المؤلفون: Shaghyegh Taghavi, Simin Rahimi-Aliabadi, Haleh Akhavan-Niaki, Neda Shahmohammadibeni, Javad Jamshidi, Ramin Pouriran, Farhad Ramezani Nejad, Ehteram Khademi, Parasto Shokraeian, Elham Alehabib, Coro Paisán-Ruiz, Ehsan Esmaili Shandiz, Mina Ohadi, Monavvar Andarva, Nader Mansoori, Azadeh Ahmadifard, Hossein Darvish

المصدر: Genetic Testing and Molecular Biomarkers. 21:485-490

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Iran, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Gene expression, Genotype, Guanine Nucleotide Exchange Factors, Humans, SNP, Allele, Promoter Regions, Genetic, Gene, Alleles, Genetic Association Studies, Genetics (clinical), Genetics, Promoter, General Medicine, Middle Aged, humanities, 030104 developmental biology, Case-Control Studies, Schizophrenia, Microsatellite, Female, Cell Adhesion Molecules, 030217 neurology & neurosurgery, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927af9cfb798cda161819115f2722fc7
https://doi.org/10.1089/gtmb.2016.0422

المؤلفون: Behnam Safarpour Lima, Shaghayegh Taghavi, Monavvar Andarva, Mahmoud Shekari Khaniani, Parasto Shokraeian, Tannaz Safaralizadeh, Peyman Petramfar, Ali Kowsari, Minoo Atakhorrami, Abolfazl Movafagh, Gholam Ali Shahidi, Azadeh Ahmadifard, Tahereh Dadkhah, Mina Ohadi, Marzieh Motallebi, Babak Emamalizadeh, Hossein Darvish, Elham Alehabib, Neda Shahmohammadibeni, Ali Khaligh, Javad Jamshidi, Mohammad Javad Soltani Banavandi, Somayyeh Kazeminasab, Mehdi Khorrami, Ehteram Khademi, Akbar Biglarian, Abbas Tafakhori, Arash Mirabzadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli

المصدر: Molecular Neurobiology. 54:2234-2240

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Bipolar Disorder, Parkinson's disease, Neurology, Genotype, Essential Tremor, Neuroscience (miscellaneous), Genome-wide association study, Single-nucleotide polymorphism, Disease, Bioinformatics, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Asian People, Risk Factors, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Autistic Disorder, Aged, Monomeric GTP-Binding Proteins, Genetics, Essential tremor, Parkinson Disease, Middle Aged, medicine.disease, 030104 developmental biology, Autism, Female, Psychology, 030217 neurology & neurosurgery, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ea67477b0995804e8ecfd77416a757
https://doi.org/10.1007/s12035-016-9815-4

المؤلفون: Yousef Daneshmandpour, Babak Emamalizadeh, Javad Jamshidi, Hossein Darvish, Parasto Shokraeian

المصدر: Meta Gene. 22:100609

مصطلحات موضوعية: 0301 basic medicine, Genetics, Single-nucleotide polymorphism, Biology, medicine.disease, Genetic analysis, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Schizophrenia, 030220 oncology & carcinogenesis, Genetic model, Genotype, medicine, Allele, Allele frequency, Gene, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::ca961833214508c9adbd831ebe28a4f5
https://doi.org/10.1016/j.mgene.2019.100609

المؤلفون: Peyman Petramfar, Arman Habibi, Faranak Madadi, Zahra Taherian-Esfahani, Hossein Ehsanbakhsh, Banafsheh Mohammad Hossein Pour, Marzieh Motallebi, Saeed Askarpour, Shiva Askarpour, Monavvar Andarva, Mona Ahmadi, Mahdis Bayat, Mehdi Khorrami, Luis J. Azcona, Hajar Eftekhari, Zahra Azimzadeh, Reza Ebrahimi Rad, Jalal Rezaeidian, Gholam Ali Shahidi, Azadeh Ahmadifard, Safa Najmi, Javad Jamshidi, Seyed Erfan Mortazavi, Rita Chaouni, Ahmad Chitsaz, Zahra Dehghani-Tafti, Hossein Darvish, Elham Alehabib, Faraz Mohammadi, Samareh Omidvari, Abbas Tafakhori, Amir Mohammad Besharati, Seyed Amir Hassan Habibi, Minoo Atakhorrami, Saghar Ghasemi Firouzabadi, Mir Davood Omrani, Babak Emamalizadeh, Hossein Ali Shahmohammadibeni, Coro Paisán-Ruiz, Saeed Mohammadihosseinabad, Parasto Shokraeian, Ehsan Esmaili Shandiz, Shaghayegh Taghavi, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Hamid Noorollahi Moghaddam, Mohammad Ali Harati-Ghavi

