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CURRICULUM VITAE

DR. EVERLYN COXIN SIEW
DR. EVERLYN COXIN SIEW
Medical Lecturer
Department of Paediatrics
Faculty of Medicine
0379677022
ResearcherID
ORCID ID

ACADEMIC QUALIFICATION

  • MASTER OF PAEDIATRICS, (Paediatrics)
    Universiti Malaya (UM)
  • MBBS, (Medicine and Surgery)
    Manipal Academy of Higher Education (mahe), India

MEMBERSHIPS

  • LIFETIME MEMBERSHIP OF MALAYSIAN PAEDIATRIC ASSOCIATION, MEMBER
    Since 2023 (National)

AWARD AND STEWARDSHIP

  • Certificate of Excellent Service
    2026, Universiti Malaya
  • Asian Young Investigator Award
    2025, ICIEM 2025,  (International)

PUBLICATIONS

Article in Journal
WoS
  1. Chan, SH; Iness, AN; Rosenfeld, JA; Bekheirnia, MR; Burrage, LC; Chau, MHK; Htoo, CEMC; Kao, EC; Ketkar, S; Lim, WW; Luo, X; Mazlan, R; Mizerik, E; Mun, KS; Patel, KR; Potocki, L; Rapp, CK; Roca, X; Saianda, A; Iglesias-Serrano, I; Siew, EC; Sim, DY; Spielberg, DR; Tae, SK; Teo, JX; Warfsmann, J; Xia, F; Jamuar, SS; Tan, ES; Griese, M; Lim, WK; Thong, MK; Machol, K; chILD-EU Registry; Undiagnosed Dis Network (2026). Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder, AMERICAN JOURNAL OF HUMAN GENETICS. 113, 12. doi:10.1016/j.ajhg.2026.05.008

RESEARCH PROJECT

University
  1. 2026 - 2028, Universiti Malaya Translational Research Grant (UM TRG) - PPUM
    Strengthening Diagnostic Capacity for Newborn Screening of Lysosomal Storage Disorders in Malaysia ( Co-Researcher)
  2. 2025 - 2027, Bantuan Khas Penyelidikan (BKP Special)
    Breaking Barriers to Newborn Screening for Inherited Metabolic Disorders in Malaysia: A Study of Parental Knowledge, Attitudes, and Practices ( Principal Investigator(PI))

PAPER PRESENTED

Poster Presenter
  1. Ten-Year Experience with Expanded Newborn Screening for Inborn Errors of Metabolism at a Malaysian University Hospital: Challenges, Outcomes, and Opportunities, International Congress of Inborn Errors of Metabolism (ICIEM), Japanese Society of Inherited Metabolic Disorders (JSIMD) (International) (02 Sep 2025 - 06 Sep 2025)
  2. Whole Genome Sequencing Unravels the Molecular Bases of Rare Variants in Duchenne Muscular Dystrophy, Wellcome Connecting Science: Genomics of Rare Disease 2025, Wellcome Connecting science (International) (09 Apr 2025 - 11 Apr 2025)

COURSE ATTENDED

External Course
NATIONAL
  1. Seminar perubatan genomik dalam kanser dan penyakit jarang jumpa, Hospital Tunku Azizah, Kl (22 Sep 2025 - 23 Sep 2025)
  2. Variant Analysis Workshop, Hospital Tunku Azizah Kl (11 Sep 2025 - 12 Sep 2025)
  3. DKSH Paediatric Endocrinologist Workshop, St Giles Garden Hotel Kl (10 Sep 2025 - 10 Sep 2025)
  4. Short Course in Clinical Genetics, Nih Setia Alam, Selangor (07 Aug 2025 - 08 Aug 2025)