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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:

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

Showing 21 citing articles:

Novel islands of GGC and GCC repeats coincide with human evolution
Nahid Tajeddin, Masoud Arabfard, Samira Alizadeh, et al.
Gene (2024) Vol. 902, pp. 148194-148194
Open Access | Times Cited: 4
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
Dyads of GGC and GCC form hotspot colonies that coincide with the evolution of human and other great apes
Masoud Arabfard, Nahid Tajeddin, Samira Alizadeh, et al.
BMC Genomic Data (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 3
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
DNA MARKERS AND MICROSATELLITE CODE (review)
В. И. Глазко
Sel skokhozyaistvennaya Biologiya (2023) Vol. 58, Iss. 2, pp. 223-248
Open Access | Times Cited: 4
ДНК МАРКЕРЫ И «МИКРОСАТЕЛЛИТНЫЙ КОД» (обзор)
В.И. ГЛАЗКО
Sel skokhozyaistvennaya Biologiya (2023) Vol. 58, Iss. 2, pp. 223-248
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
CG-rich trinucleotide two-repeats signify novel recombination hotspots conserved across primates and mouse
Mina Ohadi, Nahid Tajeddin, Masoud Arabfard, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 1
Dyads of GGC and GCC form hotspot colonies that coincide with the evolution of human and other great apes.
Masoud Arabfard, Nahid Tajeddin, Samira Alizadeh, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
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
Comparative analysis of microsatellites in coding regions provides insights into the adaptability of the giant panda, polar bear and brown bear
Mei‐Ling Cheng, Daxin Xie, Megan Price, et al.
Genetica (2022) Vol. 150, Iss. 6, pp. 355-366
Closed Access | Times Cited: 2
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
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
Unprecedented islands of GGC and GCC repeats coincide with human evolution.
Nahid Tajeddin, Masoud Arabfard, Samira Alizadeh, et al.
Research Square (Research Square) (2023)
Open Access
Novel islands of GGC and GCC repeats coincide with human evolution
Nahid Tajeddin, Masoud Arabfard, Samira Alizadeh, et al.
Research Square (Research Square) (2023)
Open Access
Two-repeat units of CG-rich trinucleotides form long-sought hotspot loci shared across primates and mouse
Mina Ohadi, Nahid Tajeddin, Hadi Bayat, 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
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
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