A118G Single Nucleotide Polymorphism of Human μ-Opioid Receptor Gene Influences Pain Perception and Patient-controlled Intravenous Morphine Consumption after Intrathecal Morphine f... by SIA, Alex T, LIM, Yvonne, LIM, Eileen C. P, GOH, Rachelle W. C, HAI YANG LAW, LANDAU, Ruth, TEO, Yik-Ying, ENE CHOO TAN

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Ethnicity and OPRM Variant Independently Predict Pain Perception and Patient-Controlled Analgesia Usage for Post-Operative Pain by Tan, Ene-choo, Lim, Eileen CP, Teo, Yik-ying, Lim, Yvonne, Law, Hai-yang, Sia, Alex T

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Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event by Brett, Maggie, Korovesis, George, Lai, Angeline H M, Lim, Eileen C P, Tan, Ene-Choo

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Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients by Lim, Eileen C P, Brett, Maggie, Lai, Angeline H M, Lee, Siew-Peng, Tan, Ee-Shien, Jamuar, Saumya S, Ng, Ivy S L, Tan, Ene-Choo

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De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability by Brett, Maggie S., Ng, Ivy S.L., Lim, Eileen C.P., Yong, Min Hwee, Li, Zhihui, Lai, Angeline, Tan, Ene-Choo

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De novo trisomy 12p in twin girls with different levels of mosaicism by Lim, Eileen C.P., Ng, Ivy S.L., Yong, Min-Hwee, Yon, Hui-Yi, Brett, Maggie S.Y., Tan, Ene-Choo

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A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family with Van der Woude Syndrome by Tan, Ene-Choo, Lim, Hwee-Woon, Lim, Eileen C.P., Lee, Seng-Teik

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A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein–Taybi syndrome by Lai, Angeline H.M., Brett, Maggie S., Chin, Wai-Hoe, Lim, Eileen C.P., Ng, Jasmine S.H., Tan, Ene-Choo

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Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation by Nagaputra, Jerry C., Koh, Mark J.A., Brett, Maggie, Lim, Eileen C.P., Lim, Hwee-Woon, Tan, Ene-Choo

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De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus by Tan, Ene-Choo, Lim, Eileen Cp, Lee, Seng-Teik

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Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern by Tan, Ee-Shien, Yong, Min-Hwee, Lim, Eileen Cp, Li, Zhi-Hui, Brett, Maggie Sy, Tan, Ene-Choo

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Piebaldism with multiple café-au-lait-like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation by Nagaputra, Jerry C, Koh, Mark J A, Brett, Maggie, Lim, Eileen C P, Lim, Hwee-Woon, Tan, Ene-Choo

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Narcissism, extraversion and adolescents’ self-presentation on Facebook by Ong, Eileen Y.L., Ang, Rebecca P., Ho, Jim C.M., Lim, Joylynn C.Y., Goh, Dion H., Lee, Chei Sian, Chua, Alton Y.K.

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From Narcissistic Exploitativeness to Bullying Behavior: The Mediating Role of Approval-of-aggression Beliefs by Ang, Rebecca P., Ong, Eileen Y. L., Lim, Joylynn C. Y., Lim, Eulindra W.

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A Novel Severe Acute Respiratory Syndrome Coronavirus Protein, U274, Is Transported to the Cell Surface and Undergoes Endocytosis by TAN, Yee-Joo, TENG, Eileen, SHEN, Shuo, TAN, Timothy H. P, GOH, Phuay-Yee, FIELDING, Burtram C, OOI, Eng-Eong, TAN, Hwee-Cheng, SENG GEE LIM, WANJIN HONG

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Comparison of self-reported and register-based hospital medical data on comorbidities in women by Ho, Peh Joo, Tan, Chuen Seng, Shawon, Shajedur Rahman, Eriksson, Mikael, Lim, Li Yan, Miao, Hui, Png, Eileen, Chia, Kee Seng, Hartman, Mikael, Ludvigsson, Jonas F., Czene, Kamila, Hall, Per, Li, Jingmei

