1. New insights into short peptides derived from the collagen nc1 a1, a2, and a3 (iv) domains: an experimental and md simulations study

Reyhane Chamani, Seyed mohammad hossein Taleqani, Aylar Imanpour, Mehri Khatami (2022), Biochimica et biophysica acta-proteins and proteomics , 1870(), 140769-1-140769-10 (No: 26705) (10.1016/j.bbapap.2022.140769)

2. In-silico study to identify the pathogenic single nucleotide polymorphisms in the coding region of cdkn2a gene

Farzane Ghasemi, Mehri Khatami, Mohammad Mehdi Heidari, Reyhane Chamani, Zare-Zardini Hadi (2021), Iranian journal of pediatric hematology and oncology , 11(2), 114-133 (No: 24876) (10.18502/ijpho.v11i2.5844)

3. Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the apc gene in patients with familial adenomatous polyposis (fap)

Faranak Ghadamyari, Mohammad Mehdi Heidari, Sirous Zeinali, Mehri Khatami, Shahin Merat, Hamideh Bagherian, Leili Rejali, Farzane Ghasemi (2021), Journal of clinical laboratory analysis , 35(35), 1-13 (No: 25472) (10.1002/jcla.23768)

4. Novel point mutations in 3-untranslated region of gata4 gene are associated with sporadic non-syndromic atrial and ventricular septal defects

Mehri Khatami, Sajede Ghorbani, MOJGAN REZAEIADERYANI, Sahar Bahaloo, Mehri Azaminaeini, Mohammad Mehdi Heidari, Mehdi Hadadzadeh (2021), Current medical science , 1(), 1-15 (No: 26162) (10.1007/s11596-021-2428-9)

6. Micrornas as a new molecular biomarker for diagnosis and prognosis of t-cell acute lymphoblastic leukemia (t-all): a systematic review

Parisa sadat Naji esfahani, Mohammad Mehdi Heidari, Mehri Khatami, Hadi Zare-Zardini, Reyhane Chamani (2020), Iranian journal of pediatric hematology and oncology , 10(3), 184-199 (No: 22900)

8. Relationship of hypomethylation cpg islands in interleukin-6 gene promoter with il-6 mrna levels in patients with coronary atherosclerosis

Monireh Mohammadpanah, Mohammad Mehdi Heidari, Mehri Khatami, Mehdi Hadadzadeh (2020), Journal of cardiovascular and thoracic research , 12(3), 221-228 (No: 23348) (10.34172/jcvtr.2020.37)

10. Association of pathogenic missense and nonsense mutations in mitochondrial coii gene with familial adenomatous polyposis (fap)

Zahra Shaker ardakani, Mohammad Mehdi Heidari, Mehri Khatami, Morteza Bitaraf Sani (2020), International journal of molecular and cellular medicine , 9(4), 1-11 (No: 23577)

11. Identification of novel missense mutations of the tsh-b subunit gene in pediatric patients with congenital central hypothyroidism

Seyede Fateme Talebi, Mohammad Mehdi Heidari, Mehri Khatami, Mahtab Ordooei (2020), Jentashapir journal of cellular and molecular biology , 11(3), e108948-1-e108948-9 (No: 23578) (10.5812/jjcmb.108948)

13. Protective effect of berberis vulgaris on fenton reaction-induced dna cleavage

Noushin Asadi, Mohammad Mehdi Heidari, Mehri Khatami (2019), Avicenna journal of phytomedicine , 9(3), 213-220 (No: 20602)

15. Detection of novel mitochondrial mutations in cytochrome c oxidase subunit 1 (cox1) in patients with familial adenomatous polyposis (fap)

Elham Afkhami, Mohammad Mehdi Heidari, Mehri Khatami, Faranak Ghadamyari, Sima Dianatpour (2019), Clinical and translational oncology , 1(1), 1-11 (No: 21126) (10.1007/s12094-019-02208-6)

16. Novel point mutations of cited2 gene are associated with non-familial congenital heart disease (chd) in sporadic pediatric patients

Sima Dianatpour, Mehri Khatami, Mohammad Mehdi Heidari, Mehdi Hadadzadeh (2019), Applied biochemistry and biotechnology , 1(), 1-8 (No: 21127) (10.1007/s12010-019-03125-8)

17. Induced pluripotent stem cells (ipscs) based approaches for hematopoietic cancer therapy

Bardia Khandani, Mohammad Mehdi Heidari, Mehri Khatami (2019), Iranian journal of pediatric hematology and oncology , 9(2), 117-130 (No: 20603)

18. Identification of a novel non-sense mutation in tbx5 gene in pediatric patients with congenital heart defects

Mehri Khatami, Mohammad Mehdi Heidari, Fatemeh Kazeminasab, Razieh Zare bidoky (2018), Journal of cardiovascular and thoracic research , 10(1), 41-45 (No: 17635)

