Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts von Yong, Rita Y.Y., Mustaffa, Su'Aidah B., Wasan, Pavandip S., Sheng, Liang, Marshall, Christian R., Scherer, Stephen W., Teo, Yik-Ying, Yap, Eric P.H.

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Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia von Khor, Chiea Chuen, Miyake, Masahiro, Chen, Li Jia, Shi, Yi, Barathi, Veluchamy A, Qiao, Fan, Nakata, Isao, Yamashiro, Kenji, Zhou, Xin, Tam, Pancy O S, Cheng, Ching-Yu, Tai, E Shyong, Vithana, Eranga N, Aung, Tin, Teo, Yik-Ying, Wong, Tien-Yin, Moriyama, Muka, Ohno-Matsui, Kyoko, Mochizuki, Manabu, Matsuda, Fumihiko, Yong, Rita Y Y, Yap, Eric P H, Yang, Zhenglin, Pang, Chi Pui, Saw, Seang-Mei, Yoshimura, Nagahisa

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Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats von Ballantyne, Kaye N., Ralf, Arwin, Aboukhalid, Rachid, Achakzai, Niaz M., Anjos, Maria J., Ayub, Qasim, Balažic, Jože, Ballantyne, Jack, Berger, Burkhard, Bobillo, Cecilia, Burri, Helen, Capal, Tomas, Caratti, Stefano, Cárdenas, Jorge, Carvalho, Monica, Comas, David, Corach, Daniel, D'Amato, Maria E., Davison, Sean, de Knijff, Peter, De Ungria, Maria Corazon A., Decorte, Ronny, Dobosz, Tadeusz, Dupuy, Berit M., Grol, Laurens, Haas, Cordula, Hanson, Erin, Henke, Jürgen, Henke, Lotte, Herrera-Rodríguez, Fabiola, Hill, Carolyn R., Holmlund, Gunilla, Honda, Katsuya, Inokuchi, Shota, Jobling, Mark A., Kaddura, Mahmoud, Kim, Jong S., Kim, Soon H., Kim, Wook, King, Turi E., Kling, Daniel, Kovačević, Lejla, Kovatsi, Leda, Krajewski, Paweł, Kravchenko, Sergey, Larmuseau, Maarten H. D., Lee, Eun Young, Lessig, Ruediger, Livshits, Ludmila A., Marjanović, Damir, Minarik, Marek, Mukherjee, Meeta, Munier, Patrick, Nagaraju, Javaregowda, Neuhuber, Franz, Nie, Shengjie, Nilasitsataporn, Premlaphat, Nishi, Takeki, Oh, Hye H., Palo, Jukka U., Pamjav, Horolma, Parson, Walther, Petlach, Michal, Phillips, Christopher, Ploski, Rafal, Primorac, Dragan, Purnomo, Gludhug A., Purps, Josephine, Rębała, Krzysztof, Rerkamnuaychoke, Budsaba, Robino, Carlo, Roewer, Lutz, Rosa, Alexandra, Sajantila, Antti, Sala, Andrea, Sanz, Paula, Schmitt, Cornelia, Sharma, Anil K., Shin, Kyoung-Jin, Sirker, Miriam, Siváková, Daniela, Solano-Matamoros, Carlos, Souto, Luis, Stenzl, Vlastimil, Sudoyo, Herawati, Syndercombe-Court, Denise, Tagliabracci, Adriano, Taylor, Duncan, Tillmar, Andreas, Tsybovsky, Iosif S., Tyler-Smith, Chris, van der Gaag, Kristiaan J., Vanek, Daniel, Völgyi, Antónia, Ward, Denise, Willemse, Patricia, Yap, Eric P.H., Yong, Rita Y.Y., Pajnič, Irena Zupanič, Kayser, Manfred

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Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females von Tong, Terry Y.Y, Yong, Rita Y.Y, Goh, Victor H.H, Liang, Shen, Chong, Alicia P.L, Mok, Helen P.P, Yong, Eu Leong, Yap, Eric P.H, Moochhala, Shabbir

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Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations von Yong, Rita Y Y, Gan, Linda S H, Chang, Yuet Meng, Yap, Eric P H

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A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Yp11.2 (DYS458-MSY1-AMEL-Y) deletion von Chang, Yuet Meng, Perumal, Revathi, Keat, Phoon Yoong, Yong, Rita Y.Y., Kuehn, Daniel L.C., Burgoyne, Leigh

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Malignant Hyperthermia and Ryanodine Receptor Type 1 Gene (RyR1) Mutation in a Family in Singapore von Li, Daphne Wy, Lai, Poh San, Lee, Delice W, Yong, Rita Yy, Lee, Tat Leang

