Heidari E - Search Results

1

Identification of novel loss of function variants in MBOAT7 resulting in intellectual disability.

Heidari E, Caddeo A, Zarabadi K, Masoudi M, Tavasoli AR, Romeo S, Garshasbi M. Heidari E, et al. Genomics. 2020 Nov;112(6):4072-4077. doi: 10.1016/j.ygeno.2020.07.008. Epub 2020 Jul 6. Genomics. 2020. PMID: 32645526 Free article.

2

Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family.

Heidari E, Razmara E, Hosseinpour S, Tavasoli AR, Garshasbi M. Heidari E, et al. Ann Hum Genet. 2020 Jul;84(4):315-323. doi: 10.1111/ahg.12378. Epub 2020 Feb 20. Ann Hum Genet. 2020. PMID: 32077500

3

A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients.

Farajollahi Z, Razmara E, Heidari E, Jafarinia E, Garshasbi M. Farajollahi Z, et al. Among authors: heidari e. J Gene Med. 2020 Nov;22(11):e3253. doi: 10.1002/jgm.3253. Epub 2020 Aug 3. J Gene Med. 2020. PMID: 32666583

4

Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.

Heidari E, Harrison AN, Jafarinia E, Tavasoli AR, Almadani N, Molday RS, Garshasbi M. Heidari E, et al. Hum Mutat. 2021 May;42(5):491-497. doi: 10.1002/humu.24180. Epub 2021 Mar 14. Hum Mutat. 2021. PMID: 33565221

5

Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy.

Heidari E, Rasoulinezhad M, Pak N, Reza Ashrafi M, Heidari M, Banwell B, Garshasbi M, Reza Tavasoli A. Heidari E, et al. Among authors: heidari m. Mitochondrion. 2021 Sep;60:12-20. doi: 10.1016/j.mito.2021.07.001. Epub 2021 Jul 9. Mitochondrion. 2021. PMID: 34252606

6

Dehnavi AZ, Heidari E, Rasulinezhad M, Heidari M, Ashrafi MR, Hosseini MM, Sadeghzadeh F, Fallah MS, Rostampour N, Bahraini A, Garshasbi M, Tavasoli AR. Dehnavi AZ, et al. Among authors: heidari e, heidari m. Hum Genomics. 2021 Jul 19;15(1):45. doi: 10.1186/s40246-021-00345-0. Hum Genomics. 2021. PMID: 34281620 Free PMC article.

7

Novel splicing variant and gonadal mosaicism in DYRK1A gene identified by whole-genome sequencing in multiplex autism spectrum disorder families.

Agha Gholizadeh M, Behjati F, Ghasemi Firouzabadi S, Heidari E, Razmara E, Almadani N, Sharifi Zarchi A, Garshasbi M. Agha Gholizadeh M, et al. Among authors: heidari e. Neurogenetics. 2024 Oct;25(4):377-391. doi: 10.1007/s10048-024-00768-6. Epub 2024 Jul 8. Neurogenetics. 2024. PMID: 38976082

8

Comparisons of lumbar spine loads and kinematics in healthy and non-specific low back pain individuals during unstable lifting activities.

Heidari E, Arjmand N, Kahrizi S. Heidari E, et al. J Biomech. 2022 Nov;144:111344. doi: 10.1016/j.jbiomech.2022.111344. Epub 2022 Oct 10. J Biomech. 2022. PMID: 36270086

9

Co-delivery of curcumin and Bcl-2 siRNA to enhance therapeutic effect against breast cancer cells using PEI-functionalized PLGA nanoparticles.

Mohammad Gholinia Sarpoli L, Zare-Karizi S, Heidari E, Hasanzadeh A, Bayandori M, Azedi F, Hamblin MR, Karimi M. Mohammad Gholinia Sarpoli L, et al. Among authors: heidari e. Pharm Dev Technol. 2022 Sep;27(7):785-793. doi: 10.1080/10837450.2022.2120003. Epub 2022 Sep 7. Pharm Dev Technol. 2022. PMID: 36043390

10

Evaluation of the focus reduction neutralization and ELISA tests compared to the plaque reduction neutralization test for the detection of antibodies against measles virus.

Yaghoobizad S, Norouzbabaei Z, Shafiei Jandaghi NZ, Rahimi Foroushani A, Sadeghi K, Izadi S, Fatemi-Nasab GS, Heidari E, Salimi V, Mokhtari-Azad T. Yaghoobizad S, et al. Among authors: heidari e. Biologicals. 2024 Oct 5;88:101795. doi: 10.1016/j.biologicals.2024.101795. Online ahead of print. Biologicals. 2024. PMID: 39369472

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