Publications

2012

1) Abbas Basiri, Nasser Shakhssalim, Massoud Houshmand, Amir H Kashi,
Mohaddeseh Azadvari, Banafsheh Golestan, Esmaeel Mohammadi Pargoo,
Hamid Pakmanesh. Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease (2012) Urol Res. 40(1):35-40. (IF: 1.172)

2) Falah M, Houshmand M, Mahmoudian S, Emamdjomeh H, Ghavami Y, Farhadi M. The Anticipation and Inheritance Pattern of c.487A>G Mutation in the GJB2 Gene. (2012) Arch Iran Med.; 15(1): 49 – 51. (IF: 0.87)

3) Alessandro Achilli, Anna Olivieri, Hovirag Lancioni, Baharak Hooshiar Kashani, Ugo A. Perego, Solomon G. Nergadze, Valeria Carossa, Marco Santagostino, Katia Cappelli, Michela Felicetti, Walid Al-Achkar, Cecilia Penedo, Ernie Bailey, Andrea Verini-Supplizi, Massoud Houshmand, Scott R. Woodward, Ornella Semino, Maurizio Silvestrelli, Elena Giulotto, Hans-Jürgen Bandelt, and Antonio Torroni. Mitochondrial Genomes Reveal That at Least 17 Matrilineal Lineages from Wild Horses Underwent Domestication (2012) Accepted in PNAS. (IF: 9.77)

4) Anders G. Holst; Siamak Saber; Massoud Houshmand; Elena V. Zaklyazminskaya; Yinman Wang; HenrikKjærulf Jensen; Lena Refsgaard; StigHaunsø; JesperHastrup Svendsen; Morten S. Olesen; Jacob Tfelt-Hansen. Sodium current and Potassium Transient Outward Current Genes in Brugada Syndrome: Screening and Bioinformatics (2012) Accept for publication in Canadian Journal of Cardiology (IF: 2.224)

5) Maria Pala, Anna Olivieri, Alessandro Achilli, Matteo Accetturo,Ene Metspalu, Kristiina Tambets, Baharak Hooshiar Kashani, Ugo A. Perego,Valeria Carossa, Francesca Gandini, Joana B. Pereira, Sergei Rychkov, Oksana Naumova, Pedro Soares, Nadia Al-Zahery, Valerio Carelli, Massoud Houshmand, Jiři Hatina, Vincent Macaulay,1Luísa Pereira, Scott R. Woodward, Douglas Baird, Ornella Semino, Richard Villems, Antonio Torroni, and Martin B. Richards. Mitochondrial DNA signals of Late Glacial re-colonisation of Europe from Near Eastern refugia (2012) Submit for publication in The American Journal of Human Genetics(IF: 11.68 )

6) Safinejad K, Darbouy M, Kalantar SM, Zeinali S, Mirfakhraie R, Yadegar L, Houshmand M. The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques. (2012) Accepted in J Assist Reprod Genet. (IF: 1.253)

7) Piryaei F, Houshmand M, Dadgar S, Aryani O, Sohili H. Association of the Mitochondrial ATPase 6/8 and tRNALys Genes Mutations with Autism in Iranian Patients (2012) accept for publication in Yakhteh. (IF: 0.442)

8 ) Didari E, Rezvani Z, Arasteh A, Ghodsinejad V, Houshmand M. Spectrum the three LHON primary mutations in Iranian patients with Leber’s hereditary optic neuropathy (2012) accept for publication in Iranian Journal of Public Health. (IF: 0.321)

9) Aryan H, Aryani O, Houshmand M. Novel mutation in Iranian Tay-Sachs Patient. (2012) accept for publication in Iranian Journal of Public Health.(IF: 0.321)

10) Esmaeel  Mohammadi Pargoo , Omid Aryani , Seyyed Hassan Tonekaboni , Parichehr Yaghmaei , Behnam Kamalidehghan , Massoud Houshmand. A novel mutation in the GDAP1 associated with Charcot-Marie-Tooth disease in an Iranian family (2012) accept for publication in Iranian Journal of Child Neurology.

11) Siiri Rootsi, Natalie M. Myres, Alice A. Lin, Mari Järve, Roy J. King, Ildus Kutuev, Vicente M. Cabrera, Elza K. Khusnutdinova, Kärt Varendi, Hovhannes Sahakyan, Doron Behar, Rita Khusainova, Oleg Balanovsky, Elena Balanovska, Pavao Rudan, Levon Yepiskoposyan, Ardeshir Bahmanimehr, Shirin Farjadian, Alena Kushniarevich, Rene J. Herrera, Viola Grugni, Vincenza Battaglia, Carmela Nici, Francesca Crobu, Sena Karacanak, Massoud Houshmand, Mohammad H. Sanati, Baharak Hooshiar Kashani, Draga Toncheva, Antonella Lisa, Ornella Semino, Jacques Chiaroni, Julie Di Cristofaro, Richard Villems, Toomas Kivisild, and Peter A. Underhill . Distinguishing co-ancestries of European and Caucasian human Y-chromosomes within haplogroup G (2012) Submit for publication in European Journal of Human Genetics (IF: 4.38 )

12) Naseroleslami M, Parivar K, Sanjarian S, Aryani O, Houshmand M. Study of FRDA gene in suspect Friedreich Ataxia patients. (2012) Med Sci J IAU , Vol 21:4, 275-280

13) Leila Akbari, Parisa Azadfar, Samira Sheibaninia, Maryam Nourozian, Farhad Asarzadegan, Massoud Houshmand. Investigation of hot spot region of PSNa and PSN2 gene in Iranian eraly onset Alzheimer. (2012) Accepted for publication in Zah J Res Med Sci.

