Mina Ohadi - Publications, H-index & Citations

Mina Ohadi

Roozbeh Hospital

23H指数

140论文数

1.6K被引数

收录论文 26

发表时间

A zinc finger MYM-type containing 3 (ZMYM3) allele is associated with autism spectrum disorder in Iranian people 包含3个锌指MYM型（ZMYM3）等位基因与伊朗人群中的自闭症谱系障碍相关

Journal of Neurogenetics

IF2

2026-04-03

PREAI

Razavi, Maryam; Tabibian, Mobina; Lakpour, Zahra; Mehrabi, Shiva; Salmanian, Maryam; Ghamari, Rana; Mohammad-Zadeh, Azar; Tehrani-Doost, Mehdi; Ohadi, Mina; Alizadeh, Fatemeh

Novel crossover and recombination hotspots massively spread across primate genomes

BIOLOGY DIRECT

IF4.9

2024-08-21

OAAI

Ohadi, Mina; Arabfard, Masoud; Khamse, Safoura; Alizadeh, Samira; Vafadar, Sara; Bayat, Hadi; Tajeddin, Nahid; Maddi, Ali M. A.; Delbari, Ahmad; Khorshid, Hamid R. Khorram

CRISPR/Cas9-mediated deletion of a GA-repeat in human GPM6B leads to disruption of neural cell differentiation from NT2 cells

SCIENTIFIC REPORTS

IF3.9

2024-01-25

OAAI

Bayat, Hadi; Mirahmadi, Maryam; Azarshin, Zohreh; Ohadi, Hamid; Delbari, Ahmad; Ohadi, Mina

A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder

SCIENTIFIC REPORTS

IF3.9

2022-09-14

OAAI

Khamse, Safoura; Alizadeh, Samira; Bernhart, Stephan H.; Afshar, Hossein; Delbari, Ahmad; Ohadi, Mina

Novel implications of a strictly monomorphic (GCC) repeat in the human PRKACB gene

SCIENTIFIC REPORTS

IF3.9

2021-10-19

OAAI

Khamse, Safoura; Jafarian, Zahra; Bozorgmehr, Ali; Tavakoli, Mostafa; Afshar, Hossein; Keshavarz, Maryam; Moayedi, Razieh; Ohadi, Mina

Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder

SCIENTIFIC REPORTS

IF3.9

2021-09-28

OAAI

Jafarian, Z.; Khamse, S.; Afshar, H.; Khorshid, H. R. Khorram; Delbari, A.; Ohadi, M.

Global Single Clustering of Phenotype-Associated Human Aging Genes in the Co-Expression and Physical Interaction Networks: An OMIM-Based Investigative Review

ARCHIVES OF GERONTOLOGY AND GERIATRICS

IF3.8

2021-09-01

PREAI

Rahimi, M.; Arabfard, M.; Borna, H.; Ohadi, M.

Evolving evidence on a link between the ZMYM3 exceptionally long GA-STR and human cognition

SCIENTIFIC REPORTS

IF3.9

2020-11-10

OAAI

Afshar, H.; Khamse, S.; Alizadeh, F.; Delbari, A.; Najafipour, R.; Bozorgmehr, A.; Khazaei, M.; Adelirad, F.; Alizadeh, A.; Kowsari, A.; Ohadi, M.

Natural Selection at the NHLH2 Core Promoter Exceptionally Long CA-Repeat in Human and Disease-Only Genotypes in Late-Onset Neurocognitive Disorder

GERONTOLOGY

IF3

2020-09-02

PREAI

Afshar, Hossein; Adelirad, Fatemeh; Kowsari, Ali; Kalhor, Naser; Delbari, Ahmad; Najafipour, Reza; Foroughan, Mahshid; Bozorgmehr, Ali; Khamse, Safoura; Nazaripanah, Neda; Ohadi, Mina

How obsessive-compulsive and bipolar disorders meet each other? An integrative gene-based enrichment approach

general psychiatry

IF3.1

2020-05-09

OAAI

Hamidian, Sajedeh; Pourshahbaz, Abbas; Bozorgmehr, Ali; Ananloo, Esmaeil Shahsavand; Dolatshahi, Behrooz; Ohadi, Mina

The ATF6-calreticulin axis: a prime model for the contribution of low frequency deleterious mutations to major psychiatric disorders

EUROPEAN PSYCHIATRY

IF6.7

2020-04-15

PREAI

Ohadi, M.

