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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:

Evolving evidence on a link between the ZMYM3 exceptionally long GA-STR and human cognition
Hossein Afshar, Safoura Khamse, Fatemeh Alizadeh, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 20

Showing 20 citing articles:

Zinc Finger Proteins in Neuro-Related Diseases Progression
Siyuan Bu, Yihan Lv, Yu‐Sheng Liu, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 69
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: 5
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
A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder
Safoura Khamse, Samira Alizadeh, Stephan Wolf, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 17
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
Novel implications of a strictly monomorphic (GCC) repeat in the human PRKACB gene
Safoura Khamse, Zahra Jafarian, Ali Bozorgmehr, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 21
A GCC repeat in RAB26 undergoes natural selection in human and harbors divergent genotypes in late-onset Alzheimer’s disease
Samira Alizadeh, Safoura Khamse, Nahid Tajeddin, et al.
Gene (2023) Vol. 893, pp. 147968-147968
Closed Access | Times Cited: 7
Comparative physiological anthropogeny: exploring molecular underpinnings of distinctly human phenotypes
Michael Vaill, Kunio Kawanishi, Nissi Varki, et al.
Physiological Reviews (2023) Vol. 103, Iss. 3, pp. 2171-2229
Open Access | Times Cited: 4
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
Integrated Bioinformatics Analysis Identifies Hub Genes Associated with Viral Infection and Alzheimer’s Disease
Xiaoru Sun, Hui Zhang, Dongdong Yao, et al.
Journal of Alzheimer s Disease (2021) Vol. 85, Iss. 3, pp. 1053-1061
Closed Access | Times Cited: 9
A primate-specific (GCC) repeat in SMAD9 undergoes natural selection in humans and harbors unambiguous genotypes in late-onset neurocognitive disorder.
Samira Alizadeh, Safoura Khamse, Stephan Wolf, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 5
The human SMAD9 (GCC) repeat links to natural selection and late-onset neurocognitive disorders
Samira Alizadeh, Safoura Khamse, Sara Vafadar, et al.
Neurological Sciences (2024)
Closed Access
A (GCC) Repeat in the Untranslated Region of Human SBF1 Departs from Hardy-Weinberg Equilibrium in Human and Links to Late-onset Neurocognitive Disorder.
Mina Ohadi, Safoura Khamse, Samira Alizadeh, et al.
Research Square (Research Square) (2022)
Closed Access | Times Cited: 1
A primate-specific (CCG) repeat in DISP2 is subject to natural selection in human and harbors unambiguous genotypes in late-onset neurocognitive disorder
Safoura Khamse, Samira Alizadeh, Bernhart SH, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 1
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
A primate-specific (CCG) repeat in DISP2 is subject to natural selection in human and harbors divergent genotypes in late-onset neurocognitive disorder.
Safoura Khamse, Samira Alizadeh, Hamid Reza Khorram Khorshid, et al.
Research Square (Research Square) (2023)
Open Access
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
A primate-specific (GCC) repeat in the untranslated region of SMAD9 undergoes natural selection and links with late-onset neurocognitive disorder in human
Samira Alizadeh, Safoura Khamse, Hossein Afshar, et al.
Research Square (Research Square) (2022)
Open Access
Natural Selection at an Exceptionally Long GGC Repeat in the Human RASGEF1C and Divergent Genotypes in Late-onset Neurocognitive Disorder
Zahra Jafarian, Safoura Khamse, Hossein Afshar, et al.
Research Square (Research Square) (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
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