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Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling.
Chin HL, Benton MC, Yang L, Poon KS, Tan KML, Jamuar SS, Foo R, Law HY, Goh DL, Chong SS, de Sessions PF
Mol Genet Genomic Med, 12(1):e2285, 23 Sep 2023
Cited by: 1 article | PMID: 37740604 | PMCID: PMC10767580
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Safety, Tolerability, and Pharmacokinetics of β-Cryptoxanthin Supplementation in Healthy Women: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial.
Tan KML, Chee J, Lim KLM, Ng M, Gong M, Xu J, Tin F, Natarajan P, Lee BL, Ong CN, Tint MT, Kee MZL, Müller-Riemenschneider F, Gluckman PD, Meaney MJ, Kumar M, Karnani N, Eriksson JG, Nandanan B, [...] Cameron-Smith D
Nutrients, 15(10):2325, 16 May 2023
Cited by: 0 articles | PMID: 37242207 | PMCID: PMC10222860
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Dietary Supplement Intake and Fecundability in a Singapore Preconception Cohort Study.
Ku CW, Ku CO, Tay LPC, Xing HK, Cheung YB, Godfrey KM, Colega MT, Teo C, Tan KML, Chong YS, Shek LP, Tan KH, Chan SY, Lim SX, Chong MF, Yap F, Chan JKY, Loy SL
Nutrients, 14(23):5110, 01 Dec 2022
Cited by: 1 article | PMID: 36501137 | PMCID: PMC9739604
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Metabolic health status and fecundability in a Singapore preconception cohort study.
Loy SL, Chan DWK, Ku CW, Cheung YB, Godfrey KM, Tan KML, Chong YS, Shek LP, Tan KH, Chan SY, Chan JKY, Yap F
Am J Obstet Gynecol, 226(5):714.e1-714.e16, 16 Dec 2021
Cited by: 4 articles | PMID: 34921802 | PMCID: PMC7612690
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Associations Between Eczema and Attention Deficit Hyperactivity Disorder Symptoms in Children.
Loo EXL, Ooi DSQ, Ong M, Ta LDH, Lau HX, Tay MJY, Yap QV, Chan YH, Tham EH, Goh AEN, Van Bever H, Teoh OH, Eriksson JG, Chong YS, Gluckman P, Yap FKP, Karnani N, Xu J, Tan KML, [...] Broekman BFP
Front Pediatr, 10:837741, 30 Mar 2022
Cited by: 1 article | PMID: 35433544 | PMCID: PMC9007142
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Variability in newborn telomere length is explained by inheritance and intrauterine environment.
Chen L, Tan KML, Gong M, Chong MFF, Tan KH, Chong YS, Meaney MJ, Gluckman PD, Eriksson JG, Karnani N
BMC Med, 20(1):20, 25 Jan 2022
Cited by: 11 articles | PMID: 35073935 | PMCID: PMC8787951
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Role of maternal tryptophan metabolism in allergic diseases in the offspring.
Lau HX, El-Heis S, Yap QV, Chan YH, Tan CPT, Karnani N, Tan KML, Tham EH, Goh AEN, Teoh OH, Tan KH, Eriksson JG, Chong YS, Chong MF, Van Bever H, Lee BW, Shek LP, Godfrey KM, Loo EXL
Clin Exp Allergy, 51(10):1346-1360, 24 Jun 2021
Cited by: 3 articles | PMID: 34033173 | PMCID: PMC7611755
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Association of Cord Blood Thyroid-Stimulating Hormone Levels with Maternal, Delivery and Infant Factors.
Tan KML, Chu AHY, Loy SL, Rajadurai VS, Ho CKM, Chong YS, Karnani N, Lee YS, Yap FKP, Chan SY
Ann Acad Med Singap, 49(12):937-947, 01 Dec 2020
Cited by: 5 articles | PMID: 33463651
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Cohort profile: Singapore Preconception Study of Long-Term Maternal and Child Outcomes (S-PRESTO).
Loo EXL, Soh SE, Loy SL, Ng S, Tint MT, Chan SY, Huang JY, Yap F, Tan KH, Chern BSM, Tan HH, Meaney MJ, Karnani N, Godfrey KM, Lee YS, Chan JKY, Gluckman PD, Chong YS, Shek LP, [...] Cheng ZR
Eur J Epidemiol, 36(1):129-142, 21 Nov 2020
Cited by: 26 articles | PMID: 33222050 | PMCID: PMC7116651
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CEBPA mutational analysis in acute myeloid leukaemia by a laboratory-developed next-generation sequencing assay.
Ng CWS, Kosmo B, Lee PL, Lee CK, Guo J, Chen Z, Chiu L, Lee HK, Ho S, Zhou J, Lin M, Tan KML, Ban KHK, Tan TW, Chng WJ, Yan B
J Clin Pathol, 71(6):522-531, 27 Nov 2017
Cited by: 3 articles | PMID: 29180507
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Desacetyl-α-melanocyte stimulating hormone and α-melanocyte stimulating hormone are required to regulate energy balance.
Mountjoy KG, Caron A, Hubbard K, Shome A, Grey AC, Sun B, Bould S, Middleditch M, Pontré B, McGregor A, Harris PWR, Kowalczyk R, Brimble MA, Botha R, Tan KML, Piper SJ, Buchanan C, Lee S, Coll AP, Elmquist JK
Mol Metab, 9:207-216, 24 Nov 2017
Cited by: 14 articles | PMID: 29226825 | PMCID: PMC5869732
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Improved Discrimination of Patients with Breast Cancer from Healthy Controls Using Paper-Based microRNA Expression Profiling of Plasma, Following Precipitation.
Tan KML, Tay SP, Chua HW, Sufyan Bin Masroni M, Tucker S, Koay ES, Leong SM
Clin Chem, 63(12):1899-1901, 18 Sep 2017
Cited by: 1 article | PMID: 28923847
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Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease.
Lee SY, Goh JH, Tan KML, Liu TC
Hemoglobin, 41(3):209-212, 01 May 2017
Cited by: 0 articles | PMID: 28791912
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Functional characterization of naturally occurring human mutations causing insulin resistance and obesity
Tan KML
University of Cambridge, 01 Jan 2007
Cited by: 0 articles | ETH: 612991
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1-14 of 14 results

Search life-sciences literature (45,100,050 articles, preprints and more)

Search results

Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling.

Safety, Tolerability, and Pharmacokinetics of β-Cryptoxanthin Supplementation in Healthy Women: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial.

Dietary Supplement Intake and Fecundability in a Singapore Preconception Cohort Study.

Metabolic health status and fecundability in a Singapore preconception cohort study.

Associations Between Eczema and Attention Deficit Hyperactivity Disorder Symptoms in Children.

Variability in newborn telomere length is explained by inheritance and intrauterine environment.

Role of maternal tryptophan metabolism in allergic diseases in the offspring.

Association of Cord Blood Thyroid-Stimulating Hormone Levels with Maternal, Delivery and Infant Factors.

Cohort profile: Singapore Preconception Study of Long-Term Maternal and Child Outcomes (S-PRESTO).

CEBPA mutational analysis in acute myeloid leukaemia by a laboratory-developed next-generation sequencing assay.

Desacetyl-α-melanocyte stimulating hormone and α-melanocyte stimulating hormone are required to regulate energy balance.

Improved Discrimination of Patients with Breast Cancer from Healthy Controls Using Paper-Based microRNA Expression Profiling of Plasma, Following Precipitation.

Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease.

Functional characterization of naturally occurring human mutations causing insulin resistance and obesity

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