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Won Chan Jeong

Showing results (1-10 of 11) with videos related to

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Studies in Health Technology and Informatics|May 17, 2025
Understanding Stain Separation Improves Cross-Scanner Adenocarcinoma Segmentation with Joint Multi-Task LearningHo Heon Kim, Won Chan Jeong, Youngjin Park, et al.
JMIR Medical Informatics|February 4, 2026
Ranking-Aware Multiple Instance Learning for Histopathology Slide Classification: Development and Validation StudyHo Heon Kim, Gisu Hwang, Won Chan Jeong, et al.
Journal of Pathology Informatics|October 28, 2025
Evaluating the robustness of slide-level AI predictions on out-of-focus whole slide images: A retrospective observational studyHo Heon Kim, Young Sin Ko, Won Chan Jeong, et al.
JMIR Formative Research|November 5, 2024
A Deep Learning Model to Predict Breast Implant Texture Types Using Ultrasonography Images: Feasibility Development StudyHo Heon Kim, Won Chan Jeong, Kyungran Pi, et al.
Cardiovascular Diagnosis and Therapy|January 9, 2026
Identification of recurrent <i>MYH7</i> variant hypertrophic cardiomyopathy patients in Korea: a case seriesSeung Woo Ryu, Seokhui Jang, Jang-Won Son, et al.
NPJ Genomic Medicine|January 22, 2025
Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disordersHeonjong Han, Go Hun Seo, Seong-In Hyun, et al.
Frontiers in Cardiovascular Medicine|July 22, 2024
High prevalence of <i>ALPK3</i> premature terminating variants in Korean hypertrophic cardiomyopathy patientsSeung Woo Ryu, Won Chan Jeong, Geu Ru Hong, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Biallelic loss of function variants in <i>WBP4</i>, encoding a spliceosome protein, result in a variable neurodevelopmental delay syndromeEden Engal, Kaisa Teele Oja, Reza Maroofian, et al.
American Journal of Human Genetics|November 14, 2023
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndromeEden Engal, Kaisa Teele Oja, Reza Maroofian, et al.
Ebiomedicine|August 27, 2024
Clinical and neuroradiological spectrum of biallelic variants in NOTCH3Pablo Iruzubieta, César Augusto Pinheiro Ferreira Alves, Aisha M Al Shamsi, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Studies in Health Technology and Informatics|May 17, 2025
Understanding Stain Separation Improves Cross-Scanner Adenocarcinoma Segmentation with Joint Multi-Task LearningHo Heon Kim, Won Chan Jeong, Youngjin Park, et al.
JMIR Medical Informatics|February 4, 2026
Ranking-Aware Multiple Instance Learning for Histopathology Slide Classification: Development and Validation StudyHo Heon Kim, Gisu Hwang, Won Chan Jeong, et al.
Journal of Pathology Informatics|October 28, 2025
Evaluating the robustness of slide-level AI predictions on out-of-focus whole slide images: A retrospective observational studyHo Heon Kim, Young Sin Ko, Won Chan Jeong, et al.
JMIR Formative Research|November 5, 2024
A Deep Learning Model to Predict Breast Implant Texture Types Using Ultrasonography Images: Feasibility Development StudyHo Heon Kim, Won Chan Jeong, Kyungran Pi, et al.
Cardiovascular Diagnosis and Therapy|January 9, 2026
Identification of recurrent <i>MYH7</i> variant hypertrophic cardiomyopathy patients in Korea: a case seriesSeung Woo Ryu, Seokhui Jang, Jang-Won Son, et al.
NPJ Genomic Medicine|January 22, 2025
Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disordersHeonjong Han, Go Hun Seo, Seong-In Hyun, et al.
Frontiers in Cardiovascular Medicine|July 22, 2024
High prevalence of <i>ALPK3</i> premature terminating variants in Korean hypertrophic cardiomyopathy patientsSeung Woo Ryu, Won Chan Jeong, Geu Ru Hong, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Biallelic loss of function variants in <i>WBP4</i>, encoding a spliceosome protein, result in a variable neurodevelopmental delay syndromeEden Engal, Kaisa Teele Oja, Reza Maroofian, et al.
American Journal of Human Genetics|November 14, 2023
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndromeEden Engal, Kaisa Teele Oja, Reza Maroofian, et al.
Ebiomedicine|August 27, 2024
Clinical and neuroradiological spectrum of biallelic variants in NOTCH3Pablo Iruzubieta, César Augusto Pinheiro Ferreira Alves, Aisha M Al Shamsi, et al.
Pageof 2