Definition and refinement Loss of Heterozygosity (LOH) of 8p22 region in diffuse type of gastric cancer. Hosseini HA, Ahani A, Galehdari H, Froughmand AM, Hosseini M, Masjedizadeh A, Zali MR.World J Gastroenterol. 2007 Jun 28;13(24):3354-8.

Emery’s Elements of Medical Genetics. Book, 13th edition, Churchill Livingstone publication. 2007. (Translated to Persian).

RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations. Ali Ahani, Babak Behnam, Hamid Reza Khorram Khorshid, Mohammad Taghi Akbari. Cancer Genetics 204 (2011) 316-322

Report of a novel mutation in RB1 gene from an Iranian retinoblastoma patient and its effect on splicing pattern. Journal of Shahrekord university of medical sciences. Ali Ahani, Hamid Reza Khorram Khorshid, Babak Behnam, Mohammad Taghi Akbari. J Sharekord Univ Med Sci. 2012 Oct, Nov; 14(4): 88-95.

Emery’s Elements of Medical Genetics. Book, 14th edition, Churchill Livingstone publication. 2012. (Translated to Persian).
Thompson & Thompson Genetics in Medicine. Book, 6th edition, Elsevier Publication. 2007 (Translated to Persian).

Molecular Diagnostic of Y Chromosome Microdeletions: New Candidate STS Markers.Saliminejad K, Ahani A, Khorram Khorshid HR. J Androl. 2012 Apr 19.
Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population. Saman Mohamad Zahery, Kioomars Saliminejad, Hamid Reza Khorram Khorshid, Ali Ahani. Avicenna J Med Biotech 2012; 4(4): 199-205.

Screening for large rearrangements of the RB1 gene in Iranian retinoblastoma patients using Multiplex Ligation-dependent Probe Amplification. Ali Ahani, Mohammad Taghi Akbari, Kioomars Saliminejad, Babak Behnam, Mohammad Mehdi Akhondi, Parvaneh Vosoogh, Farriba Ghassemi, Masood Naseripour, Gholamreza Bahoush, Hamid Reza Khorram Khorshid. Molecular Vision 2013; 19:454-462.

Rapid detection of RB1 recurrent mutations in retinoblastoma patients. Saliminejad K., Behnam B., Akbari M. T., Khorram Khorshid H. R., Ghassemi F., Amoli F. A., Akhondi M. M., Vosoogh P., Naseripour M. and Ahani A. 2013 J. Genet. 92, e36–e40.

Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome. Babak Behnam, Marjan Shakiba, Ali Ahani, Maryam Razzaghy Azar. Hepat Mon. 2013;13(6):e10124.

Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification. Fereshteh Ashtari, Kioomars Saliminejad, Ali Ahani, Koorosh Kamali, Zhamak Pahlevanzadeh, and Hamid Reza Khorram Khorshid. Avicenna Journal of Medical Biotechnology, Vol. 5, No. 4, October-December 2013.

Comparative evaluation of differentiation potential of menstrual blood- versus bone marrow-derived stem cells into hepatocyte-like cells. Khanjani S, Khanmohammadi M, Zarnani AH, Akhondi MM, Ahani A, Ghaempanah Z, Naderi MM, Eghtesad S, Kazemnejad S. PLoS One. 2014 Feb 5;9(2):e86075. doi: 10.1371/journal.pone.0086075. eCollection 2014.

Methionine synthase A2756G variation is associated with the risk of retinoblastoma in Iranian children. Akbari MT, Naderi A, Saremi L, Sayad A, Irani S, Ahani A. Cancer Epidemiol. 2015 Nov 17;39(6):1023-1025. doi: 10.1016/j.canep.2015.11.002. [Epub ahead of print].

An ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree. Mehrpour M, Gohari F, Dizaji MZ, Ahani A, Malicdan MC, Behnam B. J Mol Genet Med. 2016 Jun;10(2). pii: 222. Epub 2016 Jun 19.

Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia. Alimardanian L, Saliminejad K, Razi S, Ahani A. Andrologia. 2016 Nov;48(9):890-894. doi: 10.1111/and.12527. Epub 2016 Jan 14.

Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma. Soleimani E, Saliminejad K, Akbari MT, Kamali K, Ahani A. Ophthalmic Genet. 2016 Dec;37(4):384-387. Epub 2016 Feb 25.

Genetic screening in Iranian patients with retinoblastoma. Shahraki K, Ahani A, Sharma P, Faranoush M, Bahoush G, Torktaz I, Gahl WA, Naseripour M, Behnam B. Eye (Lond). 2016 Dec 16. doi: 10.1038/eye.2016.289. [Epub ahead of print].

Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development. Shojaei A, Ebrahimzadeh-Vesal R, Ahani A, Razzaghy-Azar M, Khakpour G, Ghazi F, Tavakkoly-Bazzaz J. Rep Biochem Mol Biol. 2017 Oct;6(1):59-65.

Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma. Soleimani E, Saliminejad K, Akbari MT, Kamali K, Ahani A. Ophthalmic Genet. 2016 Dec;37(4):384-387. Epub 2016 Feb 25.

The Association between TNF-alpha Gene Polymorphisms and Endometriosis in An Iranian Population. Babak Babaabasi, Ali Ahani, Faegheh Sadeghi, Haniyeh Bashizade-Fakhar, Hamid Reza Khorram Khorshid. International Journal of Fertility and Sterility. Vol 13, No 1, Apr-Jun 2019, Pages:6-11.