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

Tekijä Pouresmaeili, Farkhondeh, Jamshidi, Javad, Azargashb, Eznollah, Samangouee, Shahdokht
Julkaistu 2013

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

Tekijä Jamshidi, Javad, Naderi, Hamed, Taghavi, Shaghayegh, Emamalizadeh, Babak, Darvish, Hossein
Julkaisussa Int J Mol Cell Med (2016)

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

Tekijä Ahmadifard, Azadeh, Jamshidi, Javad, Tafakhori, Abbas, Mollazadeh, Reza, Falsafi, Zeinab, Darvish, Hossein
Julkaisussa 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

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

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

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

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

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

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

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

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

Tekijä 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
Julkaisussa Genet Test Mol Biomarkers (2016)

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

Tekijä 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
Julkaisussa Mov Disord (2016)

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

Tekijä 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
Julkaisussa 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

Tekijä 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
Julkaisussa 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

Tekijä 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
Julkaisussa 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

Tekijä 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
Julkaisussa Mol Neurobiol (2017)