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Mahdi Malekpour
Mahdi Malekpour
University of Texas
Verified email at vanderbilt.edu
Title
Cited by
Cited by
Year
Epigenetically deregulated microRNA-375 is involved in a positive feedback loop with estrogen receptor α in breast cancer cells
P de Souza Rocha Simonini, A Breiling, N Gupta, M Malekpour, M Youns, ...
Cancer research 70 (22), 9175-9184, 2010
3172010
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out
HPH Neumann, Z Erlic, CC Boedeker, LA Rybicki, M Robledo, ...
Cancer research 69 (8), 3650-3656, 2009
2142009
Head and neck paragangliomas: clinical and molecular genetic classification
C Offergeld, C Brase, S Yaremchuk, I Mader, HC Rischke, S Gläsker, ...
Clinics 67, 19-28, 2012
2062012
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome
Y Zhang, M Malekpour, N Al-Madani, K Kahrizi, M Zanganeh, M Mohseni, ...
Journal of medical genetics 44 (4), 233-240, 2007
1272007
GJB2 mutations: Passage through Iran
H Najmabadi, C Nishimura, K Kahrizi, Y Riazalhosseini, M Malekpour, ...
American Journal of Medical Genetics Part A 133 (2), 132-137, 2005
1112005
Analgesic choice in management of rib fractures: paravertebral block or epidural analgesia?
M Malekpour, A Hashmi, J Dove, D Torres, J Wild
Anesthesia & Analgesia 124 (6), 1906-1911, 2017
832017
Elucidating the spectrum of α-thalassemia mutations in Iran
V Hadavi, AH Taromchi, M Malekpour, B Gholami, HY Law, N Almadani, ...
haematologica 92 (7), 992-993, 2007
762007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus
NC Meyer, F Alasti, CJ Nishimura, P Imanirad, K Kahrizi, Y Riazalhosseini, ...
American Journal of Medical Genetics Part A 143 (14), 1623-1629, 2007
602007
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis
HJ Garringer, M Malekpour, F Esteghamat, SMJ Mortazavi, SI Davis, ...
American Journal of Physiology-Endocrinology and Metabolism 295 (4), E929-E937, 2008
572008
Two novel GALNT3 mutations in familial tumoral calcinosis
HJ Garringer, SMJ Mortazavi, F Esteghamat, M Malekpour, H Boztepe, ...
American Journal of Medical Genetics Part A 143 (20), 2390-2396, 2007
502007
Lateral supracerebellar infratentorial approach for microsurgical resection of large midline pineal region tumors: techniques to expand the operative corridor
C Kulwin, K Matsushima, M Malekpour, AA Cohen-Gadol
Journal of Neurosurgery 124 (1), 269-276, 2016
482016
Epilepsy surgery: challenges for developing countries
J Qiu
The Lancet Neurology 8 (5), 420-421, 2009
332009
High prevalence of low bone density in young Iranian healthy individuals
I Salehi, S Khazaeli, SR Najafizadeh, H Ashraf, M Malekpour
Clinical rheumatology 28, 173-177, 2009
332009
Murine membranous nephropathy: Immunization with α3 (IV) collagen fragment induces subepithelial immune complexes and FcγR-independent nephrotic syndrome
JJ Zhang, M Malekpour, W Luo, L Ge, F Olaru, XP Wang, M Bah, Y Sado, ...
The Journal of Immunology 188 (7), 3268-3277, 2012
322012
An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4
K Kahrizi, H Najmabadi, R Kariminejad, P Jamali, M Malekpour, ...
European journal of human genetics 17 (1), 125-128, 2009
292009
A novel DFNA5 mutation does not cause hearing loss in an Iranian family
L Van Laer, NC Meyer, M Malekpour, Y Riazalhosseini, M Moghannibashi, ...
Journal of human genetics 52 (6), 549-552, 2007
272007
Diagnostic values of GHSR DNA methylation pattern in breast cancer
SK Botla, AM Gholami, M Malekpour, EA Moskalev, M Fallah, P Jandaghi, ...
Breast cancer research and treatment 135, 705-713, 2012
262012
The effect of sarcopenia on outcomes in geriatric blunt trauma
M Malekpour, K Bridgham, K Jaap, R Erwin, K Widom, M Rapp, ...
The American Surgeon 83 (11), 1203-1208, 2017
242017
Utility of prophylactic antibiotics in nonoperative facial fractures
M Malekpour, K Bridgham, N Neuhaus, K Widom, M Rapp, D Leonard, ...
Journal of Craniofacial Surgery 27 (7), 1677-1680, 2016
212016
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome
Y Zhang, M Malekpour, N Al-Madani, K Kahrizi, M Zanganeh, M Mohseni, ...
Case Reports 2009, bcr0820080645, 2009
212009
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Articles 1–20