List of Publications: Manually uptadted

Preimplantation High Resolution HLA Sequencing Using Next Generation Sequencing.

Rafati M, Akhondi MM, Sadeghi MR, Tara SZ, Ghaffari SR.

Biol Blood Marrow Transplant. 2018 Apr 9. pii: S1083-8791(18)30158-7. doi: 10.1016/j.bbmt.2018.03.024.

 

Mohamadhashem F, Rafati M, Hoseininasab F, Rostami S, Tabatabaie R, Rezai S, Keramatipour M, Ghaffari SR.

Climacteric. 2017 Oct;20(5):498-502. doi: 10.1080/13697137.2017.1316255. Epub 2017 Apr 28.

A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia.

Rafati M, Mohamadhashem F, Hoseini A, Hoseininasab F, Ghaffari SR.

Eur J Med Genet. 2016 Jun;59(6-7):330-6. doi: 10.1016/j.ejmg.2016.05.007. Epub 2016 May 13.

Experiences of Infertile Women Seeking Assisted Pregnancy in Iran: A Qualitative Study.

Ranjbar F, Behboodi-Moghadam Z, Borimnejad L, Ghaffari SR, Akhondi MM.

J Reprod Infertil. 2015 Oct-Dec;16(4):221-8.

Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing.

Rafati M, Mohamadhashem F, Hoseini A, Ramandi SD, Ghaffari SR.

Fetal Pediatr Pathol. 2016;35(4):282-5. doi: 10.3109/15513815.2016.1167149. Epub 2016 Apr 19.

Paradox of Modern Pregnancy: A Phenomenological Study of Women’s Lived Experiences from Assisted Pregnancy.

Ranjbar F, Akhondi MM, Borimnejad L, Ghaffari SR, Behboodi-Moghadam Z.

J Pregnancy. 2015;2015:543210. doi: 10.1155/2015/543210. Epub 2015 May 3.

A method for semi-automatic nuchal translucency thickness measurement.

Pakdaman N, Arabalibeik H, Ghaffari SR, Tahmasbpour AR.

Stud Health Technol Inform. 2014;196:307-11.

Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies.

Eisenberger T, Neuhaus C, Khan AO, Decker C, Preising MN, Friedburg C, Bieg A, Gliem M, Charbel Issa P, Holz FG, Baig SM, Hellenbroich Y, Galvez A, Platzer K, Wollnik B, Laddach N, Ghaffari SR, Rafati M, Botzenhart E, Tinschert S, Börger D, Bohring A, Schreml J, Körtge-Jung S, Schell-Apacik C, Bakur K, Al-Aama JY, Neuhann T, Herkenrath P, Nürnberg G, Nürnberg P, Davis JS, Gal A, Bergmann C, Lorenz B, Bolz HJ.

PLoS One. 2013 Nov 12;8(11):e78496. doi: 10.1371/journal.pone.0078496. eCollection 2013. Erratum in: PLoS One. 2014;9(11):e108840.

Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290.

Ghaffari SR, Rafati M, Ghaffari G, Morra M, Tekin M.

Clin Genet. 2014 Oct;86(4):387-90. doi: 10.1111/cge.12296. Epub 2013 Oct 31. No abstract available.

Correlation of nuchal translucency and thyroxine at 11-13 weeks of gestation.

Hantoushzadeh S, Tara F, Salmanian B, Gharedaghi MH, Nasri K, Ganjizadeh M, Ghaffari SR, Tahmasebpour AR, Farrokhi B, Abdollahi A, Sheikh M, Javadian P.

J Matern Fetal Neonatal Med. 2013 Nov;26(16):1586-9. doi: 10.3109/14767058.2013.784259. Epub 2013 Apr 17.

Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophy.

Korzebor A, Derakhshandeh-Peykar P, Meshkani M, Hoseini A, Rafati M, Purhoseini M, Ghaffari SR.

Mol Biol Rep. 2013 Jan;40(1):67-72. doi: 10.1007/s11033-012-2011-3. Epub 2012 Nov 7.

Normal ranges for fetal femur and humerus diaphysis length during the second trimester in an Iranian population.

Tahmasebpour AR, Pirjani R, Rahimi-Foroushani A, Ghaffari SR, Rahimi-Sharbaf F, Masrour FF.

J Ultrasound Med. 2012 Jul;31(7):991-5.

Familial Williams-Beuren syndrome ascertained by screening rather than targeted diagnosis.

Rafati M, Seyyedaboutorabi E, Brujerdi R, Moossavi S, Ghaffari SR.

Clin Dysmorphol. 2012 Jul;21(3):118-23. doi: 10.1097/MCD.0b013e3283520539.

“Familial” versus “Sporadic” intellectual disability: contribution of common microdeletion and microduplication syndromes.

