Mohammad Yahya Vahidi Mehrjardi

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Topics

Autism Spectrum Disorder

Long Noncoding Rna

Top Venues

Molecular genetics & genomic medicine

Physiological reports

Biochemical genetics

Diabetes, metabolic syndrome and obesity : targets and therapy

This page only lists publications with an associated author ORCID identifier.

Publications

Masoumeh Heidari Feizabadi, Masoome Alerasool, Atieh Eslahi, Emran Esmaeilzadeh, Mohammad Yahya Vahidi Mehrjardi, Mitra Saket, Shima Farokhi, Zohreh Fattahi, Hamid Reza Khorram Khorshid, Majid Mojarrad
Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A. Biochemical genetics (2024)
Erfan Zaker, Negar Nouri, Mojtaba Movahedinia, Ali Dadbinpour, Mohammad Yahya Vahidi Mehrjardi
Type 1 early infantile epileptic encephalopathy: A case report and literature review. Molecular genetics & genomic medicine 12 (2) (2024)
Erfan Zaker, Negar Nouri, Mojtaba Movahedinia, Ali Dadbinpour, Mohammad Yahya Vahidi Mehrjardi
Type 1 early infantile epileptic encephalopathy: A case report and literature review. Molecular genetics & genomic medicine 12 (2) (2024)
Maria Bejerholm Christensen, Amanda M Levy, Nazanin A Mohammadi, Marcello Niceta, Rauan Kaiyrzhanov, Maria Lisa Dentici, Chadi Al Alam, Viola Alesi, Valérie Benoit, Kailash P Bhatia, Tatjana Bierhals, Christian Malte Boßelmann, Julien Buratti, Bert Callewaert, Berten Ceulemans, Perrine Charles, Matthias De Wachter, Mohammadreza Dehghani, Erika D'haenens, Martine Doco-Fenzy, Michaela Geßner, Cyrielle Gobert, Ulviyya Guliyeva, Tobias B Haack, Trine B Hammer, Tilman Heinrich, Maja Hempel, Theresia Herget, Ute Hoffmann, Judit Horvath, Henry Houlden, Boris Keren, Christina Kresge, Candy Kumps, Damien Lederer, Alban Lermine, Francesca Magrinelli, Reza Maroofian, Mohammad Yahya Vahidi Mehrjardi, Mahdiyeh Moudi, Amelie J Müller, Anna J Oostra, Beth A Pletcher, David Ros-Pardo, Shanika R Samarasekera, Tartaglia Marco, Kristof Van Schil, Julie Vogt, Evangeline Wassmer, Juliane Winkelmann, Maha Saad Zaki, Michael Zech, Holger Lerche, Francesca Clementina Radio, Paulino Gómez-Puertas, Rikke Steensjerre Moller, Zeynep Tümer
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Clinical genetics 102 (2) (2022)
Zakieh Yazdanpanah, Nasrin Kazemipour, Seyed Mehdi Kalantar, Mohammad Yahya Vahidi Mehrjardi
Plasma miR-21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus. Physiological reports 10 (2) (2022)
Masoud Dehghan Tezerjani, Behdokht Fathi Dizaji, Zahra Metanat, Mohammad Yahya Vahidi Mehrjardi
Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous family. Ophthalmic genetics 42 (6) (2021)
Seyed Mohsen Aghaei Zarch, Masoud Dehghan Tezerjani, Mehrdad Talebi, Mohammad Yahya Vahidi Mehrjardi
Molecular biomarkers in diabetes mellitus (DM). Medical journal of the Islamic Republic of Iran 34 (2020)
Salman Sadeghzadeh, Mahmood Dehghani Ashkezari, Seyed Morteza Seifati, Mohammad Yahya Vahidi Mehrjardi, Masoud Dehghan Tezerjani, Sara Sadeghzadeh, Seyed Amir Behtash Ladan
Circulating miR-15a and miR-222 as Potential Biomarkers of Type 2 Diabetes. Diabetes, metabolic syndrome and obesity : targets and therapy 13 (2020)