Author:
Tajeddin N.,Arabfard M.,Alizadeh S.,Salesi M.,Khamse S.,Delbari A.,Ohadi M.
Subject
Genetics,General Medicine
Reference45 articles.
1. A primate-specific (GCC) repeat in SMAD9 undergoes natural selection in humans and harbors unambiguous genotypes in late-onset neurocognitive disorder;Alizadeh;Research Square,2022
2. Unravelling the link between neurodevelopmental disorders and short tandem CGG-repeat expansions;Annear;Emerg. Top Life Sci.,2023
3. Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease;Annear;Sci. Rep.,2021
4. Non-Mendelian inheritance patterns and extreme deviation rates of CGG repeats in autism;Annear;Genome Res.,2022
5. Link between short tandem repeats and translation initiation site selection;Arabfard;Hum. Genomics,2018