Novel evidence of the involvement of calreticulin in major psychiatric disorders von Ohadi, M., Mirabzadeh, A., Esmaeilzadeh-Gharehdaghi, E., Rezazadeh, M., Hosseinkhanni, S., Oladnabi, M., Firouzabadi, S. Ghasemi, Darvish, H.

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HLA-DRA is associated with Parkinson's disease in Iranian population von Jamshidi, J., Movafagh, A., Emamalizadeh, B., Zare Bidoki, A., Manafi, A., Ghasemi Firouzabadi, S., Shahidi, G.-A., Kazeminasab, S., Petramfar, P., Fazeli, A., Motallebi, M., Mortazavi-Tabatabaei, S. A., Kowsari, A., Jafarian, Z., Darvish, H.

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A clinical and molecular genetic study of 112 Iranian families with primary microcephaly von Darvish, H, Esmaeeli-Nieh, S, Monajemi, G B, Mohseni, M, Ghasemi-Firouzabadi, S, Abedini, S S, Bahman, I, Jamali, P, Azimi, S, Mojahedi, F, Dehghan, A, Shafeghati, Y, Jankhah, A, Falah, M, Soltani Banavandi, M J, Ghani-Kakhi, M, Garshasbi, M, Rakhshani, F, Naghavi, A, Tzschach, A, Neitzel, H, Ropers, H H, Kuss, A W, Behjati, F, Kahrizi, K, Najmabadi, H

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Investigation of genetic causes of intellectual disability in kerman province, South East of Iran von Fayruzabadi, S. Ghasemi, Jafari, E., Ghadami, Sh, Sabbagh, F., Kavoosi, Gh. R., Najmabadi, H., Abedinni, S. Sedigheh, Bahman, I., Darvish, H., Muhseni, M., Behjati, F., Banavandi, M. J. Sultani, Kahrizi, K.

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Exceptional human core promoter nucleotide compositions von Darvish, H., Nabi, M. Olad, Firouzabadi, S. Ghasemi, Karimlou, M., Heidari, A., Najmabadi, H., Ohadi, M.

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Core promoter STRs: Novel mechanism for inter-individual variation in gene expression in humans von Heidari, A., Nariman Saleh Fam, Z., Esmaeilzadeh-Gharehdaghi, E., Banan, M., Hosseinkhani, S., Mohammadparast, S., Oladnabi, M., Ebrahimpour, M.R., Soosanabadi, M., Farokhashtiani, T., Darvish, H., Firouzabadi, S. Ghasemi, Farashi, S., Najmabadi, H., Ohadi, M.

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HLA ‐ DRA is associated with P arkinson's disease in I ranian population von Jamshidi, J., Movafagh, A., Emamalizadeh, B., Zare Bidoki, A., Manafi, A., Ghasemi Firouzabadi, S., Shahidi, G.‐A., Kazeminasab, S., Petramfar, P., Fazeli, A., Motallebi, M., Mortazavi‐Tabatabaei, S. A., Kowsari, A., Jafarian, Z., Darvish, H.

