Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing von Aristidou, Constantia, Koufaris, Costas, Theodosiou, Athina, Bak, Mads, Mehrjouy, Mana M, Behjati, Farkhondeh, Tanteles, George, Christophidou-Anastasiadou, Violetta, Tommerup, Niels, Sismani, Carolina

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Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis von Najafi, Maryam, Kordi-Tamandani, Dor Mohammad, Behjati, Farkhondeh, Sadeghi-Bojd, Simin, Bakey, Zeineb, Karimiani, Ehsan Ghayoor, Schüle, Isabel, Azarfar, Anoush, Schmidts, Miriam

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BOD1 Is Required for Cognitive Function in Humans and Drosophila von Esmaeeli-Nieh, Sahar, Fenckova, Michaela, Porter, Iain M, Motazacker, M Mahdi, Nijhof, Bonnie, Castells-Nobau, Anna, Asztalos, Zoltan, Weißmann, Robert, Behjati, Farkhondeh, Tzschach, Andreas, Felbor, Ute, Scherthan, Harry, Sayfati, Seyed Morteza, Ropers, H Hilger, Kahrizi, Kimia, Najmabadi, Hossein, Swedlow, Jason R, Schenck, Annette, Kuss, Andreas W

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Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans von Pak, ChangHui, Garshasbi, Masoud, Kahrizi, Kimia, Gross, Christina, Apponi, Luciano H, Noto, John J, Kelly, Seth M, Leung, Sara W, Tzschach, Andreas, Behjati, Farkhondeh, Abedini, Seyedeh Sedigheh, Mohseni, Marzieh, Jensen, Lars R, Hu, Hao, Huang, Brenda, Stahley, Sara N, Liu, Guanglu, Williams, Kathryn R, Burdick, Sharon, Feng, Yue, Sanyal, Subhabrata, Bassell, Gary J, Ropers, Hans-Hilger, Najmabadi, Hossein, Corbett, Anita H, Moberg, Kenneth H, Kuss, Andreas W

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The Genotoxic and Cytotoxic Effects of Bisphenol-A (BPA) in MCF-7 Cell Line and Amniocytes von Aghajanpour-Mir, Seyed Mohsen, Zabihi, Ebrahim, Akhavan-Niaki, Haleh, Keyhani, Elahe, Bagherizadeh, Iman, Biglari, Sajjad, Behjati, Farkhondeh

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Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature von Tafazoli, Alireza, Behjati, Farkhondeh, Farhud, Dariush D, Abbaszadegan, Mohammad Reza

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Overexpression of HER-2/neu in Malignant Mammary Tumors: Translation of Clinicopathological Features from Dog to Human von Muhammadnejad, Ahad, Keyhani, Elahe, Mortazavi, Pejman, Behjati, Farkhondeh, Haghdoost, Iraj Sohrabi

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A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family von Nozari, Ahoura, Aghaei-Moghadam, Ehsan, Zeinaloo, Aliakbar, Alavi, Afagh, Ghasemi Firouzabdi, Saghar, Minaee, Shohre, Eskandari Hesari, Marzieh, Behjati, Farkhondeh

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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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COVID-19; History, Taxonomy, and Diagnostic Molecular and Immunological Techniques von Taghizadeh, Sara, Behjati, Farkhondeh

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A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East von Najafi, Maryam, Tamandani, Dor Mohammad Kordi, Azarfar, Anoush, Bakey, Zeineb, Behjati, Farkhondeh, Antony, Dinu, Schüle, Isabel, Sadeghi-Bojd, Simin, Karimiani, Ehsan Ghayoor, Schmidts, Miriam

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Relationship Between PIK3CA Amplification and P110α and CD34 Tissue Expression as Angiogenesis Markers in Iranian Women with Sporadic Breast Cancer von Hosseini, Shadi, Behjati, Farkhondeh, Rahimi, Maryam, Taheri, Nazanin, Khoram Khorshid, Hamidreza, Aghakhani Moghaddam, Fatemeh, Ghasemi, Saghar, Karimlou, Masoud, Sirati, Fereidoon, Keyhani, Elahe

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Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family von Hadipour, Fatemeh, Shafeghati, Yousef, Bagherizadeh, Eiman, Behjati, Farkhondeh, Hadipour, Zahra

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Mutation Screening of BRCA Genes in 10 Iranian Males with Breast Cancer von Zorrieh Zahra, Atieh, Kadkhoda, Sepideh, Behjati, Farkhondeh, Aghakhani Moghaddam, Fatemeh, Badiei, Azadeh, Sirati, Fereidoon, Afshin Alavi, Hossein, Atri, Morteza, Omranipour, Ramesh, Keyhani, Elahe

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

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Expression of ERBB1 gene in Iranian women with sporadic breast cancer and its relationship with clinicopathological features of the disease von Pazhoomand, Reza, Keihani, Elahe, Behjati, Farkhondeh

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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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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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Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease von Soosanabadi, Mohsen, Ghahfarokhi, Arezoo Mosharraf, Pourghazi, Farzad, Ehtesham, Naeim, Mirfakhraie, Reza, Atanesyan, Lilit, Keyhani, Elahe, Behjati, Farkhondeh

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Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability von Fattahi, Mahshid, Bushehri, Ata, Alavi, Afagh, Asghariazar, Vahid, Nozari, Ahoura, Ghasemi Firouzabadi, Saghar, Motamedian Dehkordi, Parisa, Javid, Marzieh, Farajzadeh Valiliou, Saeed, Karimian, Javad, Behjati, Farkhondeh

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