Kariminejad R - Search Results

1

Evaluating the Plausibility of Euploid Embryos Transfer on Day-5 by Reanalysis of Day-3 Single Aneuploid Embryos: A Case Series.

Bazrgar M, Kariminejad R, Eftekhari-Yazdi P, Gourabi H. Bazrgar M, et al. Among authors: kariminejad r. J Reprod Infertil. 2024 Jan-Mar;25(1):56-59. doi: 10.18502/jri.v25i1.15200. J Reprod Infertil. 2024. PMID: 39157285 Free PMC article.

2

Frequency of Sperm Aneuploidy in Oligoasthenoteratozoospermic (OAT) Patients by Comprehensive Chromosome Screening: A Proof of Concept.

Saei P, Bazrgar M, Gourabi H, Kariminejad R, Eftekhari-Yazdi P, Fakhri M. Saei P, et al. Among authors: kariminejad r. J Reprod Infertil. 2021 Jan-Mar;22(1):57-64. doi: 10.18502/jri.v22i1.4996. J Reprod Infertil. 2021. PMID: 33680886 Free PMC article.

3

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.

Najafi K, Gholami S, Moshtagh A, Bazrgar M, Sadatian N, Abbasi G, Rostami P, Khalili S, Babanejad M, Nourmohammadi B, Faramarzi Garous N, Najmabadi H, Kariminejad R. Najafi K, et al. Among authors: kariminejad r. Mol Genet Genomic Med. 2019 Aug;7(8):e820. doi: 10.1002/mgg3.820. Epub 2019 Jun 18. Mol Genet Genomic Med. 2019. PMID: 31210028 Free PMC article.

4

Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis.

Najafi K, Kariminejad R, Hosseini K, Moshtagh A, Abbassi GM, Sadatian N, Bazrgar M, Kariminejad A, Kariminejad MH. Najafi K, et al. Among authors: kariminejad mh, kariminejad r, kariminejad a. Case Rep Genet. 2017;2017:2706098. doi: 10.1155/2017/2706098. Epub 2017 Jan 4. Case Rep Genet. 2017. PMID: 28133555 Free PMC article.

5

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.

Behjati F, Firouzabadi SG, Kariminejad R, Vameghi R, Sajedi F, Shafaghati Y, Ghasemlou BE, Shojaei A, Jamali P, Bahman I, Najmabadi H. Behjati F, et al. Among authors: kariminejad r. Indian J Hum Genet. 2013 Oct;19(4):443-8. doi: 10.4103/0971-6866.124373. Indian J Hum Genet. 2013. PMID: 24497710 Free PMC article.

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

High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations.

Kariminejad R, Lind-Thomsen A, Tümer Z, Erdogan F, Ropers HH, Tommerup N, Ullmann R, Møller RS. Kariminejad R, et al. Hum Mutat. 2011 Dec;32(12):1427-35. doi: 10.1002/humu.21585. Epub 2011 Sep 23. Hum Mutat. 2011. PMID: 21882292

8

Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome.

Ghaffari M, Tahmasebi Birgani M, Kariminejad R, Saberi A. Ghaffari M, et al. Among authors: kariminejad r. Ann Hum Genet. 2018 Nov;82(6):469-476. doi: 10.1111/ahg.12278. Epub 2018 Aug 29. Ann Hum Genet. 2018. PMID: 30155880

9

Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.

Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: kariminejad r. Eur J Hum Genet. 2024 Oct;32(10):1238-1249. doi: 10.1038/s41431-024-01533-x. Epub 2024 Jan 26. Eur J Hum Genet. 2024. PMID: 38278869

10

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. Sci Rep. 2021 Mar 26;11(1):6952. doi: 10.1038/s41598-021-86309-9. Sci Rep. 2021. PMID: 33772059 Free PMC article.

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