azimatun noor aizuddin, abdul rahman ramdzan, sharifah azween syed omar, zuria mahmud, zarina a. latiff, salleh amat, keng wee teik, ch ng gaik siew, haniza rais, syed mohamed aljunid.  (2021).  genetic testing for cancer risk: is the community willing to pay for it?.  - international journal of environmental research and public health.  1-11. 

zarina al, juriza i, sharifah azween so, azli i, mohd fadly ma, zubaidah z, chia wk, clarence ko ch, julia mi, khairunisa k, sharifah noor akmal sh.  (2010).  cri-du-chat syndrome: application of array cgh in diagnostic evaluation.  - medicine & health.  108-113. 

aizuddin an, syed rusli sas, ramdzan ar, syed omar sa, mahmud z, abdul latiff z, shah sa, amat s, ismail f, keng wt, ch ng gs, rais h, aljunid sm.  (2021).  willingness to pay for cancer genetic testing in a tertiary healthcare centre.  - iium medical journal malaysia.  5-12. 

azimatun noor aizuddin, abdul rahman ramdzan, sharifah azween syed omar, zuria mahmud, zarina a. latiff, salleh amat, keng wee teik, ch ng gaik siew, haniza rais, syed mohamed aljunid.  (2021).  genetic testing for cancer risk: is the community willing to pay for it?.  - international journal of environmental research and public health.  1-11. 

zarina a. latiff, sharifah azween s. omar, doris lau, sau wei wong.  (2013).  alpha-thalassemia mental retardation syndrome: a case report of two affected siblings.  - journal of pediatric neurology.  11(1):67-70. 

siti aishah sulaiman, nor azian abdul murad, yock ping chow, muhammad-redha abdullah-zawawi, zam zureena mohd rani, siti nurmi nasir, salwati shuib, dayang anita abdul aziz, hana azhari, sharifah azween syed omar, zarina abdul latiff, rahman jamal.  (2024).  penjujukan eksom bagi penyakit jarang jumpa, mullerian agenesis dan agenesis anotectal anomaly: kajian kes.  - jurnal sains kesihatan malaysia.  18 - 38. 

cheah fc, syed omar sa, lee j, md zin wn, ng bk, chiang sc, chien ys, borhanuddin b.  (2024).  a pilot study to evaluate the use of umbilical cord blood in dried blood spot test for newborn screening of infantile-onset pompe disease.  - the 23rd congress of the federation of the asia and oceania perinatal societies.  . 

iman zaki, adli ali, sharifah azween omar, wong sau wei, nor asyikin mohd tahir, shamin saffian, a’dina rizal, nurazwa rizal.  (2024).  awareness of and attitudes toward pharmacogenetic testing for hla-b*15:02 among parents/guardians of epileptic patients in malaysia: a qualitative study.  - 26th medical & health research week.  . 

vicneswary balakrishnan, sharifah azween syed omar, nadiah sulaiman, chai-eng tan, adli ali .  (2024).  practice and perceived challenges among clinical immunologists toward genetic testing and genetic counseling in malaysia: a qualitative study.  - 26th medical & health research week.  . 

alia elsaddig mohamed salman, sharifah azween syed omar ,doris lau sie chong, loh c-khai .  (2024).  knowledge and attitude towards carrier screening and genetic counselling among parents of children diagnosed with inherited diseases in hpkk.  - 5th bcm-cuhk-um joint symposium in clinical genetics.  . 

vicneswary balakrishnan, sharifah azween syed omar, nadiah sulaiman, chai-eng tan, adli ali.  (2024).  practice and perceived challenges among clinical immunologists toward genetic testing and genetic counseling in malaysia: a qualitative study.  - 5th bcm-cuhk-um joint symposium in clinical genetics.  .