Masoud Tajamolian

Cited by

	All	Since 2019
Citations	52	40
h-index	4	4
i10-index	3	2

2016201720182019202020212022202320243 2 5 8 10 8 7 5 2

Co-authors

Parisa Kolahdouzstudent of MSc-shahid sadoughi university of medical scienceVerified email at ssu.ac.ir
Mohammad Yahya Vahidi MehrjardiAssistant Professor in Molecular Genetics, Shahid Sadoughi University of Medical SciencesVerified email at ssu.ac.ir
Mohammad Hasan SheikhhaProfessor of Medical Genetics, Shahid Sadoughi University of Medical SciencesVerified email at ssu.ac.ir
Ehsan Farashahi YazdStem Cell Biology Research Center, Yazd Reproductive Sciences InstituteVerified email at ssu.ac.ir
Mohmmadreza DehghaniAssociated professor of Medical Genetics ,Shahid Sadough University of Medical SciencesVerified email at unipv.it
Seyed Mehdi HoseiniDepartment of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, IranVerified email at mail.um.ac.ir
mahsa kolahdouzMSc of human genetics

Masoud Tajamolian

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran

Verified email at uswr.ac.ir

Medical Genetics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity MR Dehghani, MYV Mehrjardi, N Dilaver, M Tajamolian, S Enayati, ... European journal of medical genetics 61 (8), 465-467, 2018	20	2018
Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia M Kolahdouz, Z Mohammadi, P Kolahdouz, M Tajamolian, H Khanahmad Advanced biomedical research 4 (1), 189, 2015	15	2015
The rs3917779 polymorphism of P-selectin’s significant association with proliferative diabetic retinopathy in Yazd, Iran P Kolahdouz, E Farashahi Yazd, M Tajamolian, MR Manaviat, ... Graefe's Archive for Clinical and Experimental Ophthalmology 253, 1967-1972, 2015	13	2015
A rare missense mutation and a polymorphism with high frequency in LDLR gene among iranian patients with familial hypercholesterolemia M Tajamolian, P Kolahdouz, P Nikpour, SK Forouzannia, MH Sheikhha, ... Advanced Biomedical Research 7 (1), 37, 2018	4	2018
The association of RBX1 and BAMBI gene expression with oocyte maturation in PCOS women K Monshizadeh, M Tajamolian, F Anbari, MYV Mehrjardi, SM Kalantar, ... BMC Medical Genomics 17 (1), 24, 2024		2024
The effect of angiotensin-converting enzyme insertion/deletion polymorphism on severity and death rate of COVID-19 in Iranian patients M Samet, M Yazdi, M Tajamolian, M Beygi, MH Sheikhha, SM Hoseini Biochemical Genetics, 2023		2023
Immunologic Factors and Genomic Considerations in Recurrent Pregnancy Loss: A Review F Montazeri, M Tajamolian, ES Hosseini, SM Hoseini International Journal of Medical Laboratory 10 (4), 279-305, 2023		2023

The system can't perform the operation now. Try again later.

Articles 1–7

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Follow

Cited by

Co-authors