Neda Shahmohammadibeni

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations

Shaghayegh Taghavi, Rita Chaouni, Abbas Tafakhori et al. · Molecular Neurobiology · 2017 · 86 citations · Full text

Mendelian Disorder, Molecular Genetic Study, Genetic Disorder +10

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

Matias Wagner, Daniel P. S. Osborn, Ina Gehweiler et al. · Nature Communications · 2019 · 51 citations · Full text

RIT2 Polymorphisms: Is There a Differential Association?

Babak Emamalizadeh, Javad Jamshidi, Abolfazl Movafagh et al. · Molecular Neurobiology · 2016 · 36 citations

Genetic Determinant, Genotype-phenotype Association, Genetics +5

Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population

Leyla Haghnejad, Babak Emamalizadeh, Javad Jamshidi et al. · Journal of the Neurological Sciences · 2015 · 27 citations

Systems Biology, Developmental Biology, Iranian Population +7

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder

Minoo Atakhorrami, Simin Rahimi-Aliabadi, Javad Jamshidi et al. · Journal of Neural Transmission · 2015 · 20 citations

Camkk2 Gene, Genetic Variant, Psychiatry +9