Concepedia

Mohammadreza Dehghani

MD

7

Publications

260

Citations

7

H-Index

2013

Active since

Affiliations

Shahid Sadoughi University of Medical Sciences and Health Services(Current)

Royal Devon & Exeter NHS Foundation Trust

University of Pavia

University College London

National Hospital for Neurology and Neurosurgery

Mohammadreza Dehghani is an author at Shahid Sadoughi University of Medical Sciences and Health Services specializing in medicine, genetics, and molecular genetics.

ORCID

Top concepts

Publications per year

2013–2020

7

Publications

7

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

Annalisa Vetro, Mohammadreza Dehghani, Lilia Kraoua et al. · European Journal of Human Genetics · 2014 · 108 citations · Full text

, , +13

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

Caroline Dias, Jaya Punetha, Céline Zheng et al. · The American Journal of Human Genetics · 2019 · 57 citations · Full text

, , +17

Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1

Bart Appelhof, Matias Wagner, Julia Hoefele et al. · European Journal of Human Genetics · 2020 · 29 citations · Full text

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

Maria M. Alves, Danny Halim, Reza Maroofian et al. · European Journal of Human Genetics · 2016 · 24 citations · Full text

, , +12

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

Baran Bayindir, Elena Piazza, Erika Della Mina et al. · European Journal of Medical Genetics · 2013 · 16 citations

, , +10

Rows per page

1–5 of 7