14) Viola Grugni; Vincenza Battaglia; Baharak Hooshiar Kashani; Silvia Parolo; Nadia Al-Zahery; Alessandro Achilli; Anna Olivieri; Francesca Gandini; Massoud Houshmand; Mohammad Hossein Sanati; Antonio Torroni; Ornella Semino. “Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians”(2012) PLOS One Vol 7, Issue 7; e41252 1-14 (IF: 4.41)

15) Al-Kashwan TA, Houshmand M, Al-Janabi A, Melconian AK, Al-Abbasi D, Al-Musawi MN, Rostami M, Yasseen AA. Specific-mutational patterns of p53 gene in bladder transitional cell carcinoma among a group of Iraqi patients exposed to war environmental hazards. (2012) BMC Res Notes. 2012 Aug 28;5:466. (IF: 1.63)

16) Dowlati MA, Derakhshandeh-Peykar P, Houshmand M, Farhadi M, Shojaei A, Bazzaz JT. Novel human mitochondrial tRNA(phe) mutation in a patient with hearing impairment: A case study. (2012) Accepted for publication in Mitochondrial DNA (IF: 1.48)

17) Hosseini Mojgan, Houshmand Massoud, Ebrahimi Ahmad. ERCC1 intron 1 was associated with breast cancer risk (2012) Arch Med Sci; 8, 4: 655-658 (IF: 1.24)

18) Nayereh Nouri, Narges Nouri, Omid Aryani, Behnam Kamalidehghan, Maryam Sedghi and Massoud Houshmand. A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease (2012) Iranian Biomedical Journal 16 (4): .(IF:0.031)

19) Hosseini M, Houshmand M, Ebrahimi A. RAD51 polymorphisms and breast cancer risk. Mol Biol Rep. (2012) Oct 13. (IF: 2.929)

20) Aryani O, Houshmand M, Fatehi F A novel PANK2 gene mutation in a Persian boy: The first report from Iran. (2012) Clin Neurol Neurosurg. pii: S0303-8467(12) (IF: 1.75)

21) Kamalidehghan B, Houshmand M, Kamalidehghan F, Jafarzadeh N, Azari S, Akmal SN, Rosli R. Establishment and characterisation of two human breast carcinoma cell lines by spontaneous immortalization: discordance between Estrogen (ER), progesterone (PR) and HER2/neu receptors of breast carcinoma tissues with derived cell lines. Cancer Cell Int. 2012 Oct 29;12(1):43. (IF: 1.97)

22) Azadfar P, Akbari L, Shibaninia S, Nourozian M, Asarzadegan F, Houshmand M. Investigation of hot spot exons in APP gene in Iranian patients with early onset Alzheimer disease. (2012) Accept for publication in Journal of Modern Genetic

23) Dowlati MA, Derakhshandeh-Peykar P, Houshmand M, Farhadi M, Shojaei A, Bazzaz JT. Novel nucleotide changes in mutational analysis in mitochondrial 12sRNA in patients with nonsyndromic and aminoglycoside-induced hearing loss. (2012) acceoted for publication in Mol Biol Rep. (IF: 2.92)

24) Behnam Kamalidehghan, Massoud Houshmand. Pitfalls for Common Mitochondrial DNA Deletion (ΔmtDNA4977) As a Biomarker of Cancer (2012) Accepted for publication in Archives of Medical Research (IF: 1.73)

25) Parvaneh Karimzadeh, Seyed Hassan Tonekaboni, Mahmoud Reza Ashrafi, Yousef Shafeghati, Alireza Rezayi, Shadab Salehpour, Mohammad Ghofrani, Mohammad Mehdi Taghdiri, Ali Rahmanifar, Talieh Zaman, Omid Aryani, Babak Najaf Shoar, Farideh Shiva, Alireza Tavasoli and Massoud Houshmand. Effects of Miglustat on Stabilization of Neurological Disorder in Niemann-Pick Disease Type C : Iranian Pediatric Case Series (2012) Journal of Child Neurology
(IF: 1.7.8)

2011

1) Seyed Mohammad Seyedhassani, Massoud Houshmand, Seyed Mehdi Kalantar, Abbas Aflatoonian, Glayol Modabber, Fatemeh Hadipour, Mohammad Hossein Falahzadeh. BAX Pro-apoptotic Gene Alterations in Repeated Pregnancy Loss. (2011) Arch Med Sci; 7, 1: 117-122 (IF: 1.199)

2) Hosseini M., Houshmand M., Ebrahimi A. MTHFR and breast cancer risk. (2011) Arch Med Sci; 7, 1: 134-137 (IF: 1.199)

3) Houshmand M, Montazeri M, Kuchekian N, Moohi F, Givtaj N, Zamani A. Is 8860 variation a rare polymorphism or associate as a secondary effect of HCM disease? (2011) Arch Med Sci; 7, 2: 242-246 (IF: 1.199)

