Author = Leila Mehdizadeh Fanid
The rs6323 and uVNTR Polymorphisms in the MAOA Gene are Associated with Attention Deficit Hyperactivity Disorder in Iranian Azeri Children

Volume 10, Issue 9, September 2022, Pages 16712-16718

10.22038/ijp.2022.65546.4938

Leila Mehdizadeh Fanid; Samaneh Tayefeh_gholami; Sama Akbarzadeh; Nazila Valatabar; MohammadAli HosseinpourFeizi


Polymorphism of dopamine transporter gene 3'-UTR VNTR in Iranian Azeri Turkish patients with ADHD

Volume 10, Issue 2, February 2022, Pages 15466-15473

10.22038/ijp.2022.59297.4621

Adel Abdi; Narges Zeinalzadeh; Leila Mehdizadeh Fanid; Nava Khalilinejad


The Survey of DBH Gene Polymorphism Rs5320 in Children with Attention Deficit Hyperactivity Disorder (ADHD)

Volume 6, Issue 9, September 2018, Pages 8177-8184

10.22038/ijp.2018.29296.2566

Shahrokh Amiri; Seyed Mahmoud Tabatabaei; Asghar Arfaie; Maryam Parvizi Aghdam; Habibeh Barzegar; Leila Mehdizadeh Fanid


Evaluating Sleep Disorders amongst Children with Attention Deficit/ Hyperactivity Disorder (ADHD)

Volume 5, Issue 10, October 2017, Pages 5907-5917

10.22038/ijp.2017.25322.2149

Khalil Esmaeilpour; Leila Mehdizadeh Fanid; Azam Hosein nejad


Study of Polymorphism of the DRD2 Gene (-141C Ins/Del, rs1799732) with Attention Deficit Hyperactivity Disorder a Population Sample of Children in Iranian-Azeri

Volume 5, Issue 3, March 2017, Pages 4569-4574

10.22038/ijp.2016.21049.1764

Leila Mehdizadeh Fanid; Mina Adampourezare; Mohammad Ali HosseinpourFeizi; SeyedGholamreza Noorazar


An Association Analysis of Reelin Gene (RELN) Exon 22 (G/C), Rs.362691, Polymorphism with Autism Spectrum Disorder among Iranian-Azeri Population

Volume 4, Issue 7, July 2016, Pages 2027-2033

10.22038/ijp.2016.6856

Leila Mehdizadeh Fanid; Mohammad Ali Hosseinpour Feizi; Mina Adampour Zare; Hasan Shahrokhi


The Association of DRD2 Gene TaqI Polymorphism with Attention Deficit Hyperactivity Disorder a Population Sample of Iranian Azeri-children

Volume 4, Issue 5, May 2016, Pages 1803-1807

10.22038/ijp.2016.6726

Leila Mehdizadeh Fanid; Mina Adampurzare; 3. SeyedGholamreza Noorazar; Mohammad Ali HosseinpourFeizi


Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

Volume 3, Issue 6.1, November 2015, Pages 1065-1071

10.22038/ijp.2015.5668

Leila Mehdizadeh Fanid; Hassan Shahrokhi; Mina Adampourezare; Mohamad Ali Hosseinpour Feizi; Mortaza Bonyadi; A Eslami