학력

• 2011.02

  충남대학교 의학과 학사

• 2016.02

  성균관대학교 의학 석사

• 성균관대학교 의학 박사 과정

주요경력

• 2019.03 ~ 현재

  인하대병원 소아청소년과 조교수

• 2018.03 ~ 2019.02

  인하대학교병원 소아청소년과 임상강사

• 2016.03 ~ 2018.02

  삼성서울병원 소아청소년과 내분비, 유전 대사 분야 전임의

• 2012.03 ~ 2016.02

  삼성서울병원 소아청소년과 전공의

• 2011.03 ~ 2012.02

  가톨릭중앙의료원 인턴

학회활동

• -

  뮤코다당증 연구학회 정회원

• -

  APPES (아시아태평양 소아내분비학회) 정회원

• -

  대한의학유전학회 정회원

• -

  대한유전성대사질환학회 정회원

• -

  대한소아내분비학회 정회원

수상경력

• 2017.01

  2017 June, Young investigation award by KISMD

• 2016.01

  2016 March, Young investigation award by KISMD

주요 논문 및 저서

• 2017

  Lipoid Congenital Adrenal Hyperplasia Diagnosed in an Infant with Hyperpigmentation Only by Targeted Exome Sequencing. Kim J, Yang A, Jang JH, Cho SY, Jin DK. J Mucopolysacch Rare Dis. 2017;3(1):28-32

• 2017

  2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis. Cho EK, Kim J, Yang A, Cho SY, Jin DK. Ann Pediatr Endocrinol Metab. 2017 Jun;22(2):129-132

• 2017

  An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing. Kim J, Cho SY, Yang A, Jang JH, Choi Y, Lee JE, Jin DK. Ann Pediatr Endocrinol Metab. 2017 Sep;22(3):203-207

• 2017

  Prevalence and Epidemiological Characteristics of Endoscopically Proven Reflux Esophagitis in Children in Korea. Yang A, Kang B, Choe JY, Kim HS, Kim K, Choe YH. Pediatr Gastroenterol Hepatol Nutr. 2017 Sep;20(3):160-166

• 2017

  Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience. Yang A, Kim J, Cho SY, Jin DK. Orphanet J Rare Dis. 2017 Aug 30;12(1):146.

• 2017

  HDR Syndrome with a Novel Mutation in GATA3 Mimicking a Congenital X-linked Stapes Gusher: a case report. Yang A, Kim J, Ki CS, Hong SH, Cho SY, Jin DK. BMC Medical genetics. 2017 Oct 26;18(1):121

• 2016

  Clinical Features, Molecular Analysis, and Outcome of ERT in Korean Patients with Mucopolysaccharidosis Type VI. Wichajarn K, Kim J, Yang A, Sohn YB, Lee BH, Yoo HW, Cho SY, Jin DK. Journal of the Korean Society of Inherited Metabolic Disease. 2016;16(1):24~33

• 2016

  Introduction to the New Version of PWS Application and It’s Use in Medical Practice. Kim J, Yang A, Cho SY, Jin DK. J Mucopolysacch Rare Dis. 2016;2(2):41-42

• 2016

  A Patient with Propionic Acidemia with a Novel mutation who was Successfully Managed by Home Care-Based Fluid Therapy. Yang A, Nam SY, Kim J, Kim HY, Park HD, Jin DK, Cho SY. Journal of the Korean Society of Inherited Metabolic Disease. 2016;16(1):52~56

• 2016

  Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study. Cho EK, Kim J, Yang A, Ki CS, Lee JE, Cho SY, Jin DK. Orphanet J Rare Dis. 2016 Aug 9;11(1):113

• 2016

  Further delineation of COG8-CDG: A case with novel compound heterozygous mutations diagnosed by targeted exome sequencing. Yang A, Cho SY, Jang JH, Kim J, Kim SZ, Lee BH, Yoo HW, Jin DK. Clin Chim Acta. 2017 Aug;471:191-195.

• 2015

  Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion. Yang A, Lee YH, Nam SY, Jeong YJ, Kyung Y, Huh R, Lee J, Kwun Y, Cho SY, Jin DK. Ann Pediatr Endocrinol Metab. 2015 Mar;20(1):40-5.

• 2015

  Acute Necrotizing Pancreatitis Associated with Mycoplasma pneumoniae Infection in a Child. Yang A, Lee YH, Nam SY, Jeong YJ, Kyung Y, Huh R, Lee J, Kwun Y, Cho SY, Jin DK. Pediatr Gastroenterol Hepatol Nutr. 2015 Sep;18(3):209-15