Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes by Sadeghzadeh, Salman, Dehghani Ashkezari, Mahmood, Seifati, Seyed Morteza, Vahidi Mehrjardi, Mohammad Yahya, Dehghan Tezerjani, Masoud, Sadeghzadeh, Sara, Ladan, Seyed Amir Behtash

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B.02 Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy by McMillan, HJ, Telegrafi, A, Singleton, A, Cho, M, Lelli, D, Lynn, FC, Griffin, J, Asamoah, A, Rinne, T, Erasmus, CE, Koolen, DA, Haaxma, CA, Keren, B, Doummar, D, Mignot, C, Thompson, I, Velsher, L, Dehghani, M, Vahidi Mehrjardi, M, Maroofian, R, Tchan, M, Simons, C, Christodoulou, J, Martín-Hernández, E, Guillen Sacoto, MJ, Henderson, LB, McLaughlin, H, Molday, LL, Molday, RS, Yoon, G

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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder by Christensen, Maria B., Levy, Amanda M., Mohammadi, Nazanin A., Niceta, Marcello, Kaiyrzhanov, Rauan, Dentici, Maria Lisa, Al Alam, Chadi, Alesi, Viola, Benoit, Valérie, Bhatia, Kailash P., Bierhals, Tatjana, Boßelmann, Christian M., Buratti, Julien, Callewaert, Bert, Ceulemans, Berten, Charles, Perrine, De Wachter, Matthias, Dehghani, Mohammadreza, D'haenens, Erika, Doco‐Fenzy, Martine, Geßner, Michaela, Gobert, Cyrielle, Guliyeva, Ulviyya, Haack, Tobias B., Hammer, Trine B., Heinrich, Tilman, Hempel, Maja, Herget, Theresia, Hoffmann, Ute, Horvath, Judit, Houlden, Henry, Keren, Boris, Kresge, Christina, Kumps, Candy, Lederer, Damien, Lermine, Alban, Magrinelli, Francesca, Maroofian, Reza, Vahidi Mehrjardi, Mohammad Yahya, Moudi, Mahdiyeh, Müller, Amelie J., Oostra, Anna J., Pletcher, Beth A., Ros‐Pardo, David, Samarasekera, Shanika, Tartaglia, Marco, Van Schil, Kristof, Vogt, Julie, Wassmer, Evangeline, Winkelmann, Juliane, Zaki, Maha S., Zech, Michael, Lerche, Holger, Radio, Francesca Clementina, Gomez‐Puertas, Paulino, Møller, Rikke S., Tümer, Zeynep

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Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder by Dias, Caroline M., Punetha, Jaya, Zheng, Céline, Mazaheri, Neda, Rad, Abolfazl, Efthymiou, Stephanie, Petersen, Andrea, Dehghani, Mohammadreza, Pehlivan, Davut, Partlow, Jennifer N., Posey, Jennifer E., Salpietro, Vincenzo, Gezdirici, Alper, Malamiri, Reza Azizi, Al Menabawy, Nihal M., Selim, Laila A., Vahidi Mehrjardi, Mohammad Yahya, Banu, Selina, Polla, Daniel L., Yang, Edward, Rezazadeh Varaghchi, Jamileh, Mitani, Tadahiro, van Beusekom, Ellen, Najafi, Maryam, Sedaghat, Alireza, Keller-Ramey, Jennifer, Durham, Leslie, Coban-Akdemir, Zeynep, Karaca, Ender, Orlova, Valeria, Schaeken, Lieke L.M., Sherafat, Amir, Jhangiani, Shalini N., Stanley, Valentina, Shariati, Gholamreza, Galehdari, Hamid, Gleeson, Joseph G., Walsh, Christopher A., Lupski, James R., Seiradake, Elena, Houlden, Henry, van Bokhoven, Hans, Maroofian, Reza

