Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sajedeh Masjoudi"'
Autor:
Mahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, Mina Jahangiri, Hossein Lanjanian, Danial Habibi, Sajedeh Masjoudi, Parisa Riahi, Sahand Tehrani Fateh, Farideh Neshati, Asiyeh Sadat Zahedi, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Seyedeh Fatemeh Mousavi, Sara Asgarian, Maryam Zarkesh, Mohammad Reza Moghaddas, Albert Tenesa, Anoshirvan Kazemnejad, Hassan Vahidnezhad, Hakon Hakonarson, Fereidoun Azizi, Mehdi Hedayati, Maryam Sadat Daneshpour, Mahdi Akbarzadeh
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-12 (2024)
Abstract This study aims to assess the effect of familial structures on the still-missing heritability estimate and prediction accuracy of Type 2 Diabetes (T2D) using pedigree estimated risk values (ERV) and genomic ERV. We used 11,818 individuals (T
Externí odkaz:
https://doaj.org/article/d1778760f30742c2868c53ce140b1d16
Autor:
Sara Asgarian, Hossein Lanjanian, Shiva Rahimipour Anaraki, Farzad Hadaegh, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Zarkesh, Bita Shalbafan, Mahdi Akbarzadeh, Sahand Tehrani Fateh, Davood Khalili, Amirabbas Momenan, Narges Sarbazi, Mehdi Hedayati, Fereidoun Azizi, Maryam S. Daneshpour
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Maturity-onset diabetes of the young (MODY) is an uncommon monogenic type of diabetes mellitus. Detecting genetic variants for MODY is a necessity for precise diagnosis and treatment. The majority of MODY genetic predisposition has been docu
Externí odkaz:
https://doaj.org/article/9cffd875dd33497eb13b7e36d072b360
Autor:
Mahdi Akbarzadeh, Parisa Riahi, Amir Hossein Saeidian, Maryam Zarkesh, Sajedeh Masjoudi, Sara Asgarian, Kamran Guity, Hamed Moheimani, Homayoon Masoudi, Mahmoud Amiri Roudbar, Davood Khalili, Farhad Hosseinpanah, Maryam Barzin, Carolyn T. Hogan, Hakon Hakonarson, Mehdi Hedayati, Maryam S. Daneshpour, Fereidoun Azizi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Dyslipidemia, as a metabolic risk factor, with the strongest and most heritable independent cause of cardiovascular diseases worldwide. We investigated the familial transmission patterns of dyslipidemia through a longitudinal family-based co
Externí odkaz:
https://doaj.org/article/d720967d10a146a6b8c4f2051ea969de
Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case–control study and meta-analysis
Autor:
Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Sajedeh Masjoudi, Maryam Tohidi, Mehdi Hedayati, Fereidoun Azizi, Maryam S. Daneshpour
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Due to the central role in insulin secretion, the potassium inwardly-rectifying channel subfamily J member 11 (KCNJ11) gene is one of the essential genes for type 2 diabetes (T2D) predisposition. However, the relevance of this gene to T2D de
Externí odkaz:
https://doaj.org/article/ed3cd4cc543e48049355e937cde1c7bb
Autor:
Hossein Lanjanian, Leila Najd Hassan Bonab, Mahdi Akbarzadeh, Maryam Moazzam-Jazi, Asiyeh Sadat Zahedi, Sajedeh Masjoudi, Maryam S. Daneshpour
Publikováno v:
Biology of Sex Differences, Vol 13, Iss 1, Pp 1-10 (2022)
Abstract Biological processes involving environmental and genetic factors drive the interplay between age- and sex-regulating lipid profile. The relation between variations in the LPA gene with increasing the risk of coronary heart disease is depende
Externí odkaz:
https://doaj.org/article/3f4a0a0cab7142d6a993c381824246e4
Autor:
Sajedeh Masjoudi, Bahareh Sedaghati-khayat, Niloufar Javanrouh Givi, Leila Najd Hassan Bonab, Fereidoun Azizi, Maryam S. Daneshpour
