A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families

מאת Dehghani, Mohammadreza, Dehghan Tezerjani, Masoud, Metanat, Zahra, Vahidi Mehrjardi, Mohammad Yahya
הוצא לאור ב Int J Mol Cell Med (2017)

A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)

מאת Dehghan Tezerjani, Masoud, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Rahmanian, Masoud
הוצא לאור ב Front Pediatr (2020)

Molecular biomarkers in diabetes mellitus (DM)

מאת Aghaei Zarch, Seyed Mohsen, Dehghan Tezerjani, Masoud, Talebi, Mehrdad, Vahidi Mehrjardi, Mohammad Yahya
הוצא לאור ב Med J Islam Repub Iran (2020)

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report

מאת VAHIDI MEHRJARDI, Mohammad Yahya, DEHGHAN TEZERJANI, Masoud, NORI-SHADKAM, Mahmoud, KALANTAR, Seyed Mehdi, DEHGHANI, Mohammadreza
הוצא לאור ב Iran J Public Health (2016)

A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family

מאת Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Kalantar, Seyed M., Jaafarinia, Mojtaba, Chilton, John, Dehghani, Mohammadreza
הוצא לאור ב Mol Syndromol (2017)

Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes

מאת Sadeghzadeh, Salman, Dehghani Ashkezari, Mahmood, Seifati, Seyed Morteza, Vahidi Mehrjardi, Mohammad Yahya, Dehghan Tezerjani, Masoud, Sadeghzadeh, Sara, Ladan, Seyed Amir Behtash
הוצא לאור ב Diabetes Metab Syndr Obes (2020)

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

מאת 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
הוצא לאור ב PLoS One (2021)

A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report

מאת 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
הוצא לאור ב Iran J Public Health (2016)

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...

מאת 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
הוצא לאור ב Trials (2020)

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum

מאת 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
הוצא לאור ב Brain (2021)

Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration

מאת 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
הוצא לאור ב Neurology (2018)

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

מאת 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
הוצא לאור ב Orphanet J Rare Dis (2018)

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

מאת 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
הוצא לאור ב Am J Hum Genet (2019)