Хайлтын үр дүнгүүд - Vahidi Mehrjardi, Mohammad Yahya

A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families -н Dehghani, Mohammadreza, Dehghan Tezerjani, Masoud, Metanat, Zahra, Vahidi Mehrjardi, Mohammad Yahya

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A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) -н Dehghan Tezerjani, Masoud, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Rahmanian, Masoud

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Plasma miR‐21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus -н Yazdanpanah, Zakieh, Kazemipour, Nasrin, Kalantar, Seyed Mehdi, Vahidi Mehrjardi, Mohammad Yahya

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Molecular biomarkers in diabetes mellitus (DM) -н Aghaei Zarch, Seyed Mohsen, Dehghan Tezerjani, Masoud, Talebi, Mehrdad, Vahidi Mehrjardi, Mohammad Yahya

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Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report -н VAHIDI MEHRJARDI, Mohammad Yahya, DEHGHAN TEZERJANI, Masoud, NORI-SHADKAM, Mahmoud, KALANTAR, Seyed Mehdi, DEHGHANI, Mohammadreza

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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 -н Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Kalantar, Seyed M., Jaafarinia, Mojtaba, Chilton, John, Dehghani, Mohammadreza

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Evaluation of NF1 and RASA1 gene expression in endometriosis -н Yarahmadi, Ghafour, Dehghanian, Mehran, Sandoghsaz, Reyhaneh Sadat, Savaee, Mohamadreza, Shamsi, Farimah, Vahidi Mehrjardi, Mohammad Yahya

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Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families -н Moudi, Mahdiyeh, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Metanat, Zahra, Kalantar, Seyed Mehdi, Taheri, Mohsen, Ghasemi, Nasrin, Dehghani, Mohammadreza

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Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes -н 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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Circulating microRNA-122, microRNA-126-3p and microRNA-146a are associated with inflammation in patients with pre-diabetes and type 2 diabetes mellitus: A case control study -н Zeinali, Fahime, Aghaei Zarch, Seyed Mohsen, Jahan-Mihan, Alireza, Kalantar, Seyed Mehdi, Vahidi Mehrjardi, Mohammad Yahya, Fallahzadeh, Hossein, Hosseinzadeh, Mahdieh, Rahmanian, Masoud, Mozaffari-Khosravi, Hassan

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A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report -н DEHGHAN TEZERJANI, Masoud, MAROOFIAN, Reza, VAHIDI MEHRJARDI, Mohammad Yahya, CHIOZA, Barry A., ZAMANINEJAD, Shiva, KALANTAR, Seyed Mehdi, NORI-SHADKAM, Mahmoud, GHADIMI, Hamidreza, BAPLE, Emma L., CROSBY, Andrew H., DEHGHANI, Mohammadreza

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Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study prot... -н Zeinali, Fahime, Aghaei Zarch, Seyed Mohsen, Vahidi Mehrjardi, Mohammad Yahya, Kalantar, Seyed Mehdi, Jahan-mihan, Alireza, Karimi-Nazari, Elham, Fallahzadeh, Hossein, Hosseinzadeh-Shamsi-Anar, Mahdieh, Rahmanian, Masoud, Fazeli, Mohammad Reza, Mozaffari-Khosravi, Hassan

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Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum -н Kaiyrzhanov, Rauan, Wortmann, Saskia, Reid, Taryn, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Alhaddad, Bader, Wagner, Matias, Deschauer, Marcus, Cordts, Isabell, Fernandez-Murray, J Pedro, Treffer, Veronika, Metanat, Zahra, Pittman, Alan, Houlden, Henry, Meitinger, Thomas, Carroll, Christopher, McMaster, Christopher R, Maroofian, Reza

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Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration -н Muto, Valentina, Flex, Elisabetta, Kupchinsky, Zachary, Primiano, Guido, Galehdari, Hamid, Dehghani, Mohammadreza, Cecchetti, Serena, Carpentieri, Giovanna, Rizza, Teresa, Mazaheri, Neda, Sedaghat, Alireza, Vahidi Mehrjardi, Mohammad Yahya, Traversa, Alice, Di Nottia, Michela, Kousi, Maria M., Jamshidi, Yalda, Ciolfi, Andrea, Caputo, Viviana, Malamiri, Reza Azizi, Pantaleoni, Francesca, Martinelli, Simone, Jeffries, Aaron R., Zeighami, Jawaher, Sherafat, Amir, Di Giuda, Daniela, Shariati, Gholam Reza, Carrozzo, Rosalba, Katsanis, Nicholas, Maroofian, Reza, Servidei, Serenella, Tartaglia, Marco

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Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy -н McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace

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Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder -н 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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