19. A novel heteroplasmic mutation in mitochondrial trnaarg gene associated with non-dystrophic myotonias

Mohammad Mehdi Heidari, Abolfazl Keshmirshekan, Mozhgan Bidakhavidi, Azam Khosravi, Zeinab Bandari, Mehri Khatami, Shahriar Nafissi (2018), Acta neurologica belgica , (1), 1-8 (No: 18524) (10.1007/s13760-018-1042-5)

20. Novel point mutations in the nkx2.5 gene in pediatric patients with non-familial congenital heart disease

Mehri Khatami, Mansoure Mazidi, , Mohammad Mehdi Heidari, Mehdi Hadadzadeh (2018), Medicina , 54(), 46-56 (No: 18683) (10.3390/medicina54030046)

21. Novel and heteroplasmic mutations in mitochondrial trna genes in brugada syndrome

MAHSAALSADAT FALLAHTAFTI, Mehri Khatami, Shiva Rezaee, Mohammad Mehdi Heidari, Mehdi Hadadzadeh (2018), Cardiology journal , 25(1), 113-119 (No: 16146) (10.5603/CJ.a2017.0104)

22. Simultaneous genotyping of the rs4762 and rs699 polymor-phisms in angiotensinogen gene and correlation with iranian cad patients with novel hexa-primer arms-pcr

Mehri Khatami, Mohammad Mehdi Heidari, Mehdi Hadadzadeh, Barbara SCHEIBER-MOJDEHKAR, Morteza BITARAF SANI, Massoud Houshmand (2017), Iranian journal of public health , 46(6), 811-819 (No: 15227)

23. Relationship of the mthfd1 (rs2236225) enos (rs1799983) cbs (rs2850144) and ace (rs4343) gene polymorphisms in a population of iranian pediatric patients with congenital heart defects

Mehri Khatami, Farzaneh Morteza ratky, Saba Tajfar, (2017), Kaohsiung journal of medical sciences , 33(), 442-448 (No: 15471) (10.1016/j.kjms.2017.05.016)

24. Molecular analysis of rs2070744 and rs1799983 polymorphisms of nos3 gene in iranian patients with multiple sclerosis

Mohammad Mehdi Heidari, Mehri Khatami, Yaser Tahamtan (2017), Basic and clinical neuroscience , 4(8), 279-284 (No: 15472)

25. Designing and validation of one-step t-arms-pcr for genotyping the enos rs1799983 snp

Mohammad Mehdi Heidari, Mehri Khatami (2017), Iranian journal of biotechnology , 15(3), 208-212 (No: 15652)

26. The association of reninangiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss

Mohammad Mehdi Heidari, Mozhgan Sheikholeslami, Mahdiye Yavari, Mehri Khatami, Seyed Mohammad Seyedhassani (2017), Human fertility , 0(0), 1-7 (No: 15782) (10.1080/14647273.2017.1388545)

28. Mutation analysis of the nkx2.5 gene in iranian pediatric patients with congenital hypothyroidism

Mehri Khatami, Mohammad Mehdi Heidari, Fatemeh Tabesh, Mahtab Ordooei, Zohreh Salehifar (2017), Journal of pediatric endocrinology and metabolism , 30(), 1-6 (No: 15470) (10.1515/jpem-2017-0084)

29. A novel nonsense mutation in exon 5 of kind1 gene in an iranian family with kindler syndrome

Mohammad Mehdi Heidari, Mehri Khatami, Kargar saeed, , Hasan Hossein Zadeh, Hamideh Fallah ali abadi (2016), Archives of iranian medicine , 19(6), 403-408 (No: 12144)

30. Upregulation of mir-222 in both helicobacter pylori-infected and noninfected gastric cancer patients

Mina Noormohammad, SADEGHI SAMIRA, TABATABAEIAN HOSSEIN, GHAEDI KAMRAN, TALEBI ARDESHIR , MANSOUREH AZADEH, Mehri Khatami, Mohammad Mehdi Heidari (2016), Journal of genetics , 95(4), 991-995 (No: 12963)

31. Mitochondrial genetic variation in iranian infertile men with varicocele

Mohammad Mehdi Heidari, Mehri Khatami, Amirhossein Danafar, , Ghazaleh Farahmand, Ali Reza Talebi (2016), International journal of fertility and sterility , 10(3), 303-309 (No: 12964)

32. Common rs5918 (pla1/a2) polymorphism in the itgb3 gene and risk of coronary artery disease

Mehri Khatami, Mohammad Mehdi Heidari (2016), Archives of medical science , (1), 9-15 (No: 12158)

33. Polymorphisms in nos3 mthfr apob and tnf-a genes and risk of coronary atherosclerotic lesions in iranian patients

Mohammad Mehdi Heidari, Mehri Khatami, Hadadzade Mehdi, Mahboobe Kazemi, Sahar Mahamed, , (2016), Research in cardiovascular medicine , 5(1), 1-6 (No: 12159)

34. The polg polyglutamine tract variants in iranian patients

Mehri Khatami, Mohammad Mehdi Heidari, , (2015), Iranian journal of child neurology , 1(9), 37-41 (No: 9972)