Kariminejad A - Search Results

1

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: kariminejad a. Sci Rep. 2024 Dec 2;14(1):29880. doi: 10.1038/s41598-024-76815-x. Sci Rep. 2024. PMID: 39622884 Free PMC article.

2

Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 gene.

Fadaee M, Kariminejad A, Fattahi Z, Nafissi S, Godarzi HR, Beheshtian M, Vazehan R, Akbari MR, Kahrizi K, Najmabadi H. Fadaee M, et al. Among authors: kariminejad a. Neuromuscul Disord. 2016 Apr-May;26(4-5):277-82. doi: 10.1016/j.nmd.2016.02.003. Epub 2016 Feb 15. Neuromuscul Disord. 2016. PMID: 27020652

3

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.

Najafi K, Mehrjoo Z, Ardalani F, Ghaderi-Sohi S, Kariminejad A, Kariminejad R, Najmabadi H. Najafi K, et al. Among authors: kariminejad r, kariminejad a. Sci Rep. 2021 Mar 26;11(1):6952. doi: 10.1038/s41598-021-86309-9. Sci Rep. 2021. PMID: 33772059 Free PMC article.

4

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: kariminejad a. 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.

5

Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathy.

Fattahi Z, Kahrizi K, Nafissi S, Fadaee M, Abedini SS, Kariminejad A, Akbari MR, Najmabadi H. Fattahi Z, et al. Among authors: kariminejad a. Arch Iran Med. 2015 Jan;18(1):60-4. Arch Iran Med. 2015. PMID: 25556389

6

Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.

Rostami P, Valizadegan S, Ghalandary M, Mehrjouy MM, Esmail-Nia G, Khalili S, Shahmoradi SS, Imanian H, Hadavi V, Ghaderi-Sohi S, Almadani N, Afroozan F, Kariminejad A, Kariminejad R, Najmabadi H. Rostami P, et al. Among authors: kariminejad r, kariminejad a. Arch Iran Med. 2015 May;18(5):296-303. Arch Iran Med. 2015. PMID: 25959911

7

Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations.

Beheshtian M, Izadi N, Kriegshauser G, Kahrizi K, Mehr EP, Rostami M, Hosseini M, Azad M, Montajabiniat M, Kariminejad A, Nemeth S, Oberkanins C, Najmabadi H. Beheshtian M, et al. Among authors: kariminejad a. J Genet. 2016 Sep;95(3):667-74. doi: 10.1007/s12041-016-0682-6. J Genet. 2016. PMID: 27659338

8

Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.

Taghizadeh S, Vazehan R, Beheshtian M, Sadeghinia F, Fattahi Z, Mohseni M, Arzhangi S, Nafissi S, Kariminejad A, Najmabadi H, Kahrizi K. Taghizadeh S, et al. Among authors: kariminejad a. Arch Iran Med. 2020 Jul 1;23(7):426-433. doi: 10.34172/aim.2020.39. Arch Iran Med. 2020. PMID: 32657593 Free article.

9

COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum.

Hesami O, Ramezani M, Ghasemi A, Fatehi F, Okhovat AA, Ziaadini B, Kariminejad A, Nafissi S. Hesami O, et al. Among authors: kariminejad a. Orphanet J Rare Dis. 2024 Mar 12;19(1):113. doi: 10.1186/s13023-024-03116-x. Orphanet J Rare Dis. 2024. PMID: 38475910 Free PMC article.

10

Mutation profile of BBS genes in Iranian patients with Bardet-Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes.

Fattahi Z, Rostami P, Najmabadi A, Mohseni M, Kahrizi K, Akbari MR, Kariminejad A, Najmabadi H. Fattahi Z, et al. Among authors: kariminejad a. J Hum Genet. 2014 Jul;59(7):368-75. doi: 10.1038/jhg.2014.28. Epub 2014 May 22. J Hum Genet. 2014. PMID: 24849935

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