4) Lashgary Z, Khodadadi A, Singh Y, Houshmand M, Mahjoubi F, Sharma P, Singh Sh, Seyedin M, Sirvastava A, Ataei M, Mohammadi Z, Rezaei M, Bamzai M, Sanati MH. T chromosome diversity among the Iranian religious group: A reservoir of genetic variation (2011) Annals of Human Biology; Vol. 38, No. 3: Pages 364-371 (IF: 1.064)

5) Houshmand M, Kasraei S, Etemad Ahari S, Moein M, Bahar MA, Zamani A. Investigation of tRNALys/Leu and ATPase 6/8 genes mutations in Iranian Ataxia Telangiectasia patients. (2011) Arch Med Sci; 7, 3: 523-527. (IF: 1.199)

6) Sepideh Safaei, Zahra Pourpak, Mostafa Moin, Massoud Houshmand. Novel Protocol to Identify Mutations in SCID Patients with IL7R and RAG1/2 Deficiency (2011) Iran J Allergy Asthma Immunol. 10(2):129-32 (IF: 0.98 )

7) Mirfakhraie R, Kalantar SM, Mirzajani F, Montazeri M, Salsabili N, Houshmand M, Hashemi-Gorji F, Pourmand G. A novel mutation in the transactivation-regulating domain of the androgen receptor in a patient with azoospermia. (2011) J Androl. 2011 Jul-Aug;32(4):367-70 (IF: 1.422)

8 ) Basiri A, Shakhssalim N, Houshmand M, Kashi AH, Azadvari M, Golestan B, Mohammadi Pargoo E, Pakmanesh H. Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease. (2011). Accept for publication Urol Res. (IF: 1.172)

9) Maryam Sadat Daneshpour, Ahmed Rebai, Massoud Houshmand, Suad Alfadhli, Sirous Zeinali, Mehdi Hedayati, Maryam Zarkesh, and Fereidoun Azizi. 8q24.3 and 11q25 chromosomal loci association with low HDL-C in metabolic syndrome (2011) Eur J Clin Invest.;41(10):1105-1112 (IF: 2.643)

10) Arman Ardalan, Cornelya Klütsch, Ai-bing Zhang, Metin Erdogan, Mathias Uhlén, Massoud Houshmand, Cafer Tepeli, Seyed Reza Miraei Ashtiani, Peter Savolainen. Indication of dog-wolf hybridization, but not independent domestication, in Southwest Asia (2011) Oppen access Journal of Ecology and Evolution. (1-13)

11) Mansoureh Akouchekian, Massoud Houshmand, Mohammad Hassan Hosseini Akbari, Behnam Kamalidehghan,Masoumeh Dehghan. Analysis of mitochondrial ND1 gene in human colorectal cancer (2011) JRMS; 16(1): 50-55

12) Mehdi Moghaddasi, Mansoureh Mamarabadi, Ahmad Ebrahimi, Seyed Hassan Tonekaboni, Sirous Zainali and Massoud Houshmand. Dravet Syndrome: A case report with a new missense substitution as 1274 Tyr > Asp (2011) J. Pediatrics Neurology.9: 115-118

13) S. Salehpour, F. Rohani, O. Aryani, M. Houshmand, F. Hashemzad, M. Rezvani Kashani, F. Mahvelati Shamsabadi, Z. Pournasisi. Effects of growth hormone on muscle strength, tone, and mobility of children with Prader-Willi syndrome (2011) Iran J Child Neurology Vol 5 No1 27-31

14) Masoumeh Falah, Massoud Houshmand, Susan Akbaroghli, Saeid Mahmodian, Yaser Ghavami, 1Mohammad Farhadi. Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation. (2011) Iranian Journal of Basic Medical Sciences Vol. 14, No. 3,  213-218

15) Farajieilanjegh, Abolfazl, Maryam Mobaraki, Yazdi, AmirReza; Seyedhassani, seyed Mohammad, O. Aryani; Houshmand, Massoud. Case Reports of TGM1 Mutations in Iranian Patients with Lamellar Ichthyosis (2011) Iran J Child Neurology Vol 5 No1 45-48

16) Malakoutian T, Asgari M, Houshmand M, Mohammadi R, Aryani O, Mohammadi Pargoo E, Ghods AJ. Recurrence of primary hyperoxaluria after kidney transplantation. (2011) Iran J Kidney Dis.5(6):429-33.

17) Heidari MM, Khatami M, Houshmand M, Mahmoudi E, Nafissi Sh. Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia (2011) IJCN 5 (4): 25-33

18 ) Ashrafi MR, Nikkhah A, Houshmand M, Aryani O. L-2-Hydroxyglutaric Aciduria is a Diagnostic Indicator of Leukodystrophy: A Case Report (2011) 5 (4): 37-38

19) Shejbaninya S, Azadfar P, Akbari L, Asarzadegan F, Houshmand M. New mutation in mitochondrial 22 tRNA genes in alzheimer patients. (2011) G.T.M (9) 2:33, pp 2367-2373

20) Mohammadi Poorgo E, Aryani O, Tonekaboni S.H, Yaghmaei P, Sadeghizadeh M, Houshmand M. Investigation of PMP 22 duplication in CMT patients by PCR-RFLP and MLPA methods. (2011) G.T.M (9) 2:33, pp 2379-2386

2010
1) Khatami M, Houshmand M, Sadeghizadeh M, Eftekharzadeh M, Heidari MM, Saber S, Banihashemi K, Scheiber-Mojdehkar B. .Accumulation of Mitochondrial Genome Variations in Persian LQTS Patients: A Possible Risk Factor? (2010) Cardiovasc Pathol;19(2):21-7. (IF: 1.626)