Rafati M, Seyyedaboutorabi E, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Javadi GR, Dastan J, Mosavi-Jarrahi A, Hoseini A, Purhoseini M, Ghaffari SR.

Mol Cytogenet. 2012 Jan 29;5(1):9. doi: 10.1186/1755-8166-5-9.

Rafati M, Ghadirzadeh MR, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian MR, Dastan J, Hoseini A, Purhoseini M, Ghaffari SR.

Mol Cytogenet. 2012 Jan 19;5(1):4. doi: 10.1186/1755-8166-5-4.

First-trimester screening for chromosomal abnormalities by integrated application of nuchal translucency, nasal bone, tricuspid regurgitation and ductus venosus flow combined with maternal serum free β-hCG and PAPP-A: a 5-year prospective study.

Ghaffari SR, Tahmasebpour AR, Jamal A, Hantoushzadeh S, Eslamian L, Marsoosi V, Fattahi F, Rajaei M, Niroomanesh S, Borna S, Beigi A, Khazardoost S, Saleh-Gargari S, Rahimi-Sharbaf F, Farrokhi B, Bayani N, Tehrani SE, Shahsavan K, Farzan S, Moossavi S, Ramezanzadeh F, Dastan J, Rafati M.

Ultrasound Obstet Gynecol. 2012 May;39(5):528-34. doi: 10.1002/uog.10051.

Rafati M, Ravanbod S, Hoseini A, Rassoulzadegan M, Jazebi M, Enayat MS, Ala FA, Ghaffari SR.

Haemophilia. 2011 Jul;17(4):705-7. doi: 10.1111/j.1365-2516.2010.02476.x. Epub 2011 Mar 4. No abstract available.

 

Investigation of QF-PCR Application for Rapid Prenatal Diagnosis of Chromosomal Aneuploidies in Iranian Population.

Nasiri H, Noori-Dalooi MR, Dastan J, Ghaffari SR.

Iran J Pediatr. 2011 Mar;21(1):15-20.

Normal ranges of fetal nasal bone length during the second trimester in an Iranian population.

Rahimi-Sharbaf F, Tahmasebpour AR, Pirjani R, Ghaffari SR, Rahimi-Foroushani A.

Prenat Diagn. 2011 Apr;31(4):401-4. doi: 10.1002/pd.2704. Epub 2011 Feb 3.

Tracing human papilloma virus in breast tumors of Iranian breast cancer patients.

Ghaffari SR, Sabokbar T, Meshkat Z, Fereidooni F, Dastan J, Rafati M, Zendehdel K.

Breast J. 2011 Mar-Apr;17(2):218-9. doi: 10.1111/j.1524-4741.2010.01053.x. Epub 2011 Jan 31. No abstract available.

A novel truncating mutation in the E-cadherin gene in the first Iranian family with hereditary diffuse gastric cancer.

Ghaffari SR, Rafati M, Sabokbar T, Dastan J.

Eur J Surg Oncol. 2010 Jun;36(6):559-62. doi: 10.1016/j.ejso.2010.04.001. Epub 2010 May 14.

Human papillomavirus in saliva of patients with oral squamous cell carcinoma.

SahebJamee M, Boorghani M, Ghaffari SR, AtarbashiMoghadam F, Keyhani A.

Med Oral Patol Oral Cir Bucal. 2009 Oct 1;14(10):e525-8.

Novel human pathological mutations. Gene symbol: CDH1. Disease: gastric cancer.

Ghaffari SR, Dastan J, Rafati M, Sabokbar T.

Hum Genet. 2009 Apr;125(3):337. No abstract available.

Molecular cytogenetic analysis of urothelial carcinomas using urine samples.

Ayati M, Tousi VN, Sabokba T, Vaziri-Nasab H, Mehrkhani F, Jamshidian H, Dastan J, Mosavi-Jarrahi AR, Ghaffari SR.

Asian Pac J Cancer Prev. 2008 Oct-Dec;9(4):687-90.

Chromosomal radiosensitivity in patients with common variable immunodeficiency.

Aghamohammadi A, Moin M, Kouhi A, Mohagheghi MA, Shirazi A, Rezaei N, Tavassoli S, Esfahani M, Cheraghi T, Dastan J, Nersesian J, Ghaffari SR.

Immunobiology. 2008;213(5):447-54. doi: 10.1016/j.imbio.2007.10.018. Epub 2007 Dec 31.

Comparative genomic hybridization (CGH) analysis of chromosomal aberrations in Iranian patients with invasive ductal carcinoma breast cancer.

Ghaffari SR, Sabokbar T, Pour PN, Dastan J, Mehrkhani F, Shoraka S, Mohagheghi MA, Tirgari F, Mosavi-Jarrahi A.

