| Sanfilippo syndrome: Overall review F Andrade, L Aldámiz‐Echevarría, M Llarena, ML Couce Pediatrics International 57 (3), 331-338, 2015 | 133 | 2015 |
| A double-blind, placebo-controlled comparison of letrozole to oxandrolone effects upon growth and puberty of children with constitutional delay of puberty and idiopathic short … S Salehpour, P Alipour, M Razzaghy-Azar, L Ardeshirpour, A Shamshiri, ... Hormone research in paediatrics 74 (6), 428-435, 2010 | 75 | 2010 |
| FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome B Felder, B Radlwimmer, A Benner, A Mincheva, G Tödt, KS Beyer, ... American Journal of Medical Genetics Part A 149 (5), 952-959, 2009 | 55 | 2009 |
| Cyclic pamidronate therapy in children with osteogenesis imperfecta S Salehpour, S Tavakkoli J Pediatr Endocrinol Metab 23 (1-2), 73-80, 2010 | 50 | 2010 |
| Biodegradation and ecotoxicological impact of cellulose nanocomposites in municipal solid waste composting S Salehpour, M Jonoobi, M Ahmadzadeh, V Siracusa, F Rafieian, ... International journal of biological macromolecules 111, 264-270, 2018 | 42 | 2018 |
| Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication L Bernardini, M Castori, A Capalbo, V Mokini, R Mingarelli, P Simi, ... American Journal of Medical Genetics Part A 143 (24), 2937-2943, 2007 | 39 | 2007 |
| Craniosynostosis: another feature of the 22q11. 2 deletion syndrome DM McDonald‐McGinn, KW Gripp, RE Kirschner, MK Maisenbacher, ... American Journal of Medical Genetics Part A 136 (4), 358-362, 2005 | 39 | 2005 |
| Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis A Kariminejad, R Kariminejad, A Tzschach, R Ullmann, A Ahmed, ... American Journal of Medical Genetics Part A 149 (7), 1544-1549, 2009 | 37 | 2009 |
| Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population T Shirzadeh, AH Saeidian, H Bagherian, S Salehpour, A Setoodeh, ... Journal of inherited metabolic disease 41, 1159-1167, 2018 | 36 | 2018 |
| Micronutrient status in obese patients: A narrative review IA Lapik, AV Galchenko, KM Gapparova Obesity Medicine 18, 100224, 2020 | 35 | 2020 |
| Etiology of precocious puberty, 10 years study in Endocrine Research Center (Firouzgar), Tehran F Rohani, S Salehpur, F Saffari Iran J Reprod Med 10 (1), 1-6, 2012 | 31 | 2012 |
| Effects of miglustat on stabilization of neurological disorder in Niemann–Pick disease type C: Iranian pediatric case series P Karimzadeh, SH Tonekaboni, MR Ashrafi, Y Shafeghati, A Rezayi, ... Journal of Child Neurology 28 (12), 1599-1606, 2013 | 30 | 2013 |
| Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa H Vahidnezhad, L Youssefian, AH Saeidian, S Zeinali, A Touati, M Abiri, ... Experimental Dermatology 28 (10), 1118-1121, 2019 | 29 | 2019 |
| Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat) B Levy, TM Dunn, JH Kern, K Hirschhorn, NB Kardon American journal of medical genetics 108 (3), 192-197, 2002 | 29 | 2002 |
| Distal 5q trisomy resulting from an X; 5 translocation detected by chromosome painting DN Abuelo, AN Ahsanuddin, HFL Mark American journal of medical genetics 94 (5), 392-399, 2000 | 28 | 2000 |
| Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients. S Khatami, SR Dehnabeh, S Zeinali, B Thöny, M Alaei, S Salehpour, ... JIMD Rep, 2016 | 26 | 2016 |
| Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes L Youssefian, H Vahidnezhad, AH Saeidian, S Sotoudeh, H Mahmoudi, ... European Journal of Human Genetics 25 (11), 1282-1285, 2017 | 25 | 2017 |
| Craniosynostosis associated with distal 5q‐trisomy: Further evidence that extra copy of MSX2 gene leads to craniosynostosis JC Wang, M Steinraths, L Dang, B Lomax, P Eydoux, T Stockley, SL Yong, ... American Journal of Medical Genetics Part A 143 (24), 2931-2936, 2007 | 25 | 2007 |
| Two concurrent chromosomal aberrations involving interstitial deletion in 1q24. 2q25. 2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with … T Kibe, Y Mori, T Okanishi, K Shimojima, K Yokochi, T Yamamoto American Journal of Medical Genetics Part A 155 (1), 215-220, 2011 | 24 | 2011 |
| Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis O Villa, M Del Campo, M Salido, B Gener, L Astier, J Del Valle, ... American Journal of Medical Genetics Part A 143 (10), 1108-1113, 2007 | 24 | 2007 |
Mohammad Miryounesishahid beheshti university of medical sciencesVerified email at sbmu.ac.ir
