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105. Identifying and correcting epigenetics measurements for systematic sources of variation

106. Rare variants in the MECP2gene in girls with central precocious puberty: a translational cohort study

108. Newborn body composition and child cardiovascular risk markers: a prospective multi-ethnic Asian cohort study

110. Maternal obesity increases hypothalamic miR-505-5p expression in mouse offspring leading to altered fatty acid sensing and increased intake of high-fat food

111. Using genetic variation to disentangle the complex relationship between food intake and health outcomes

115. Associations between Children's Genetic Susceptibility to Obesity, Infant's Appetite and Parental Feeding Practices in Toddlerhood

116. Metabolomics in early life and the association with body composition at age 2 years

121. Damaging missense variants in IGF1R implicate a role for IGF-1 resistance in the aetiology of type 2 diabetes

122. ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbance

128. Transforming Obesity Prevention for CHILDren (TOPCHILD) Collaboration: protocol for a systematic review with individual participant data meta-analysis of behavioural interventions for the prevention of early childhood obesity

133. Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan

135. Extensive Study of Breast Milk and Infant Growth: Protocol of the Cambridge Baby Growth and Breastfeeding Study (CBGS-BF)

141. Sixty-Five Common Genetic Variants and Prediction of Type 2 Diabetes

144. Genetic studies of body mass index yield new insights for obesity biology

145. New genetic loci link adipose and insulin biology to body fat distribution

148. Correction: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

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