Examining the common and specific grey matter abnormalities in childhood maltreatment and peer victimisation

por Lim, Lena, Khor, Chiea Chuen
Publicado 2022

Revealing the molecular signatures of host-pathogen interactions

por Khor, Chiea-Chuen, Hibberd, Martin L
Publicado 2011

Plateau iris syndrome and angle-closure glaucoma in a patient with nail-patella syndrome

por Gardin, Margot A., Khor, Chiea Chuen, Silva, Luis, Krefting, Einar A., Ritch, Robert
Publicado 2020

Combined genotype and haplotype tests for region-based association studies

por Zakharov, Sergii, Wong, Tien Yin, Aung, Tin, Vithana, Eranga Nishanthie, Khor, Chiea Chuen, Salim, Agus, Thalamuthu, Anbupalam
Publicado 2013

Plasma endothelin-1 and single nucleotide polymorphisms of endothelin-1 and endothelin type A receptor genes as risk factors for normal tension glaucoma

por Kosior-Jarecka, Ewa, Wróbel-Dudzińska, Dominika, Łukasik, Urszula, Aung, Tin, Khor, Chiea Chuen, Kocki, Janusz, Żarnowski, Tomasz
Publicado 2016

Characterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India

por Ali, Mohammad, Liu, Xuanyao, Pillai, Esakimuthu Nisha, Chen, Peng, Khor, Chiea-Chuen, Ong, Rick Twee-Hee, Teo, Yik-Ying
Publicado 2014

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

por Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Publicado 2018

A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family

por Kausar, Mehran, Chew, Elaine Guo Yan, Ullah, Hazrat, Anees, Mariam, Khor, Chiea Chuen, Foo, Jia Nee, Makitie, Outi, Siddiqi, Saima
Publicado 2019

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

por Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam
Publicado 2019

An Evaluation of DNA Methyltransferase 1 (DNMT1) Single Nucleotide Polymorphisms and Chemotherapy-Associated Cognitive Impairment: A Prospective, Longitudinal Study

por Chan, Alexandre, Yeo, Angie, Shwe, Maung, Tan, Chia Jie, Foo, Koon Mian, Chu, Pat, Khor, Chiea Chuen, Ho, Han Kiat
Publicado 2019

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

por Ajmal, Muhammad, Mir, Asif, Wahid, Sughra, Khor, Chiea Chuen, Foo, Jia Nee, Siddiqi, Saima, Kauser, Mehran, Malik, Salman Akbar, Nasir, Muhammad
Publicado 2017

Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study

por Ho, Peh Joo, Tan, Iain BeeHuat, Chong, Dawn Qingqing, Khor, Chiea Chuen, Yuan, Jian-Min, Koh, Woon-Puay, Dorajoo, Rajkumar, Li, Jingmei
Publicado 2023

Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease

por Ravindran, Ethiraj, Ullah, Noor, Mani, Shyamala, Chew, Elaine Guo Yan, Tandiono, Moses, Foo, Jia Nee, Khor, Chiea Chuen, Kaindl, Angela M., Siddiqi, Saima
Publicado 2022

Impact of Measurement Error on Testing Genetic Association with Quantitative Traits

por Liao, Jiemin, Li, Xiang, Wong, Tien-Yin, Wang, Jie Jin, Khor, Chiea Chuen, Tai, E. Shyong, Aung, Tin, Teo, Yik-Ying, Cheng, Ching-Yu
Publicado 2014

Genetic associations with healthy ageing among Chinese adults

por Chang, Xuling, Zhou, Yan-Feng, Wang, Ling, Liu, Jianjun, Yuan, Jian-Min, Khor, Chiea-Chuen, Heng, Chew-Kiat, Pan, An, Koh, Woon-Puay, Dorajoo, Rajkumar
Publicado 2022

Whole-Genome Sequencing Analysis of Serially Isolated Multi-Drug and Extensively Drug Resistant Mycobacterium tuberculosis from Thai Patients

por Faksri, Kiatichai, Tan, Jun Hao, Disratthakit, Areeya, Xia, Eryu, Prammananan, Therdsak, Suriyaphol, Prapat, Khor, Chiea Chuen, Teo, Yik-Ying, Ong, Rick Twee-Hee, Chaiprasert, Angkana
Publicado 2016

Global gene expression profiling identifies new therapeutic targets in acute Kawasaki disease

por Hoang, Long Truong, Shimizu, Chisato, Ling, Ling, Naim, Ahmad Nazri Mohamed, Khor, Chiea Chuen, Tremoulet, Adriana H, Wright, Victoria, Levin, Michael, Hibberd, Martin L, Burns, Jane C
Publicado 2014

Lens Status Influences the Association between CFH Polymorphisms and Age-Related Macular Degeneration: Findings from Two Population-Based Studies in Singapore

por Wong, Chee Wai, Liao, Jiemin, Cheung, Gemmy C., Khor, Chiea Chuen, Vithana, Eranga N., Wang, Jie Jin, Mitchell, Paul, Aung, Tin, Wong, Tien Y., Cheng, Ching-Yu
Publicado 2015

Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese population

por Chang, Xuling, Dorajoo, Rajkumar, Sun, Ye, Wang, Ling, Ong, Choon Nam, Liu, Jianjun, Khor, Chiea Chuen, Yuan, Jian-Min, Koh, Woon Puay, Friedlander, Yechiel, Heng, Chew-Kiat
Publicado 2020

LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets

por Wilm, Andreas, Aw, Pauline Poh Kim, Bertrand, Denis, Yeo, Grace Hui Ting, Ong, Swee Hoe, Wong, Chang Hua, Khor, Chiea Chuen, Petric, Rosemary, Hibberd, Martin Lloyd, Nagarajan, Niranjan
Publicado 2012