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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia von Wiessner, M, Maroofian, R, Ni, M-Y, Pedroni, A, Müller, JS, Beetz, C, Santorelli, FM, Alfares, AA, Zhu, C, Alehabib, E, Bakhtiari, S, Janecke, AR, Otero, MG, Chen, JYH, Peterson, JT, Strom, TM, De Jonghe, P, Deconinck, T, De Ridder, W, De Winter, J, Ricca, I, Alfadhel, M, van de Warrenburg, BP, Portier, R, Bergmann, C, Ghasemi Firouzabadi, S, Jin, SC, Bilguvar, K, Hamed, S, Abdelhameed, M, Maqbool, S, Rahman, F, Anwar, N, Carmichael, J, Pagnamenta, A, Wood, NW, Tran Mau-Them, F, Haack, T, Genomics England Research Consortium, PREPARE network, Di Rocco, M, Ceccherini, I, Iacomino, M, Zara, F, Salpietro, V, Scala, M, Rusmini, M, Xu, Y, Wang, Y, Suzuki, Y, Koh, K, Nan, H, Ishiura, H, Tsuji, S, Lambert, L, Schmitt, E, Lacaze, E, Küpper, H, Dredge, D, Skraban, C, Goldstein, A, Willis, MJH, Grand, K, Graham, JM, Lewis, RA, Millan, F, Duman, Ö, Dündar, N, Uyanik, G, Schöls, L, Nürnberg, P, Nürnberg, G, Seeman, P, Kuchar, M, Darvish, H, Rebelo, A, Bouçanova, F, Medard, J-J, Chrast, R, Auer-Grumbach, M, Alkuraya, FS, Shamseldin, H, Al Tala, S, Rezazadeh Varaghchi, J, Najafi, M, Deschner, S, Gläser, D, Hüttel, W, Kruer, MC, Takiyama, Y, Züchner, S, Baets, J, Synofzik, M, Schüle, R, Horvath, R, Houlden, H, Bartesaghi, L, Lee, H-J, Ampatzis, K, Pierson, TM, Senderek, J

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders von Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman, Zecha, Agnes, Mohseni, Marzieh, Püttmann, Lucia, Vahid, Leyla Nouri, Jensen, Corinna, Moheb, Lia Abbasi, Bienek, Melanie, Larti, Farzaneh, Mueller, Ines, Weissmann, Robert, Darvish, Hossein, Wrogemann, Klaus, Hadavi, Valeh, Lipkowitz, Bettina, Esmaeeli-Nieh, Sahar, Wieczorek, Dagmar, Kariminejad, Roxana, Firouzabadi, Saghar Ghasemi, Cohen, Monika, Fattahi, Zohreh, Rost, Imma, Mojahedi, Faezeh, Hertzberg, Christoph, Dehghan, Atefeh, Rajab, Anna, Banavandi, Mohammad Javad Soltani, Hoffer, Julia, Falah, Masoumeh, Musante, Luciana, Kalscheuer, Vera, Ullmann, Reinhard, Kuss, Andreas Walter, Tzschach, Andreas, Kahrizi, Kimia, Ropers, H. Hilger

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COL18A1 is a candidate eye iridocorneal angle-closure gene in humans von Suri, Fatemeh, Yazdani, Shahin, Chapi, Marjan, Safari, Iman, Rasooli, Paniz, Daftarian, Narsis, Jafarinasab, Mohammad Reza, Ghasemi Firouzabadi, Saghar, Alehabib, Elham, Darvish, Hossein, Klotzle, Brandy, Fan, Jian-Bing, Turk, Casey, Elahi, Elahe

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Novel splicing variant and gonadal mosaicism in DYRK1A gene identified by whole-genome sequencing in multiplex autism spectrum disorder families von Agha Gholizadeh, Mehdi, Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Heidari, Erfan, Razmara, Ehsan, Almadani, Navid, Sharifi Zarchi, Ali, Garshasbi, Masoud

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ANXA1 with Anti‐Inflammatory Properties Might Contribute to Parkinsonism von Darvish, Hossein, Azcona, Luis J., Taghavi, Shaghayegh, Firouzabadi, Saghar Ghasemi, Tafakhori, Abbas, Alehabib, Elham, Mohajerani, Fatemeh, Zardadi, Safoura, Paisán‐Ruiz, Coro

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Nitrogen reduction and foliar application of zinc sulfate improve the physiological and biochemical characteristics of two autumn-sown sugar beet (Beta vulgaris L.) von Haqshenas, Amene, Azizi, Khosro, Ghasemi, Soraya, Firouzabadi, Farhad Nazarian, Hosseinpour, Mostafa

