Jisook Yim

Clinical assistant professor

Yonsei University College of Medicine

South Korea

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About

Jisook Yim is a Clinical Assistant Professor at the College of Medicine, Korea University. Her research areas include genetic testing, muscle mass impact on health, and various renal disorders, as evidenced by her recent publications on genetic mutations and case reports in pediatric conditions. Jisook contributes significantly to the understanding of complex syndromes and genetic conditions through her clinical and academic work.

Articles (14)

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

Collaborators (7)

Jeong-Ho Kim

Professor/Director

Severance Hospital, Yonsei University College of Medicine

SOUTH KOREA

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Myungshin Kim

Professor

Catholic University of Korea School of Medicine

SOUTH KOREA

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Jung Hwan Lee

SOUTH KOREA

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Ja Un Moon

Clinical Assistant Professor

Catholic University of Korea School of Medicine

SOUTH KOREA

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Il-Jung Park

Associate Professor

Catholic University of Korea Eunpyeong St Mary's Hospital

SOUTH KOREA

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Taeyoung Kyong

Yonsei University College of Medicine

SOUTH KOREA

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Ji Soo Park

Seoul National University Hospital

SOUTH KOREA

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Jisook Yim

Research Interests

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About

Articles (14)

Current Landscape and Perspectives of Direct-to-Consumer Genetic Testing

Renal hypouricemia as the cause of exercise-induced acute kidney injury

Muscle mass has a greater impact on serum creatinine levels in older males than in females

A Novel HNPP Phenotype in Charcot-Marie-Tooth Type 2E With c.1319C>T Missense Mutation in the NEFL Gene

18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review

Andersen–Tawil Syndrome With Novel Mutation in KCNJ2: Case Report

Hereditary renal hypouricemia with SLC22A12 mutation: A case report

Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report

Multilevel Airway Stenosis Being Bypassed by a Customized Tracheostomy Tube in an Infant with Myhre Syndrome

Total and exchangeable copper assay using inductively coupled plasma mass spectrometry and establishment of a pediatric reference interval

Novel WTX nonsense mutation in a family diagnosed with osteopathia striata with cranial sclerosis: Case report

Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage

Case Report: Co-occurrence of Duchenne Muscular Dystrophy and Frontometaphyseal Dysplasia 1

Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report

Collaborators (7)

Jeong-Ho Kim

Myungshin Kim

Jung Hwan Lee

Ja Un Moon

Il-Jung Park

Taeyoung Kyong

Ji Soo Park

Make your next move.

Jisook Yim

Research Interests

Explore related searches

Contact this professor

About

Articles (14)

Current Landscape and Perspectives of Direct-to-Consumer Genetic Testing

Renal hypouricemia as the cause of exercise-induced acute kidney injury

Muscle mass has a greater impact on serum creatinine levels in older males than in females

A Novel HNPP Phenotype in Charcot-Marie-Tooth Type 2E With c.1319C&gt;T Missense Mutation in the NEFL Gene

18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review

Andersen–Tawil Syndrome With Novel Mutation in KCNJ2: Case Report

Hereditary renal hypouricemia with SLC22A12 mutation: A case report

Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report

Multilevel Airway Stenosis Being Bypassed by a Customized Tracheostomy Tube in an Infant with Myhre Syndrome

Total and exchangeable copper assay using inductively coupled plasma mass spectrometry and establishment of a pediatric reference interval

Novel WTX nonsense mutation in a family diagnosed with osteopathia striata with cranial sclerosis: Case report

Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage

Case Report: Co-occurrence of Duchenne Muscular Dystrophy and Frontometaphyseal Dysplasia 1

Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report

Collaborators (7)

Jeong-Ho Kim

Myungshin Kim

Jung Hwan Lee

Ja Un Moon

Il-Jung Park

Taeyoung Kyong

Ji Soo Park

Make your next move.

A Novel HNPP Phenotype in Charcot-Marie-Tooth Type 2E With c.1319C>T Missense Mutation in the NEFL Gene