Ohadi M - Search Results

1

The human SMAD9 (GCC) repeat links to natural selection and late-onset neurocognitive disorders.

Alizadeh S, Khamse S, Vafadar S, Bernhart SH, Afshar H, Vahedi M, Rezaei O, Delbari A, Ohadi M. Alizadeh S, et al. Among authors: ohadi m. Neurol Sci. 2024 Nov;45(11):5241-5251. doi: 10.1007/s10072-024-07637-y. Epub 2024 Jun 14. Neurol Sci. 2024. PMID: 38877206

2

Aberrant expression of Activating Transcription Factor 6 (ATF6) in major psychiatric disorders.

Kazeminasab S, Esmaeilzadeh-Gharehdaghi E, Oladnabi M, Ohadi M, Mirabzadeh A, Hosseinkhani S. Kazeminasab S, et al. Among authors: ohadi m. Psychiatry Res. 2012 Dec 30;200(2-3):1086-7. doi: 10.1016/j.psychres.2012.04.006. Epub 2012 May 7. Psychiatry Res. 2012. PMID: 22572160 No abstract available.

3

A mutation in the calreticulin gene promoter in a family case of schizoaffective disorder leads to its aberrant transcriptional activation.

Nunes A, Ohadi M, Rahimi A, Aghajani A, Najmabadi H, Currais A, Soriano S. Nunes A, et al. Among authors: ohadi m. Brain Res. 2008 Nov 6;1239:36-41. doi: 10.1016/j.brainres.2008.08.064. Epub 2008 Sep 4. Brain Res. 2008. PMID: 18801343

4

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

Anvar NE, Saliminejad K, Ohadi M, Kamali K, Daneshmand P, Khorshid HR. Anvar NE, et al. Among authors: ohadi m. J Neurol Sci. 2015 Nov 15;358(1-2):324-7. doi: 10.1016/j.jns.2015.09.344. Epub 2015 Sep 11. J Neurol Sci. 2015. PMID: 26386715

5

Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeats.

Nazaripanah N, Adelirad F, Delbari A, Sahaf R, Abbasi-Asl T, Ohadi M. Nazaripanah N, et al. Among authors: ohadi m. Hum Genomics. 2018 Apr 5;12(1):17. doi: 10.1186/s40246-018-0149-3. Hum Genomics. 2018. PMID: 29622039 Free PMC article.

6

Link between short tandem repeats and translation initiation site selection.

Arabfard M, Kavousi K, Delbari A, Ohadi M. Arabfard M, et al. Among authors: ohadi m. Hum Genomics. 2018 Oct 29;12(1):47. doi: 10.1186/s40246-018-0181-3. Hum Genomics. 2018. PMID: 30373661 Free PMC article.

7

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

Alizadeh F, Moharrami T, Mousavi N, Yazarlou F, Bozorgmehr A, Shahsavand E, Delbari A, Ohadi M. Alizadeh F, et al. Among authors: ohadi m. J Affect Disord. 2019 May 15;251:86-90. doi: 10.1016/j.jad.2019.03.056. Epub 2019 Mar 20. J Affect Disord. 2019. PMID: 30909162

8

Genome-wide prediction and prioritization of human aging genes by data fusion: a machine learning approach.

Arabfard M, Ohadi M, Rezaei Tabar V, Delbari A, Kavousi K. Arabfard M, et al. Among authors: ohadi m. BMC Genomics. 2019 Nov 9;20(1):832. doi: 10.1186/s12864-019-6140-0. BMC Genomics. 2019. PMID: 31706268 Free PMC article.

9

Proposed minimal essential co-expression and physical interaction networks involved in the development of cognition impairment in human mid and late life.

Salehi Z, Arabfard M, Sadatpour O, Ohadi M. Salehi Z, et al. Among authors: ohadi m. Neurol Sci. 2021 Mar;42(3):951-959. doi: 10.1007/s10072-020-04594-0. Epub 2020 Jul 16. Neurol Sci. 2021. PMID: 32676761

10

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

Afshar H, Adelirad F, Kowsari A, Kalhor N, Delbari A, Najafipour R, Foroughan M, Bozorgmehr A, Khamse S, Nazaripanah N, Ohadi M. Afshar H, et al. Among authors: ohadi m. Gerontology. 2020;66(5):514-522. doi: 10.1159/000509471. Epub 2020 Sep 2. Gerontology. 2020. PMID: 32877896

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