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Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population.
Khanbazi A, Beheshtian M, Azad M, Akbari Kelishomi M, Afroozan F, Fatehi F, Noudehi K, Zamanian Najafabadi S, Omrani M, Habibi H, Taghdiri M, Abdi Rad I, Nafissi S, Jankhah A, Yazdan H, Daneshmand P, Saberi SH, Kahrizi K, Kariminejad A, Najmabadi H. Khanbazi A, et al. Among authors: kahrizi k. Sci Rep. 2024 Dec 2;14(1):29880. doi: 10.1038/s41598-024-76815-x. Sci Rep. 2024. PMID: 39622884 Free PMC article.
Super-enhancer profiling reveals ThPOK/ZBTB7B, a CD4 + cell lineage commitment factor, as a master regulator that restricts breast cancer cells to a luminal non-migratory phenotype.
Arcuschin CD, Kahrizi K, Sayaman RW, DiBenedetto C, Shen Y, Salaberry PJ, Zakroui O, Schwarzer C, Scapozza A, Betancur P, Saba JD, Coppé JP, Barcellos-Hoff MH, Kappes D, van 't Veer L, Schor IE, Muñoz DP. Arcuschin CD, et al. Among authors: kahrizi k. bioRxiv [Preprint]. 2024 Sep 25:2024.09.21.614267. doi: 10.1101/2024.09.21.614267. bioRxiv. 2024. PMID: 39386673 Free PMC article. Preprint.
Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups.
Alinaghi S, Mohseni M, Fattahi Z, Beheshtian M, Ghodratpour F, Zare Ashrafi F, Arzhangi S, Jalalvand K, Najafipour R, Khorram Khorshid HR, Kahrizi K, Najmabadi H. Alinaghi S, et al. Among authors: kahrizi k. Arch Iran Med. 2024 Feb 1;27(2):79-88. doi: 10.34172/aim.2024.13. Arch Iran Med. 2024. PMID: 38619031 Free PMC article.
Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene.
Rashvand Z, Najmabadi H, Kahrizi K, Mozhdehipanah H, Moradi M, Estaki Z, Taherkhani K, Nikzat N, Najafipour R, Omrani MD. Rashvand Z, et al. Among authors: kahrizi k. Iran J Child Neurol. 2024 Winter;18(1):25-41. doi: 10.22037/ijcn.v18i1.42188. Epub 2024 Jan 18. Iran J Child Neurol. 2024. PMID: 38375126 Free PMC article.
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H. Abolhassani A, et al. Among authors: kahrizi k. NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0. NPJ Genom Med. 2024. PMID: 38374194 Free PMC article.
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.
Mehvari S, Karimian Fathi N, Saki S, Asadnezhad M, Arzhangi S, Ghodratpour F, Mohseni M, Zare Ashrafi F, Sadeghian S, Boroumand M, Shokohizadeh F, Rostami E, Boroumand R, Najafipour R, Malekzadeh R, Riazalhosseini Y, Akbari M, Lathrop M, Najmabadi H, Hosseini K, Kahrizi K. Mehvari S, et al. Among authors: kahrizi k. Clin Genet. 2024 Jun;105(6):611-619. doi: 10.1111/cge.14491. Epub 2024 Feb 3. Clin Genet. 2024. PMID: 38308583
172 results