Full Articles
1.Mochida GH,Rajab A,Eyaid W,Lu A, Al-Nouri D,Kosaki K,Noruzinia M,Sarda P,Ishihara J,Bodell A,K Apse,C A Walsh.Broader geographical spectrum of Cohen syndrome due to COH1 mutations.Journal of medical genetics 2004, 41(6):e87.
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2. Noruzinia M, Coupier I,Pujol P.Is BRCA1/BRCA2-related breast carcinogenesis estrogen dependent?.Cancer 2005;104(8):1567-1574.
3. Pujol P, This P, Noruzinia M, Stoppa-Lyonnet D, Maudelonde T.Les formes héréditaires de cancer du sein liées à BRCA1 et BRCA2 sont-elles sensibles aux œstrogènes ?.Bulletin du cancer 2004;91(7-8):583-591.
4. Rey JM, Noruzinia M, Brouillet JP, Sarda P, Maudelonde T,Pujol P.Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer.Cancer genetics and cytogenetics 2004;155(2):149-151.
5. Pouranvari S,Noruzinia M,Zeinaloo AA,Ghaffari SR,Houshmand M,Kaviani S.Detection of 22q11.2 microdeletions by SemiQuantitaive MultiplexPCR (SQMPCR).Modares Journal of Medical Sciences 2008;10(2):71-78
6. Vasli N,Noruzinia M,Saremi A,Azmi M,Mahjoubi F.Mutation screening of APC gene in patients with Familial Adenomatous Polyposis by Conformation Sensitive Gel Electrophoresis (CSGE)).Modares Journal of Medical Sciences 2008.10(1)
7. Noruzinia M,Akbari MT,Ghofrani M,Sheikhha H.Rett syndrome molecular diagnosis and implications in genetic counseling.Report of a case Indian Journal of Human Genetics 2008. 13(3):119-121
8. Mehrdad Noruzinia,Lefort Genevieve,Chaze Anne Marie,Puechberty Jacques,Pellestor Franck,Blanchet Patricia,Cacheux Valerie,Sarda Pierre.Phenotypic and cytogenetic variety of pure partial trisomy of chromosome 16p.Acta Medica Iranica 2009;47(3):240-233
9.Jenny Chang-Claude,Nadine Andrieu,Matti Rookus,Richard Brohet,Antonis C. Antoniou,Susan Peock,Rosemarie Davidson,Louise Izatt,Trevor Cole,Catherine Nogue`s,Elisabeth Luporsi,Laetitia Huiart,Nicoline Hoogerbrugge,Flora E. Van Leeuwen,Ana Osorio,Jorunn Eyfjord,Paolo Radice,Noruzinia M.Age at menarche and menopause and breast cancer risk in the International BRCA1/2 Carrier Cohort Study.Cancer Epidemiology Biomarkers and Prevention 2007;16(4):740-746
10.Pouranvari Sara, Noruzinia Mehrdad, Ghafari S. Reza, Zeinaloo Ali Akbar, Kaviani Saeed.Atypical 22q11 microdeletions in Iranian patients with congenital truncal cardiac defects.SMJ 2008;29(10):1514-1519
11. Azad m, Kaviani S, Soleimani M, Noruzinia M, Hajfathali A.Common thiopurine S-methyltransferase (TPMT) polymorphisms` analysis in an Iranian population. Yakhteh Medical J2009;11(3):311-316
12. Klaus Dieterich, Raoudha Zouari, Radu Harbuz, François Vialard , Delphine Martinez, Hanane Bellayou, Nadia Prisant, Abdelali Zoghmar , Marie Roberte Guichaoua, Isabelle Koscinski, Mahmoud Kharouf, Mehrdad Noruzinia, Sellama Nadifi, Abdelaziz Sefiani, Jacqueline Lornage, Mohamed Zahi, Stéphane Viville, Bernard Sèle, Pierre-Simon Jouk, Marie-Christine Jacob,Denise Escalier, Yorgos Nikas, Sylviane Hennebicq, Joël Lunardi and Pierre F Ray.The Aurora Kinase C c.144delC mutation causes Meiosis I arrest in men and is frequent in the North African population.Hum Mol Genet.2009 Apr;18(7):1301-1309
13. Khazamipour N, Noruzinia M, Fatehmanesh P, Keyhanee M, Pujol P.MTHFR promoter hypermethylation in testicular biopsies of patients with non-obstructive azoospermia: the role of epigenetics in male infertility.Human Reproduction2009;24(9):2361-2364
14.V Laugel,C Dalloz,M Durand,F Sauvanaud,U Kristensen,MC Vincent,L Pasquier,Odent,V Cormier-Daire,B Gener,ES Tobias,JL Tolmie,D Martin-Coignard,V Drouin-,D Heron,H Journel,E Raffo,J Vigneron,S Lyonnet,V Murday,D Gubser Mercati,B Funalot,L Brueton,J Sanchez del Pozo,E Mu oz,AR Gennery,M Salih,Noruzinia-M.Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.Human mutation2010;31(2):113-126.
