Ji Yoon Han

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 29

Top Topics

Urinary Tract Infection

Intellectual Disability

Peripheral Blood

Top Venues

International journal of molecular sciences

Children (Basel, Switzerland)

Diagnostics (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Kyung Hee Kim, Ji Yoon Han, Joonhong Park, Jung Sun Cho
The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant. International journal of molecular sciences 25 (7) (2024)
Ji Yoon Han, Joonhong Park
Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review. Genes 15 (4) (2024)
Kyung Hee Kim, Ji Yoon Han, Joonhong Park, Jung Sun Cho
The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant. International journal of molecular sciences 25 (7) (2024)
Kyung Hee Kim, Ji Yoon Han, Joonhong Park, Jung Sun Cho
The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant. International journal of molecular sciences 25 (7) (2024)
Ji Yoon Han, Joonhong Park
Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review. Genes 15 (4) (2024)
Ji Yoon Han, Joonhong Park
Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review. Genes 15 (4) (2024)
Ji Yoon Han, Joonhong Park
Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review. Genes 15 (4) (2024)
Ji Yoon Han, Yong Gon Cho, Dae Sun Jo, Joonhong Park
Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome. International journal of molecular sciences 25 (1) (2023)
Yong Gon Cho, Joonhong Park, Ji Yoon Han, Tae Yun Kim
Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations. Genes 14 (6) (2023)
Jee Min Kim, Ji Yoon Han, Seung-Beom Han
Acute COVID-19 in unvaccinated children without a history of previous infection during the delta and omicron periods. Postgraduate medicine (2023)
Ji Yoon Han, Yong Gon Cho, Dae Sun Jo, Joonhong Park
Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome. International journal of molecular sciences 25 (1) (2023)
Yong Gon Cho, Joonhong Park, Ji Yoon Han, Tae Yun Kim
Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations. Genes 14 (6) (2023)
Namsu Kim, Tae Yun Kim, Ji Yoon Han, Joonhong Park
Five Years' Experience with Gene Panel Sequencing in Hereditary Hemolytic Anemia Screened by Routine Peripheral Blood Smear Examination. Diagnostics (Basel, Switzerland) 13 (4) (2023)
Namsu Kim, Tae Yun Kim, Ji Yoon Han, Joonhong Park
Five Years' Experience with Gene Panel Sequencing in Hereditary Hemolytic Anemia Screened by Routine Peripheral Blood Smear Examination. Diagnostics (Basel, Switzerland) 13 (4) (2023)
Yong Gon Cho, Joonhong Park, Ji Yoon Han, Tae Yun Kim
Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations. Genes 14 (6) (2023)
Yong Gon Cho, Joonhong Park, Ji Yoon Han, Tae Yun Kim
Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations. Genes 14 (6) (2023)
Ji Yoon Han, Yong Gon Cho, Dae Sun Jo, Joonhong Park
Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome. International journal of molecular sciences 25 (1) (2023)
Ji Yoon Han, Woori Jang, Joonhong Park
Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1. Genes 13 (8) (2022)
Ja Un Moon, Ji Yoon Han
Effectiveness of Chloral Hydrate on Brain MRI in Children with Developmental Delay/Intellectual Disability Comparing with Normal Intelligence: Single Tertiary Center Experience. Children (Basel, Switzerland) 8 (12) (2021)
Ji Yoon Han, Eun-Ae Yang, Jung-Woo Rhim, Seung-Beom Han
Effects of Antiviral Therapy and Glucocorticoid Therapy on Fever Duration in Pediatric Patients with Influenza. Medicina (Kaunas, Lithuania) 57 (12) (2021)
Ji Yoon Han, Joonhong Park
A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review. Genes 12 (9) (2021)
Ji Yoon Han, Joonhong Park
Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review. Genes 12 (7) (2021)
Ji Yoon Han, Hyun Joo Lee, Young-Mock Lee, Joonhong Park
Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report. Children (Basel, Switzerland) 8 (4) (2021)
Ji Yoon Han, Seung-Beom Han
Seizures Related to Influenza in Pediatric Patients: A Comparison with Seizures Associated with Other Respiratory Viral Infections. Journal of clinical medicine 10 (14) (2021)
Ja Un Moon, Ji Yoon Han
Comparative Efficacy of Levetiracetam for Epilepsy in School-Aged Children with Intellectual Disability and Normal Intelligence. Brain sciences 11 (11) (2021)
Ji Yoon Han, Joonhong Park
Phenotypic Diversity of 15q11.2 BP1-BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review. Diagnostics (Basel, Switzerland) 11 (4) (2021)
Ji Yoon Han, Seung-Beom Han
Febrile Seizures and Respiratory Viruses Determined by Multiplex Polymerase Chain Reaction Test and Clinical Diagnosis. Children (Basel, Switzerland) 7 (11) (2020)
Ji Yoon Han, Hyun Joo Lee, Young-Mock Lee, Joonhong Park
Identification of Missense ADGRV1 Mutation as a Candidate Genetic Cause of Familial Febrile Seizure 4. Children (Basel, Switzerland) 7 (9) (2020)
Joonhong Park, Woori Jang, Ji Yoon Han
Differing disease phenotypes of Duchenne muscular dystrophy and Moyamoya disease in female siblings of a Korean family. Molecular genetics & genomic medicine 7 (9) (2019)