Yassaee VR - Search Results

1

Delineating the expanding phenotype of HERC2-related disorders: The impact of biallelic loss of function versus missense variation.

Vincent KM, Eaton A, Yassaee VR, Miryounesi M, Hashemi-Gorji F, Rudichuk L, Goez H, Leonard N, Lazier J. Vincent KM, et al. Among authors: yassaee vr. Clin Genet. 2021 Nov;100(5):637-640. doi: 10.1111/cge.14039. Epub 2021 Aug 9. Clin Genet. 2021. PMID: 34370298

2

Screening for genomic rearrangements at BRCA1 locus in Iranian women with breast cancer using multiplex ligation-dependent probe amplification.

Yassaee VR, Emamalizadeh B, Omrani MD. Yassaee VR, et al. J Genet. 2013 Apr;92(1):131-4. doi: 10.1007/s12041-013-0223-5. J Genet. 2013. PMID: 23640417 No abstract available.

3

A new approach for molecular diagnosis of TAR syndrome.

Yassaee VR, Hashemi-Gorji F, Soltani Z, Poorhosseini SM. Yassaee VR, et al. Clin Biochem. 2014 Jun;47(9):835-9. doi: 10.1016/j.clinbiochem.2014.04.018. Epub 2014 Apr 24. Clin Biochem. 2014. PMID: 24769264

4

A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A.

Yassaee VR, Khojaste A, Hashemi-Gorji F, Ravesh Z, Toosi P. Yassaee VR, et al. Gene. 2016 Feb 10;577(1):8-13. doi: 10.1016/j.gene.2015.08.071. Epub 2015 Nov 19. Gene. 2016. PMID: 26602028

5

Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.

Yassaee VR, Hashemi-Gorji F, Boosaliki S, Parvaneh N. Yassaee VR, et al. Hum Immunol. 2016 Feb;77(2):191-5. doi: 10.1016/j.humimm.2015.11.019. Epub 2015 Nov 27. Hum Immunol. 2016. PMID: 26639818

6

Mutation Spectra of BRCA Genes in Iranian Women with Early Onset Breast Cancer - 15 Years Experience.

Yassaee VR, Ravesh Z, Soltani Z, Hashemi-Gorji F, Poorhosseini SM, Anbiaee R, Joulaee A. Yassaee VR, et al. Asian Pac J Cancer Prev. 2016;17(S3):149-53. doi: 10.7314/apjcp.2016.17.s3.149. Asian Pac J Cancer Prev. 2016. PMID: 27165220 Free article.

7

New Gene Profiling in Determination of Breast Cancer Recurrence and Prognosis in Iranian Women.

Poorhosseini SM, Hashemi M, Alipour Olyaei N, Izadi A, Moslemi E, Ravesh Z, Hashemi-Gorji F, Kheiri HR, Yassaee VR. Poorhosseini SM, et al. Among authors: yassaee vr. Asian Pac J Cancer Prev. 2016;17(S3):155-60. doi: 10.7314/apjcp.2016.17.s3.155. Asian Pac J Cancer Prev. 2016. PMID: 27165221 Free article.

8

First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population.

Soltani Z, Karami F, Yassaee V, Hashemi Gorji F, Talebzadeh M, Miryounesi M. Soltani Z, et al. Iran Red Crescent Med J. 2016 Jan 1;18(2):e21633. doi: 10.5812/ircmj.21633. eCollection 2016 Feb. Iran Red Crescent Med J. 2016. PMID: 27175306 Free PMC article.

9

A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β.

Hashemi-Gorji F, Ghafouri-Fard S, Salehpour S, Yassaee VR, Miryounesi M. Hashemi-Gorji F, et al. Among authors: yassaee vr. J Pediatr Endocrinol Metab. 2016 Aug 1;29(8):991-3. doi: 10.1515/jpem-2016-0032. J Pediatr Endocrinol Metab. 2016. PMID: 27180337

10

Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI.

Seyedhassani SM, Hashemi-Gorji F, Yavari M, Harazi F, Yassaee VR. Seyedhassani SM, et al. Among authors: yassaee vr. Fetal Pediatr Pathol. 2016;35(5):353-358. doi: 10.1080/15513815.2016.1191567. Epub 2016 Jun 30. Fetal Pediatr Pathol. 2016. PMID: 27362741

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