2) Isaian A, Bogdanova NV, Houshmand M, Movahadi M, Agamohammadi A, Rezaei N, Atarod L, Sadeghi-Shabestari M, Tonekaboni SH, Chavoshzadeh Z, Hassani SM, Mirfakhrai R, Cheraghi T, Kalantari N, Ataei M, Dork-Bousset T, Sanati MH. BAK, BAX, and NBK/BIK Proapoptotic Gene Alterations in Iranian Patients with Ataxia Telangiectasia. (2010) J Clin Immunol.;30(1):132-7 (IF: 3.583)

3) Seyed Mohammad Seyedhassani, Massoud Houshmand, Seyed Mehdi Kalantar, Abbas Aflatoonian, Glayol Modabber, Fatemeh Hadipour, Mohammad Hossein Falahzadeh. The point mutations of mitochondrial tRNA theronine and praline in idiopathic repeated pregnancy loss. (2010) IJRM Vol. 8 No 1 45-50 (IF: 0.183)

4) Seyedhassani Seyed Mohammad, Houshmand Massoud, Kalantar Seyed Mehdi, Modabber Glayol, Aflatoonian Abbas. No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss (2010) Journal of Assisted Reproduction and Genetics, V 27, Nr 11, 641-648. (IF: 1.359)

5) Ahmad Ebrahimi; Massoud Houshmand, Seyed Hassan Tonekaboni, Mohammd Sadegh Fallah Mahboob Passand, Sirous Zainali, Mehdi Moghadasi. Two Novel Mutations in SCN1A Gene in Iranian Patient with Epilepsy. (2010) Archives of Medical Research 41:207-214 (IF: 1.884)

6) Reza Mirfakhraie, Farzaneh Mirzajani, Sayed Mahdi Kalantar , Maryam Montazeri, Nasser Salsabili, Gholam Reza Pourmand, and Massoud Houshmand. High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermia
(2010) Indian J Med Res. 132:265-70 (IF: 1.516)
7) Shakhssalim N, Kazemi B, Basiri A, Houshmand M, Pakmanesh H, Golestan B, Eilanjegh AF, Kashi AH, Kilani M, Azadvari M. Association between calcium-sensing receptor gene polymorphisms and recurrent calcium kidney stone disease: a comprehensive gene analysis. (2010) Scand J Urol Nephrol. 44(6):406-12 (IF: 0.88 )

8 ) Ataei M, Zare Mehrjerdi M.A, Yazdi A.R, Zamani A, Faraje Ilanjegh A,   Houshmand M. Mutations in Corneal carbohydrate Sulfotransferase 6 gene (CHST6) among Iranian Macular corneal dystrophy (MCD) Patients: report of 7 patients from Iran. (2010)  IJCN. l4: 2; 55-58

9) M.S Daneshpour, S Alfadhli, M Houshmand, S Zeinali, M Hedayati, M Zarkesh, and F Azizi. Allele frequency distribution for D11S1304, D11S1998 and D11S934 and metabolic syndrome in TLGS. (2010) European Journal of Lipid Science and Technology. Volume 112, Issue 12,  1302–1307 (IF: 1.831)

10) Fakhraz MR, Tavalaei M, Houshmand M, Sajadian A. Role of mitochondrial markers in crime detection. (2010) Journal of Military Medicine. 12 (3) :161-165

11) Sobhani S, Ghaffarpour M, Mostakhdemin Hosseini Z, Kamali F, Nour Mohammadi Z, Houshmand M. The prevalence of common mutation frequency in K-ras codons 12, 13 in Iranian Colorectal Cancer patients (2010) Genetic in the 3rd millennium; Vol 8; No 2, 2011-2018.

12) Sanjarian S, Nour Mohammadi Z, Naser Eslami M, Aryani O, Houshmand M. Clinical anf Molecular investigation of Friedreich Ataxia in Iranian patients (2010) Genetic in the 3rd millennium; Vol 8; No 2, 2023-2027.

13)  A. Aleyasin, M Ghazanfari, M Houshmand. Leber Hereditary Optic Neuropathy: Do Folate Pathway Gene Alterations Influence the Expression of Mitochondrial DNA Mutation? (2010) Iranian J Publ Health, Vol. 39, No.3, pp. 53-60 (IF: 0.341)

2009
1) Safaei S, Houshmand M, Banoei MM, Panahi MS, Nafisi S, Parivar K, Rostami M, Shariati P. Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias. (2009) Neurodegener Dis.;6(1-2):16-22. (IF: 1.044)

2) Mansoureh Akouchekian, Massoud Houshmand, Simin Hemati, Mehdi Shafa. Appearance of large scale mitochondrial DNA deletion in human colorectal cancer, (2009) Dis Colon Rectum 2009; 52: 526Y530 (IF:2.536)
.
3) Mansoureh Akouchekian, Massoud Houshmand, Simin Hemati, Mohammad Ansaripour, Mehdi Shafa. High Rate of Mutation in Mitochondrial DNA Displacement Loop Region in Human Colorectal Cancer,(2009) Dis Colon Rectum. 52(3):526-30. (IF:2.536)

4) Birgani SA, Salehi Z, Houshmand M, Mohamadi MJ, Promehr LA, Mozafarzadeh Z. Novel mutations of CHST6 in Iranian patients with macular corneal dystrophy. (2009) Mol Vis.;15:373-7. (IF: 2.33)