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The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations by Rodríguez Cruz, Pedro M, Cossins, Judith, Estephan, Eduardo de Paula, Munell, Francina, Selby, Kathryn, Hirano, Michio, Maroofin, Reza, Mehrjardi, Mohammad Yahya Vahidi, Chow, Gabriel, Carr, Aisling, Manzur, Adnan, Robb, Stephanie, Munot, Pinki, Wei Liu, Wei, Banka, Siddharth, Fraser, Harry, De Goede, Christian, Zanoteli, Edmar, Conti Reed, Umbertina, Sage, Abigail, Gratacos, Margarida, Macaya, Alfons, Dusl, Marina, Senderek, Jan, Töpf, Ana, Hofer, Monika, Knight, Ravi, Ramdas, Sithara, Jayawant, Sandeep, Lochmüller, Hans, Palace, Jacqueline, Beeson, David

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Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locus by Maroofian, Reza, Pagnamenta, Alistair T., Navabazam, Alireza, Schwessinger, Ron, Roberts, Hannah E., Lopopolo, Maria, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Haerian, Alireza, Soltanianzadeh, Mojtaba, Noori Kooshki, Mohammad Hadi, Knight, Samantha J.L., Miller, Kerry A., McGowan, Simon J., Chatron, Nicolas, Timberlake, Andrew T., Melo, Uirá Souto, Mundlos, Stefan, Buck, David, Twigg, Stephen R.F., Taylor, Jenny C., Wilkie, Andrew O.M., Calpena, Eduardo

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A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family by Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Kalantar, Seyed M., Jaafarinia, Mojtaba, Chilton, John, Dehghani, Mohammadreza

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B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycan... by Maroofian, Reza, Riemersma, Moniek, Jae, Lucas T, Zhianabed, Narges, Willemsen, Marjolein H, Wissink-Lindhout, Willemijn M, Willemsen, Michèl A, de Brouwer, Arjan P M, Mehrjardi, Mohammad Yahya Vahidi, Ashrafi, Mahmoud Reza, Kusters, Benno, Kleefstra, Tjitske, Jamshidi, Yalda, Nasseri, Mojila, Pfundt, Rolph, Brummelkamp, Thijn R, Abbaszadegan, Mohammad Reza, Lefeber, Dirk J, van Bokhoven, Hans

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Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity by Dehghani, Mohammad Reza, Mehrjardi, Mohammad Yahya Vahidi, Dilaver, Nafi, Tajamolian, Masoud, Enayati, Samaneh, Ebrahimi, Pirooz, Amoli, Mahsa M., Farooqi, Sadaf, Maroofian, Reza

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Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment by Kaiyrzhanov, Rauan, Thompson, Kyle, Efthymiou, Stephanie, Mukushev, Askhat, Zharylkassyn, Akbota, Prasad, Chitra, Ghayoor Karimiani, Ehsan, Alvi, Javeria Raza, Niyazov, Dmitriy, Alahmad, Ahmad, Babaei, Meisam, Tajsharghi, Homa, Albash, Buthaina, Alaqeel, Ahmad, Charif, Majida, Hashemi, Narges, Heidari, Morteza, Kalantar, Seyed Mehdi, Lenaers, Guy, Mehrjardi, Mohammad Yahya Vahidi, Srinivasan, Varunvenkat M., Gowda, Vykuntaraju K., Mirabutalebi, Seyed Hamidreza, Carere, Deanna Alexis, Movahedinia, Mojtaba, Murphy, David, McFarland, Robert, Abdel-Hamid, Mohamed S., Elhossini, Rasha M., Alavi, Shahryar, Napier, Melanie, Belanger-Quintana, Amaya, Prasad, Asuri N., Jakobczyk, Jessica, Roubertie, Agathe, Rupar, Tony, Sultan, Tipu, Toosi, Mehran Beiraghi, Sazanov, Leonid, Severino, Mariasavina, Houlden, Henry, Taylor, Robert W., Maroofian, Reza

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