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Identification of an I Na -dependent and I to -mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient von Ma, Dongrui, Liu, Zhenfeng, Loh, Li Jun, Zhao, Yongxing, Li, Guang, Liew, Reginald, Islam, Omedul, Wu, Jianjun, Chung, Ying Ying, Teo, Wee Siong, Ching, Chi Keong, Tan, Boon Yew, Chong, Daniel, Ho, Kah Leng, Lim, Paul, Yong, Rita Yu Yin, Panama, Brian K, Kaplan, Aaron D, Bett, Glenna C L, Ware, James, Bezzina, Connie R, Verkerk, Arie O, Cook, Stuart A, Rasmusson, Randall L, Wei, Heming

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A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Y(p)11.2 (DYS458-MSY1-AMEL-Y) deletion von Chang, Yuet Meng, Perumal, Revathi, Keat, Phoon Yoong, Yong, Rita Y Y, Kuehn, Daniel L C, Burgoyne, Leigh

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Young men driving dangerously: Development of the Motives for Dangerous Driving Scale (MDDS) von Ho, Robert, Gee, Rita Yong

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Polymorphism studies of six miniSTR loci for three ethnic populations in Singapore von Yong, Rita Y.Y, Gan, Linda S.H, Chua, Elizabeth M.Y, Yap, Eric P.H

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A Novel Susceptibility Locus On Chromosome 2 in the (New Zealand Black x New Zealand White)F1 Hybrid Mouse Model of Systemic Lupus Erythematosus von Rahman, Ziaur SM, Tin, Soe-Kyaw, Buenaventura, Pia-Nina L, Ho, Chiu-Han, Yap, Eric P. H, Yong, Rita Y. Y, Koh, Dow-Rhoon

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Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore von Yong, Rita Y.Y, Gan, Linda S.H, Coble, Mike D, Yap, Eric P.H

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Identification of an INa-dependent and Ito-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient von Ma, Dongrui, Liu, Zhenfeng, Loh, Li Jun, Zhao, Yongxing, Li, Guang, Liew, Reginald, Islam, Omedul, Wu, Jianjun, Chung, Ying Ying, Teo, Wee Siong, Ching, Chi Keong, Tan, Boon Yew, Chong, Daniel, Ho, Kah Leng, Lim, Paul, Yong, Rita Yu Yin, Panama, Brian K., Kaplan, Aaron D., Bett, Glenna C. L., Ware, James, Bezzina, Connie R., Verkerk, Arie O., Cook, Stuart A., Rasmusson, Randall L., Wei, Heming

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Announcement of Population Data: Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore von Yong, Rita Y Y, Gan, Linda S H, Coble, Mike D, Yap, Eric P H

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Brugada Syndrome and SCN5A-Encoded Cardiac Sodium Channel Mutations in Singapore von Yew Tan, Boon, Yong, Rita, Uttamchandani, Mahesh, Qi Wong, Wei, Liew, Reginald, Chong, Daniel, Chong Seow, Swee, Ling Neo, Jia, Hui Yap, Shiao, Gan, Linda, Keong Ching, Chi, Siong Teo, Wee

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Compound Heterozygosity in Brugada Syndrome: A Case Study von Yew Tan, Boon, Yong, Rita, Uttamchandani, Mahesh, Qi Wong, Wei, Liew, Reginald, Chong, Daniel, Chong Seow, Swee, Ling Neo, Jia, Hui Yap, Shiao, Gan, Linda, Keong Ching, Chi, Siong Teo, Wee

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Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts: HUMAN MUTATION von Yong, Rita Y.Y., Mustaffa, Su'Aidah B., Wasan, Pavandip S., Sheng, Liang, Marshall, Christian R., Scherer, Stephen W., Teo, Yik-Ying, Yap, Eric P.H.

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A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore von Tan, Boon Yew, Yong, Rita Yu Yin, Barajas-Martinez, Hector, Dumaine, Robert, Chew, Ying Xia, Wasan, Pavandip Singh, Ching, Chi Keong, Ho, Kah Leng, Gan, Linda Seo Hwee, Morin, Nathalie, Chong, Alicia Poh Leng, Yap, Shiao Hui, Neo, Jia Ling, Yap, Eric Peng Huat, Moochhala, Shabbir, Chong, Daniel Thuan Tee, Chow, Weien, Seow, Swee Chong, Hu, Dan, Uttamchandani, Mahesh, Teo, Wee Siong

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A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome von Tan, Boon Yew, Wang, Luokai, Uttamchandani, Mahesh, Barajas-Martinez, Hector, Dumaine, Robert, Morin, Nathalie, Ching, Chi Keong, Ho, Kah Leng, Chong, Daniel Thuan Tee, Chow, Weien, Yap, Eric Peng Huat, Moochhala, Shabbir, Hu, Dan, Yong, Rita Yu Yin, Teo, Wee Siong

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