Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing

由 Tomar, S, Sethi, R, Lai, PS
出版 2020

Pharmaceutical care issues encountered by post-menopausal osteoporotic women prescribed bisphosphonates

由 Lai, P.S., Chua, S.S., Chan, S.P.
出版 2012

Impact of pharmaceutical care on knowledge, quality of life and satisfaction of postmenopausal women with osteoporosis

由 Lai, P.S., Chua, S.S., Chan, S.P.
出版 2013

Detection of Low Numbers of Neuroblastoma Cells in Vitro

由 Lai, P.S., Chee, S., Chiu, L.L., Sano, K.
出版 2013

Gold nanostructures for the multiplex detection of glucose-6-phosphate dehydrogenase gene mutations

由 Seow, N., Lai, P.S., Yung, L.-Y.L.
出版 2014

J’Accuse…. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing

由 Reichardt, JKV, Patrinos, GP, Lai, PS, Novelli, G
出版 2022

Efficient mining of haplotype patterns for linkage disequilibrium mapping

由 Lin, L., Wong, L., Leong, T.-Y., Lai, P.S.
出版 2013

Validation of the diabetes, hypertension and hyperlipidemia (DHL) knowledge instrument in Malaysia

由 Lai, P.S., Chua, S.S., Tan, C.H., Chan, S.P.
出版 2012

The impact of pharmacist intervention on the use of activated vitamin D in a tertiary referral hospital in Malaysia

由 Siow, J.Y., Lai, P.S., Chua, S.S., Chan, S.P.
出版 2009

The validity and reliability of the Malaysian osteoporosis knowledge Tool in postmenopausal women

由 Lai, P.S., Chua, S.S., Chan, S.P., Low, W.Y.
出版 2008

Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing

由 Chen, H.Y., Kathirvel, P., Yee, W.C., Lai, P.S.
出版 2011

Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report

由 Hettiarachchi, D., Panchal, H., Lai, P.S., Dissanayake, V.H.W.
出版 2021

Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell lines

由 Tay, S.K.H., Khng, H.H., Low, P.S., Lai, P.S.
出版 2011

Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy

由 Qin, W.J., Yung, L.-Y.L., Yim, O.S., Lai, P.S.
出版 2011

Development and validation of the osteoporosis patient satisfaction questionnaire (OPSQ)

由 Lai, P.S., Chua, S.S., Chan, S.P., Low, W.Y., Wong, I.C.
出版 2010

Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.

由 Lai, P.S., Chiu, L.L., Low, P.S., Lee, W.L., Tay, J.S.
出版 2013

Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys

由 Hettiarachchi, D, Subasinghe, SMV, Anandagoda, GG, Panchal, H, Lai, PS, Dissanayake, VHW
出版 2022

The contributions of oxytocin and vasopressin pathway genes to human behavior

由 Ebstein, R.P., Knafo, A., Mankuta, D., Chew, S.H., Lai, P.S.
出版 2014

Erratum: Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults (BMC Psychol (2019) 7:47 DOI: 10.1186/s40359-019-0323-y)

由 Keng, S.-L., Yim, O.S., Lai, P.S., Chew, S.H., Ebstein, R.P.
出版 2021

Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling

由 Tomar S., Sethi R., Sundar G., Quah T.C., Quah B.L., Lai P.S.
出版 2019