Mohammad Hossein Sanati
Mohammad Hossein Sanati
Professor of medical genetic, National Institute for Genetic Engineering and Biotechnology: Tehran, Tehran, Iran
Verified email at nigeb.ac.ir
TitleCited byYear
Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia
M Pala, A Olivieri, A Achilli, M Accetturo, E Metspalu, M Reidla, E Tamm, ...
The American journal of human genetics 90 (5), 915-924, 2012
1592012
Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus
S Rootsi, NM Myres, AA Lin, M Järve, RJ King, I Kutuev, VM Cabrera, ...
European Journal of Human Genetics 20 (12), 1275-1282, 2012
962012
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family
F Alasti, A Sadeghi, MH Sanati, M Farhadi, E Stollar, T Somers, ...
The American Journal of Human Genetics 82 (4), 982-991, 2008
822008
Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians
V Grugni, V Battaglia, BH Kashani, S Parolo, N Al-Zahery, A Achilli, ...
PloS one 7 (7), 2012
802012
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes
F Chitsazian, BK Tusi, E Elahi, HA Saroei, MH Sanati, S Yazdani, ...
The Journal of Molecular Diagnostics 9 (3), 382-393, 2007
692007
Heat-Induced Production of Human Growth Hormone by High Cell Density Cultivation of Recombinant Escherichia Coli
F Tabandeh, SA Shojaosadati, A Zomorodipour, M Khodabandeh, ...
Biotechnology letters 26 (3), 245-250, 2004
662004
MiRNA-375 promotes beta pancreatic differentiation in human induced pluripotent stem (hiPS) cells
R Lahmy, M Soleimani, MH Sanati, M Behmanesh, F Kouhkan, N Mobarra
Molecular biology reports 41 (4), 2055-2066, 2014
652014
Three major glucose‐6‐phosphate dehydrogenase‐deficient polymorphic variants identified in Mazandaran state of Iran
SA Mesbah‐Namin, MH Sanati, A Mowjoodi, PJ Mason, TJ Vulliamy, ...
British journal of haematology 117 (3), 763-764, 2002
572002
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11
N Hilgert, F Alasti, N Dieltjens, B Pawlik, B Wollnik, O Uyguner, ...
Clinical genetics 74 (3), 223-232, 2008
562008
Distinctive audiometric profile associated with DFNB21 alleles of TECTA
S Naz, F Alasti, A Mowjoodi, S Riazuddin, MH Sanati, TB Friedman, ...
Journal of medical genetics 40 (5), 360-363, 2003
552003
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations
A Amiri-Yekta, C Coutton, ZE Kherraf, T Karaouzène, P Le Tanno, ...
Human Reproduction, 1-9, 2016
522016
Contributions of MYOC and CYP1B1 mutations to JOAG
B Bayat, S Yazdani, A Alavi, M Chiani, F Chitsazian, BK Tusi, F Suri, ...
Molecular vision 14, 508, 2008
512008
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families
F Alasti, MH Sanati, AH Behrouzifard, A Sadeghi, APM De Brouwer, ...
International journal of pediatric otorhinolaryngology 72 (2), 249-255, 2008
492008
A thermodynamic study on the interaction between magnesium ion and human growth hormone
AA Saboury, MS Atri, MH Sanati, AA Moosavi‐Movahedi, GH Hakimelahi, ...
Biopolymers: Original Research on Biomolecules 81 (2), 120-126, 2006
492006
Effects of calcium binding on the structure and stability of human growth hormone
AA Saboury, MS Atri, MH Sanati, AA Moosavi-Movahedi, K Haghbeen
International journal of biological macromolecules 36 (5), 305-309, 2005
482005
Application of a simple calorimetric data analysis on the binding study of calcium ions by human growth hormone
A Saboury, M Atri, M Sanati, M Sadeghi
Journal of thermal analysis and calorimetry 83 (1), 175-179, 2006
422006
Molecular identification of mutations in G6PD gene in patients with favism in Iran
MR Noori-Daloii, L Najafi, SM Ganji, Z Hajebrahimi, MH Sanati
Journal of physiology and biochemistry 60 (4), 273, 2004
422004
Complex I deficiency in Persian multiple sclerosis patients
HH Kumleh, GH Riazi, M Houshmand, MH Sanati, K Gharagozli, M Shafa
Journal of the neurological sciences 243 (1-2), 65-69, 2006
382006
A haplotype framework for cystic fibrosis mutations in Iran
E Elahi, A Khodadad, I Kupershmidt, F Ghasemi, B Alinasab, ...
The Journal of Molecular Diagnostics 8 (1), 119-127, 2006
382006
A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north …
MR Noori-Daloii, Z Hajebrahimi, L Najafi, SA Mesbah-Namin, A Mowjoodi, ...
Clinical biochemistry 40 (9-10), 699-704, 2007
352007
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