Works by Vahidi Mehrjardi, Mohammad Yahya

Results: 38

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.

Published in:

2021

By:

Kaiyrzhanov, Rauan;
Wortmann, Saskia;
Reid, Taryn;
Dehghani, Mohammadreza;
Mehrjardi, Mohammad Yahya Vahidi;
Alhaddad, Bader;
Wagner, Matias;
Deschauer, Marcus;
Cordts, Isabell;
Fernandez-Murray, J Pedro;
Treffer, Veronika;
Metanat, Zahra;
Pitman, Alan;
Houlden, Henry;
Meitinger, Thomas;
Carroll, Christopher;
McMaster, Christopher R;
Maroofian, Reza;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Letter

Evaluation of the relationship between miR-337-3p and RAP1A gene in endometriosis.

Published in:

Journal of Endometriosis & Pelvic Pain Disorders, 2022, v. 14, n. 4, p. 178, doi. 10.1177/22840265221099622

By:

Dehghanian, Mehran;
Yarahmadi, Ghafour;
Fazeli, Javad;
Vahidi Mehrjardi, Mohammad Yahya;
Javaheri, Atiyeh;
Kalantar, Seyed Mehdi;
Dehghani, Mohammadreza

Publication type:

Article

Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report.

Published in:

Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00293-x

By:

Moudi, Mahdiyeh;
Vahidi Mehrjardi, Mohammad Yahya;
Kalantar, Seyed Mehdi;
Taheri, Mohsen;
Metanat, Zahra;
Ghasemi, Nasrin;
Dehghani, Mohammadreza

Publication type:

Article

Characterizing Homozygous Variants in Bardet-Biedl Syndrome-Associated Genes Within Iranian Families: Unveiling a Founder Variant in BBS2, c.471G>A.

Published in:

2025

By:

Feizabadi, Masoumeh Heidari;
Alerasool, Masoome;
Eslahi, Atieh;
Esmaeilzadeh, Emran;
Mehrjardi, Mohammad Yahya Vahidi;
Saket, Mitra;
Farokhi, Shima;
Fattahi, Zohreh;
Khorshid, Hamid Reza Khorram;
Mojarrad, Majid

Publication type:

Case Study

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant.

Published in:

2018

By:

Helal, Mayada;
Mazaheri, Neda;
Shalbafan, Bita;
Malamiri, Reza Azizi;
Dilaver, Nafi;
Buchert, Rebecca;
Mohammadiasl, Javad;
Golchin, Neda;
Sedaghat, Alireza;
Mehrjardi, Mohammad Yahya Vahidi;
Haack, Tobias B.;
Riess, Olaf;
Chung, Wendy K.;
Galehdari, Hamid;
Shariati, Gholamreza;
Maroofian, Reza

Publication type:

journal article

Association of NFKB1 gene polymorphism (rs28362491) with cardiometabolic risk factor in patients undergoing coronary angiography.

Published in:

Journal of Cardiovascular & Thoracic Research, 2023, v. 15, n. 3, p. 161, doi. 10.34172/jcvtr.2023.31834

By:

Darabi, Zahra;
Jambarsang, Sara;
Vahidi Mehrjardi, Mohammad Yahya;
Seyed Hosseini, Seyed Mostafa;
Sarebanhassanabadi, Mohammadtaghi;
Hosseinzadeh, Mahdieh;
Beigrezaei, Sara;
Ahmadi Vasmehjani, Azam;
Taftian, Marzieh;
Arabi, Vahid;
Motallaei, Maryam;
Golvardi Yazdi, Faezeh;
Salehi-Abargouei, Amin;
Nadjarzadeh, Azadeh

Publication type:

Article

The impact of Polymorphisms of rs689 and rs757110 in Familial Type 2 Diabetes: A Case-Control Study in the Iranian Population.

Published in:

Iranian Journal of Diabetes & Obesity (IJDO), 2025, v. 17, n. 1, p. 19, doi. 10.18502/ijdo.v17i1.18030

By:

Haghighi, Amin;
Javid, Amaneh;
Khodadadian, Ali;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

MiR-194-5p might be a Potential Biomarker for Type 2 Diabetes Mellitus.

Published in:

Iranian Journal of Diabetes & Obesity (IJDO), 2024, v. 16, n. 3, p. 167, doi. 10.18502/ijdo.v16i3.16324

By:

Dadbinpour, Ali;
Dehghanian, Mehran;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

Antibody Engineering to Enhancement of Ranibizumab Binding Affinity for the Prevention and Treatment of Diabetic Retinopathy.