المصدر: Molecular neurobiology. 55(4)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Ubiquitin-Protein Ligases, Neuroscience (miscellaneous), Consanguinity, Biology, medicine.disease_cause, Parkin, Article, Frameshift mutation, 03 medical and health sciences, Cellular and Molecular Neuroscience, Young Adult, 0302 clinical medicine, Parkinsonian Disorders, Molecular genetics, medicine, Missense mutation, Humans, Family, Amino Acid Sequence, Gene, Genetics, Mutation, Base Sequence, Parkinsonism, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Exons, Middle Aged, medicine.disease, Phosphoric Monoester Hydrolases, 030104 developmental biology, Neurology, Female, Protein Kinases, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::819e7d2c518a5ea5ad689dd00a5d651b
https://pubmed.ncbi.nlm.nih.gov/28502045

المؤلفون: Parasto Shokraeian, Javad Jamshidi, Alireza Zare Bidoki, Fatemeh Mohajerani, Hossein Darvish, Shaghayegh Taghavi, Mohammad Reza Eslami Amirabadi, Saeid Ganji, Babak Emamalizadeh, Mahjoubeh Zarrabi Alhosseini

المصدر: Neurological research. 38(11)

مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Pediatrics, Adolescent, Genotype, Synaptosomal-Associated Protein 25, Single-nucleotide polymorphism, Iran, Impulsivity, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Age Distribution, Polymorphism (computer science), medicine, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, Sex Distribution, Psychiatry, Child, Genotyping, Gene, Chi-Square Distribution, Snap, General Medicine, medicine.disease, 030104 developmental biology, Neurology, Attention Deficit Disorder with Hyperactivity, Case-Control Studies, Female, Neurology (clinical), medicine.symptom, Psychology, 030217 neurology & neurosurgery, Sex ratio

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce2ae2996d05501e772fb5d9e616816f
https://pubmed.ncbi.nlm.nih.gov/27627841

المؤلفون: Simin Rahimi-Aliabadi, Hamid Ghaedi, Hossein Darvish, Abbas Tafakhori, Parasto Shokraeian, Tahereh Dadkhah, Haleh Akhavan-Niaki, Mina Ohadi, Shaghyegh Taghavi, Javad Jamshidi

المصدر: Journal of affective disorders. 208

مصطلحات موضوعية: 0301 basic medicine, Oncology, Untranslated region, Adult, Male, Risk, medicine.medical_specialty, Genotype, Single-nucleotide polymorphism, MiRNA binding, Biology, Receptors, Metabotropic Glutamate, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Internal medicine, medicine, Humans, Allele, Allele frequency, Genetics, Depressive Disorder, Major, Binding Sites, Brain, Middle Aged, medicine.disease, Genotype frequency, Psychiatry and Mental health, Clinical Psychology, MicroRNAs, 030104 developmental biology, Major depressive disorder, Female, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9ec948f9240635a529c04f59cf5e6b
https://pubmed.ncbi.nlm.nih.gov/27792966

المؤلفون: Azadeh Ahmadifard, Hossein Darvish, Monavvar Andarva, Babak Emamalizadeh, Elham Alehabib, Hamid Ahmadieh, Abbas Tafakhori, Hamid Ghaedi, Simin Rahimi-Aliabadi, Parasto Shokraeian, Rezvan Noroozi, Javad Jamshidi, Shaghyegh Taghavi, Narsis Daftarian, Minoo Atakhorrami

المصدر: Eye (London, England). 30(11)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, genetic structures, Photophobia, Amelogenesis Imperfecta, DNA Mutational Analysis, Vision Disorders, Consanguinity, Polymerase Chain Reaction, Nystagmus, Pathologic, 03 medical and health sciences, Jalili syndrome, Ophthalmology, Retinitis pigmentosa, medicine, Electroretinography, Humans, Point Mutation, Amelogenesis imperfecta, Cation Transport Proteins, business.industry, Macular coloboma, Dystrophy, Macular dystrophy, medicine.disease, eye diseases, Pedigree, 030104 developmental biology, Phenotype, Clinical Study, Female, sense organs, medicine.symptom, business, Cone-Rod Dystrophies, Retinitis Pigmentosa

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a2c7b6da3bb6818e2155dbf3edde7f6
https://pubmed.ncbi.nlm.nih.gov/27419834