Serotonin transporter functional polymorphisms potentially increase risk of schizophrenia separately and as a haplotype

por Ghamari, Rana, Yazarlou, Fatemeh, Khosravizadeh, Zahra, Moradkhani, Atefeh, Abdollahi, Elaheh, Alizadeh, Fatemeh
Publicado 2022

Neuregulin1 types mRNA level changes in autism spectrum disorder, and is associated with deficit in executive functions

por Abbasy, Samane, Shahraki, Fazlollah, Haghighatfard, Arvin, Qazvini, Masoume Ghasemzadeh, Rafiei, Sahel Towfigh, Noshadirad, Elnaz, Farhadi, Mahdi, Rezvani asl, Horie, Shiryazdi, Atena alsadat, Ghamari, Rana, Tabrizi, Zeinab, Mehrfard, Rashed, Esmaili kakroudi, Fereshteh, Azarnoosh, Mahsima, Younesi, Faeghe, Parsamehr, Narges, Garaei, Nooriyeh, Abyari, Soroush, Salehi, Maede, Gholami, Maryam, Zolfaghari, Pardis, Bagheri, Seyede Mahsa, Pourmehrabi, Melika, Rastegarimogaddam, Elham, Nobakht, Elnaz, Nobakht, Elmira, Partovi, Rayan
Publicado 2018