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Chew, Elaine Guo Yan
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Showing results 10 to 12 of 12
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Issue Date
Title
Author(s)
2019
A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family
Kausar, Mehran
;
Chew, Elaine Guo Yan
;
Ullah, Hazrat
;
Anees, Mariam
;
Khor, Chiea Chuen
;
Foo, Jia Nee
;
Makitie, Outi
;
Siddiqi, Saima
2022
Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia
Chew, Elaine Guo Yan
;
Lim, Tze Chiun
;
Leong, Meng Fatt
;
Liu, Xingliang
;
Sia, Yee Yen
;
Leong, See Ting
;
Yan-Jiang, Benjamin C.
;
Stoecklin, Celine
;
Borhan, Rosa
;
Heilmann-Heimbach, Stefanie
;
Nöthen, Markus M.
;
Viasnoff, Virgile
;
Ng, Shyh-Chang
;
Wan, Andrew C. A.
;
Philpott, Michael P.
;
Hillmer, Axel M.
2022
Trans-interaction of risk loci 6p24.1 and 10q11.21 is associated with endothelial damage in coronary artery disease
Tay, Kai Yi
;
Wu, Kan Xing
;
Chioh, Florence Wen Jing
;
Autio, Matias Ilmari
;
Pek, Nicole Min Qian
;
Narmada, Balakrishnan Chakrapani
;
Tan, Sock-Hwee
;
Low, Adrian Fatt-Hoe
;
Lian, Michelle Mulan
;
Chew, Elaine Guo Yan
;
Lau, Hwee Hui
;
Kao, Shih Ling
;
Teo, Adrian Kee Keong
;
Foo, Jia Nee
;
Foo, Roger Sik Yin
;
Heng, Chew Kiat
;
Chan, Mark Yan Yee
;
Cheung, Christine