Published in:

Iranian Journal of Diabetes & Obesity (IJDO), 2024, v. 16, n. 2, p. 112, doi. 10.18502/ijdo.v16i2.15710

By:

Sefid, Fateme;
Monshizadeh, Kimia;
Azamirad, Ghasem;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

Common Polymorphisms Identified In Patients with Type 2 Diabetes Mellitus Revealed From Next-Generation Sequencing Analysis.

Published in:

Iranian Journal of Diabetes & Obesity (IJDO), 2023, v. 15, n. 2, p. 73, doi. 10.18502/ijdo.v15i2.12964

By:

Sefid, Fateme;
Azamirad, Ghasem;
Asadollahi, Samira;
Kalantar, Seyed Mehdi;
Khalilzade, Saeed Hosein;
Mehrjardi, Mohammad Yahya Vahidi

Publication type:

Article

Investigating the Relation between LCK Gene Expression with Type 2 Diabetes Patients in Yazd Diabetes Research Center.

Published in:

Iranian Journal of Diabetes & Obesity (IJDO), 2022, v. 14, n. 1, p. 14, doi. 10.18502/ijdo.v14i1.8736

By:

Rahvarzadeh, Zahra;
Dehghanian, Mehran;
Mehrjardi, Mohammad Yahya Vahidi;
Ashkezari, Mahmood Dehghani

Publication type:

Article

Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.

Published in:

Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 2, p. 1, doi. 10.1002/jcla.24241

By:

Moudi, Mahdiyeh;
Vahidi Mehrjardi, Mohammad Yahya;
Hozhabri, Hossein;
Metanat, Zahra;
Kalantar, Seyed Mehdi;
Taheri, Mohsen;
Ghasemi, Nasrin;
Dehghani, Mohammadreza

Publication type:

Article

Evaluation of Rap1GAP and EPAC1 Gene Expression in Endometriosis Disease.

Published in:

Advanced Biomedical Research, 2023, v. 12, n. 4, p. 1, doi. 10.4103/abr.abr_86_22

By:

Dehghanian, Mehran;
Yarahmadi, Ghafour;
Sandoghsaz, Reyhaneh Sadat;
Khodadadian, Ali;
Shamsi, Farimah;
Mehrjardi, Mohammad Yahya Vahidi

Publication type:

Article

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

Published in:

Diabetes, Metabolic Syndrome & Obesity: Targets & Therapy, 2020, v. 13, p. 3461, doi. 10.2147/DMSO.S263883

By:

Sadeghzadeh, Salman;
Ashkezari, Mahmood Dehghani;
Seifati, Seyed Morteza;
Mehrjardi, Mohammad Yahya Vahidi;
Tezerjani, Masoud Dehghan;
Sadeghzadeh, Sara;
Ladan, Seyed Amir Behtash

Publication type:

Article

The association of RBX1 and BAMBI gene expression with oocyte maturation in PCOS women.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01800-2

By:

Monshizadeh, Kimia;
Tajamolian, Masoud;
Anbari, Fatemeh;
Mehrjardi, Mohammad Yahya Vahidi;
Kalantar, Seyed Mehdi;
Dehghani, Mohammadreza

Publication type:

Article

Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous family.

Published in:

Ophthalmic Genetics, 2021, v. 42, n. 6, p. 787, doi. 10.1080/13816810.2021.1955276

By:

Dehghan Tezerjani, Masoud;
Fathi Dizaji, Behdokht;
Metanat, Zahra;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the FLVCR1 gene.

Published in:

2020

By:

Beigi, Fahimeh;
Del Pozo-Valero, Marta;
Martin-Merida, Inmaculada;
Vahidi Mehrjardi, Mohammad Yahya;
Manaviat, Masoud Reza;
Sherafat, Amir;
Ayuso, Carmen;
Ghasemi, Nasrin

Publication type:

Letter

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

Published in:

Molecular Syndromology, 2017, v. 8, n. 5, p. 261, doi. 10.1159/000477752

By:

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

Publication type:

Article

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 protocol for a double-blind controlled randomized clinical trial.

Published in:

2020

By:

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

Publication type:

journal article

Repurposing doxycycline for a case of CONDSIAS Syndrome with a novel ADPRHL2 missense mutation.

Published in:

2025

By:

Eslamiyeh, Hosein;
Vahidi Mehrjardi, Mohammad Yahya;
Poursalehi, Negareh;
Dehghan Tezerjani, Masoud

Publication type:

Letter

Uncovering the genetic architecture of inherited retinal disease in a consanguineous Iranian cohort.

