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Author

Aram Yang

Observed names: A Ram Yang, Yang, Aram
ORCID: 0000-0003-4731-3701
Observed ORCID: 0000-0003-4731-3701
OpenAlex ID: A5007715890
2022 Clinical practice guidelines for central precocious puberty of Korean children and adolescents
2023 · Su Jin Kim, Ji Hyun Kim, et al. · Annals of Pediatric Endocrinology & Metabolism · 47
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Impact of BMI on peak growth hormone responses to provocative tests and therapeutic outcome in children with growth hormone deficiency
2019 · Aram Yang, Sung Yoon Cho, et al. · Scientific Reports · 41
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Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea
2020 · Haena Kim, Jung Yeon Shim, et al. · Journal of Korean Medical Science · 36
Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial
2019 · Aram Yang, Jin-Ho Choi, et al. · Orphanet Journal of Rare Diseases · 33
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Clinical and endocrine characteristics and genetic analysis of Korean children with McCune–Albright syndrome: a retrospective cohort study
2016 · Eun-Kyung Cho, Jinsup Kim, et al. · Orphanet Journal of Rare Diseases · 31
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Prevalence and risk factors for type 2 diabetes mellitus with Prader–Willi syndrome: a single center experience
2017 · Aram Yang, Jinsup Kim, et al. · Orphanet Journal of Rare Diseases · 28
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Etiological trends in male central precocious puberty
2018 · Jisun Lee, Jinsup Kim, et al. · Annals of Pediatric Endocrinology & Metabolism · 26
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Trends of Sensitization to Inhalant Allergens in Korean Children Over the Last 10 Years
2020 · Yea Ji Kim, Mi Yeon Lee, et al. · Yonsei Medical Journal · 23
Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center
2020 · Aram Yang, Sung Yoon Cho, et al. · Frontiers in Endocrinology · 20
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Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review
2020 · Su Jin Kim, Aram Yang, et al. · Frontiers in Genetics · 18
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A case of de novo 18p deletion syndrome with panhypopituitarism
2019 · Aram Yang, Jinsup Kim, et al. · Annals of Pediatric Endocrinology & Metabolism · 17
Acute Necrotizing Pancreatitis Associated withMycoplasma pneumoniaeInfection in a Child
2015 · Aram Yang, Ben Kang, et al. · Pediatric Gastroenterology Hepatology & Nutrition · 16
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Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review
2021 · Soyoung Bae, Aram Yang, et al. · BMC Medical Genomics · 15
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Oculodentodigital Dysplasia with a Novel Mutation in GJA1 Diagnosed by Targeted Gene Panel Sequencing: A Case Report and Literature Review.
2018 · Jaeyoung Choi, Aram Yang, et al. · PubMed · 12
Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III
2022 · Min-Sun Kim, Aram Yang, et al. · Journal of Personalized Medicine · 11
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Further delineation of COG8-CDG: A case with novel compound heterozygous mutations diagnosed by targeted exome sequencing
2017 · Aram Yang, Sung Yoon Cho, et al. · Clinica Chimica Acta · 11
A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets
2018 · Misun Yang, Jinsup Kim, et al. · Annals of Pediatric Endocrinology & Metabolism · 10
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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
2017 · Eun-Kyung Cho, Jinsup Kim, et al. · Annals of Pediatric Endocrinology & Metabolism · 9
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Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature
2019 · Sun Kim, Yeong Seok Lee, et al. · Annals of Pediatric Endocrinology & Metabolism · 8
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Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center
2018 · Min-Sun Kim, Ari Song, et al. · Korean Journal of Pediatrics · 8
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First Korean Case of Renpenning Syndrome with Novel Mutation in PQBP1 Diagnosed by Targeted Exome Sequencing, and Literature Review.
2018 · Hye-In Jeong, Aram Yang, et al. · PubMed · 8
HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report
2017 · Aram Yang, Jinsup Kim, et al. · BMC Medical Genetics · 8
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Prevalence and Epidemiological Characteristics of Endoscopically Proven Reflux Esophagitis in Children in Korea
2017 · Aram Yang, Ben Kang, et al. · Pediatric Gastroenterology Hepatology & Nutrition · 8
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Coexistence of Growth Hormone Deficiency and Pituitary Microadenoma in a Child with Unique Mosaic Turner Syndrome: A Case Report and Literature Review
2020 · Eu Gene Park, Eun-Jung Kim, et al. · Diagnostics · 7
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Impact of 6-month triptorelin formulation on predicted adult height and basal gonadotropin levels in patients with central precocious puberty
2023 · Eunjoo Yoo, Sinae Kim, et al. · Frontiers in Endocrinology · 6
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Works count: 61
Citation count: 507
H-index: 13
I10-index: 17
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