5) Hosseini M., Houshmand M., Ebrahimi A. Breast cancer risk not only was not associated with CYP17/ A2 allele But also was related to A1 allele (2009) Archives of Medical Science.Vol 5 Issue 1; 103-106 (IF: 1.199)

6) R. Shahsavari, A. Ehsani-Zonouz, M. Houshmand, A. Salehnia, G. Ahangari and M. Firoozrai   Plasma Glucose Lowering Effect of the Wild Satureja khuzestanica Jamzad Essential Oil in Diabetic Rats: Role of Decreased Gluconeogenesis (2009) Pakistan Journal of Biological Sciences, Volume: 12; Issue: 2; 140-145

7) Heidari MM, Houshmand M, Hosseinkhani S, Nafissi S, Khatami M. Complex I and ATP content deficiency in lymphocytes from Friedreich’s ataxia. (2009) Can J Neurol Sci.;36(1):26-31. (IF: 1.04)

8 ) Mohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, Shahriar Nafissi, Barbara Scheiber-Mojdehkar, Mehri Khatami. A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia, (2009) Cell Mol Neurobiol. ;29(2):225-33. (IF: 2.107)

9) Rasi H, Houshmand M, Hashemi M, Majidzadeh AK, Hosseini Akbari MH.
Investigation of Mitochondrial common deletion and BRAC mutations for detection of familial breast cancers in archival breast cancer materials. (2009) IJCP Vol 2, No 2, 77-83. (IF: 2.245)

10) Jamali Sh, Bahar M.A, Houshmand M. Detection of Bla gene among imipenem – resistant Pseudomonas aeruginosa Isolated from Burn wounds from Tehran Shahid Motahari Hospital. (2009) Microbiology Knowledge Vol 1 No 1 19-27

11) Daneshpour MS, Alfadhli S, Houshmand M, Zeinali S, Hedayati M, Zarkesh M, Momenan AA, Azizi F. Allele frequency distribution data for D8S1132, D8S1779, D8S514, and D8S1743 in four ethnic groups in relation to metabolic syndrome: Tehran Lipid and Glucose Study. (2009) Biochem Genet. 2009 Oct;47(9-10):680-7. (IF: 0,887)

12) Ghabaee M, Bayati A, Amri Saroukolaei S, Sahraian MA, Sanaati MH, Karimi P, Houshmand M, Sadeghian H, Hashemi Chelavi L. Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) Haplotypes in Iranian Patients with Multiple Sclerosis. (2009)  Cell Mol Neurobiol. ;29(1):109-14. (IF: 2.107)

13) Ghabaee M, Omranisikaroudi M, Amrisaroukolaei S, Meysamie A, Sahraian MA, Bayati A, Sanati MH, Houshmand M, Sadeghian H, Vajihazaman K. Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations. (2009) Cell Mol Neurobiol. ;29(3):341-6. (IF: 2.107)

14) Narooie-Nejad M, Chitsazian F, Khoramian Tusi B, Mousavi F, Houshmand M, Rohani MR, Hosseinipour AS, Rismanchian A, Elahi E. Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist.. (2009) Mol Vis. 22;15:2155-61. (IF: 2.33)

15) Fereshteh Ghasemi and Massoud Houshmand . Cystic Fibrosis: Genetic view (2009). Genetic in 3rd millennium. Volume 7, Number 1 1604-7

2008
1) Achilli A, Olivieri A, Pellecchia M, Uboldi C, Colli L, Al-Zahery N, Accetturo M, Pala M, Kashani BH, Perego UA, Battaglia V, Fornarino S, Kalamati J, Houshmand M, Negrini R, Semino O, Richards M, Macaulay V, Ferretti L, Bandelt HJ, Ajmone-Marsan P, Torroni A. Mitochondrial genomes of extinct aurochs survive in domestic cattle. (2008 ) Curr Biol. 26;18(4):R157-8. (IF: 11.571)

2) Banihashemi Kambiz, Houshmand Massoud, Rostami Maryam, Khosroheidari Mahdieh. Molecular genetics of fetal organogenesis in the Quran: Tracking a modern concept in an orginal religious text (2008 ) Pak J Med Sci , Vol. 24 No. 1 163-166

3) Ali Mohammad Ahadi, Majid Sadeghizadeh, Massoud Houshmand, Kurosh Gharagoozli, Mehdi Shafa Shariat panahi. An A8296G mutation in mitochondrial tRNALys gene in a patient with epilepsy; “a disease- causing mutation” or rare polymorphism?!. (2008 ) Neurol Neurochir Pol (0) 42: 263-266.  (IF: 0.597)

4) Mohammad Mehdi Banoei, Morteza Hashemzadeh Chaleshtori, Mohammad Hossein Sanati, Parvin Shariati, Massoud Houshmand, Tayebeh Majidizadeh, Niloofar Jahangir Soltani, and Massoud Golalipour. Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region (2008 ) Human Biology, v. 80, no. 1, pp. 73–81. (IF: 0.87)

5)  Sadaf Kasraie, Massoud Houshmand, Mohammad Mehdi Banoei, Mehdi Shafa Shariat Panahi,  Solmaz Etemad Ahari, Mostafa Moin,  Mohammad Bahar,  Parvin Shariati. Investigation of tRNALeu/Lys and ATPase 6 Genes Mutations in Huntington’s Disease (2008 ) Cell Mol Neurobiol  DOI 10.1007/s10571-008-9261-6 (IF: 2.107)

6) Rassi H, Houshmand M, Hashemi M, Majidzadeh K, Akbari MH, Panahi MS.
Application of multiplex PCR with histopathologic features for detection of familial breast cancer in formalin-fixed, paraffin-embedded histologic specimens.
Tsitol Genet. (2008 );42(2):55-62.

