Babak Emamalizadeh - Concepedia

Author

Babak Emamalizadeh

Shahid Beheshti University of Medical Sciences ORCID

Also Known As

B Emamalizadeh, B. Emamalizadeh, BABAK EMAMALIZADEH, Babak Emamalizadeh, Shaghayegh Taghavi

Publications

647

Citations

H-Index

Concepts

All Affiliations

Shahid Beheshti University of Medical Sciences Fasa University of Medical Sciences Tehran University of Medical Sciences Tabriz University of Medical Sciences University of Social Welfare and Rehabilitation Sciences

About

Babak Emamalizadeh is an author at Shahid Beheshti University of Medical Sciences specializing in genetics, medicine, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	257
2	Public Health	3	3	83
3	Natural Sciences	1	1	21
4	Biostatistics	1	1	37
5	Cell Biology	1	1	27

Babak Emamalizadeh

Publications

405

Citations

H-Index

Page 1

	Year	Citations
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, Molecular Neurobiology Mendelian DisorderMolecular Genetic StudyGenetic DisorderParkinson DiseaseGenetics	2017	86
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients Hossein Darvish, Abolfazl Movafagh, Mir Davood Omrani, Neuroscience Letters Genetic AnalysisIranian PatientsMendelian DisorderGenetic DisorderMedicine	2013	37
RIT2 Polymorphisms: Is There a Differential Association? Babak Emamalizadeh, Javad Jamshidi, Abolfazl Movafagh, Molecular Neurobiology Genetic DeterminantGenotype-phenotype AssociationGeneticsRit2 PolymorphismsGenetic Epidemiology	2016	36
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, Journal of the Neurological Sciences Systems BiologyDevelopmental BiologyIranian PopulationRisk FactorFibroblast Growth Factor	2015	27
<i><scp>HLA</scp>‐<scp>DRA</scp></i> is associated with <scp>P</scp>arkinson's disease in <scp>I</scp>ranian population Javad Jamshidi, Abolfazl Movafagh, Babak Emamalizadeh, International Journal of Immunogenetics	2014	27
The human RIT2 core promoter short tandem repeat predominant allele is species-specific in length: a selective advantage for human evolution? Babak Emamalizadeh, Abolfazl Movafagh, Hossein Darvish, Molecular Genetics and Genomics Allelic VariantMolecular EcologySelective AdvantageNatural SciencesGenetics	2017	21
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder Minoo Atakhorrami, Simin Rahimi-Aliabadi, Javad Jamshidi, Journal of Neural Transmission Camkk2 GeneGenetic VariantPsychiatryGenetic DisorderGenetics	2015	20
Incomplete penetrance of <i>CRX</i> gene for autosomal dominant form of cone-rod dystrophy Marjan Chapi, Hamideh Sabbaghi, Fatemeh Suri, Ophthalmic Genetics	2019	18
Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes Hossein Darvish, Luís Azcona, Abbas Tafakhori, Scientific Reports	2020	16
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population Neda Shahmohammadibeni, Simin Rahimi-Aliabadi, Javad Jamshidi, Neurological Sciences Neurodegenerative DiseasesIranian PopulationMendelian DisorderGenetic DisorderParkinson Disease	2016	15

Page 1