Zou D, Zeng Q, Liu P, Wei Y, Guo R, Zhu Y
Front Genet. 2024; 15:1348387.
PMID: 38544802
PMC: 10965694.
DOI: 10.3389/fgene.2024.1348387.
Kessi M, Duan H, Xiong J, Chen B, He F, Yang L
Front Mol Neurosci. 2022; 15:925049.
PMID: 36211978
PMC: 9532551.
DOI: 10.3389/fnmol.2022.925049.
Adil K, Gonzales E, Remonde C, Boo K, Jeon S, Shin C
Biomol Ther (Seoul). 2021; 30(3):232-237.
PMID: 34702791
PMC: 9047488.
DOI: 10.4062/biomolther.2021.133.
Balestra S, Eugster B, Liebert H
Health Econ. 2020; 29(5):591-607.
PMID: 32052533
PMC: 9328428.
DOI: 10.1002/hec.4005.
Won J, Jin Y, Choi J, Park S, Lee T, Lee S
Int J Mol Sci. 2017; 18(6).
PMID: 28632163
PMC: 5486135.
DOI: 10.3390/ijms18061314.
Prenatal antidepressant use and risk of attention-deficit/hyperactivity disorder in offspring: population based cohort study.
Man K, Chan E, Ip P, Coghill D, Simonoff E, Chan P
BMJ. 2017; 357:j2350.
PMID: 28566274
PMC: 5450015.
DOI: 10.1136/bmj.j2350.
Beneficial effect of interventional exercise on autistic Fragile X syndrome.
Lee S, Won J, Park S, Lee S, Chang K, Kim J
J Phys Ther Sci. 2017; 29(4):760-762.
PMID: 28533625
PMC: 5430288.
DOI: 10.1589/jpts.29.760.
Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population.
Safari M, Omrani M, Noroozi R, Sayad A, Sarrafzadeh S, Komaki A
J Mol Neurosci. 2016; 61(3):305-311.
PMID: 27888397
DOI: 10.1007/s12031-016-0860-2.
Benefits of Physical Exercise for Individuals with Fragile X Syndrome in Humans.
Lee M, Won J, Lee S, Hong Y, Kim J, Hong Y
J Lifestyle Med. 2016; 5(2):35-8.
PMID: 26770889
PMC: 4711957.
DOI: 10.15280/jlm.2015.5.2.35.
A knowledge network for a dynamic taxonomy of psychiatric disease.
Krishnan R
Dialogues Clin Neurosci. 2015; 17(1):79-87.
PMID: 25987866
PMC: 4421904.
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.
Codina-Sola M, Rodriguez-Santiago B, Homs A, Santoyo J, Rigau M, Aznar-Lain G
Mol Autism. 2015; 6:21.
PMID: 25969726
PMC: 4427998.
DOI: 10.1186/s13229-015-0017-0.
Shared familial transmission of autism spectrum and attention-deficit/hyperactivity disorders.
Musser E, Hawkey E, Kachan-Liu S, Lees P, Roullet J, Goddard K
J Child Psychol Psychiatry. 2014; 55(7):819-27.
PMID: 24444366
PMC: 4211282.
DOI: 10.1111/jcpp.12201.
Speech-Sound Disorders and Attention-Deficit/Hyperactivity Disorder Symptoms.
Lewis B, Short E, Iyengar S, Taylor H, Freebairn L, Tag J
Top Lang Disord. 2013; 32(3):247-263.
PMID: 24363479
PMC: 3868495.
DOI: 10.1097/tld.0b013e318261f086.
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders.
Paemka L, Mahajan V, Skeie J, Sowers L, Ehaideb S, Gonzalez-Alegre P
PLoS One. 2013; 8(12):e80737.
PMID: 24312498
PMC: 3849077.
DOI: 10.1371/journal.pone.0080737.
Association between the GRM7 rs3792452 polymorphism and attention deficit hyperacitiveity disorder in a Korean sample.
Park S, Jung S, Kim B, Cho S, Shin M, Kim J
Behav Brain Funct. 2013; 9:1.
PMID: 23295062
PMC: 3680053.
DOI: 10.1186/1744-9081-9-1.
The association of child mental health conditions and parent mental health status among U.S. Children, 2007.
Bennett A, Brewer K, Rankin K
Matern Child Health J. 2011; 16(6):1266-75.
PMID: 21948199
DOI: 10.1007/s10995-011-0888-4.
Regional differences in cerebral perfusion associated with the alpha-2A-adrenergic receptor genotypes in attention deficit hyperactivity disorder.
Kim B, Kim J, Kang H, Cho S, Shin M, Yoo H
J Psychiatry Neurosci. 2010; 35(5):330-6.
PMID: 20731965
PMC: 2928286.
DOI: 10.1503/jpn.090168.
The role of genetics in the etiology of schizophrenia.
Gejman P, Sanders A, Duan J
Psychiatr Clin North Am. 2010; 33(1):35-66.
PMID: 20159339
PMC: 2826121.
DOI: 10.1016/j.psc.2009.12.003.
ADHD familial loading and abnormal EEG alpha asymmetry in children with ADHD.
Hale T, Smalley S, Dang J, Hanada G, Macion J, McCracken J
J Psychiatr Res. 2009; 44(9):605-15.
PMID: 20006344
PMC: 2878884.
DOI: 10.1016/j.jpsychires.2009.11.012.
Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder.
Vegt R, Bertoli-Avella A, Tulen J, de Graaf B, Verkerk A, Vervoort J
Eur J Hum Genet. 2009; 18(2):206-11.
PMID: 19707245
PMC: 2987191.
DOI: 10.1038/ejhg.2009.148.