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Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia von Husain, Ralf A., Grimmel, Mona, Wagner, Matias, Hennings, J. Christopher, Marx, Christian, Feichtinger, René G., Saadi, Abdelkrim, Rostásy, Kevin, Radelfahr, Florentine, Bevot, Andrea, Döbler-Neumann, Marion, Hartmann, Hans, Colleaux, Laurence, Cordts, Isabell, Kobeleva, Xenia, Darvish, Hossein, Bakhtiari, Somayeh, Kruer, Michael C., Besse, Arnaud, Ng, Andy Cheuk-Him, Chiang, Diana, Bolduc, Francois, Tafakhori, Abbas, Mane, Shrikant, Ghasemi Firouzabadi, Saghar, Huebner, Antje K., Buchert, Rebecca, Beck-Woedl, Stefanie, Müller, Amelie J., Laugwitz, Lucia, Nägele, Thomas, Wang, Zhao-Qi, Strom, Tim M., Sturm, Marc, Meitinger, Thomas, Klockgether, Thomas, Riess, Olaf, Klopstock, Thomas, Brandl, Ulrich, Hübner, Christian A., Deschauer, Marcus, Mayr, Johannes A., Bonnen, Penelope E., Krägeloh-Mann, Ingeborg, Wortmann, Saskia B., Haack, Tobias B.

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A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family von Nozari, Ahoura, Aghaei-Moghadam, Ehsan, Zeinaloo, Aliakbar, Mollazadeh, Reza, Majnoon, Mohammad-Taghi, Alavi, Afagh, Ghasemi Firouzabadi, Saghar, Mohammadzadeh, Akbar, Banihashemi, Susan, Nikzaban, Mehrnoush, Najmabadi, Hossein, Behjati, Farkhondeh

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Detection of novel PPP1R1B::STARD3 fusion transcript in acute myeloid leukemia: a case report von Firouzabadi, Elahe Dehghani, Allami, Mohammed, Mohammed, Eman Jassim, Barzegar, Hossein, Dastpak, Mahtab, Alemohammad, Reza, Moghimi, Vahid, Mahmoudian, Reihaneh Alsadat, Nasrabadi, Fatemeh, Arghiani, Nahid, Kitamura, Yohei, Hosseini, Seyed Abolfazl, Ghasemi, Ali, Farshchian, Moein

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The Use of Hexokinase 2-Displacing Peptides as an Anti-Neoplastic Approach for Malignant Peripheral Nerve Sheath Tumors von Ciscato, Francesco, Masgras, Ionica, Gori, Alessandro, Fantuz, Marco, Bergamaschi, Greta, Komarov, Denis, La Spina, Martina, Ghasemi-Firouzabadi, Shiva, Pizzi, Marco, Dei Tos, Angelo Paolo, Chiara, Federica, Carrer, Alessandro, Rasola, Andrea

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Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism von Sanchez, Elena, Darvish, Hossein, Mesias, Roxana, Taghavi, Shaghyegh, Firouzabadi, Saghar Ghasemi, Walker, Ruth H., Tafakhori, Abbas, Paisán-Ruiz, Coro

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Association of -460C/T and +405 G/C polymorphisms of vascular endothelial growth factor gene and susceptibility to ovarian hyperstimulation syndrome von Ghasemi, Nasrin, Dehghani Firouzabadi, Razieh, Ahmadi, Shahnaz

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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies von Mohammadzadeh, Akbar, Akbaroghli, Susan, Aghaei-Moghadam, Ehsan, Mahdieh, Nejat, Badv, Reza Shervin, Jamali, Payman, Kariminejad, Roxana, Chavoshzadeh, Zahra, Ghasemi Firouzabadi, Saghar, Mansour Ghanaie, Roxana, Nozari, Ahoura, Banihashemi, Sussan, Hadipour, Fatemeh, Hadipour, Zahra, Kariminejad, Ariana, Najmabadi, Hossein, Shafeghati, Yousef, Behjati, Farkhondeh

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