15. Alizadeh Shaban,Kaviani Saeid,Soleimani Masoud,Kouhka Fatemeh,Pourfatollah Ali Akbar,Amirizadeh Naser,Abroun Saeid,Noruzinia-M. Evaluation of Mir-150 downregulation by miRCURY LNA microRNA inhibitor can express alpha chain hemoglobins expression in erythroleukemia K562 Cell line.International journal of hematology oncology and stem cell research.Jan 2010
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16. Akbari-Mohammad Taghi,Noruzinia M,Mozdarani-H,Hamid-Mohammad .Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR.Journal of Genetics.2011May;90(5):20-24
17. Tarfiee GH, Noruzinia M,Soleimani M,Kaviani S,Mahmodinia M,Farshdosti M,Paskal Pojal.ROR2 promoter methylation change in osteoblastic differentiation of mesenchymal stem cells.Yakhtae Medical Journal.spring 2011;13(1):11-18
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18. Totty-steve, Robinson-Nigel, Waldron-Kevin, Firbank-Susan, Bessant-conrad, Noruzinia M.sociey for experimental biology annual main meeting 28th june-1st july 2009,Glasgow,uk.Comparative biochemistry and physiology2009;153:159-164
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19. Mehdi-Azad, Kaviani-Saeid, Masoud Soleimani, Noruzinia M, Abbas-Hajfathali. Common Polymorphism's Analysis of Thiopurine S-Methylteransferase (TMPT )in Iranian Population. Yakhteh Medical Journal2009;11(3):312-316
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20.Sayad Azadeh,Noruzinia Mehrdad,Zamani Mahdi,Harirchian Mohammad Hosein,KazemNezhadAnoushiravan.LRP C766T polymorphism in Iranian patients with late-onset Alzheimer's Disease.Journal of Modares Medical Science.Accepted
21.Ahmadvand M, Noruzinia Mehrdad,Soleimani M,Kaviani S,Abron S,Dehghani fard A,Mahmodinia M.In vitro induction of gamma globin gene in erythroid cells derived from CD133+ by thalidomide and sodium butyrate.Journal of Genetics in the 3rd Millennium.Accepted
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Abstracts :
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1. Vasli-N,Noruzinia-M.The place of genetic analysis in medical mangement of patients with Familial Adenomatous Polyposis.The 1 international congress on Health Genomics and Biotechnology.Iran.Tehran24November2007
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2. Vasli-N,Noruzinia-M.mutation screening of APC gene in FAP patients by a novel CSGE technique. دومين كنگره بيوشيمي و بيولوژي مولكولي ايران.Iran.Shiraz4October2007
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3. Noruzinia-M,Akbari-MT.Hereditary Multiple Exostoses: report of a case and a novel mutation in EXT1 in Iran. European Society of Human Genetics.France.Nice16June2007
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4. Noruzinia-M,Akbari-MT. Rett syndrome molecular diagnosis and implications in genetic counseling: report of a case.European Society of Human Genetics.France.Nice16June2007
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5. Noruzinia-M,Poranvari-S,Kaviani-S,Hoshmand-M.Genetic basis of cogenital heart disease.First International congress on health genomics and biotechnology.Iran.Tehran.26 November2007
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6. Poranvari-S, Noruzinia-M,Zeinalo-A,Ghafari-S,Hoshmand-M.Molecular diagnosis of DiGeorge syndrome : 3M common deletion by Semi Quantitative PCR and its comparison with FISH.نهمين كنگره بيوشيمي ايران و دومين كنگره بين المللي بيوشيمي و بيولوژي مولكولIran.Shiraz 4November2007
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7. Khodabande S,Noruzinia-M.UV-absorbing compounds extracted from the Persian sturgeon caviar and Artemia urmiana cysts and their UV protective effects on human skin fibroblasts.Society for Experimental Biology Annual Main Meeting.UK.Glasko28June2009
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8. Kaviani S,Atashi A,Soleimani M, Noruzinia-M,Haj Fathaliha A.IN VITRO INDUCTION OF FETAL HEMOGLOBIN BY TRANSFORMING GROWTH FACTOR-B AND STEM CELL FACTOR IN ERYTHROID CELLS DERIVED FROM CD133+ CELLS. European Hematology Association.Germany.Berlin4June2009
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9.Fatemeh Hadipour,Zahra Hadipour, Noruzinia-M, Farkhonde Behjati,Yousef Shafeghati. Prader-willi syndrome: A case report. نقش اپي ژنتيك در سندرمهاي ژنتيكي شايع.Iran. Tehran.Autumn2009
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10. Zahra Hadipour, Fatemeh Hadipour, Noruzinia-M, Farkhonde Behjati, Yousef Shafeghati. Angelman syndrome: A case report. نقش اپي ژنتيك در سندرمهاي ژنتيكي شايع. Iran. Tehran.Autumn2009
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11. Noruzinia-M. The role of epigenetics in human genome and imprinting defect syndromes. نقش اپي ژنتيك در سندرمهاي ژنتيكي شايع. Iran. Tehran.Autumn2009