Published in:

NPJ Genomic Medicine, 2025, v. 10, n. 1, p. 1, doi. 10.1038/s41525-025-00473-9

By:

Vincke, Lieselot;
Van Schil, Kristof;
Ahmadieh, Hamid;
Moghaddasi, Afrooz;
Sabbaghi, Hamideh;
Daftarian, Narsis;
Motevasseli, Tahmineh;
Javanparast Sheykhani, Leila;
Dehghani, Mohammadreza;
Vahidi Mehrjardi, Mohammad Yahya;
De Zaeytijd, Julie;
De Bruyne, Marieke;
Mahieu, Quinten;
Al-Hajj, Ebrahim;
Del Pozo-Valero, Marta;
Rosseel, Toon;
Van Heetvelde, Mattias;
Maroofian, Reza;
Suri, Fatemeh;
Bauwens, Miriam

Publication type:

Article

Interaction of dietary patterns with rs28362491 on severity of coronary artery stenosis in patients undergoing coronary angiography.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41438-1

By:

Darabi, Zahra;
Seyed Hosseini, Seyed Mostafa;
Sarebanhassanabadi, Mohammadtaghi;
Jambarsang, Sara;
Vahidi Mehrjardi, Mohammad Yahya;
Hosseinzadeh, Mahdieh;
Beigrezaei, Sara;
Vasmehjani, Azam Ahmadi;
Taftian, Marzieh;
Arabi, Vahid;
Motallaei, Maryam;
Yazdi, Faezeh Golvardi;
Salehi-Abargouei, Amin;
Nadjarzadeh, Azadeh

Publication type:

Article

Interaction of dietary patterns with rs28362491 on severity of coronary artery stenosis in patients undergoing coronary angiography.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41438-1

By:

Darabi, Zahra;
Seyed Hosseini, Seyed Mostafa;
Sarebanhassanabadi, Mohammadtaghi;
Jambarsang, Sara;
Vahidi Mehrjardi, Mohammad Yahya;
Hosseinzadeh, Mahdieh;
Beigrezaei, Sara;
Vasmehjani, Azam Ahmadi;
Taftian, Marzieh;
Arabi, Vahid;
Motallaei, Maryam;
Yazdi, Faezeh Golvardi;
Salehi-Abargouei, Amin;
Nadjarzadeh, Azadeh

Publication type:

Article

The Relationship between Mutation in HOXB1 Gene and Acute Myeloid Leukemia.

Published in:

Iranian Journal of Pediatric Hematology & Oncology, 2019, v. 9, n. 4, p. 229

By:

Vahidi Mehrjardi, Mohammad Yahya;
Aghaei Zarch, Seyed Mohsen;
Dehghani, Mohammadreza

Publication type:

Article

B3GALNT2 mutations associated with nonsyndromic autosomal recessive intellectual disability reveal a lack of genotype- phenotype associations in the muscular dystrophy-dystroglycanopathies.

Published in:

Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0505-2

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.;
Vahidi Mehrjardi, Mohammad Yahya;
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

Publication type:

Article

Investigation of rs328 polymorphism of lipoprotein lipase and rs1260326 polymorphism of glucokinase regulatory genes in individuals with type 2 diabetes in Yazd, Iran.

Published in:

Egyptian Journal of Medical Human Genetics, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s43042-025-00682-y

By:

Rezazadeh Khabaz, Mohammad Javad;
Dastghaib, Sanaz;
Vahidi Mehrjardi, Mohammad Yahya;
Sheikhha, Mohammad Hasan

Publication type:

Article

The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.

Published in:

2019

By:

Cruz, Pedro M. Rodríguez;
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;
Liu, Wei Wei;
Banka, Siddharth;
Fraser, Harry;
Goede, Christian De;
Zanoteli, Edmar;
Reed, Umbertina Conti;
Sage, Abigail

Publication type:

journal article

GGPS1-associated muscular dystrophy with and without hearing loss.

