Baik-lin L. Eun

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 42 publications

Improving CNV Detection Performance Except for Software-Specific Problematic Regions.

Improving CNV Detection Performance Except for Software-Specific Problematic Regions.

Journal: Genes

Published: September 30, 2025

Adjunctive cannabidiol in intractable pediatric epilepsy: A retrospective study on tolerability, efficacy, and safety across genetic and nongenetic etiologies.

Adjunctive cannabidiol in intractable pediatric epilepsy: A retrospective study on tolerability, efficacy, and safety across genetic and nongenetic etiologies.

Journal: Medicine

Published: February 08, 2025

Tuberous Sclerosis Complex Caused by TSC2 Inversion and Deletions Identified Using Whole-genome Sequencing: A Case Study.

Tuberous Sclerosis Complex Caused by TSC2 Inversion and Deletions Identified Using Whole-genome Sequencing: A Case Study.

Journal: Annals of laboratory medicine

Published: February 02, 2025

Clinical implementation of a multidisciplinary pipeline for genome sequencing in rare diseases: A prospective, multicenter, observational cohort study.

Clinical implementation of a multidisciplinary pipeline for genome sequencing in rare diseases: A prospective, multicenter, observational cohort study.

Journal: Clinical and translational medicine

Published: December 17, 2024

Evaluation of users' level of satisfaction for an artificial intelligence-based diagnostic program in pediatric rare genetic diseases.

Evaluation of users' level of satisfaction for an artificial intelligence-based diagnostic program in pediatric rare genetic diseases.

Journal: Medicine

Published: July 15, 2022

Korean Developmental Screening Test for Infants and Children (K-DST): development, applications, and implications for future early childhood development interventions.

Korean Developmental Screening Test for Infants and Children (K-DST): development, applications, and implications for future early childhood development interventions.

Journal: Clinical and experimental pediatrics

Published: June 29, 2022

Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.

Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.

Journal: Molecular medicine (Cambridge, Mass.)

Published: December 23, 2021

Novel Pathogenic Variant (c.1171A>T) in PHF21A in a Female with Intellectual Disability and Craniofacial Anomalies.

Novel Pathogenic Variant (c.1171A>T) in PHF21A in a Female with Intellectual Disability and Craniofacial Anomalies.

Journal: Molecular syndromology

Published: July 22, 2021

Percutaneous Endoscopic Gastrostomy and Nutritional Interventions by the Pediatric Nutritional Support Team Improve the Nutritional Status of Neurologically Impaired Children.

Percutaneous Endoscopic Gastrostomy and Nutritional Interventions by the Pediatric Nutritional Support Team Improve the Nutritional Status of Neurologically Impaired Children.

Journal: Journal of clinical medicine

Published: September 04, 2020

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.

Journal: Clinical genetics

Published: May 08, 2020

Development of the Korean Developmental Screening Test for Infants and Children (K-DST).

Development of the Korean Developmental Screening Test for Infants and Children (K-DST).

Journal: Clinical and experimental pediatrics

Published: April 12, 2020

The long journey toward improving children's health: from 'Korean Journal of Pediatrics' to 'Clinical and Experimental Pediatrics'.

The long journey toward improving children's health: from 'Korean Journal of Pediatrics' to 'Clinical and Experimental Pediatrics'.

Journal: Clinical and experimental pediatrics

Published: December 14, 2019

Showing 1-12 of 42

Last Updated: 09/26/2026