7) Ghorashi, S. A., Fatemi, S. M.1, Amini, F, Houshmand, M., Salehi Tabar, R. and Hazaie, K. Phylogenetic analysis of anemone fishes of the Persian Gulf using mtDNA sequences. African Journal of Biotechnology (2008 ) Vol. 7 (12), pp. 2074-2080

8 ) Heidari MM, Houshmand M, Hosseinkhani S, Nafissi S, Scheiber-Mojdehkar B, Khatami M. Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients. Neurol Sci. (2008 ) Dec;29(6):489-93. (IF: 1.12)

9 ) Mahzad Akbarpour, Masoud Houshmand, Ali Ghorashi, Hossein Hayatgheybi, Screening for FecGH Mutation of Growth Differentiation Factor 9 Gene in Iranian Ghezel Sheep Population (2008 ) INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY, Volume: 2, Number: 3, 139-144.

10) Hossein R, Houshmand M.  Diagnostic algorithm for identification of individuals with hereditary predisposition to breast cancer. Lik Sprava. 2008 Jan-Feb;(1-2):103-8. Review.

11) Daneshpour MS, Hedayati M, Eshraghi P, Houshmand M and Azizi F. Asociation of
apolipoprotein E gene polymorphism and lipid level in an Iranian population: Tehran Lipid and Glucose study. (2008 ) Iranian j of diabet and lipid 2008;7:399-405.

2007
1) Houshmand M, Banoei MM, Tabarsi P, Panahi MS, Kashani BH, Ebrahimi G, Zargar L, Farnia P, Morris MW, Mansouri D, Velayati AA, Mirsaeidi MS. Do mitochondrial DNA haplogroups play a role in susceptibility to tuberculosis? Respirology. 2007 Nov;12(6):823-7. (IF: 1.853)

2) Banoei MM, Houshmand M, Panahi MS, Shariati P, Rostami M, Manshadi MD, Majidizadeh T. Huntington’s Disease and Mitochondrial DNA Deletions: Event or Regular Mechanism for Mutant Huntingtin Protein and CAG Repeats Expansion?!Cell Mol Neurobiol. 2007: 27:867–875
(IF: 2.107)

3) Fesahat F, Houshmand M, Panahi MS, Gharagozli K, Mirzajani F. Do haplogroups h and u act to increase the penetrance of Alzheimer’s disease? (2007)Cell Mol Neurobiol.;27(3):329-34 (IF: 2.107)

4) Ahari SE, Houshmand M, Panahi MS, Kasraie S, Moin M, Bahar MA. Investigation on Mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients. (2007) Cell Mol Neurobiol. 27(6):695-700 (IF: 2.107)

5) Houshmand M, Panahi MS, Fesahat F, Gharagozli K. Lack of association between mitochondrial A4336G/ haplogroup and Parkinson’s disease. (2007) J. Chin. Clin. Med. Vol 21. No 51,

6) Bayat B, Houshmand M, Sanati MH, Moin M, Panahi MS. Aleyasin SA, Farhoodi A, Eesaian A. Use of D11S2179 and D11S1343 Markers as Informatiove Markers for Prenatal Diagnosis in Iranian Ataxia Telengiectasia Patients. (2007) Arch. Med. Res. 38: 803e805 (IF: 1.884)

7) Solmaz Etemad Ahari, Massoud Houshmand, Sadaf Kasraie, Mostafa Moin, Mohammad Ali Bahar, Mehdi Shafa Shariat Panahi, Ghasem Ahangari.  Investigation for point mutations on different parts of Mitochondrial DNA, relating to adjunct of pathogenesis of FA, on 20 Iranian patients with Friedreich’s ataxia.(2007) IJCN vol. 5.

8 ) Sara pouranvari, Mehrdad Nourosinia, Aliakbar Zinalou, SaeedREza Ghafari, Massoud Houshmand, Saeed Keivani. Detection of 22q11.2 micro deletions by semi quantitative multiplex PCR (2007) Modares Journal of Medical Sciences, Vol 10 No 2 71-77

2006

1) Shafa Shariat Panahi M, Houshmand M, Tabassi AR Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors. (2006) Arch Med Res.;37(8 ):1028-33 (IF: 1.884)

2) Kamalidehghan B, Houshmand M, Panahi MS, Abbaszadegan MR, Ismail P, Shiroudi MB. Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer.( 2006)Arch Med Res.;37(7):848-53. (IF: 1.884)

3) Kamalidehghan B, Houshmand M, Ismail P, Panahi MS, Akbari MH. Delta mtDNA4977 is more common in non-tumoral cells from gastric cancer sample. (2006) Arch Med Res.;37(6):730-5. (IF: 1.884)

4) Houshmand M, Shafa Shariat Panahi M, Hosseini BN, Dorraj Gh, Tabassi AR, Investigation on mtDNA deletion and Twinkle gene mutation (G1423C) in Iranian CPEO patients. (2006) Neurology India. Vol 54- Issue 2 178-182 (IF: 0.733)

