Feyzollah Hashemi-Gorji, MSc - Shahid Beheshti University of Medical Sciences - Research assistant

Feyzollah Hashemi-Gorji

MSc

Shahid Beheshti University of Medical Sciences

Research assistant

Tehran, Tehran | Iran (Islamic Republic of)

Main Specialties: Biochemical Genetics, Medical Genetics, Molecular Genetic Pathology

Additional Specialties: Molecular Genetics

ORCID logohttps://orcid.org/0000-0002-9996-9406

Feyzollah Hashemi-Gorji, MSc - Shahid Beheshti University of Medical Sciences - Research assistant

Feyzollah Hashemi-Gorji

MSc

Introduction

Primary Affiliation: Shahid Beheshti University of Medical Sciences - Tehran, Tehran , Iran (Islamic Republic of)

Specialties:

Additional Specialties:

Research Interests:


View Feyzollah Hashemi-Gorji’s Resume / CV

Metrics

Number of Publications

21

Publications

Number of Profile Views

17

Profile Views

Number of Article Reads

108

Reads

Number of PubMed Central Citations

21

PubMed Central Citations

Education

Sep 2006 - Jan 2009
Islamic Azad University Science and Research Branch
Sep 2002 - Feb 2006
Islamic Azad University - Tonekabon Branch

Experience

Oct 2011 - Oct 2011
Shahid Beheshti University of Medical Sciences
Research assistant
Dec 2009 - Dec 2009
Pasteur Institute of Iran
Research assistant

Top co-authors

Vahid Reza Yassaee
Vahid Reza Yassaee

Shaheed Beheshti Medical University

11
Mohammad Miryounesi
Mohammad Miryounesi

Shahid Beheshti University of Medical Sciences

9
Soudeh Ghafouri-Fard
Soudeh Ghafouri-Fard

Shahid Beheshti University of Medical Sciences

6
Seyed Mohammad Poorhosseini
Seyed Mohammad Poorhosseini

Shahid Beheshti University of Medical Sciences

4
Zeinab Ravesh
Zeinab Ravesh

University of Tübingen

4
Ziba Soltani
Ziba Soltani

Taleghani Hospital

4
Seyed Mohammad Seyedhassani
Seyed Mohammad Seyedhassani

National Institute of Genetic Engineering and Biotechnology

3
Shadab Salehpour
Shadab Salehpour

Shaheed Beheshti University of Medical Sciences

3
Reza Mirfakhraie
Reza Mirfakhraie

Shahid Beheshti University of Medical Sciences

2
Alireza Rezayi
Alireza Rezayi

Pediatric Neurology Research Center

2

Publications

21Publications

108Reads

21PubMed Central Citations

Novel LAMA2 Gene Mutations Associated with Merosin-Deficient Congenital Muscular Dystrophy

Iran Biomed J 2018 11 30;22(6):408-14. Epub 2018 Apr 30.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
November 2018
2 Reads

Association of the Risk of Dental Caries and Polymorphism of MBL2 rs11003125 Gene in Iranian Adults.

Caries Res 2018 Jun 14;53(1):60-64. Epub 2018 Jun 14.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
June 2018
2.28 Impact Factor

Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia

Iran Biomed J 2018 03 23;22(2):117-22. Epub 2017 Jul 23.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

View Article
March 2018
9 Reads
1 PubMed Central Citation(source)

Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series.

Clin Chim Acta 2017 Nov 24;474:88-95. Epub 2017 Aug 24.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Department of Pediatrics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address:

View Article
November 2017
7 Reads
2.82 Impact Factor

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

Asian Pac J Cancer Prev 2016 ;17(S3):149-53

Genomic Research Center, Department of Medical Genetic,Shahid Beheshti University of Medical Sciences, Tehran, Iran E-mail:

View Article
February 2017
1.50 Impact Factor

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

Asian Pac J Cancer Prev 2016 ;17(S3):155-60

Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran E-mail:

View Article
February 2017
1 Read
2 PubMed Central Citations(source)
1.50 Impact Factor

Limb Girdle Muscular Dystrophy Type 2E Due to a Novel Large Deletion in SGCB Gene.

Iran J Child Neurol 2017 ;11(3):57-60

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
January 2017
7 Reads

Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome.

