Mahmoud Shekari Khaniani
Tabriz University of Medical Sciences
H-index: 17
Asia-Iran
Top articles of Mahmoud Shekari Khaniani
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Over-expression of mir-181a-3p in serum of breast cancer patients as diagnostic biomarker | Molecular Biology Reports | Hadi Fouladi Amir Ebrahimi Sima Mansoori Derakhshan Mahmoud Shekari Khaniani | 2024/12 |
Mutual interaction of lncRNAs and epigenetics: Focusing on cancer | Maryam Ranjbar Samaneh Heydarzadeh Mahmoud Shekari Khaniani Zahra Foruzandeh Farhad Seif | 2023/3/6 | |
A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case | BMC Medical Genomics | Tohid Ghasemnejad Mahmoud Shekari Khaniani Jafar Nouri Nojadeh Sima Mansoori Derakhshan | 2022/2/1 |
Molecular evaluation of Ex3 VNTR polymorphism of the DRD4 gene in patients with autism spectrum disorder | Iranian Journal of Child Neurology | Shahrokh Amiri Mahmoud Shekari Khaniani Arman Mohammadi Mahan Asadian Leila Mehdizadeh Fanid | 2022 |
Evaluating the relationship between Ex3 vNTR and rs3758653 polymorphisms in DRD4 genes in children with attention deficit hyperactivity disorder with respect to the dose of … | Medical Journal of Tabriz University of Medical Sciences | Shahrokh Amiri Sardari Mamaghani Negar Sara Farhang Sima Mansouri Derakhshan Mahmoud Shekari Khaniani | 2022/11/1 |
WITHDRAWN: In silico and Experimental Analysis of miR-125b-5 and miR-485-5p Expression in Serum of Patients with Breast Cancer | Microrna (Shariqah, United Arab Emirates) | Zahra Bahmanpour Roghayeh Sheervalilou Mahmoud Shekari Khaniani Arash Poursheikhani Vahid Montazeri | 2022/5/23 |
A Novel Missense Variant in the ESRRB Gene Causing Nonsyndromic Hearing Loss: In Silico Analyses of a Case | Tohid Ghasemnejad Mahmoud Shekari Khaniani Jafar Nouri Nojadeh Sima Mansoori Derakhshan | 2021/7/15 | |
Analysis of Association Between the Effects of Methylphenidate and DRD4 Gene Polymorphisms in Patients with Attention Deficit Hyperactivity Disorder | Journal of Comprehensive Pediatrics | Shahrokh Amiri Sara Farhang Mahmoud Shekari Khaniani Sima Mansouri Derakhshan Aziz Zadfattah | 2021/11 |
Identification of multi-exon deletion in the COL7A1 gene underlying dystrophic epidermolysis bullosa by whole-exome sequencing | Our Dermatology Online/Nasza Dermatologia Online | Mahdieh Taghizadeh Sima Mansoori Derakhshan Mahmoud Shekari Khaniani Yeganeh Eshaghkhani Zahra Golchehre | 2021/10/1 |
Association between the rs8028440 polymorphism of CYFIP 1 gene in autism patients | Biomedical and Translational Science | Hossein Ghahramani Almanghadim Marjan Assefi Shahab Masoumi Parisa Vakili Zinat Shams | 2021/7/28 |
Molecular Analysis of STin2 (Intron 2) Variant of The SLC6A4 Gene in Children and Adolescents With Attention Deficit Hyperactivity Disorder | Shahrokh Amiri Mahan Asadian Mahmoud Shekari Khaniani Sima Mansouri Derakhshan Negar Pourhossein Rahmani | 2021/7/27 |
Co-Authors