5) F. Mirzajani, R. Mirfakhraie, F. Nabati, N. Naghibzadeh Tabatabaei, E. Talachian, M. Houshmand. “The first study of galactose-1phosphate uridyl transferase mutations in Iranian gactosemia patients.” (2006) Clin Biochem;39(7):697-9 (IF: 2.019)

6) Kumleh H.H, Houshmand M, Shafa M Riazi Gh-H,  Sanati M-H, Gharagozli K,.Ghabaee, M    Mitochondrial d-loop variation in Persian multiple sclerosis patients: k and a haplogroups as a risk  factor!!(2006) Cell Mol Neurobiol.;26(2):119-25 (IF: 1.884)

7) Houshmand M, Mahmoudi T, Shafa M, Saber S, Seyedena Y, Ataie M. Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene. (2006) Braz J Med Biol Res;39(6):725-30 (IF: 1.075)

8 ) Elahi E, Kalhor R, Banihosseini SS, Torabi N, Pour-Jafari H, Houshmand M, Amini SS, Ramezani A, Loeys B. Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.(2006) J Invest Dermatol.;126(7):1506-9. (IF: 5.543)

9) Houshmand M, Shafa M, Nafisi SH, Soltanzadeh A, Alkandari F.M. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich ataxia. (2006) Mitochondrion; 6(2):87-93 (IF: 4.145)

10) Kumleh H.H, Riazi Gh-H, Houshmand M, Sanati M-H, Gharagozli K, Shafa M.  Complex I deficiency in Persian multiple sclerosis patients. (2006) J. Neurol. Sci. 243: 65-69 (IF: 2.324)

11) Mirzaei M, Salami F, Rahmaniani F, Jafari A, Houshmand M, Shafa M. Correlation between CK and LDH changes and mtDNA deletion in Blood leukocytes after exhaustive aerobic exercise, (2006) Olampic, Vol 13, No 4; 73-81

12) Mehdi Shafa Shariat Panahi, Massoud Houshmand.”Friedreich’s Ataxia Disease” (2006) Genetic in the third millennium.; 2(3):367-370

13) M Houshmand, MH Sanati, B Hooshiar Kashani, M Shafa Shariat Panahi, Y Eisaian, M. Moien, M Farhoudi. Investigation of mitochondrial deletions and Haplogroups in Iranian Ataxia-Telangiectasia patients. (2006) I. J. B., Vol. 4, No. 1, 64-68

14) MH Salehi, M Houshmand, A Bidmeshkipour, M Shafa shariat panahi. Low Sperm Motility due to mitochondrial DNA multiple deletions. (2006) J. Ch. Clin. Med; Vol. 1, No. 4, 181-185

15) Fawziah M.A Mohammed, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Laila Bastaki, Kamal Naguib, Baharak Houshyar, Anna Olivieri, Antonio Torroni.
Mitochondrial DNA haplogroups in Kuwaiti infertile males.(2006) Korean Journal of Genetics; Vol. 28, No. 3, 261-267 (IF: 0.308 )

16) Mirsaeidi SM, Houshmand M, Tabarsi P, Banoei MM, Zargari L, Amiri M, Mansouri SD, Sanati MH, Masjedi MR.. Lack of association between interferon-gamma receptor-1 polymorphism and pulmonary TB in Iranian population sample. (2006) J Infect.; Vol. 52, 374-377.
2005

1) Houshmand M, M-H Sanati, F. Babrzadeh, A Ardalan, M Teimori, M Vakilian, M  Akuchekian, D Farhud and J Lotfi.  Population scanning for association of mitochondrial haplogroup BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients. (2005) Multiple Sclerosis Volume 11 Issue 6,  728-730 (IF: 3.279)

2) Bagher Larijani, Massoud Houshmand, Ghamar Soltan Dorraj, Farzaneh Darvishzadeh. Prevalence of mtDNA Mutation in Type II Diabetes Mellitus. I. (2005) J. Diab and Lip. Dis. Vol 4. No. 3.

3) Jafari A, Hosseinpourfaizi MA, Houshmand M, Ravasi AA. Effect of aerobic exercise training on mtDNA deletion in soleus muscle of trained and untrained Wistar rats. (2005 Aug ) Br J Sports Med.;39(8 ):517-20. (IF: 2.547)

4) Montazeri M, Houshmand M, Shafa Shariat Panahi M, Givtaj N, Nohi F, Sanati M-H, Zaklyazminskaya E. V. Polymorphism in non-coding Region of Human Mitochondrial DNA in 31 Persian  HCM Patients.(2005) I. J. B..Vol 3, No. 3. 157-162

5) Mirzaei M, Salami F, Rahmaniani F, Jafari A, Houshmand M, Shafa M.  Correlation between lactate and mtDNA deletion in Blood leukocytes after exhaustive aerobic exercise, (2005) Harkat, Vol 25, 83-99.

