Personal information

Other IDs

Scopus Author ID: 57188860314

Countries

Iran

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Employment (3)

Shahid Sadoughi  University of Medical Sciences and Health Services: Yazd, Yazd, IR

2017 to present | faculty member (Genetics)
Employment
Source: Self-asserted source
Mohammadreza Dehghani

Shahid Sadoughi  University of Medical Sciences and Health Services: Yazd, Yazd, IR

2014 to present | Head (Medical Genetic research Center)
Employment
Source: Self-asserted source
Mohammadreza Dehghani

Shahid Sadoughi  University of Medical Sciences and Health Services: Yazd, Yazd, IR

2013 to 2014 | manager (Shahid Sadoughi Hospital)
Employment
Source: Self-asserted source
Mohammadreza Dehghani

Education and qualifications (2)

Università degli Studi di Pavia: Pavia, Lombardia, IT

2008-11 to 2012-11 | PhD (Medical Genetics)
Education
Source: Self-asserted source
Mohammadreza Dehghani

Islamic Azad University Science and Research Branch: Tehran, Tehran, IR

1989 to 1996 | MD (Medical school)
Education
Source: Self-asserted source
Mohammadreza Dehghani

Works (10)

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

Public Health Genomics
2017 | Journal article
DOI: 10.1159/000477560
EID:

2-s2.0-85025460321
Contributors: Dehghani, M.R.; Mojarad, M.; Karimiani, E.G.; Mehrjardi, M.Y.V.; Sahebalzamani, A.; Ashrafzadeh, F.; Toosi, M.B.; Eslahi, A.; Ahangari, N.; Yassini, S.M. et al.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

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

Molecular Syndromology
2017 | Journal article
DOI: 10.1159/000477752
EID:

2-s2.0-85021663877
Contributors: Vahidi Mehrjardi, M.Y.; Maroofian, R.; Kalantar, S.M.; Jaafarinia, M.; Chilton, J.; Dehghani, M.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

A novel missense mutation in the ALDH13 gene causes anophthalmia in two unrelated Iranian consanguineous families

International Journal of Molecular and Cellular Medicine
2017 | Journal article
EID:

2-s2.0-85021856438
Contributors: Dehghani, M.; Tezerjani, M.D.; Metanat, Z.; Mehrjardi, M.Y.V.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

A novel mutation in the OFD1 gene in a family with oral-facial-digital syndrome type 1: A case report

Iranian Journal of Public Health
2016 | Journal article
EID:

2-s2.0-84992316304
Contributors: Dehghan Tezerjani, M.; Maroofian, R.; Vahidi Mehrjardi, M.Y.; Chioza, B.A.; Zamaninejad, S.; Kalantar, S.M.; Nori-Shadkam, M.; Ghadimi, H.; Baple, E.L.; Crosby, A.H. et al.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder

European Journal of Human Genetics
2016 | Journal article
DOI: 10.1038/ejhg.2016.58
EID:

2-s2.0-84976342612
Contributors: Alves, M.M.; Halim, D.; Maroofian, R.; De Graaf, B.M.; Rooman, R.; Van Der Werf, C.S.; Van De Vijver, E.; Mehrjardi, M.Y.V.; Aflatoonian, M.; Chioza, B.A. et al.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

Newborn with supernumerary marker chromosome derived from chromosomes 11 and 22- A case report

Iranian Journal of Public Health
2016 | Journal article
EID:

2-s2.0-84963826941
Contributors: Vahidi Mehrjardi, M.Y.; Dehghan Tezerjani, M.; Nori-Shadkam, M.; Kalantar, S.M.; Dehghani, M.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

Genetic susceptibility to transient and permanent neonatal diabetes mellitus

International Journal of Pediatrics
2015 | Journal article
DOI: 10.22038/ijp.2015.5628
EID:

2-s2.0-85015953889
Contributors: Tezerjani, M.D.; Mehrjardi, M.Y.V.; Kalantar, S.M.; Dehghani, M.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

Testis development in the absence of SRY: Chromosomal rearrangements at SOX9 and SOX3

European Journal of Human Genetics
2015 | Journal article
DOI: 10.1038/ejhg.2014.237
EID:

2-s2.0-84937526184
Contributors: Vetro, A.; Dehghani, M.R.; Kraoua, L.; Giorda, R.; Beri, S.; Cardarelli, L.; Merico, M.; Manolakos, E.; Parada-Bustamante, A.; Castro, A. et al.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

X chromosome skewness in neurological disorders

Genetics in the Third Millennium
2014 | Journal article
EID:

2-s2.0-84933545135
Contributors: Negahdari, S.; Rasti, A.; Dehghani, M.; Froughmand, A.; Montazeri, F.; Ghadimi, H.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier

Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene

European Journal of Medical Genetics
2013 | Journal article
DOI: 10.1016/j.ejmg.2013.08.003
EID:

2-s2.0-84885382157
Contributors: Bayindir, B.; Piazza, E.; Della Mina, E.; Limongelli, I.; Brustia, F.; Ciccone, R.; Veggiotti, P.; Zuffardi, O.; Dehghani, M.R.
Source: Self-asserted source
Mohammadreza Dehghani via Scopus - Elsevier
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