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Cited by in F6Publishing
For: Jafarian Z, Khamse S, Afshar H, Khorshid HRK, Delbari A, Ohadi M. Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder. Sci Rep 2021;11:19235. [PMID: 34584172 DOI: 10.1038/s41598-021-98725-y] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Khamse S, Alizadeh S, Sh B, Afshar H, Delbari A, Ohadi M. A primate-specific (CCG) repeat in DISP2 is subject to natural selection in human and harbors unambiguous genotypes in late-onset neurocognitive disorder.. [DOI: 10.21203/rs.3.rs-2197976/v1] [Reference Citation Analysis]
2 Alizadeh S, Khamse S, Bernhart SH, Vahedi M, Afshar H, Rezaei O, Delbari A, Ohadi M. A primate-specific (GCC) repeat in SMAD9 undergoes natural selection in humans and harbors unambiguous genotypes in late-onset neurocognitive disorder.. [DOI: 10.21203/rs.3.rs-2144796/v1] [Reference Citation Analysis]
3 Khamse S, Alizadeh S, Bernhart SH, Afshar H, Delbari A, Ohadi M. A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder. Sci Rep 2022;12. [DOI: 10.1038/s41598-022-19878-y] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Khamse S, Arabfard M, Salesi M, Behmard E, Jafarian Z, Afshar H, Khazaei M, Ohadi M. Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment. Genetica 2022. [PMID: 34984576 DOI: 10.1007/s10709-021-00143-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Arabfard M, Salesi M, Nourian YH, Arabipour I, Maddi AMA, Kavousi K, Ohadi M. Global non-random abundance of short tandem repeats in rodents and primates.. [DOI: 10.1101/2021.11.24.469825] [Reference Citation Analysis]
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