Ali Ahani

Ali Ahani

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Ali Ahani

Ali Ahani

Publications by authors named "Ali Ahani"

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17Publications

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The Association between TNF-alpha Gene Polymorphisms and Endometriosis in An Iranian Population.

Int J Fertil Steril 2019 Apr 6;13(1):6-11. Epub 2019 Jan 6.

Genetic Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

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http://dx.doi.org/10.22074/ijfs.2019.5542DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334017PMC
April 2019

A soft computing approach for diabetes disease classification.

Health Informatics J 2018 12 14;24(4):379-393. Epub 2016 Nov 14.

Universiti Teknologi Malaysia, Malaysia.

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http://journals.sagepub.com/doi/10.1177/1460458216675500
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http://dx.doi.org/10.1177/1460458216675500DOI Listing
December 2018

Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development.

Rep Biochem Mol Biol 2017 Oct;6(1):59-65

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643445PMC
October 2017

Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.

Ophthalmic Genet 2016 12 25;37(4):384-387. Epub 2016 Feb 25.

b Reproductive Biotechnology Research Center, Avicenna Research Institute , Tehran , Iran.

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http://dx.doi.org/10.3109/13816810.2015.1107596DOI Listing
December 2016

Accuracy Improvement for Predicting Parkinson's Disease Progression.

Sci Rep 2016 Sep 30;6:34181. Epub 2016 Sep 30.

Department of Computer Science and Information Systems, Faculty of Computing, Johor, 81310 Skudai, Malaysia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043229PMC
http://dx.doi.org/10.1038/srep34181DOI Listing
September 2016

An Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.

J Mol Genet Med 2016 Jun 19;10(2). Epub 2016 Jun 19.

Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran; NIH Undiagnosed Diseases Program, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.4172/1747-0862.1000222DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969076PMC
June 2016

Methionine synthase A2756G variation is associated with the risk of retinoblastoma in Iranian children.

Cancer Epidemiol 2015 Dec 18;39(6):1023-5. Epub 2015 Nov 18.

Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.

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http://dx.doi.org/10.1016/j.canep.2015.11.002DOI Listing
December 2015

Perspectives and editorials: letter to the editor.

J Androl 2012 Nov-Dec;33(6):1128-9. Epub 2012 Apr 19.

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http://dx.doi.org/10.2164/jandrol.112.016717DOI Listing
October 2014

Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification.

Avicenna J Med Biotechnol 2013 Oct;5(4):251-6

Neurology Department, Isfahan Neuroscience Research Centre, Isfahan University of Medical Sciences, Isfahan, Iran ; These authors equally contributed to this work.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838770PMC
October 2013

Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.

Hepat Mon 2013 9;13(6):e10124. Epub 2013 Jun 9.

Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, IR Iran ; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, IR Iran ; Ali-Asghar Children Hospital, Iran University of Medical Sciences, Tehran, IR Iran.

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http://dx.doi.org/10.5812/hepatmon.10124DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759778PMC
September 2013

Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR.

J Genet 2013 May 29;92(2):e36-40. Epub 2013 May 29.

Reproductive Biotechnology Research Center, Avicenna Research Institute, Academic Center for Education Culture and Research (ACECR), 1936773493 Tehran, Iran.

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May 2013

Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.

Avicenna J Med Biotechnol 2012 Oct;4(4):193-9

Reproductive Biotechnology Research Center, Avicenna Research Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran ; Monoclonal Antibody Research Center, Avicenna Research Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran ; These authors equally contributed to this work.

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http://www.ajmb.org/pdf/en/fulltext/99.pdf
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558219PMC
October 2012

The role of IL-6 for predicting neonatal sepsis: a systematic review and meta-analysis.

Iran J Pediatr 2011 Dec;21(4):411-7

Golestan Research Center of Gastroenterology and Hepatology, Golestan University of Medical Sciences, Gorgan, Iran ; Department of Pediatrics, Golestan University of Medical Sciences, Gorgan, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446138PMC
December 2011

RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations.

Cancer Genet 2011 Jun;204(6):316-22

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

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http://dx.doi.org/10.1016/j.cancergen.2011.04.007DOI Listing
June 2011