Published in:

Annals of Clinical & Translational Neurology, 2022, v. 9, n. 9, p. 1465, doi. 10.1002/acn3.51633

By:

Kaiyrzhanov, Rauan;
Perry, Luke;
Rocca, Clarissa;
Zaki, Maha S.;
Hosny, Heba;
Martins Moreno, Cristiane Araujo;
Phadke, Rahul;
Zaharieva, Irina;
Camelo Gontijo, Clara;
Beetz, Christian;
Pini, Veronica;
Movahedinia, Mojtaba;
Zanoteli, Edmar;
DiTroia, Stephanie;
Vuillaumier-Barrot, Sandrine;
Isapof, Arnaud;
Mehrjardi, Mohammad Yahya Vahidi;
Ghasemi, Nasrin;
Sarkozy, Anna;
Muntoni, Francesco

Publication type:

Article

Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment.

Published in:

Brain Communications, 2025, v. 7, n. 1, p. 1, doi. 10.1093/braincomms/fcae453

By:

Kaiyrzhanov, Rauan;
Thompson, Kyle;
Efthymiou, Stephanie;
Mukushev, Askhat;
Zharylkassyn, Akbota;
Prasad, Chitra;
Karimiani, Ehsan Ghayoor;
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

Publication type:

Article

Plasma miR‐21 as a potential predictor in prediabetic individuals with a positive family history of type 2 diabetes mellitus.

Published in:

Physiological Reports, 2022, v. 10, n. 2, p. 1, doi. 10.14814/phy2.15163

By:

Yazdanpanah, Zakieh;
Kazemipour, Nasrin;
Kalantar, Seyed Mehdi;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

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.

Published in:

PLoS ONE, 2021, v. 16, n. 6, p. 1, doi. 10.1371/journal.pone.0251697

By:

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

Publication type:

Article

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

Published in:

2018

By:

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

Publication type:

journal article

Testicular expression of TDRD1, TDRD5, TDRD9 and TDRD12 in azoospermia.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0970-0

By:

Babakhanzadeh, Emad;
Khodadadian, Ali;
Rostami, Saadi;
Alipourfard, Iraj;
Aghaei, Mohsen;
Nazari, Majid;
Hosseinnia, Mehdi;
Mehrjardi, Mohammad Yahya Vahidi;
Jamshidi, Yalda;
Ghasemi, Nasrin

Publication type:

Article

A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report.

Published in:

International Journal of Reproductive Biomedicine, 2019, v. 17, n. 6, p. 449, doi. 10.18502/ijrm.v17i6.4817

By:

Nazari, Majid;
Mehrjardi, Mohammad Yahya Vahidi;
Neghab, Nosrat;
Aghabagheri, Mahdi;
Ghasemi, Nasrin

Publication type:

Article

Is there any relationship between mutation in CPS1 Gene and pregnancy loss?

Published in:

International Journal of Reproductive Biomedicine, 2019, v. 17, n. 5, p. 371, doi. 10.18502/ijrm.v17i5.4604

By:

Talebi, Mehrdad;
Vahidi Mehrjardi, Mohammad Yahya;
Kalhor, Kambiz;
Dehghani, Mohammadreza

Publication type:

Article

Type 1 early infantile epileptic encephalopathy: A case report and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 2, p. 1, doi. 10.1002/mgg3.2412

By:

Zaker, Erfan;
Nouri, Negar;
Movahedinia, Mojtaba;
Dadbinpour, Ali;
Vahidi Mehrjardi, Mohammad Yahya

Publication type:

Article

A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.

Published in:

Public Health Genomics, 2017, v. 20, n. 3, p. 188, doi. 10.1159/000477560

By:

Dehghani, MohammadReza;
Mojarad, Majid;
Ghayoor Karimiani, Ehsan;
Vahidi Mehrjardi, Mohammad Yahya;
Sahebalzamani, afsaneh;
ashrafzadeh, Farah;
Beiraghi Toosi, Mehran;
Eslahi, atiyeh;
ahangari, Najmeh;
Yassini, Seyed Mojtaba;
Hassanbeigi, afsaneh;
Rasti, azam;
Kalantar, Seyed Mehdi;
Maroofian, Reza

Publication type:

Article

A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.

Published in:

Public Health Genomics, 2017, v. 20, n. 2, p. 188, doi. 10.1159/000477560

By:

Dehghani, MohammadReza;
Mojarad, Majid;
Karimiani, Ehsan Ghayoor;
Mehrjardi, Mohammad Yahya Vahidi;
Sahebalzamani, Afsaneh;
Ashrafzadeh, Farah;
Toosi, Mehran Beiraghi;
Eslahi, Atiyeh;
Ahangari, Najmeh;
Yassini, Seyed Mojtaba;
Hassanbeigi, Afsaneh;
Rasti, Azam;
Kalantar, Seyed Mehdi;
Maroofian, Reza

Publication type:

Article