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

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Whole genome sequencing identifies a novel homozygous exon deletion in the NT5C2 gene in a family with intellectual disability and spastic paraplegia by Darvish, Hossein, Azcona, Luis J., Tafakhori, Abbas, Ahmadi, Mona, Ahmadifard, Azadeh, Paisán-Ruiz, Coro

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Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals by Ahmadifard, Azadeh, Jamshidi, Javad, Tafakhori, Abbas, Mollazadeh, Reza, Falsafi, Zeinab, Darvish, Hossein

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Genome editing in K562 cells suggests a functional role for the XmnI Gγ polymorphism: a widely used genetic marker in β-thalassemia and sickle cell disease patients by Azadeh Ahmadifard, Nahal Maroofi, Maryam Maleki Tehrani, Tahere Dabestani, Masoumeh Sadat Mousavi Maleki, Sepideh Bayrami, Mehdi Banan

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A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations by 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, Shafiei Zarneh, Amir Ehtesham, Mohammadihosseinabad, Saeed, Khorrami, Mehdi, Najmi, Safa, Chitsaz, Ahmad, Shokraeian, Parasto, Ehsanbakhsh, Hossein, Rezaeidian, Jalal, Ebrahimi Rad, Reza, 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, Mohammad Hossein Pour, Banafsheh, Noorollahi Moghaddam, Hamid, Esmaili Shandiz, Ehsan, Habibi, Arman, Taherian-Esfahani, Zahra, Darvish, Hossein, Paisán-Ruiz, Coro

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RIT2 Polymorphisms: Is There a Differential Association? by Emamalizadeh, Babak, Jamshidi, Javad, Movafagh, Abolfazl, Ohadi, Mina, khaniani, Mahmoud Shekari, Kazeminasab, Somayyeh, Biglarian, Akbar, Taghavi, Shaghayegh, Motallebi, Marzieh, Fazeli, Atena, Ahmadifard, Azadeh, Shahidi, Gholam-Ali, Petramfar, Peyman, Shahmohammadibeni, Neda, Dadkhah, Tahereh, Khademi, Ehteram, Tafakhori, Abbas, Khaligh, Ali, Safaralizadeh, Tannaz, Kowsari, Ali, Mirabzadeh, Arash, Zarneh, Amir Ehtesham Shafiei, Khorrami, Mehdi, Shokraeian, Parasto, Banavandi, Mohammad Javad Soltani, Lima, Behnam Safarpour, Andarva, Monavvar, Alehabib, Elham, Atakhorrami, Minoo, Darvish, Hossein

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A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder by Atakhorrami, Minoo, Rahimi-Aliabadi, Simin, Jamshidi, Javad, Moslemi, Elham, Movafagh, Abolfazl, Ohadi, Mina, Mirabzadeh, Arash, Emamalizadeh, Babak, Ghaedi, Hamid, Gholipour, Fatemeh, Fazeli, Atena, Motallebi, Marzieh, Taghavi, Shaghayegh, Ahmadifard, Azadeh, Mohammadihosseinabad, Saeed, Shafiei Zarneh, Amir Ehtesham, Shahmohammadibeni, Neda, Madadi, Faranak, Andarva, Monavvar, Darvish, Hossein

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The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population by Shahmohammadibeni, Neda, Rahimi-Aliabadi, Simin, Jamshidi, Javad, Emamalizadeh, Babak, Shahmohammadibeni, Hossein Ali, Zare Bidoki, Alireza, Akhavan-Niaki, Haleh, Eftekhari, Hajar, Abdollahi, Shokoufeh, Shekari Khaniani, Mahmoud, Shahmohammadibeni, Mahnaz, Fazeli, Atena, Motallebi, Marzieh, Taghavi, Shaghayegh, Ahmadifard, Azadeh, Shafiei Zarneh, Amir Ehtesham, Andarva, Monavvar, Dadkhah, Tahereh, Khademi, Ehteram, Alehabib, Elham, Rahimi, Mahnoosh, Tafakhori, Abbas, Atakhorrami, Minoo, Darvish, Hossein

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c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness by Safarpour Lima, Behnam, Ghaedi, Hamid, Daftarian, Narsis, Ahmadieh, Hamid, Jamshidi, Javad, Khorrami, Mehdi, Noroozi, Rezvan, Sohrabifar, Nasim, Assarzadegan, Farhad, Hesami, Omid, Taghavi, Shaghayegh, Ahmadifard, Azadeh, Atakhorrami, Minoo, Rahimi-Aliabadi, Simin, Shahmohammadibeni, Neda, Alehabib, Elham, Andarva, Monavvar, Darvish, Hossein, Emamalizadeh, Babak

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Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE... by Setoodeh, Aria, Panjeh-Shahi, Samareh, Bahmani, Fariba, Vand-Rajabpour, Fatemeh, Jalilian, Nazanin, Sayarifard, Fatemeh, Abbasi, Farzaneh, Sayarifard, Azadeh, Rostami, Parastoo, Parvaneh, Nima, Akhavan-Niaki, Haleh, Ahmadifard, Mohamadreza, Tabrizi, Mina

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