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Metabolic syndrome (MetS) is one of the most important risk factors for cardiovascular disease. The 11p23.3 chromosomal region plays a potential role in the pathogenesis of MetS. The present study aimed to assess the association between 18 s
Externí odkaz:
https://doaj.org/article/893b53e9665f4e0ba3b3066260911243
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract Obesity is the most crucial phenotype in metabolic syndrome (MetS), and waist circumference (WC) and body mass index (BMI) are two common indexes to define obesity. It is an accepted fact that genetic and environmental interaction influence
Externí odkaz:
https://doaj.org/article/ab1676bf2cf3496fb4dd121e9021ae69
Autor:
Maryam S. Daneshpour, Mahdi Akbarzadeh, Hossein Lanjanian, Bahar Sedaghati-khayat, Kamran Guity, Sajedeh Masjoudi, Asiyeh Sadat Zahedi, Maryam Moazzam-Jazi, Leila Najd Hassan Bonab, Bita Shalbafan, Sara Asgarian, Goodarz Koli Farhood, Niloofar Javanrooh, Maryam Zarkesh, Parisa Riahi, Mohammad Reza Moghaddas, Parvaneh Arbab Dehkordi, Azar Delbarpour Ahmadi, Firoozeh Hosseini, Sara Jalali Farahani, Farzad Hadaegh, Parvin Mirmiran, Fahimeh Ramezani Tehrani, Arash Ghanbarian, Mohammad Sadegh Fallah Mahboob Pasand, Parisa Amiri, Majid Valizadeh, Farhad Hosseipanah, Maryam Tohidi, Asghar Ghasemi, Azita Zadeh-Vakili, Mohammad Piryaei, Shahram Alamdari, Davood Khalili, Amirabbas Momenan, Maryam Barzin, Sirous Zeinali, Mehdi Hedayati, Fereidoun Azizi
Publikováno v:
European Journal of Epidemiology, 38(6), 699-711. Springer Netherlands
The Tehran cardiometabolic genetic study (TCGS) is a large population-based cohort study that conducts periodic follow-ups. TCGS has created a comprehensive database comprising 20,367 participants born between 1911 and 2015 selected from four main on
Title: Cohort profile update: Tehran Cardiometabolic Genetic Study, a path toward precision medicine
Autor:
Maryam S Daneshpour, Mahdi Akbarzadeh, Hossein Lanjanian, Bahar Sedaghati-khayat, Kamran Guity, Sajedeh Masjoudi, Asieh Sadat Zahedi, Maryam Moazzam-Jazi, Leila Najd Hassan Bonab, Bita Shalbafan, Sara Asgarian, Goodarz Koli Farhood, Niloofar Javanrooh, Maryam Zarkesh, Parisa Riahi, Mohammad Reza Moghaddas, Parvaneh Arbab Dehkordi, Azar Delbarpour Ahmadi, Firoozeh Hosseini, Sara Jalali Farahani, Farzad Hadaegh, Parvin Mirmiarn, Fahimeh Ramezani Tehrani, Arash Ghanbarian, Mohammad Sadegh Fallah Mahboob Pasand, Parisa Amiri, Majid Valizadeh, Farhad Hosseipanah, Maryam Tohidi, Asghar Ghasemi, Azita Zadeh Vakili, Shahram Alamdari, Davood Khalili, Amirabbas Momenan, Maryam Barzin, Sirous Zeinali, Mehdi Hedayati, Fereidoun Azizi
The Tehran Cardiometabolic Genetic Study (TCGS) is a large population-based cohort study with periodic follow-ups, which created a comprehensive database of 20,367 participants born between 1911-2015 selected from 4 different longitudinal, ongoing, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc483ec89d41d3db645ccaf7602f13f0
https://doi.org/10.21203/rs.3.rs-2293709/v1
https://doi.org/10.21203/rs.3.rs-2293709/v1
Autor:
Maryam S. Daneshpour, Niloufar Javanrouh Givi, Sajedeh Masjoudi, Fereidoun Azizi, Bahareh Sedaghati-khayat, Leila Najd Hassan Bonab
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports
Scientific Reports
Metabolic syndrome (MetS) is one of the most important risk factors for cardiovascular disease. The 11p23.3 chromosomal region plays a potential role in the pathogenesis of MetS. The present study aimed to assess the association between 18 single nuc