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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: ghaedi h. 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
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: ghaedi h. 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
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: ghaedi h. 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
Detection of Superior Markers for Polymerase Chain Reaction Diagnosis of Breast Cancer Micrometastasis in Sentinel Lymph Nodes.
Alizadeh Shargh S, Movafagh A, Zarghami N, Sayad A, Mansouri N, Taheri M, Heidary Pour A, Iranpour M, Ghaedi H, Montazeri V, Massoudi N, Hashemi M, Mortazavi-Tabatabaei SA. Alizadeh Shargh S, et al. Among authors: ghaedi h. Asian Pac J Cancer Prev. 2016;17(S3):179-83. doi: 10.7314/apjcp.2016.17.s3.179. Asian Pac J Cancer Prev. 2016. PMID: 27165222 Free article.
A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome.
Rahimi-Aliabadi S, Daftarian N, Ahmadieh H, Emamalizadeh B, Jamshidi J, Tafakhori A, Ghaedi H, Noroozi R, Taghavi S, Ahmadifard A, Alehabib E, Andarva M, Shokraeian P, Atakhorrami M, Darvish H. Rahimi-Aliabadi S, et al. Among authors: ghaedi h. Eye (Lond). 2016 Nov;30(11):1424-1432. doi: 10.1038/eye.2016.137. Epub 2016 Jul 15. Eye (Lond). 2016. PMID: 27419834 Free PMC article.
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