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Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error by Fan, Qiao, Verhoeven, Virginie J. M., Wojciechowski, Robert, Barathi, Veluchamy A., Hysi, Pirro G., Guggenheim, Jeremy A., Höhn, René, Vitart, Veronique, Khawaja, Anthony P., Yamashiro, Kenji, Hosseini, S Mohsen, Lehtimäki, Terho, Lu, Yi, Haller, Toomas, Xie, Jing, Delcourt, Cécile, Pirastu, Mario, Wedenoja, Juho, Gharahkhani, Puya, Venturini, Cristina, Miyake, Masahiro, Hewitt, Alex W., Guo, Xiaobo, Mazur, Johanna, Huffman, Jenifer E., Williams, Katie M., Polasek, Ozren, Campbell, Harry, Rudan, Igor, Vatavuk, Zoran, Wilson, James F., Joshi, Peter K., McMahon, George, St Pourcain, Beate, Evans, David M., Simpson, Claire L., Schwantes-An, Tae-Hwi, Igo, Robert P., Mirshahi, Alireza, Bellenguez, Céline, Blettner, Maria, Raitakari, Olli, Kähönen, Mika, Seppälä, Ilkka, Zeller, Tanja, Meitinger, Thomas, Ried, Janina S., Gieger, Christian, Portas, Laura, van Leeuwen, Elisabeth M., Amin, Najaf, Uitterlinden, André G., Rivadeneira, Fernando, Hofman, Albert, Vingerling, Johannes R., Wang, Ya Xing, Wang, Xu, Tai-Hui Boh, Eileen, Ikram, M. Kamran, Sabanayagam, Charumathi, Gupta, Preeti, Tan, Vincent, Zhou, Lei, Ho, Candice E. H., Lim, Wan’e, Beuerman, Roger W., Siantar, Rosalynn, Tai, E-Shyong, Vithana, Eranga, Mihailov, Evelin, Khor, Chiea-Chuen, Hayward, Caroline, Luben, Robert N., Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Wong, Hoi-Suen, Metspalu, Andres, Aung, Tin, Young, Terri L., He, Mingguang, Pärssinen, Olavi, van Duijn, Cornelia M., Jin Wang, Jie, Williams, Cathy, Jonas, Jost B., Teo, Yik-Ying, Mackey, David A., Oexle, Konrad, Yoshimura, Nagahisa, Paterson, Andrew D., Pfeiffer, Norbert, Wong, Tien-Yin, Baird, Paul N., Stambolian, Dwight, Wilson, Joan E. Bailey, Cheng, Ching-Yu, Hammond, Christopher J., Klaver, Caroline C. W., Saw, Seang-Mei

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Soluble PD-L1 reprograms blood monocytes to prevent cerebral edema and facilitate recovery after ischemic stroke by Kim, Jennifer E., Lee, Ryan P., Yazigi, Eli, Atta, Lyla, Feghali, James, Pant, Ayush, Jain, Aanchal, Levitan, Idan, Kim, Eileen, Patel, Kisha, Kannapadi, Nivedha, Shah, Pavan, Bibic, Adnan, Hou, Zhipeng, Caplan, Justin M., Gonzalez, L. Fernando, Huang, Judy, Xu, Risheng, Fan, Jean, Tyler, Betty, Brem, Henry, Boussiotis, Vassiliki A., Jantzie, Lauren, Robinson, Shenandoah, Koehler, Raymond C., Lim, Michael, Tamargo, Rafael J., Jackson, Christopher M.

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Genome sequence of enterohaemorrhagic Escherichia coli O157:H7 by Perna, Nicole T, Plunkett, Guy, Burland, Valerie, Mau, Bob, Glasner, Jeremy D, Rose, Debra J, Mayhew, George F, Evans, Peter S, Gregor, Jason, Kirkpatrick, Heather A, Pósfai, György, Hackett, Jeremiah, Klink, Sara, Boutin, Adam, Shao, Ying, Miller, Leslie, Grotbeck, Erik J, Davis, N. Wayne, Lim, Alex, Dimalanta, Eileen T, Potamousis, Konstantinos D, Apodaca, Jennifer, Anantharaman, Thomas S, Lin, Jieyi, Yen, Galex, Schwartz, David C, Welch, Rodney A, Blattner, Frederick R

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G.3.2 is a novel allele of the gene connector enhancer of ksr ( cnk ) in Drosophila melanogaster by Chammout, Hanadi, Adkins, Delia L, Al-Olimat, Aleece K, Alsaad, Zeinab, Altopp, Beatrice M, Amer, Tuqa, Apampa, Feyi O, Avery, Gwendolyn R, Bazzi, Isaac I, Beck, Emilia D, Beier, Elise L, Belisle, B Shafer, Benton, Lane, Bolyard, Madison M, Brain, Olivia E, Buckner, Eldon T, Chowdhury, Shria Roy, Cifranic, Jennifer R, Cleary, Liam, Clum, Tyler R, Cruz, Autumn M, DeGray, Meghan V, Echeverry, Isabel L, El Dana, Haya, Elkadri, Sarah K, Estep, Paige L, Falke, Luke R, Foor, Hannah J, Gullapalli, Anika S, Hakim, Sandro S, Hazime, Hussein B, Heininger, Lauren E, Hoeft, Emma G, James, Lauren M, Jeon, Yeowon, Johnson, Megan R, Jordan, Laine P, Khan, Zayd, Kochensparger, Sydney K, Koria, Fadi J, Krasnow, Ruby M, Lilly, Veronica, Lim, Eileen, MacCormack, Ian T, Malesh, Andriy, Mariano, Mikayla G, Mentzer, Audrey C, Messner, Katelyn H, Myers, Katlyn C, Newman, Emily R, Richters, Annie M, Romero, Liliana, Rotem, Adam, Saho, Reese J, Sawaki, Kaname, Selders, Ashley N, Shockney, Elizabeth, Sobh, Farah A, Speiser, Isabelle F, Sproul, Breanna M, Sroufe, Veronica J, Tollkuci, Antonia, Trevino, Cassandra C, Vapenik, Megan A, Wagner, Erin M, Bieser, Kayla L, Siders, Jamie L, Thackeray, Justin R, Kagey, Jacob D

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