Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
BMC Medical Genomics|November 19, 2025
Long-range PCR and Nanopore sequencing for localisation and phasing variants: an end-to-end clinical application workflowJavad Jamshidi, Conor Rowntree, Shannon Fadaee, et al.
International Journal of Fertility & Sterility|February 13, 2014
FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian MenJavad Jamshidi, Farkhondeh Pouresmaeili, Hossein Darvish, et al.
Archives of Iranian Medicine|December 12, 2019
Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve AtrophyFaezeh Jamali, Hamid Ghaedi, Abbas Tafakhori, et al.
Clinical & Experimental Optometry|September 19, 2017
A novel c.240_241insGG mutation in NDP gene in a family with Norrie diseaseMonavvar Andarva, Javad Jamshidi, Hamid Ghaedi, et al.
Medical Journal of the Islamic Republic of Iran|August 31, 2018
<i>ATP2B1 rs2681472</i> and <i>STK39</i> rs35929607 polymorphisms and risk of Hypertension in Iranian PopulationJavad Jamshidi, Ali Asnaashari, Reza Alipoor, et al.
European Journal of Medical Genetics|August 16, 2017
A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndromeJavad Jamshidi, Shokoufeh Abdollahi, Hamid Ghaedi, et al.
Psychiatric Genetics|October 20, 2020
LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian populationElham Poursaei, Yousef Daneshmandpour, Ehsan Aghaei Moghadam, et al.
Psychological Medicine|April 3, 2023
Associations between mental wellbeing and fMRI neural bases underlying responses to positive emotion in a twin sampleHaeme R P Park, Miranda R Chilver, Arthur Montalto, et al.
Journal of the Neurological Sciences|September 23, 2016
SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control studyTannaz Safaralizadeh, Javad Jamshidi, Ehsan Esmaili Shandiz, et al.
Pageof 5