Asian Pac J Cancer Prev. 2008 Jan-Mar;9(1):66-70.

Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating.

Kroos M, Pomponio RJ, van Vliet L, Palmer RE, Phipps M, Van der Helm R, Halley D, Reuser A; GAA Database Consortium.

Hum Mutat. 2008 Jun;29(6):E13-26. doi: 10.1002/humu.20745.

Determination of human papillomavirus type 16 genotype and construction of cloning vector pTZ57R encoding HPV16 E7 gene.

Meshkat Z, Soleimanjahi H, Mahmoudi M, Mirshahabi H, Hassan ZM, Ghaffari SR, Sabokbar T.

Saudi Med J. 2007 Oct;28(10):1511-5.

Ataxia-telangiectasia in Iran: clinical and laboratory features of 104 patients.

Moin M, Aghamohammadi A, Kouhi A, Tavassoli S, Rezaei N, Ghaffari SR, Gharagozlou M, Movahedi M, Purpak Z, Mirsaeid Ghazi B, Mahmoudi M, Farhoudi A.

Pediatr Neurol. 2007 Jul;37(1):21-8.

Prevalence of human papillomavirus genotypes in women with normal and abnormal cervical cytology in Iran.

Ghaffari SR, Sabokbar T, Mollahajian H, Dastan J, Ramezanzadeh F, Ensani F, Yarandi F, Mousavi-Jarrahi A, Mohagheghi MA, Moradi A.

Asian Pac J Cancer Prev. 2006 Oct-Dec;7(4):529-32.

Combining mammaglobin and carcinoembryonic mRNA markers for early detection of micrometastases from breast cancers–a molecular study of 59 patients.

Ghaffari SR, Sabokbar T, Tahmasebi S, Dastan J, Shorakae S, Moradi A, Tirgari F, Mohagheghi MA, Mosavi-Jarrahi A.

Asian Pac J Cancer Prev. 2006 Jul-Sep;7(3):396-8.

Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.

Ghaffari SR, Boyd E, Connor JM, Jones AM, Tolmie JL.

J Med Genet. 1998 Oct;35(10):836-40.

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

Ghaffari SR, Boyd E, Tolmie JL, Crow YJ, Trainer AH, Connor JM.

J Med Genet. 1998 Mar;35(3):225-33.

Automatic Landmark detection on chromosomes, Images for feature extraction purposes;

Moradi M, Setarehdan SK, Ghaffari SR:

Proceeding of the IEEE symposium on computer based medical systems, pp: 56-61, 2003

 

Automatic locating the centromere on Human Chromosome pictures,

Moradi M, Setarehdan SK, Ghaffari SR:

Proceedings of the 7th world Multi-conference on systems, Cybernetics and Information, July 2003

 

Comparative Genomic Hybridization Analysis of fetal samples arising from recurrent abortion

Dastan J, Ghaffari SR et al.

Journal of Family and Reproductive Health 2007, 1; 1; 18-23

 

Investigation of RBC indices and HbA2 levels in parents of beta-Thalassemia patients.

Izadyar M, Dastan J, Ghaffari SR et al.

Journal of Family and Reproductive Health 2007, 1; 2 93-94

 

Chromosomal aberrations detected by comparative genomic Hybridization technique (CGH) in invasive ductal carcinoma of breast

Ghaffari SR et al.

Tehran University Medical Journal; Vol. 65, No. 9, Dec 2007: 7-12

 

Hematological Indices of Parents in Non-Immune Hydrops Fetalis Pregnancie

Saeed Reza Ghaffari, M.D., Ph.D.;1,2,3,4 , Farzaneh Larti, M.D.; Tayebeh Sabokbar, M.S.c.; Maryam Rafati, M.D.; Jila Dastan M.S.c, M.D.; Laleh Eslamian, M.D.; Fatemeh Rahimi, M.D.; SedigheBorna, M.D.

Journal of Family and Reproductive Health2008;2(1) : 33-36

 

Microdeletion Study in Children with Selective Congenital Heart Disease; an Iranian Multicenter Study

Akbar Zeinaloo1,2, MD; Abdorazaagh Kiani1, MD; Parvin Akbari-Asbagh1, MD; Mohammad-Reza Noori-Dalooi3, PhD; Elham Ghadami-Yazdi4,MD; Tayebeh Sabokbar5, MSc; Asgar Aghamohammadi1,2, MD; Mahmood-Gholam Alemohammad4, MD; Sima Rafeyan6, MD;    Jila Dastan7,8, MSc, MD; Saeed-Reza Ghaffari3, 4,5,7,8 , MSc, MD, PhD

Iranian Journal of Pediatrics2009;19(1) : 11-17

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