Genome-wide prediction and prioritization of human aging genes by data fusion: a machine learning approach 通过数据融合对人类衰老基因进行全基因组预测和优先级排序: 一种机器学习方法

BMC GENOMICS

IF3.7

2019-11-09

OAAI

Arabfard, Masoud; Ohadi, Mina; Tabar, Vahid Rezaei; Delbari, Ahmad; Kavousi, Kaveh

Disease-only alleles at the extreme ends of the human ZMYM3 exceptionally long 5′ UTR short tandem repeat in bipolar disorder: A pilot study

JOURNAL OF AFFECTIVE DISORDERS

IF4.9

2019-05-01

PREAI

Alizadeh, Fatemeh; Moharrami, Tamouchin; Mousavi, Negar; Yazarlou, Fatemeh; Bozorgmehr, Ali; Shahsavand, Esmaeil; Delbari, Ahmad; Ohadi, Mina

Link between short tandem repeats and translation initiation site selection 短串联重复序列与翻译起始位点选择之间的联系

HUMAN GENOMICS

IF4.3

2018-10-29

OAAI

Arabfard, Masoud; Kavousi, Kaveh; Delbari, Ahmad; Ohadi, Mina

Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeats 人类特异性核心启动子三核苷酸和四核苷酸短串联重复序列的基因组规模画像和进化意义

HUMAN GENOMICS

IF4.3

2018-04-05

OAAI

Nazaripanah, N.; Adelirad, F.; Delbari, A.; Sahaf, R.; Abbasi-Asl, T.; Ohadi, M.

SOCS gene family expression profile in the blood of multiple sclerosis patients

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2017-04-01

PREAI

Toghi, Mehdi; Taheri, Mohammad; Arsang-Jang, Shahram; Ohadi, Mina; Mirfakhraie, Reza; Mazdeh, Mehrdokht; Sayad, Arezou

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder

JOURNAL OF AFFECTIVE DISORDERS

IF4.9

2017-01-01

PREAI

Dadkhah, Tahereh; Rahimi-Aliabadi, Simin; Jamshidi, Javad; Ghaedi, Hamid; Taghavi, Shaghyegh; Shokraeian, Parasto; Akhavan-Niaki, Haleh; Tafakhori, Abbas; Ohadi, Mina; Darvish, Hossein

Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder

COGNITIVE NEURODYNAMICS

IF3.9

2015-11-27

OAAI

Farashi, S.; Ohadi, M.; Hosseinkhani, S.; Darvish, H.; Mirabzadeh, A.

Association between polymorphisms in Interleukin-16 gene and risk of late-onset Alzheimer's disease

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2015-11-01

PREAI

Anvar, Nazanin Esmaeili; Saliminejad, Kioomars; Ohadi, Mina; Kamali, Koorosh; Daneshmand, Parvaneh; Khorshid, Hamid Reza Khorram

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder

JOURNAL OF NEURAL TRANSMISSION

IF4

2015-09-09

PREAI

Atakhorrami, Minoo; Rahimi-Aliabadi, Simin; Jamshidi, Javad; Moslemi, Elham; Movafagh, Abolfazl; Ohadi, Mina; Mirabzadeh, Arash; Emamalizadeh, Babak; Ghaedi, Hamid; Gholipour, Fatemeh; Fazeli, Atena; Motallebi, Marzieh; Taghavi, Shaghayegh; Ahmadifard, Azadeh; Mohammadihosseinabad, Saeed; Zarneh, Amir Ehtesham Shafiei; Shahmohammadibeni, Neda; Madadi, Faranak; Andarva, Monavvar; Darvish, Hossein

研究方向