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.12. Maryam Mahmoodinia Maymand, Masoud Soleimani, Saeid Kaviani, Noruzinia-M. Oxidative stress and epigenetic modifications in stem cells. يازدهمين گنكره ژنتيك ایران Iran.Tehran22May2010
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13. Sahar Mohammadi Fateh,Noruzinia-M, Zahra Hadipour, Fatemeh Hadipour, Shafaghati. Molecular Diagnosis of Cystic fibrosis in a family and two prenatal diagnosis resulting in
pregnancy termination.يازدهمين گنكره ژنتيك ایران.Iran.Tehran22May2010
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14. Noruzinia-M,samira rezaee, hadi shabanloo, sahar mohamadifateh, nazila Mirfatahi. Development of a new method in BRCA1 and BRCA2 genetic analysis based in CSGE. يازدهمين گنكره ژنتيك ایران Iran.Tehran22May2010
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15. Noruzinia-M, Yousef Shafeghati, Zahra Hadipour, samira rezaee, Fatemeh Hadipour. Detection of 7q11.23 microdeletion in patients with congenital cardiac disorders by MLPA. يازدهمين گنكره ژنتيك ایران. Iran.Tehran22May2010
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16. Noruzinia-M, Hassan Tonekaboni, samira rezaee, sahar Mohamadi Fateh, Khazamipour, Nazila Mirfatahi, Yousef Shafeghati. Rett syhdrome in two families with Mental Retardation and psychomotor regression.يازدهمين گنكره ژنتيك ایران.Iran.Tehran22May2010
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17. Nastaran khazamipour, Yousef Shafeghati, sahar mohamadifateh, Noruzinia-M. A new Method in detecting pathogenic mutation in APC. يازدهمين گنكره ژنتيك ایران. Iran.Tehran22May2010
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18. H. Loghmani Khouzani, Noruzinia-M,Samareh Abolhasani. The correlation between E-Cadherin protein and estrogen receptor alpha C promoter methylation, in pathogenesis of Iranian patients with breast cancer.European Society of Human Genetics.Sweden.Gotenburg12Jun2010
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19. Noruzinia-M,g. Tarfiei.The role of methylation status of 5' UTR end of ROR2 gene in osteoblast differentiation of MSCs. European Society of Human Genetics.Sweden.Gotenburg12Jun2010
20. Javanmardi-M, Noruzinia-M,Eftekhari A, Fatehmanesh-P. Investigation the methylation status of promoter in JMJD1A of oligoazoospermia patients. European Human Genetics Conference .France.Nice16June2007
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21. Eftekhari A, Noruzinia-M, Sadeghizadeh, Majid. Failure to detect microduplication 22q11.2 among a group of Schizophrenia patients with Multiple Ligation Dependent Probe Amplification (MLPA). European Human Genetics Conference .France.Nice16June2007
22. Noruzinia-M, Keyhanee-M, Zolfaghari- Ghasem, Fatehmanesh-P, Rostami,A Shafeghati. Expansion in FMR1 5UTR CGG repeats plus recombination and mosaicism in a family with fragile X syndrome. SA Society for Human Genetics Conference.5April2009
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23. Noruzinia-M. MTFHR 5`UTR hypermethylation in testicular biopsy of Iranian patients with nonobstructive azoospermia: the role of epigenetics in male infertility. European Human Genetics Conference .France.Nice16June2007
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24. Shafeghati, Noruzinia-M. Evaluation of methylation in the 5`UTR promoter region of DBC2 gene in 50 breast cancer individuals and comparing with the normal controls in Iranian patients. European Society of Human Genetics.Sweden.Gotenburg12Jun2010
25. Noruzinia-M, Akbari-MT,Ghofrani-M, Sheikhha-H. Rett syndrom: genetic bases and the first molecular and prenatal diagnosis in Iran. The 1 international congress on Health Genomics and Biotechnology.Iran,Tehran24Novenber2007
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26. Noruzinia-M, Keihani-M, Karbasian-M. Testing for BRCA1 in Iran, Introduction of a new technique in BRCA1 analysis and cost effectiveness analysis. The 1 international congress on Health Genomics and Biotechnology.Iran,Tehran24November2007
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Full paper in Conferences :
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1. Noruzinia-M.Microdeletions and heart disease.Application of advanced molecular methods for diagnosis of human genetic diseases.Iran.Tehran16May2008
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2.Logghmani H,Karbasian M, Noruzinia-M,Rasaee MJ.Fateh Manesh P.Keihani M.The role of estrogen receptor alpha 5' UTR methylation in pathogenesis of Iranian patients with breast cancer. European Society of Human Genetics.Austria.Vienna23May2009
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3. Noruzinia-M. large deletions in BRCA1 and BRCA2 genes. تكنيك هاي نوين در ژنتيك مولكولي سيتوژنتيكي و سيتوژنتيك مولكولي و كاربرد آنها در تشخيص و پيش آگهي بيماري هاي ژنتيكي . Iran.Tehran22November2006
