Open Access Helper

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:

Genome-wide identification of human- and primate-specific core promoter short tandem repeats
Ata Bushehri, M.R. Mashhoudi Barez, Shamseddin Mansouri, et al.
Gene (2016) Vol. 587, Iss. 1, pp. 83-90
Closed Access | Times Cited: 16

Showing 16 citing articles:

LincRNA-Gm4419 knockdown ameliorates NF-κB/NLRP3 inflammasome-mediated inflammation in diabetic nephropathy
Hong Yi, Rui Peng, Luyu Zhang, et al.
Cell Death and Disease (2017) Vol. 8, Iss. 2, pp. e2583-e2583
Open Access | Times Cited: 224
CRISPR/Cas9-mediated deletion of a GA-repeat in human GPM6B leads to disruption of neural cell differentiation from NT2 cells
Hadi Bayat, Maryam Mirahmadi, Zohreh Azarshin, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 6
Suppression of lncRNA NLRP3 inhibits NLRP3-triggered inflammatory responses in early acute lung injury
Deqiang Luo, Wei‐Min Dai, Xiaojin Feng, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 10
Open Access | Times Cited: 38
Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment
Safoura Khamse, Masoud Arabfard, Mahmood Salesi, et al.
Genetica (2022) Vol. 150, Iss. 1, pp. 27-40
Closed Access | Times Cited: 17
Natural Selection at the NHLH2 Core Promoter Exceptionally Long CA-Repeat in Human and Disease-Only Genotypes in Late-Onset Neurocognitive Disorder
Hossein Afshar, Fatemeh Adelirad, Ali Kowsari, et al.
Gerontology (2020) Vol. 66, Iss. 5, pp. 514-522
Closed Access | Times Cited: 24
Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder
Zahra Jafarian, Safoura Khamse, Hossein Afshar, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 22
Link between short tandem repeats and translation initiation site selection
Masoud Arabfard, Kaveh Kavousi, Ahmad Delbari, et al.
Human Genomics (2018) Vol. 12, Iss. 1
Open Access | Times Cited: 24
Global abundance of short tandem repeats is non-random in rodents and primates
Masoud Arabfard, Mahmood Salesi, Yazdan Hassani Nourian, et al.
BMC Genomic Data (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 12
Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia
Ehteram Khademi, Elham Alehabib, Ehsan Esmaili Shandiz, et al.
Genetic Testing and Molecular Biomarkers (2017) Vol. 21, Iss. 8, pp. 485-490
Closed Access | Times Cited: 17
A Hypermutable Region in the DISP2 Gene Links to Natural Selection and Late-Onset Neurocognitive Disorders in Humans
Safoura Khamse, Samira Alizadeh, Hamid Reza Khorram Khorshid, et al.
Molecular Neurobiology (2024)
Open Access | Times Cited: 1
Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeats
Neda Sadat Nazaripanah, Fatemeh Adelirad, Ahmad Delbari, et al.
Human Genomics (2018) Vol. 12, Iss. 1
Open Access | Times Cited: 6
Transcriptional Interference Regulates the Evolutionary Development of Speech
Douglas P. Mortlock, Zhiming Fang, Kelly J. Chandler, et al.
Genes (2022) Vol. 13, Iss. 7, pp. 1195-1195
Open Access | Times Cited: 3
Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder.
Zahra Jafarian, Safoura Khamse, Hossein Afshar, et al.
Research Square (Research Square) (2021)
Open Access | Times Cited: 1
Deletion of a GA-repeat in human GPM6B disrupts differentiation of NT2 cells to neural cells
Hadi Bayat, Maryam Mirahmadi, Zohreh Azarshin, et al.
Research Square (Research Square) (2023)
Open Access
Global non-random abundance of short tandem repeats in rodents and primates
Masoud Arabfard, Mahmood Salesi, Yazdan Hassani Nourian, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder.
Zahra Jafarian, Safoura Khamse, Hossein Afshar, et al.
Research Square (Research Square) (2021)
Open Access
Page 1

Scroll to top