Tahmasebi Birgani M - Search Results

1

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing.

Nikkhah E, Safaralizadeh R, Mohammadiasl J, Tahmasebi Birgani M, Hosseinpour Feizi MA, Golchin N. Nikkhah E, et al. Among authors: tahmasebi birgani m. Cell J. 2018 Jul;20(2):284-289. doi: 10.22074/cellj.2018.5012. Epub 2018 Mar 18. Cell J. 2018. PMID: 29633607 Free PMC article.

2

Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy.

Tahmasebi-Birgani M, Hajjari M, Golchin N, Shalbafan B, Mohammadi-Asl J, Sadeghian F. Tahmasebi-Birgani M, et al. Iran J Basic Med Sci. 2019 May;22(5):576-580. doi: 10.22038/ijbms.2019.30754.7414. Iran J Basic Med Sci. 2019. PMID: 31217940 Free PMC article.

3

Whole exome sequencing identified a novel nonsense INPP4A mutation in a family with intellectual disability.

Banihashemi S, Tahmasebi-Birgani M, Mohammadiasl J, Hajjari M. Banihashemi S, et al. Among authors: tahmasebi birgani m. Eur J Med Genet. 2020 Apr;63(4):103846. doi: 10.1016/j.ejmg.2020.103846. Epub 2020 Jan 21. Eur J Med Genet. 2020. PMID: 31978615

4

Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.

Mohammadi-Asl J, Hajjari M, Tahmasebi Birgani M, Riahi K, Nasiri H, Kollaee A. Mohammadi-Asl J, et al. Among authors: tahmasebi birgani m. Ann Hum Genet. 2018 Sep;82(5):304-308. doi: 10.1111/ahg.12255. Epub 2018 Jul 24. Ann Hum Genet. 2018. PMID: 30039856

5

Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia.

Ansari H, Mohammadi-Asl J, Hajjari M, Tahmasebi-Birgani M, Kollaee A, Jassemi-Zergani F, Vakili-Hajiagha A. Ansari H, et al. Among authors: tahmasebi birgani m. J Gene Med. 2019 Aug;21(8):e3103. doi: 10.1002/jgm.3103. Epub 2019 Jul 11. J Gene Med. 2019. PMID: 31177591

6

Exome sequencing found a novel homozygous deletion in ADCK3 gene involved in autosomal recessive spinocerebellar ataxia.

Hajjari M, Tahmasebi-Birgani M, Mohammadi-Asl J, Nasiri H, Kollaee A, Mahmoodi M, Ansari H. Hajjari M, et al. Among authors: tahmasebi birgani m. Gene. 2019 Aug 5;708:10-13. doi: 10.1016/j.gene.2019.05.016. Epub 2019 May 10. Gene. 2019. PMID: 31078656

7

Long non-coding RNAs expression levels in diffuse large B-cell lymphoma: An in silico analysis.

Dousti F, Shahrisa A, Ansari H, Hajjari M, Tahmasebi Birgani Y, Mohammadiasl J, Tahmasebi Birgani M. Dousti F, et al. Among authors: tahmasebi birgani m, tahmasebi birgani y. Pathol Res Pract. 2018 Sep;214(9):1462-1466. doi: 10.1016/j.prp.2018.08.006. Epub 2018 Aug 7. Pathol Res Pract. 2018. PMID: 30104077

8

A novel infram deletion in MSH6 gene in glioma: Conversation on MSH6 mutations in brain tumors.

Deris Zayeri Z, Tahmasebi Birgani M, Mohammadi Asl J, Kashipazha D, Hajjari M. Deris Zayeri Z, et al. Among authors: tahmasebi birgani m. J Cell Physiol. 2019 Jul;234(7):11092-11102. doi: 10.1002/jcp.27759. Epub 2018 Nov 27. J Cell Physiol. 2019. PMID: 30478893

9

The pattern of gene copy number alteration (CNAs) in hepatocellular carcinoma: an in silico analysis.

Shahrisa A, Tahmasebi-Birgani M, Ansari H, Mohammadi Z, Carloni V, Mohammadi Asl J. Shahrisa A, et al. Among authors: tahmasebi birgani m. Mol Cytogenet. 2021 Jul 2;14(1):33. doi: 10.1186/s13039-021-00553-2. Mol Cytogenet. 2021. PMID: 34215297 Free PMC article.

10

HOTAIR: A Promising Long Non-coding RNA with Potential Role in Breast Invasive Carcinoma.

Avazpour N, Hajjari M, Tahmasebi Birgani M. Avazpour N, et al. Among authors: tahmasebi birgani m. Front Genet. 2017 Nov 21;8:170. doi: 10.3389/fgene.2017.00170. eCollection 2017. Front Genet. 2017. PMID: 29209357 Free PMC article. No abstract available.

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