Search Results - "Chew, Elaine G.Y."

Recurrent Fusion Genes in Gastric Cancer: CLDN18-ARHGAP26 Induces Loss of Epithelial Integrity by Yao, Fei, Kausalya, Jaya P., Sia, Yee Yen, Teo, Audrey S.M., Lee, Wah Heng, Ong, Alicia G.M., Zhang, Zhenshui, Tan, Joanna H.J., Li, Guoliang, Bertrand, Denis, Liu, Xingliang, Poh, Huay Mei, Guan, Peiyong, Zhu, Feng, Pathiraja, Thushangi Nadeera, Ariyaratne, Pramila N., Rao, Jaideepraj, Woo, Xing Yi, Cai, Shaojiang, Mulawadi, Fabianus H., Poh, Wan Ting, Veeravalli, Lavanya, Chan, Chee Seng, Lim, Seong Soo, Leong, See Ting, Neo, Say Chuan, Choi, Poh Sum D., Chew, Elaine G.Y., Nagarajan, Niranjan, Jacques, Pierre-Étienne, So, Jimmy B.Y., Ruan, Xiaoan, Yeoh, Khay Guan, Tan, Patrick, Sung, Wing-Kin, Hunziker, Walter, Ruan, Yijun, Hillmer, Axel M.

“…Genome rearrangements, a hallmark of cancer, can result in gene fusions with oncogenic properties. Using DNA paired-end-tag (DNA-PET) whole-genome sequencing,…”
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An oestrogen-receptor-α-bound human chromatin interactome by Fullwood, Melissa J., Liu, Mei Hui, Pan, You Fu, Liu, Jun, Xu, Han, Mohamed, Yusoff Bin, Orlov, Yuriy L., Velkov, Stoyan, Ho, Andrea, Mei, Poh Huay, Chew, Elaine G. Y., Huang, Phillips Yao Hui, Welboren, Willem-Jan, Han, Yuyuan, Ooi, Hong Sain, Ariyaratne, Pramila N., Vega, Vinsensius B., Luo, Yanquan, Tan, Peck Yean, Choy, Pei Ye, Wansa, K. D. Senali Abayratna, Zhao, Bing, Lim, Kar Sian, Leow, Shi Chi, Yow, Jit Sin, Joseph, Roy, Li, Haixia, Desai, Kartiki V., Thomsen, Jane S., Lee, Yew Kok, Karuturi, R. Krishna Murthy, Herve, Thoreau, Bourque, Guillaume, Stunnenberg, Hendrik G., Ruan, Xiaoan, Cacheux-Rataboul, Valere, Sung, Wing-Kin, Liu, Edison T., Wei, Chia-Lin, Cheung, Edwin, Ruan, Yijun

“…Genomes are organized into high-level three-dimensional structures, and DNA elements separated by long genomic distances can in principle interact…”
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Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia by Chew, Elaine G.Y., Tan, Joanna H.J., Bahta, Adiam W., Ho, Bryan S.-Y., Liu, Xingliang, Lim, Tze Chiun, Sia, Yee Yen, Bigliardi, Paul L., Heilmann, Stefanie, Wan, Andrew C.A., Nöthen, Markus M., Philpott, Michael P., Hillmer, Axel M.

“…Androgenetic alopecia (AGA) is a common heritable and androgen-dependent hair loss condition in men. Twelve genetic risk loci are known to date, but it is…”
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Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness by Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, del Rosario, Ricardo C. -H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M., Dedoussis, George, Richards, J. Brent, Nothnagel, Michael, Martin, Nicholas G., Becker, Tim, Hinds, David A., Nöthen, Markus M.

“…Male-pattern baldness (MPB) is a common and highly heritable trait characterized by androgen-dependent, progressive hair loss from the scalp. Here, we carry…”
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Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia by Chew, Elaine G. Y., 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, Shyh‐Chang, Ng, Wan, Andrew C. A., Philpott, Michael P., Hillmer, Axel M.

“…Androgenetic alopecia (AGA) is a prevalent hair loss condition in males that develops due to the influence of androgens and genetic predisposition. With the…”
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Identifying genes in Parkinson disease: state of the art by Chew, Elaine GY, Foo, Jia Nee, Tan, Eng‐King

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Impaired Development of Neural-Crest Cell-Derived Organs and Intellectual Disability Caused by MED13L Haploinsufficiency by Utami, Kagistia Hana, Winata, Cecilia Lanny, Hillmer, Axel M., Aksoy, Irene, Long, Hoang Truong, Liany, Herty, Chew, Elaine G. Y., Mathavan, Sinnakaruppan, Tay, Stacey K. H., Korzh, Vladimir, Sarda, Pierre, Davila, Sonia, Cacheux, Valere

“…ABSTRACT MED13L is a component subunit of the Mediator complex, an important regulator of transcription that is highly conserved across eukaryotes. Here, we…”
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Detection of chromosomal breakpoints in patients with developmental delay and speech disorders by Utami, Kagistia H, Hillmer, Axel M, Aksoy, Irene, Chew, Elaine G Y, Teo, Audrey S M, Zhang, Zhenshui, Lee, Charlie W H, Chen, Pauline J, Seng, Chan Chee, Ariyaratne, Pramila N, Rouam, Sigrid L, Soo, Lim Seong, Yousoof, Saira, Prokudin, Ivan, Peters, Gregory, Collins, Felicity, Wilson, Meredith, Kakakios, Alyson, Haddad, Georges, Menuet, Arnaud, Perche, Olivier, Tay, Stacey Kiat Hong, Sung, Ken W K, Ruan, Xiaoan, Ruan, Yijun, Liu, Edison T, Briault, Sylvain, Jamieson, Robyn V, Davila, Sonia, Cacheux, Valere

“…Delineating candidate genes at the chromosomal breakpoint regions in the apparently balanced chromosome rearrangements (ABCR) has been shown to be more…”
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