Iran J Child Neurol 2017 ;11(1):70-74

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
January 2017
7 Reads
1 PubMed Central Citation(source)

Gene expression profiling of the 8q22-24 position in human breast cancer: , , and genes are implicated in oncogenesis, while and genes may predict a risk of metastasis.

Oncol Lett 2016 Nov 30;12(5):3845-3855. Epub 2016 Sep 30.

Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717413, Iran; Molecular Diagnostic Laboratory, Genomic Research Center, Shahid Beheshti University of Medical Sciences, Ayatollah Taleghani Educational Hospital, Tehran 1985717413, Iran.

View Article
November 2016
5 Reads
2 PubMed Central Citations(source)
0.99 Impact Factor

A Novel Nonsense Mutation in Gene in Two Patients with Pantothenate Kinase-Associated Neurodegeneration.

Int J Mol Cell Med 2016 23;5(4):255-259. Epub 2016 Oct 23.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
October 2016
21 Reads

A Novel Splice Site Mutation in Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family.

Int J Mol Cell Med 2016 3;5(3):192-195. Epub 2016 Jul 3.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
July 2016
13 Reads

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

Fetal Pediatr Pathol 2016 30;35(5):353-358. Epub 2016 Jun 30.

a Genomic Research Center, Shahid Beheshti University of Medical Sciences , Tehran , Iran.

View Article
June 2016
1 Read
2 PubMed Central Citations(source)
0.40 Impact Factor

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

Gene 2016 Feb 19;577(1):8-13. Epub 2015 Nov 19.

Dept. of Dermatology, Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address:

View Article
February 2016
1 Read
1 PubMed Central Citation(source)
2.14 Impact Factor

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

Hum Immunol 2016 Feb 27;77(2):191-5. Epub 2015 Nov 27.

Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.

View Article
February 2016
3 Reads
2.14 Impact Factor

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

Iran Red Crescent Med J 2016 Feb 1;18(2):e21633. Epub 2016 Jan 1.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran.

View Article
February 2016
1 Read
0.50 Impact Factor

Novel missense mutation in the GALNS gene in an affected patient with severe form of mucopolysaccharidosis type IVA.

Clin Chim Acta 2015 Oct 11;450:121-4. Epub 2015 Aug 11.

Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Dept. of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

View Article
October 2015
16 Reads
2.82 Impact Factor

A new approach for molecular diagnosis of TAR syndrome.

Clin Biochem 2014 Jun 24;47(9):835-9. Epub 2014 Apr 24.

Dept. of Medical Genetic, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1966645643, Iran.

View Article
June 2014
1 Read
1 PubMed Central Citation(source)
2.23 Impact Factor

A novel mutation in the transactivation-regulating domain of the androgen receptor in a patient with azoospermia.

J Androl 2011 Jul-Aug;32(4):367-70. Epub 2010 Dec 2.

Biology Department, Islamic Azad University, Science and Research Branch, Tehran, Iran.

View Article
September 2011
7 Reads
6 PubMed Central Citations(source)
2.47 Impact Factor

BAX pro-apoptotic gene alterations in repeated pregnancy loss.

Arch Med Sci 2011 02 8;7(1):117-22. Epub 2011 Mar 8.

Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

View Article
February 2011
2 Reads
3 PubMed Central Citations(source)
1.89 Impact Factor

Top co-authors

Vahid Reza Yassaee
Vahid Reza Yassaee

Shaheed Beheshti Medical University

11
Mohammad Miryounesi
Mohammad Miryounesi

Shahid Beheshti University of Medical Sciences

9
Soudeh Ghafouri-Fard
Soudeh Ghafouri-Fard

Shahid Beheshti University of Medical Sciences

6
Seyed Mohammad Poorhosseini
Seyed Mohammad Poorhosseini

Shahid Beheshti University of Medical Sciences

4
Zeinab Ravesh
Zeinab Ravesh

University of Tübingen

4
Ziba Soltani
Ziba Soltani

Taleghani Hospital

4
Seyed Mohammad Seyedhassani
Seyed Mohammad Seyedhassani

National Institute of Genetic Engineering and Biotechnology

3
Shadab Salehpour
Shadab Salehpour

Shaheed Beheshti University of Medical Sciences

3
Reza Mirfakhraie
Reza Mirfakhraie

Shahid Beheshti University of Medical Sciences

2
Alireza Rezayi
Alireza Rezayi

Pediatric Neurology Research Center

2