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Ziarih Hawi
PeerJ Editor & Reviewer
1,050 Points

Contributions by role

Reviewer 15
Editor 1,035

Contributions by subject area

Computational Biology
Molecular Biology
Cognitive Disorders
Neurology
Data Science
Genetics
Dentistry
Ophthalmology
Pediatrics
Public Health
Andrology
Oncology
Urology
Medical Genetics
Orthopedics
Rheumatology
Surgery and Surgical Specialties
Epidemiology
Psychiatry and Psychology
Genomics
Sports Medicine
Cardiology
Veterinary Medicine
Bioinformatics
Diabetes and Endocrinology

Ziarih Hawi

PeerJ Editor & Reviewer

Summary

Dr Ziarih Hawi is a Senior Research Fellow in Psychiatric Genetics at the Institute of Cognitive and Clinical Neuroscience. Dr Hawi has been investigating genetic predisposition to psychiatric disorders with particular emphasis on the genetic of attention deficit hyperactivity disorder (ADHD). He has successfully identified risk gens for ADHD, narrowed down regions of associations and has functionally characterised some of the ADHD-associated genes.

Genetics Genomics Medical Genetics Neuroscience

Editorial Board Member

PeerJ - the Journal of Life & Environmental Sciences

Past or current institution affiliations

Monash University

Work details

Senior Research Fellow in Psychiatric Genetics

Monash University
May 2017
Institute of Cognitive and Clinical Neuroscience

PeerJ Contributions

  • Edited 5

Academic Editor on

December 18, 2023
Differentially expressed genes in orbital adipose/connective tissue of thyroid-associated orbitopathy
Yan Wang, Yanqiu Liu, Jiping Cai, Tianyi Zong, Ziyin Zhang, Tianhua Xie, Tong Mu, Meili Wu, Qian Yang, Yangningzhi Wang, Xiaolu Wang, Yong Yao
https://doi.org/10.7717/peerj.16569 PubMed 38130930
August 17, 2022
Complex interactions between p.His558Arg and linked variants in the sodium voltage-gated channel alpha subunit 5 (NaV1.5)
Monica Lopes-Marques, Raquel Silva, Catarina Serrano, Verónica Gomes, Ana Cardoso, Maria João Prata, Antonio Amorim, Luisa Azevedo
https://doi.org/10.7717/peerj.13913 PubMed 35996667
January 27, 2020
Association of IGF1 single-nucleotide polymorphisms with myopia in Chinese children
Tianyu Cheng, Jingjing Wang, Shuyu Xiong, Bo Zhang, Qiangqiang Li, Xun Xu, Xiangui He
https://doi.org/10.7717/peerj.8436 PubMed 32025377
January 24, 2019
Association of TIMP4 gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China
Jiaqi Wang, Feimeng An, Yuju Cao, Hongyan Gao, Mingqi Sun, Chao Ma, Hao Wu, Baoxin Zhang, Wanlin Liu, Jianzhong Wang
https://doi.org/10.7717/peerj.6270 PubMed 30697482
August 28, 2017
Mutation detection and prenatal diagnosis of XLHED pedigree
Yao Lin, Wei Yin, Zhuan Bian
https://doi.org/10.7717/peerj.3691 PubMed 28875069