Farzad Hashemi-Gorji

发表

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

H. Goez, Krista M Vincent, Alison Eaton, 2021, Clinical genetics.

Association of the P561T and C422F polymorphisms of the growth hormone receptor gene with facial dimensions.

A. Khojasteh, S. R. Motamedian, V. Yassaee, 2020 .

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

M. Houshmand, M. Montazeri, Farzad Hashemi-Gorji, 2011, Journal of andrology.

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

Seyed Mohammad Poorhosseini, V. Yassaee, Farzad Hashemi-Gorji, 2016, Asian Pacific journal of cancer prevention : APJCP.

Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case Series

Hyung-Goo Kim, M. Miryounesi, Farzad Hashemi-Gorji, 2022, Iranian journal of child neurology.

POLYMORPHISM ANALYSIS OF MALARIA SUSCEPTIBILITY BIOMARKERS IN G6PD DEFICIENCY PATIENTS

Farzad Hashemi-Gorji, H. Mehrdad, M. N. Daloii, 2010 .

A mutational and expressional analysis of DNMT3A in acute myeloid leukemia cytogenetic subgroups

M. Omrani, Farzad Hashemi-Gorji, A. Movafagh, 2015, Hematology.

BAX pro-apoptotic gene alterations in repeated pregnancy loss

M. Houshmand, A. Aflatoonian, Farzad Hashemi-Gorji, 2011, Archives of medical science : AMS.

Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran

A. Khojasteh, V. Yassaee, Farzad Hashemi-Gorji, 2022, Molecular genetics & genomic medicine.

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

Farzad Hashemi-Gorji, R. Mirfakhraie, Mahdieh Yavari, 2015, Clinica chimica acta; international journal of clinical chemistry.

A new approach for molecular diagnosis of TAR syndrome.

Seyed Mohammad Poorhosseini, V. Yassaee, Farzad Hashemi-Gorji, 2014, Clinical biochemistry.

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

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

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

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2018, Iranian biomedical journal.

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

Mohammad Hashemi, Seyed Mohammad Poorhosseini, Amir Izadi, 2016, Asian Pacific journal of cancer prevention : APJCP.

Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2022, Neurological Sciences.

Study of glucose-6-phosphate dehydrogenese (G6PD) gene mutations in patients with G6PD deficiency of Fars and Esfahan provinces

M. Alivand, M. Hashemi, Farzad Hashemi-Gorji, 2009 .

Gene expression profiling of the 8q22-24 position in human breast cancer: TSPYL5, MTDH, ATAD2 and CCNE2 genes are implicated in oncogenesis, while WISP1 and EXT1 genes may predict a risk of metastasis

Seyed Mohammad Poorhosseini, M. Akbari, V. Yassaee, 2016, Oncology letters.

Association between single nucleotide polymorphisms rs12722489 and multiple sclerosis in Iranian patients with multiple sclerosis

V. Yassaee, Farzad Hashemi-Gorji, H. Ahmadi, 2020, Current Journal of Neurology.

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

V. Yassaee, Farzad Hashemi-Gorji, P. Toosi, 2016, Gene.

Next generation sequencing elucidated a clinically undiagnosed metabolic disorder - An Iranian family with hereditary orotic aciduria

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2019, Gene Reports.

Evaluation of caries experience in two genders and ENAM polymorphism in Iranian adults

Farzad Hashemi-Gorji, M. Mokhtari, F. Koohpeima, 2018, Meta Gene.

Molecular Identification of the Most Prevalent Mutations of Glucose-6-Phosphate Dehydrogenase (G6PD) in Fars and Isfahan of Iran

Farzad Hashemi-Gorji, M. Noori-Daloii, 2009 .

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

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2017, Clinica chimica acta; international journal of clinical chemistry.

Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene

M. Miryounesi, Farzad Hashemi-Gorji, R. Mirfakhraie, 2023, Neurological Sciences.

A novel SRD5A2 mutation in an Iranian family with sex development disorder

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2020, Andrologia.

Novel mutation in the MED23 gene for intellectual disability: A case report and literature review

M. Miryounesi, Farzad Hashemi-Gorji, M. Fardaei, 2019, Clinical case reports.

Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia

B. Soltani, M. Miryounesi, Farzad Hashemi-Gorji, 2018, Iranian biomedical journal.

Neurodegeneration with brain iron accumulation 2A: Report of four independent cases

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2018 .

I. Scheffer, P. Striano, F. Alkuraya, 2023, European Journal of Human Genetics.

Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

M. Miryounesi, Farzad Hashemi-Gorji, R. Mirfakhraie, 2024, BMC medical genomics.

Genetic change investigation in DOCK1 gene in an Iranian family with sign and symptoms of temporomandibular joint disorder (TMD).

Farzad Hashemi-Gorji, S. Najafi, Nafiseh Sheykhbahaei, 2024, Clinical oral investigations.