Da-Yea相关文献与解析，生知库 | 链接生命科学的每一步

Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

出版商更正：评估家族表型偏差以衡量自闭症中新发突变的影响

Kim, Soo-Whee; Lee, Hyeji; Song, Da Yea; Lee, Gang-Hee; Han, Jae Hyun; Lee, Jee Won; Byun, Hee Jung; Son, Ji Hyun; Kim, Ye Rim; Lee, Yoojeong; Kim, Eunjoon; Werling, Donna M; Kim, So Hyun; Sanders, Stephan J; Yoo, Hee Jeong; An, Joon-Yong

自闭症

神经科学

发表日期：2025

文献求助收藏

Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

评估家族表型偏差以衡量自闭症中新发突变的影响

期刊:Genome Medicine

影响因子:11.2

doi:10.1186/s13073-025-01532-7

Combination of Two Primary Screening Instruments (K-SCQ and K-SRS-2) and Setting of New Cutoff Values to Improve Diagnostic Accuracy of Autism Spectrum Disorder in Young Children

结合两种主要筛查工具（K-SCQ 和 K-SRS-2）并设定新的临界值，以提高幼儿自闭症谱系障碍的诊断准确性

期刊:Psychiatry Investigation

影响因子:1.8

doi:10.30773/pi.2025.0015

Lee, Yoojeong; Bong, Guiyoung; Song, Da-Yea; Yoo, Heejeong

Sex differences in the prevalence of common comorbidities in autism: a narrative review

自闭症常见合并症患病率的性别差异：一项叙述性综述

期刊:

影响因子:

doi:10.12771/emj.2024.e79

Hong, Yoo Hwa; Song, Da-Yea; Yoo, Heejeong

Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism

全基因组测序分析揭示了导致自闭症表型多样性的家族模式的性别差异

期刊:Genome Medicine

影响因子:11.2

doi:10.1186/s13073-024-01385-6

Kim, Soo-Whee; Lee, Hyeji; Song, Da Yea; Lee, Gang-Hee; Ji, Jungeun; Park, Jung Woo; Han, Jae Hyun; Lee, Jee Won; Byun, Hee Jung; Son, Ji Hyun; Kim, Ye Rim; Lee, Yoojeong; Kim, Jaewon; Jung, Ashish; Lee, Junehawk; Kim, Eunha; Kim, So Hyun; Lee, Jeong Ho; Satterstrom, F Kyle; Girirajan, Santhosh; Børglum, Anders D; Grove, Jakob; Kim, Eunjoon; Werling, Donna M; Yoo, Hee Jeong; An, Joon-Yong

Short tandem repeat expansions in cortical layer-specific genes implicate in phenotypic severity and adaptability of autism spectrum disorder

皮质层特异性基因中的短串联重复序列扩增与自闭症谱系障碍的表型严重程度和适应性有关

期刊:Psychiatry and Clinical Neurosciences

影响因子:6.2

doi:10.1111/pcn.13676

Kim, Jae Hyun; Koh, In Gyeong; Lee, Hyeji; Lee, Gang-Hee; Song, Da-Yea; Kim, Soo-Whee; Kim, Yujin; Han, Jae Hyun; Bong, Guiyoung; Lee, Jeewon; Byun, Heejung; Son, Ji Hyun; Kim, Ye Rim; Lee, Yoojeong; Kim, Justine Jaewon; Park, Jung Woo; Kim, Il Bin; Choi, Jung Kyoon; Jang, Ja-Hyun; Trost, Brett; Lee, Junehawk; Kim, Eunjoon; Yoo, Hee Jeong; An, Joon-Yong

Classifying autism in a clinical population based on motion synchrony: a proof-of-concept study using real-life diagnostic interviews

基于运动同步性对临床人群中的自闭症进行分类：一项使用真实诊断访谈的概念验证研究

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-024-56098-y

Koehler, Jana Christina; Dong, Mark Sen; Song, Da-Yea; Bong, Guiyoung; Koutsouleris, Nikolaos; Yoo, Heejeong; Falter-Wagner, Christine M

Loss of Acquired Skills: Regression in Young Children With Autism Spectrum Disorders

习得技能的丧失：自闭症谱系障碍幼儿的技能倒退

期刊:Journal of the Korean Academy of Child and Adolescent Psychiatry

影响因子:1.4

doi:10.5765/jkacap.220029

Kim, Ye Rim; Song, Da-Yea; Bong, Guiyoung; Han, Jae Hyun; Yoo, Hee Jeong

Diagnostic validity of Autism Diagnostic Observation Schedule, second edition (K-ADOS-2) in the Korean population

自闭症诊断观察量表第二版（K-ADOS-2）在韩国人群中的诊断效度

期刊:Molecular Autism

影响因子:5.5

doi:10.1186/s13229-022-00506-5

Kim, So Yoon; Oh, Miae; Bong, Guiyoung; Song, Da-Yea; Yoon, Nan-He; Kim, Joo Hyun; Yoo, Hee Jeong

Exploring the Potential of a Scenario-Based Approach to Early Autism Spectrum Disorder Screening

探索基于情景的早期自闭症谱系障碍筛查方法的潜力

Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

出版商更正：评估家族表型偏差以衡量自闭症中新发突变的影响

Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism

评估家族表型偏差以衡量自闭症中新发突变的影响

Combination of Two Primary Screening Instruments (K-SCQ and K-SRS-2) and Setting of New Cutoff Values to Improve Diagnostic Accuracy of Autism Spectrum Disorder in Young Children

结合两种主要筛查工具（K-SCQ 和 K-SRS-2）并设定新的临界值，以提高幼儿自闭症谱系障碍的诊断准确性

Sex differences in the prevalence of common comorbidities in autism: a narrative review

自闭症常见合并症患病率的性别差异：一项叙述性综述

Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism

全基因组测序分析揭示了导致自闭症表型多样性的家族模式的性别差异

Short tandem repeat expansions in cortical layer-specific genes implicate in phenotypic severity and adaptability of autism spectrum disorder

皮质层特异性基因中的短串联重复序列扩增与自闭症谱系障碍的表型严重程度和适应性有关

Classifying autism in a clinical population based on motion synchrony: a proof-of-concept study using real-life diagnostic interviews

基于运动同步性对临床人群中的自闭症进行分类：一项使用真实诊断访谈的概念验证研究

Loss of Acquired Skills: Regression in Young Children With Autism Spectrum Disorders

习得技能的丧失：自闭症谱系障碍幼儿的技能倒退

Diagnostic validity of Autism Diagnostic Observation Schedule, second edition (K-ADOS-2) in the Korean population

自闭症诊断观察量表第二版（K-ADOS-2）在韩国人群中的诊断效度