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Family-based exome sequencing combined with linkage analyses identifies rare susceptibility variants of MUC4 for gastric cancer
oa mark
Choi, Yoon Jin;
Ohn, Jung Hun;
Kim, Nayoung;
Kim, Wonji;
Park, Kyungtaek;
Won, Sungho;
Sael, Lee
;
Shin, Cheol Min;
Lee, Sun Min;
Lee, Sejoon;
An, Hyun Joo;
Jang, Dong Man;
Han, Byung Woo;
Lee, Hye Seung;
Kang, Seung Joo;
Kim, Joo Sung;
Lee, Dong Ho
2020-07-01
PLoS ONE, Vol.15
Public Library of Science
Genome-Wide Association Study Identifies Genetic Variants Associated with Rotator Cuff Tear—A Pilot Study
oa mark
An, Hyun Ju;
Kim, Jae Hwa;
Yoon, Siyeong;
Choi, Junwon
;
Koo, Jeongmo;
Lee, Soonchul
2022-10-01
Diagnostics, Vol.12
Multidisciplinary Digital Publishing Institute (MDPI)
소비자 대상 직접 시행(DTC) 유전자검사에 대한 문헌고찰
박예신
2023-08
The Graduate School, Ajou University
질병 감수성 예측 유전자 검사의 유전상담 지침 개발에 대한 조사연구
서순정
2017-02
The Graduate School, Ajou University
중증 천식환자의 가래와 말초혈액에서 자가소화작용의 역할: 새로운 치료의 표적
Ban, Ga Young
2016-02
The Graduate School, Ajou University
Mitonuclear genomics and aging
oa mark
Reynolds, Joseph C.;
Bwiza, Conscience P.;
Lee, Changhan
2020-03-01
Human Genetics, Vol.139, pp.381-399
Springer
MildInt: Deep learning-based multimodal longitudinal data integration framework
oa mark
Lee, Garam;
Kang, Byungkon;
Nho, Kwangsik;
Sohn, Kyung Ah
;
Kim, Dokyoon
2019-01-01
Frontiers in Genetics, Vol.10
Frontiers Media S.A.
Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data
oa mark
Nam, Yonghyun;
Jung, Sang Hyuk;
Yun, Jae Seung;
Sriram, Vivek;
Singhal, Pankhuri;
Byrska-Bishop, Marta;
Verma, Anurag;
Shin, Hyunjung
;
Park, Woong Yang;
Won, Hong Hee;
Kim, Dokyoon
2023-01-01
Bioinformatics, Vol.39
Oxford University Press
Comorbidity scoring with causal disease networks
Jhee, Jong Ho;
Bang, Sunjoo;
Lee, Dong Gi;
Shin, Hyunjung
2019-09-01
IEEE/ACM Transactions on Computational Biology and Bioinformatics, Vol.16, pp.1627-1634
Institute of Electrical and Electronics Engineers Inc.
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