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Ng, C.G. and Mohamed, S. and See, M.H. and Harun, F. and Dahlui, M. and Sulaiman, A.H. and Zainal, N.Z. and Taib, N.A. (2015) Anxiety, depression, perceived social support and quality of life in Malaysian breast cancer patients: a 1-year prospective study. Health and Quality of Life Outcomes, 13. ISSN 1477-7525,
Kang, I.N. and Musa, M. and Harun, F. and Junit, S.M. (2010) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis. Biochemical Genetics, 48 (1-2). pp. 141-151.
Khaw, K.W. and Jalaludin, M.Y. and Suhaimi, H. and Harun, F. and Subrayan, V. (2010) Endogenous Cushing syndrome from an ectopic adrenocorticotropic hormone production as a rare cause of ocular hypertension. Journal of AAPOS, 14 (4). pp. 356-357.
Harun, F. and Taufik, I. and Omar, S.Z. (2010) Vitamin D status in multiethnic Malaysian pregnant women. Endocrine Reviews, 31 (3, 1).
Yong, P.H. and Junit, S.M. and Harun, F. and Hashim, Onn Haji (2006) Patients with congenital hypothyroidism demonstrate different altered expression of plasma fibrinogen and haptoglobin polypeptide chains. Clinical Biochemistry, 39 (2). pp. 126-132. ISSN 0009-9120, DOI https://doi.org/10.1016/j.clinbiochem.2005.11.017.
Lee, Way Seah and Lum, L.C. and Harun, F. (2003) Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice. Medical Journal of Malaysia, 58 (2). pp. 279-281. ISSN 0300-5283,
Junit, S.M. and Othman, S. and Yusof, Rohana and Billett, M.A. and Harun, F. (2003) Ala519Thr mutation in exon 11 of LDL receptor gene in members of a Malaysian family with hypercholesterolaemia. Asia Pacific Journal of Molecular Biology and Biotechnology, 11 (2). pp. 77-82. ISSN 0128-7451,
