Association between Vitamin D Receptor Gene BsmI Polymorphism and Bone Mineral Density in A Population of 146 Iranian Women

per Pouresmaeili, Farkhondeh, Jamshidi, Javad, Azargashb, Eznollah, Samangouee, Shahdokht
Publicat 2013

A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease

per Jamshidi, Javad, Naderi, Hamed, Taghavi, Shaghayegh, Emamalizadeh, Babak, Darvish, Hossein
Publicat a Int J Mol Cell Med (2016)

Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals

per Ahmadifard, Azadeh, Jamshidi, Javad, Tafakhori, Abbas, Mollazadeh, Reza, Falsafi, Zeinab, Darvish, Hossein
Publicat a Int J Mol Cell Med (2016)

Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study

per Bahramali, Ehsan, Rajabi, Mona, Jamshidi, Javad, Mousavi, Seyyed Mohammad, Zarghami, Mehrdad, Manafi, Alireza, Firouzabadi, Negar
Publicat a BMJ Open (2016)

FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men

per Jamshidi, Javad, Pouresmaeili, Farkhondeh, Darvish, Hossein, Omrani, Mir Davood, Azargashb, Eznollah, Sadeghi, Mohammad Reza, Lakpour, Niknam
Publicat 2014

A cohort study protocol to analyze the predisposing factors to common chronic non-communicable diseases in rural areas: Fasa Cohort Study

per Farjam, Mojtaba, Bahrami, Hossein, Bahramali, Ehsan, Jamshidi, Javad, Askari, Alireza, Zakeri, Habibollah, Homayounfar, Reza, Poustchi, Hossein, Malekzadeh, Reza
Publicat a BMC Public Health (2016)

ATP2B1 rs2681472 and STK39 rs35929607 polymorphisms and risk of Hypertension in Iranian Population

per Jamshidi, Javad, Asnaashari, Ali, Alipoor, Reza, Mohammadi, Sina, Roostaei, Sara, Samadian, Mohammad Mahdi, Honarmand Aliabadi, Saiedeh, Bahramali, Ehsan
Publicat a Med J Islam Repub Iran (2018)

Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population

per Madadi, Faranak, Khaniani, Mahmoud Shekari, Shandiz, Ehsan Esmaili, Ayromlou, Hormoz, Najmi, Safa, Emamalizadeh, Babak, Taghavi, Shaghayegh, Jamshidi, Javad, Tafakhori, Abbas, Shahidi, Gholam-Ali, Darvish, Hossein
Publicat a Genet Test Mol Biomarkers (2016)

PTRHD1 (C2orf79) mutations lead to autosomal recessive intellectual disability and parkinsonism

per Khodadadi, Hamidreza, Azcona, Luis J., Aghamollaii, Vajiheh, Omrani, Mir Davood, Garshasbi, Masoud, Taghavi, Shaghayegh, Tafakhori, Abbas, Shahidi, Gholam Ali, Jamshidi, Javad, Darvish, Hossein, Paisán-Ruiz, Coro
Publicat a Mov Disord (2016)

Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD)

per Alehabib, Elham, Jamshidi, Javad, Ghaedi, Hamid, Emamalizadeh, Babak, Andarva, Monavvar, Daftarian, Narsis, Rezaei Kanavi, Mozhgan, Mohammadi Torbati, Peyman, Espandar, Goldis, Alinaghi, Somayeh, Johari, Amir Hossein, Saghally, Mansoor, Mohajerani, Fatemeh, Darvish, Hossein
Publicat a Int J Mol Cell Med (2017)

Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes

per Darvish, Hossein, Azcona, Luis J., Tafakhori, Abbas, Mesias, Roxana, Ahmadifard, Azadeh, Sanchez, Elena, Habibi, Arman, Alehabib, Elham, Johari, Amir Hossein, Emamalizadeh, Babak, Jamali, Faezeh, Chapi, Marjan, Jamshidi, Javad, Kajiwara, Yuji, Paisán-Ruiz, Coro
Publicat a Sci Rep (2020)

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications

per Ghasemi Firouzabadi, Saghar, Vameghi, Roshanak, Kariminejad, Roxana, Darvish, Hossein, Banihashemi, Susan, Firouzkouhi Moghaddam, Mahboubeh, Jamali, Peyman, Farbod Mofidi Tehrani, Hassan, Dehghani, Hossein, Raeisoon, Mohammad Reza, Narooie-Nejad, Mehrnaz, Jamshidi, Javad, Tafakhori, Abbas, Sadabadi, Saeid, Behjati, Farkhondeh
Publicat a Int J Mol Cell Med (2016)

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations

per Taghavi, Shaghayegh, Chaouni, Rita, Tafakhori, Abbas, Azcona, Luis J., Firouzabadi, Saghar Ghasemi, Omrani, Mir Davood, Jamshidi, Javad, Emamalizadeh, Babak, Shahidi, Gholam Ali, Ahmadi, Mona, Habibi, Seyed Amir Hassan, Ahmadifard, Azadeh, Fazeli, Atena, Motallebi, Marzieh, Petramfar, Peyman, Askarpour, Saeed, Askarpour, Shiva, Shahmohammadibeni, Hossein Ali, Shahmohammadibeni, Neda, Eftekhari, Hajar, Zarneh, Amir Ehtesham Shafiei, Mohammadihosseinabad, Saeed, Khorrami, Mehdi, Najmi, Safa, Chitsaz, Ahmad, Shokraeian, Parasto, Ehsanbakhsh, Hossein, Rezaeidian, Jalal, Rad, Reza Ebrahimi, Madadi, Faranak, Andarva, Monavvar, Alehabib, Elham, Atakhorrami, Minoo, Mortazavi, Seyed Erfan, Azimzadeh, Zahra, Bayat, Mahdis, Besharati, Amir Mohammad, Harati-Ghavi, Mohammad Ali, Omidvari, Samareh, Dehghani-Tafti, Zahra, Mohammadi, Faraz, Pour, Banafsheh Mohammad Hossein, Moghaddam, Hamid Noorollahi, Shandiz, Ehsan Esmaili, Habibi, Arman, Taherian-Esfahani, Zahra, Darvish, Hossein, Paisán-Ruiz, Coro
Publicat a Mol Neurobiol (2017)