Ji-Eun LEE (0000-0002-7386-0015)

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Biography

2002- Present : Assistant Professor, Associated Professor, Professor, Dept of Pediatrics, College of Medicine, Inha University, Inha University Hospital
2019- Present : Director, Northwest Gyeonggi Regional Center for Rare Diseases
2019- Present : Editorial Board Member, Journal of Korean Medical Science
2016- 2019 : Editor in Chief, Annals of Pediatric Endocrinology & Metabolism
2015- 2018 : Editorial Board Member, Journal of Obesity & Metabolic Syndrome
2006- 2016 : Editorial Board Member, Korean Journal of Pediatric Endocrinology
2009-2010 : Visiting Scholar in Dept of Pharmaceutics and Pharmaceutical chemistry, University of Utah, USA
2001-2002 : Fellowship in Dept of Pediatric endocrinology & genetics, Samsung Medical Center
1998-1999 : Fellowship in Dept of Pediatrics, Inha University Hospital, Inha University college of medicine

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Northwest Gyeonggi Reginal Center for Rare Disease: Incheon, KR

2019-02-01 to present | Director

Employment

Ji-Eun LEE

https://orcid.org/0000-0002-7386-0015

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Biography

Activities

Employment (5)

Northwest Gyeonggi Reginal Center for Rare Disease: Incheon, KR

Inha University College of Medicine: Incheon, KR

Inha University Hospital: Incheon, KR

University of Utah: Salt Lake City, UT, US

Samsung Medical Center: Gangnam-gu, Seoul, KR

Education and qualifications (3)

Inha University Graduate school of medicine: Incheon, KR

Inha University Graduate school of medicine: Incheon, Incheon, KR

Inha University College of Medicine, Inha University Hospital: Incheon, KR

Works (50 of 72)

Identification of a novel splice variant in SEC23B gene in a patient with concomitant presence of congenital dyserythropoietic anemia II and Gilbert’s syndrome

Clinical efficacy of multigene panels in the management of congenital hypothyroidism with gland in situ

Case report: Development of central precocious puberty in a girl with late-diagnosed simple virilizing congenital adrenal hyperplasia complicated with Williams syndrome

Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience

2022 Clinical practice guidelines for central precocious puberty of Korean children and adolescents

Central precocious puberty with hypothalamic hamartoma: the first case reports of 2 siblings with different phenotypes of Seckel syndrome 5

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

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

The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure

Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka Syndrome

A case of follow-up of a patient with 22q11.2 distal deletion syndrome and a review of the literature

Large for Gestational Age and Obesity-Related Comorbidities

The role of growth hormone device optimization in patient-reported outcomes: real-world evidence from South Korea

A case of CHOPS syndrome accompanied with moyamoya disease and systemic vasculopathy.

Two Novel Mutations of <i>ANKRD11</i> Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review.

Machine learning-based prediction of response to growth hormone treatment in Turner syndrome: the LG Growth Study.

<p>Ease of Use, Preference, and Safety of the Recombinant Human Growth Hormone Disposable Pen Compared with the Reusable Device: A Multicenter, Single-Arm, Open-Label, Switch-Over, Prospective, Phase IV Trial</p>

Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature

Annals of Pediatric Endocrinology &amp; Metabolism is now indexed in the Emerging Sources Citation Index

Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrum.

12-Month Effects of Once-Weekly and Twice-Monthly Administration of Hybrid Fc-Fused Human Growth Hormone, GX-H9, Treatment in Pediatric with GHD Deficiency

Frequency of Self-Monitoring of Blood Glucose during the School Day Is Associated with the Optimal Glycemic Control among Korean Adolescents with Type 1 Diabetes

Thyroid function in obese Korean children and adolescents: Korea National Health and Nutrition Examination Survey 2013–2015

The effect of low-dose intravenous bisphosphonate treatment on osteoporosis in children with quadriplegic cerebral palsy

An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing

The Application of One-Hour Static Qigong Program to Decrease Needle Pain of Korean Adolescents With Type 1 Diabetes: A Randomized Crossover Design

Sleep and Obesity in Childhood

Blood Glucose Control and Related Factors at a Camp for Korean Children and Adolescents with Type 1 Diabetes

Diabetes-Specific Quality of Life of Korean Children and Adolescents With Type 1 Diabetes

Early onset of puberty in an obese boy with Klinefelter syndrome

Iron deficiency anemia in infants and toddlers

Prevalence and Relationships of Iron Deficiency Anemia with Blood Cadmium and Vitamin D Levels in Korean Women

The Diagnostic Value of Pelvic Ultrasound in Girls with Central Precocious Puberty

Clinical and endocrine characteristics and genetic analysis of Korean children with McCune–Albright syndrome: a retrospective cohort study

Clinical Predictive Factors for Metabolic Syndrome in Obese Children and Adolescents

2015 Korean Guidelines for the Management of Dyslipidemia: Executive Summary (English Translation).

Alternative biomarkers for assessing glycemic control in diabetes: fructosamine, glycated albumin, and 1,5-anhydroglucitol

Development of multifocal nodular lesions of a liver mimicking hepatic metastasis, following resection of an insulinoma in a child

Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNAS

Exploring Positive Psychology of Children with Type 1 Diabetes Focusing on Subjective Happiness and Satisfaction with Life

School Nurses’ Management for Children and Adolescents with Diabetes

The Characteristics of Severe Iron Deficiency Anemia in Children and Adolescents

A rare diabetes ketoacidosis in combined severe hypernatremic hyperosmolarity in a new-onset Asian adolescent with type I diabetes

Mosaic Turner syndrome associated with schizophrenia

Significant adverse reactions to long-acting gonadotropin-releasing hormone agonists for the treatment of central precocious puberty and early onset puberty

The ratio of estimated average glucose to fasting plasma glucose level is superior to glycated albumin, hemoglobin A1c, fructosamine, and GA/A1c ratio for assessing I��-cell function in childhood diabetes

A rare diabetes ketoacidosis in combined severe hypernatremic hyperosmolarity in a new-onset Asian adolescent with type I diabetes

Significance of Neutrophil Gelatinase-Associated Lipocalin Level as an Acute-Phase Reactant in Patients with Systemic Inflammatory Response Syndrome

Effect of Self-care Education at a Diabetes Camp on Diabetes Management Behaviors, Knowledge and Self-efficacy in Children with Type 1 Diabetes

Is It Possible to Predict the Iron Status from an Infant's Diet History?

Annals of Pediatric Endocrinology & Metabolism is now indexed in the Emerging Sources Citation Index