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VAHID REZA YASSAEE
Title
Cited by
Cited by
Year
Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer
VR Yassaee, S Zeinali, I Harirchi, S Jarvandi, MA Mohagheghi, ...
Breast Cancer Research 4, 1-6, 2002
742002
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 …
A Taghavi, ME Akbari, M Hashemi‑Bahremani, N Nafissi, A Khalilnezhad, ...
Oncology Letters 12 (5), 3845-3855, 2016
392016
Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1
VR Yassaee, F Hashemi-Gorji, S Boosaliki, N Parvaneh
Human Immunology 77 (2), 191-195, 2016
272016
Novel LAMA2 gene mutations associated with merosin-deficient congenital muscular dystrophy
F Hashemi-Gorji, VR Yassaee, P Dashti, M Miryounesi
Iranian Biomedical Journal 22 (6), 408, 2018
212018
UBD identify in paraffin tissues in patients with colorectal cancer
A IZADI, E MOSLEMI, SM POORHOSSEINI, VR YASSAEE, HR KHEIRI, ...
JOURNAL OF ISFAHAN MEDICAL SCHOOL (IUMS) 32 (291), 1-10, 2014
212014
A new approach for molecular diagnosis of TAR syndrome
VR Yassaee, F Hashemi-Gorji, Z Soltani, SM Poorhosseini
Clinical Biochemistry 47 (9), 835-839, 2014
172014
Mutation spectra of the AAAS gene in Iranian families with Allgrove Syndrome
VR Yassaee, Z Soltani, BM Ardakani
Archives of medical research 42 (2), 163-168, 2011
172011
miR‐30a promoter variation contributes to the increased risk of colorectal cancer in an Iranian population
H Sadeghi, E Nazemalhosseini‐Mojarad, M Yaghoob‐Taleghani, ...
Journal of Cellular Biochemistry 120 (5), 7734-7740, 2019
162019
Multidisciplinary management of a patient with van der Woude syndrome: A case report
A Tehranchi, H Behnia, N Nadjmi, VR Yassaee, Z Ravesh, M Mina
International Journal of Surgery Case Reports 30, 142-147, 2017
162017
Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series
VR Yassaee, F Hashemi-Gorji, M Miryounesi, A Rezayi, Z Ravesh, ...
Clinica chimica acta 474, 88-95, 2017
152017
New gene profiling in determination of breast cancer recurrence and prognosis in Iranian women
SM Poorhosseini, M Hashemi, NA Olyaei, A Izadi, E Moslemi, Z Ravesh, ...
Asian Pacific Journal of Cancer Prevention 17 (sup3), 155-160, 2016
152016
Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome
N Alipour, S Salehpour, SH Tonekaboni, M Rostami, S Bahari, V Yassaee, ...
Journal of Molecular Neuroscience 70, 21-25, 2020
132020
Investigation of CEBPA and CEBPA-AS genes expression in acute myeloid leukemia
M Gholami, S Bayat, S Manoochehrabadi, H Pashaiefar, MD Omrani, ...
Reports of Biochemistry & Molecular Biology 7 (2), 136, 2019
132019
A novel homozygous LMNA mutation (p. Met540Ile) causes mandibuloacral dysplasia type a
VR Yassaee, A Khojaste, F Hashemi-Gorji, Z Ravesh, P Toosi
Gene 577 (1), 8-13, 2016
132016
Novel long noncoding RNAs upregulation may have synergistic effects on the CYP24A1 and PFDN4 biomarker role in human colorectal cancer
H Sadeghi, E Nazemalhosseini‐Mojarad, U Sahebi, E Fazeli, ...
Journal of Cellular Physiology 236 (3), 2051-2057, 2021
122021
An intron variant in the FLT1 gene increases the risk of preeclampsia in Iranian women
M Amin-Beidokhti, M Gholami, A Abedin-Do, R Pirjani, H Sadeghi, ...
Clinical and Experimental Hypertension 41 (8), 697-701, 2019
112019
Mutation spectra of BRCA genes in Iranian women with early onset breast Cancer-15 years experience
VR Yassaee, Z Ravesh, Z Soltani, F Hashemi-Gorji, SM Poorhosseini, ...
Asian Pacific Journal of Cancer Prevention 17 (sup3), 149-153, 2016
102016
Whole-exome sequencing uncovers novel causative variants and additional findings in three patients affected by glycogen storage disease type VI and Fanconi− Bickel syndrome
M Eghbali, KS Fatemi, S Salehpour, M Abiri, H Saei, S Talebi, NA Olyaei, ...
Frontiers in Genetics 11, 601566, 2021
92021
Cloning and expression of influenza H1N1 NS1 protein in Escherichia Coli BL21
M Sadeghi, M Bandehpour, F Yarian, V Yassaee, E Torbati, B Kazemi
Iranian Journal of Biotechnology 12 (1), 25-29, 2014
82014
TAR syndrome, a rare case report with cleft lip/palate
A Naseh, A Hafizi, F Malek, H Mozdarani, V Yassaee
Internet J Pediatr Neonatol 14, 14289, 2012
82012
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Articles 1–20