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: Shahram Torkamandi, Shaghayegh Taghavi, Saeed Mohammadihosseinabad, Mohammad Reza Abbaszadegan, Neda Shahmohammadibeni, Shokoufeh Abdollahi, Marzieh Motallebi, Negar Pedram, Leyla HaghNejad, Masoumeh Amini Gavenaroudi, Ehsan Ahmadi, Abolfazl Movafagh, Hamid Ghaedi, Babak Emamalizadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Gholam Ali Shahidi, Hossein Darvish, Javad Jamshidi, Alireza Zare Bidoki, Abbas Tafakhori

المصدر: Journal of the Neurological Sciences. 355:72-74

مصطلحات موضوعية: Male, Parkinson's disease, Genotype, FGF20, Disease, Iran, Biology, Polymorphism, Single Nucleotide, Gene Frequency, Risk Factors, Polymorphism (computer science), medicine, Humans, SNP, Genetic Predisposition to Disease, Allele, Risk factor, Aged, Genetics, Chi-Square Distribution, Parkinson Disease, Middle Aged, medicine.disease, Genotype frequency, Fibroblast Growth Factors, Neurology, Female, Neurology (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60763c4a51a0fb9278bccfe9e686f52f
https://doi.org/10.1016/j.jns.2015.05.020

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: Mahnoosh Rahimi, Mahnaz Shahmohammadibeni, Hossein Ali Shahmohammadibeni, Monavvar Andarva, Javad Jamshidi, Hajar Eftekhari, Haleh Akhavan-Niaki, Babak Emamalizadeh, Mahmoud Shekari Khaniani, Azadeh Ahmadifard, Ehteram Khademi, Shaghayegh Taghavi, Alireza Zare Bidoki, Hossein Darvish, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Abbas Tafakhori, Atena Fazeli, Minoo Atakhorrami, Marzieh Motallebi, Tahereh Dadkhah, Elham Alehabib, Simin Rahimi-Aliabadi, Shokoufeh Abdollahi

المصدر: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 37(5)

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, medicine.medical_specialty, Neurology, Parkinson's disease, Genotype, Dermatology, Disease, Iran, Bioinformatics, Polymorphism, Single Nucleotide, 03 medical and health sciences, Genetic Heterogeneity, 0302 clinical medicine, Gene Frequency, Polymorphism (computer science), Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Allele frequency, Genetic Association Studies, Aged, business.industry, Genetic heterogeneity, Tumor Suppressor Proteins, Membrane Proteins, Parkinson Disease, General Medicine, Middle Aged, medicine.disease, Psychiatry and Mental health, 030104 developmental biology, Etiology, alpha-Synuclein, Female, Neurology (clinical), business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560834c8f76d74818e75ae469d17a41e
https://pubmed.ncbi.nlm.nih.gov/26732583

المؤلفون: Simin Rahimi-Aliabadi, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Neda Shahmohammadibeni, Monavvar Andarva, Mina Ohadi, Fatemeh Gholipour, Elham Moslemi, Minoo Atakhorrami, Saeed Mohammadihosseinabad, Abolfazl Movafagh, Shaghayegh Taghavi, Hamid Ghaedi, Faranak Madadi, Marzieh Motallebi, Arash Mirabzadeh, Javad Jamshidi, Babak Emamalizadeh, Azadeh Ahmadifard, Hossein Darvish

المصدر: Journal of neural transmission (Vienna, Austria : 1996). 123(3)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Bipolar Disorder, Genotype, Single-nucleotide polymorphism, Calcium-Calmodulin-Dependent Protein Kinase Kinase, Iran, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Asian People, Gene Frequency, Polymorphism (computer science), mental disorders, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Allele frequency, Gene, Biological Psychiatry, Genetics, Middle Aged, medicine.disease, Psychiatry and Mental health, 030104 developmental biology, Neurology, Schizophrenia, Female, Neurology (clinical), Psychology, 030217 neurology & neurosurgery, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b20a61d19ecd82d75dbe41af27307c
https://pubmed.ncbi.nlm.nih.gov/26354101