Tumor necrosis factor-alpha polymorphism at position -238 in preeclampsia by Naderi, Mohammad, Yaghootkar, Hanieh, Tara, Fatemeh, Tavakkol Afshari, Jalil, Farid Hosseini, Reza, Ghayour Mobarhan, Majid, Shapouri Moghadam, Abbas, Mirteimouri, Masoumeh, Tara, Seyedeh Maryam

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Effect of hemostatic agent on microshear bond strength of total-etch and self-etch adhesive systems by Hoorizad, Maryam, Heshmat, Haleh, Hosseini, Tara, Kazemi, Seyedeh, Tabatabaei, Seyedeh

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Genetics of intellectual disability in consanguineous families by Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Herwig, Ralf, Hosseini, Masoumeh, Oppitz, Cornelia, Abedini, Seyedeh Sedigheh, Suckow, Vanessa, Larti, Farzaneh, Beheshtian, Maryam, Lipkowitz, Bettina, Akhtarkhavari, Tara, Mehvari, Sepideh, Otto, Sabine, Mohseni, Marzieh, Arzhangi, Sanaz, Jamali, Payman, Mojahedi, Faezeh, Taghdiri, Maryam, Papari, Elaheh, Soltani Banavandi, Mohammad Javad, Akbari, Saeide, Tonekaboni, Seyed Hassan, Dehghani, Hossein, Ebrahimpour, Mohammad Reza, Bader, Ingrid, Davarnia, Behzad, Cohen, Monika, Khodaei, Hossein, Albrecht, Beate, Azimi, Sarah, Zirn, Birgit, Bastami, Milad, Wieczorek, Dagmar, Bahrami, Gholamreza, Keleman, Krystyna, Vahid, Leila Nouri, Tzschach, Andreas, Gärtner, Jutta, Gillessen-Kaesbach, Gabriele, Varaghchi, Jamileh Rezazadeh, Timmermann, Bernd, Pourfatemi, Fatemeh, Jankhah, Aria, Chen, Wei, Nikuei, Pooneh, Kalscheuer, Vera M., Oladnabi, Morteza, Wienker, Thomas F., Ropers, Hans-Hilger, Najmabadi, Hossein

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Is gestational hypertension associated with affective temperaments? by Rezaei Ardani, Amir, Tara, Fatemeh, Naghizadeh Kashani, Sara, Hatami, Seyedeh Behnaz, Emadzadeh, Maryam, Nahidi, Mahsa

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Affective temperaments and the risk of gestational diabetes mellitus by Rezaei Ardani, Amir, Tara, Fatemeh, Hatami, Seyedeh Behnaz, Naghizadeh Kashani, Sara, Emadzadeh, Maryam, Nahidi, Mahsa

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Re-Evaluating Risk Factors, Incidence, and Outcome of Aneurysmal and Non-Aneurysmal Subarachnoid Hemorrhage by Mortazavi, Zahra Sadat, Zandifar, Alireza, Ub Kim, Jorge Du, Tierradentro-García, Luis Octavio, Shakarami, Mehrnaz, Zamharir, Farzam Dashti, Hadipour, Maryam, Oustad, Marjan, Shafiei, Elham, Tara, Seyedeh Zahra, Shirani, Peyman, Asadi, Hamed, Vossough, Arastoo, Saadatnia, Mohammad

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Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients by Beheshtian, Maryam, Akhtarkhavari, Tara, Mehvari, Sepideh, Mohseni, Marzieh, Fattahi, Zohreh, Abedini, Seyedeh Sedigheh, Arzhangi, Sanaz, Fadaee, Mahsa, Jamali, Payman, Najafipour, Reza, Kalscheuer, Vera M., Hu, Hao, Ropers, Hans‐Hilger, Najmabadi, Hossein, Kahrizi, Kimia

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Preimplantation High-Resolution HLA Sequencing Using Next Generation Sequencing by Rafati, Maryam, Akhondi, Mohammad Mahdi, Sadeghi, Mohammad Reza, Tara, Seyedeh Zahra, Ghaffari, Saeed Reza

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Identification of a novel ALMS1 pathogenic variant in a family with Cone-Rod Dystrophy using whole exome sequencing, followed by prenatal diagnosis by Rafati, Maryam, Tara, Seyedeh Zahra, Hoseininasab, Fatemeh, Ghaffari, Saeed Reza

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