6) Dorraj Ghamarsoltan, Houshmand Massoud, Larijani Bagher, Ahmad Majd, Bibinasim Hosseini, Maryam Montazeri, Mehdi Shafa Shariat Panahi, Lack of association of mitochondrial A3243G tRNA Leu mutation in Iranian patients with type II diabetes, (2005) I. J. B, , Vol. 3, No. 4, 243-247.
2004

1) Jalalirad M, Houshmand M, Mirfakhraie R, Goharbari MH, Mirzajani F.
First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.(2004) J Trop Pediatr.;50(6):359-61 (IF: 1.112)

2) Valeh Hadavi, Mohammad H Sanati, Daroush Farhud, Masoud Hushmand, Morteza Hashemzadeh Chaleshtori, Seyed Masoud Nabavi, Masoud Younesian and Maziar Seyedian Association of apolipoprotein E polymorphism with susceptibility to multiple sclerosis. (2004) The IJB Journal, Vol. 2, No. 1,  12 pp, 1-12

3) Massoud Houshmand, Mohammad-Hossein Sanati, Mehrdad Vakilian, Mansoureh Akuchekian, Farbod Babrzadeh, Massoud Teimori and Daroush Farhud  Investigation of the mitochondrial haplogroups M, BM, N, J, K and their frequencies in five regions in Iran. (2004) The IJB Journal, Vol. 2, No. 1,  12 pp, 1-12

4) Houshmand M, Mitochondrial Disorders and Diagnosis (2004) Kyiv medical Academy for postgraduate education SHPYK, thirteenth edition, book 5; 333-339

5) Houshmand M, Sharifpanah F, Tabasi A, Sanati MH, Vakilian M, Lavasani SH, Joughehdoust S. Leber’s hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.(2004) Ann N Y Acad Sci.;1011:345-9. (IF: 2.67)

6) Houshmand M, Gardner A, Hallstrom T, Muntzing K, Oldfors A, Holme E.
Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood. (2004) Neuromuscul Disord.;14(3):195-201. (IF: 2.977)

7) Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
Lack of association between Leber’s hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran. (2004) Eur Neurol.;51(2):68-71. (IF: 2.51)

8 )  Hormozian F, Houshmand M, Sanati M.H, Ghiasvand R, Banoie M.M. Molecular analysis of the (CAG)n repeat causing Huntingtonæs disease in 34 Iranian families.( 2004) I.J.H.G: 10;2 53-57.

2003

1) Abbaszadegan MR, Gholamin M, Tabatabaee A, Farid R, Houshmand M, Abbaszadegan M. Prevalence of human T-lymphotropic virus type 1 among blood donors from Mashhad, Iran. ( 2003)J Clin Microbiol.;41(6):2593-5. (IF: 4.162)

2) Massoud Houshmand, Mitochondrial DNA Mutations, Pathogenicity and Inheritance Iranian (2003) Journal of Biotechnology, Vol. 1, No. 1, 1-18

3) Alemohammad SA, Farhoud DD, Houshmand M, Sanati MH, Derakhshandeh-Peykar P, Imam SJ, Rahmani M. Distribution of Mitochondrial DNA Intergenic COII/tRNAlys 9 bp deletionin Iranian Population. Iranian (2003)J Publ Health, Vol 32, No 2, 1-5 (IF: 0.341)

2001

Sutovsky P, Motlik J, Neuber E, Pavlok A, Schatten G, Palecek J, Hyttel P, Adebayo OT, Adwan K, Alberio R, Bagis H, Bataineh Z, Bjerregaard B, Bodo S, Bryja V, Carrington M, Couf M, de la Fuente R, Diblik J, Esner M, Forejt J, Fulka J Jr, Geussova G, Gjorret JO, Libik M, Hampl A, Hassane MS, Houshmand M, Hozak P, Jezova M, Kania G, Kanka J, Kandil OM, Kishimoto T, Klima J, Kohoutek J, Kopska T, Kubelka M, Lapathitis G, Laurincik J, Lefevre B, Mihalik J, Novakova M, Oko R, Omelka R, Owiny D, Pachernik J, Pacholikova J, Peknicova J, Pesty A, Ponya Z, Preclikova H, Sloskova A, Svoboda P, Strejcek F, Toth S, Tepla O, Valdivia M, Vodicka P, Zudova D.
Accumulation of the proteolytic marker peptide ubiquitin in the trophoblast of mammalian blastocysts.( 2001) Cloning Stem Cells.;3(3):157-61.(IF: 2.34)

1999

1) Houshmand M, Lindberg C, Moslemi AR, Oldfors A, Holme E. A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspring.    (1999) Hum Mutat.;13(3):203-9. (IF: 6887)

1997

1) Houshmand M, Holme E, Hanson C, Wennerholm UB, Hamberger L. Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection? (1997) J Assist Reprod Genet. Apr;14(4):223-7. (IF: 1.359)

1996

1) Houshmand M, Larsson NG, Oldfors A, Tulinius M, Holme E. Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A –> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gene. (1996) Hum Genet.;97(3):269-73. (IF: 4.523)

1995

1) Tulinius MH, Houshmand M, Larsson NG, Holme E, Oldfors A, Holmberg E, Wahlstrom J. De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring.(1995) Hum Genet.;96(3):290-4. (IF: 4.523)

2) Tulinius MH, Oldfors A, Holme E, Larsson NG, Houshmand M, Fahleson P, Sigstrom L, Kristiansson B. Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions. (1995) Eur J Pediatr.;154(1):35-42. (IF: 1.634)

1994

1) Houshmand M, Larsson NG, Holme E, Oldfors A, Tulinius MH, Andersen O.
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. (1994) Biochim Biophys Acta. 12;1226(1):49-55. (IF: 4.356)

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