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Abstract
ABS-391
The Role of Genetic Mutation on Schizophrenia: A Basic Review Prior to Pharmacogenomics
Dhea Nur Hikmah1, Alfian Syarifuddin1, Setiyo Budi Santoso1, Ratna Wijayatri1, Imron Wahyu Hidayat1,a
Corresponding Author: Dhea Nur Hikmah


Question & Answer to the Presentation

Question from Ms. Zaleha Rumadi
2022.12.21 14:51:33

How is the mechanism of GWAS for approachment of drug development in
Schizophrenia?
Replies:

Reply from Ms. Dhea Nur Hikmah
2022.12.21 14:55:19

Specifically, GWAS meta-analysis in schizophrenia by the
Psychiatric Genomics Consortium (PGC) schizophrenia group
has identified 128 independent associations spanning that meet
genome-wide significance in 108 genomic regions notably
including the dopamine D2 receptor locus, but also many other
neurotransmitter genes, especially those involved in central nervous
system (CNS) calcium and glutamate signalling. Thank you for your
question


Question from Ms. Henik Setiyaningsih Setiyaningsih
2022.12.21 14:51:27

How many articles are used to analyze genetic mutations in schizophrenia?
Replies:

Reply from Ms. Dhea Nur Hikmah
2022.12.21 14:54:20

There are 5 original articles used to analyze genetic mutations in
schizophrenia


Question from Ms. Setya Rini Abiyana
2022.12.21 14:50:33

How RasGRP1 mediate risk for Schizophrenia?
Replies:

Reply from Ms. Dhea Nur Hikmah
2022.12.21 14:53:51

RasGRP1 may mediate risk for SCZ by involving DLPFC and
peripheral blood, thus encouraging further studies to explore its
possible role as a biomarker of the disease and/or a target for new
medication.


Question from Ms. Salsabila Salma Zahrah
2022.12.21 14:36:33

What is the function of bioinformatical in this study?
Replies:

Reply from Ms. Dhea Nur Hikmah
2022.12.21 14:43:29

A bioinformatical approach used to find indications for drug
repositioning to produce new treatment paradigms for
schizophrenia by comparing the binding profiles of currently
available clinical compounds to targets or sets of targets derived
from genome-wide association studies (GWAS) or other genetic
studies. Thank you for your question!


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