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Page 1
Support for "Disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia.
Khademi E, Alehabib E, Shandiz EE, Ahmadifard A, Andarva M, Jamshidi J, Rahimi-Aliabadi S, Pouriran R, Nejad FR, Mansoori N, Shahmohammadibeni N, Taghavi S, Shokraeian P, Akhavan-Niaki H, Paisán-Ruiz C, Darvish H, Ohadi M. Khademi E, et al. Among authors: shahmohammadibeni n. Genet Test Mol Biomarkers. 2017 Aug;21(8):485-490. doi: 10.1089/gtmb.2016.0422. Epub 2017 Jul 19. Genet Test Mol Biomarkers. 2017. PMID: 28723299
Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia.
Rahimi-Aliabadi S, Shahmohammadibeni N, Jamshidi J, Shandiz EE, Mirfakhraie R, Ohadi M, Nejad FR, Mansoori N, Taheri M, Gholipour F, Moudi S, Tayebi G, Divsalar S, Darvish H, Movafagh A. Rahimi-Aliabadi S, et al. Among authors: shahmohammadibeni n. Genet Test Mol Biomarkers. 2017 Apr;21(4):248-251. doi: 10.1089/gtmb.2016.0262. Epub 2017 Feb 21. Genet Test Mol Biomarkers. 2017. PMID: 28384043
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.
Atakhorrami M, Rahimi-Aliabadi S, Jamshidi J, Moslemi E, Movafagh A, Ohadi M, Mirabzadeh A, Emamalizadeh B, Ghaedi H, Gholipour F, Fazeli A, Motallebi M, Taghavi S, Ahmadifard A, Mohammadihosseinabad S, Shafiei Zarneh AE, Shahmohammadibeni N, Madadi F, Andarva M, Darvish H. Atakhorrami M, et al. Among authors: shahmohammadibeni n. J Neural Transm (Vienna). 2016 Mar;123(3):323-8. doi: 10.1007/s00702-015-1456-7. Epub 2015 Sep 9. J Neural Transm (Vienna). 2016. PMID: 26354101
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
Shahmohammadibeni N, Rahimi-Aliabadi S, Jamshidi J, Emamalizadeh B, Shahmohammadibeni HA, Zare Bidoki A, Akhavan-Niaki H, Eftekhari H, Abdollahi S, Shekari Khaniani M, Shahmohammadibeni M, Fazeli A, Motallebi M, Taghavi S, Ahmadifard A, Shafiei Zarneh AE, Andarva M, Dadkhah T, Khademi E, Alehabib E, Rahimi M, Tafakhori A, Atakhorrami M, Darvish H. Shahmohammadibeni N, et al. Neurol Sci. 2016 May;37(5):731-6. doi: 10.1007/s10072-015-2420-x. Epub 2016 Jan 5. Neurol Sci. 2016. PMID: 26732583
RIT2 Polymorphisms: Is There a Differential Association?
Emamalizadeh B, Jamshidi J, Movafagh A, Ohadi M, Khaniani MS, Kazeminasab S, Biglarian A, Taghavi S, Motallebi M, Fazeli A, Ahmadifard A, Shahidi GA, Petramfar P, Shahmohammadibeni N, Dadkhah T, Khademi E, Tafakhori A, Khaligh A, Safaralizadeh T, Kowsari A, Mirabzadeh A, Zarneh AES, Khorrami M, Shokraeian P, Banavandi MJS, Lima BS, Andarva M, Alehabib E, Atakhorrami M, Darvish H. Emamalizadeh B, et al. Among authors: shahmohammadibeni n. Mol Neurobiol. 2017 Apr;54(3):2234-2240. doi: 10.1007/s12035-016-9815-4. Epub 2016 Mar 3. Mol Neurobiol. 2017. PMID: 26941103
Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population.
Haghnejad L, Emamalizadeh B, Jamshidi J, Bidoki AZ, Ghaedi H, Ahmadi E, Abdollahi S, Shahmohammadibeni N, Taghavi S, Fazeli A, Motallebi M, Zarneh AE, Mohammadihosseinabad S, Abbaszadegan MR, Torkamandi S, Gavenaroudi MA, Pedram N, Shahidi GA, Tafakhori A, Darvish H, Movafagh A. Haghnejad L, et al. Among authors: shahmohammadibeni n. J Neurol Sci. 2015 Aug 15;355(1-2):72-4. doi: 10.1016/j.jns.2015.05.020. Epub 2015 May 27. J Neurol Sci. 2015. PMID: 26070653
A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.
Taghavi S, Chaouni R, Tafakhori A, Azcona LJ, Firouzabadi SG, Omrani MD, Jamshidi J, Emamalizadeh B, Shahidi GA, Ahmadi M, Habibi SAH, Ahmadifard A, Fazeli A, Motallebi M, Petramfar P, Askarpour S, Askarpour S, Shahmohammadibeni HA, Shahmohammadibeni N, Eftekhari H, Shafiei Zarneh AE, Mohammadihosseinabad S, Khorrami M, Najmi S, Chitsaz A, Shokraeian P, Ehsanbakhsh H, Rezaeidian J, Ebrahimi Rad R, Madadi F, Andarva M, Alehabib E, Atakhorrami M, Mortazavi SE, Azimzadeh Z, Bayat M, Besharati AM, Harati-Ghavi MA, Omidvari S, Dehghani-Tafti Z, Mohammadi F, Mohammad Hossein Pour B, Noorollahi Moghaddam H, Esmaili Shandiz E, Habibi A, Taherian-Esfahani Z, Darvish H, Paisán-Ruiz C. Taghavi S, et al. Among authors: shahmohammadibeni n. Mol Neurobiol. 2018 Apr;55(4):3477-3489. doi: 10.1007/s12035-017-0535-1. Epub 2017 May 13. Mol Neurobiol. 2018. PMID: 28502045 Free PMC article.
c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.
Safarpour Lima B, Ghaedi H, Daftarian N, Ahmadieh H, Jamshidi J, Khorrami M, Noroozi R, Sohrabifar N, Assarzadegan F, Hesami O, Taghavi S, Ahmadifard A, Atakhorrami M, Rahimi-Aliabadi S, Shahmohammadibeni N, Alehabib E, Andarva M, Darvish H, Emamalizadeh B. Safarpour Lima B, et al. Among authors: shahmohammadibeni n. Eur J Med Genet. 2016 Feb;59(2):65-9. doi: 10.1016/j.ejmg.2016.01.001. Epub 2016 Jan 7. Eur J Med Genet. 2016. PMID: 26773575
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Wagner M, Osborn DPS, Gehweiler I, Nagel M, Ulmer U, Bakhtiari S, Amouri R, Boostani R, Hentati F, Hockley MM, Hölbling B, Schwarzmayr T, Karimiani EG, Kernstock C, Maroofian R, Müller-Felber W, Ozkan E, Padilla-Lopez S, Reich S, Reichbauer J, Darvish H, Shahmohammadibeni N, Tafakhori A, Vill K, Zuchner S, Kruer MC, Winkelmann J, Jamshidi Y, Schüle R. Wagner M, et al. Among authors: shahmohammadibeni n. Nat Commun. 2019 Oct 21;10(1):4790. doi: 10.1038/s41467-019-12620-9. Nat Commun. 2019. PMID: 31636353 Free PMC article.