times Cited: 6

The role of NAD metabolism in neuronal differentiation
Diogo Neves, Brian J. Goodfellow, Sandra I. Vieira, et al.
Neurochemistry International (2022) Vol. 159, pp. 105402-105402
Open Access | Times Cited: 7

Expression Analysis of Genes Involved in Transport Processes in Mice with MPTP-Induced Model of Parkinson’s Disease
Margarita M. Rudenok, М. И. Шадрина, Elena V. Filatova, et al.
Life (2022) Vol. 12, Iss. 5, pp. 751-751
Open Access | Times Cited: 6

Knockdown of the ADHD Candidate Gene Diras2 in Murine Hippocampal Primary Cells
Lena Grünewald, Andreas G. Chiocchetti, Heike Weber, et al.
Journal of Attention Disorders (2019) Vol. 25, Iss. 4, pp. 572-583
Open Access | Times Cited: 7

Genetische Risikofaktoren und ihre Auswirkungen auf die neurale Entwicklung bei Autismus-Spektrum-Störungen
Christine M. Freitag, Andreas G. Chiocchetti, Denise Haslinger, et al.
Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie (2021) Vol. 50, Iss. 3, pp. 187-202
Open Access | Times Cited: 7

Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review
Fagui Yue, Qi Xi, Xinyue Zhang, et al.
Taiwanese Journal of Obstetrics and Gynecology (2022) Vol. 61, Iss. 3, pp. 544-550
Open Access | Times Cited: 4

Page 1 - Next Page

Scroll to top