A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy von Yu, Xue-Qing, Li, Ming, Zhang, Hong, Low, Hui-Qi, Wei, Xin, Wang, Jin-Quan, Sun, Liang-Dan, Sim, Kar-Seng, Li, Yi, Foo, Jia-Nee, Wang, Wei, Li, Zhi-Jian, Yin, Xian-Yong, Tang, Xue-Qing, Fan, Li, Chen, Jian, Li, Rong-Shan, Wan, Jian-Xin, Liu, Zhang-Suo, Lou, Tan-Qi, Zhu, Li, Huang, Xiao-Jun, Zhang, Xue-Jun, Liu, Zhi-Hong, Liu, Jian-Jun

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Polygenic Risk Scores in a Prospective Parkinson's Disease Cohort von Sia, Ming‐Wei, Foo, Jia‐Nee, Saffari, Seyed‐Ehsan, Wong, Aidan Sheng‐Yong, Khor, Chiea‐Chuen, Yuan, Jian‐Min, Tan, Eng‐King, Koh, Woon‐Puay, Tan, Louis Chew‐Seng

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Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing von Wong, Lai-Ping, Lai, Jason Kuan-Han, Saw, Woei-Yuh, Ong, Rick Twee-Hee, Cheng, Anthony Youzhi, Pillai, Nisha Esakimuthu, Liu, Xuanyao, Xu, Wenting, Chen, Peng, Foo, Jia-Nee, Tan, Linda Wei-Lin, Koo, Seok-Hwee, Soong, Richie, Wenk, Markus Rene, Lim, Wei-Yen, Khor, Chiea-Chuen, Little, Peter, Chia, Kee-Seng, Teo, Yik-Ying

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Synaptic Vesicle Glycoprotein 2C: a role in Parkinson's disease von Chang, Chu Hua, Lim, Kah Leong, Foo, Jia Nee

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation von Larson, Martin G, Ji, Weizhen, Newton-Cheh, Christopher, O'Roak, Brian J, Foo, Jia Nee, Simon, David B, Zhao, Hongyu, Levy, Daniel, Lifton, Richard P, State, Matthew W

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Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy von Li, Ming, Wang, Ling, Shi, Dian-Chun, Foo, Jia-Nee, Zhong, Zhong, Khor, Chiea-Chuen, Lanzani, Chiara, Citterio, Lorena, Salvi, Erika, Yin, Pei-Ran, Bei, Jin-Xin, Wang, Li, Liao, Yun-Hua, Chen, Jian, Chen, Qin-Kai, Xu, Gang, Jiang, Geng-Ru, Wan, Jian-Xin, Chen, Meng-Hua, Chen, Nan, Zhang, Hong, Zeng, Yi-Xin, Liu, Zhi-Hong, Liu, Jian-Jun, Yu, Xue-Qing

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The Parkinson's Disease Genome‐Wide Association Study Locus Browser von Grenn, Francis P., Kim, Jonggeol J., Makarious, Mary B., Iwaki, Hirotaka, Illarionova, Anastasia, Brolin, Kajsa, Kluss, Jillian H., Schumacher‐Schuh, Artur F., Leonard, Hampton, Faghri, Faraz, Billingsley, Kimberley, Krohn, Lynne, Hall, Ashley, Diez‐Fairen, Monica, Periñán, Maria Teresa, Foo, Jia Nee, Sandor, Cynthia, Webber, Caleb, Fiske, Brian K., Gibbs, J. Raphael, Nalls, Mike A., Singleton, Andrew B., Bandres‐Ciga, Sara, Reed, Xylena, Blauwendraat, Cornelis

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Oxytocin receptor gene and parental bonding modulate prefrontal responses to cries: a NIRS Study von Cataldo, Ilaria, Neoh, Michelle Jin-Yee, Chew, Wei Fang, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca

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The Interaction between Serotonin Transporter Allelic Variation and Maternal Care Modulates Instagram Sociability in a Sample of Singaporean Users von Bonassi, Andrea, Cataldo, Ilaria, Gabrieli, Giulio, Tandiono, Moses, Foo, Jia Nee, Lepri, Bruno, Esposito, Gianluca

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Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic von Lim, Shen-Yang, Tan, Ai Huey, Ahmad-Annuar, Azlina, Okubadejo, Njideka Ulunma, Lohmann, Katja, Morris, Huw R, Toh, Tzi Shin, Tay, Yi Wen, Lange, Lara M, Bandres-Ciga, Sara, Mata, Ignacio, Foo, Jia Nee, Sammler, Esther, Ooi, Joshua Chin Ern, Noyce, Alastair J, Bahr, Natascha, Luo, Wei, Ojha, Rajeev, Singleton, Andrew B, Blauwendraat, Cornelis, Klein, Christine

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X chromosome‐wide association study of follicular lymphoma von Conde, Lucia, Foo, Jia‐Nee, Riby, Jacques, Liu, Jianjun, Darabi, Hatef, Hjalgrim, Henrik, Bracci, Paige M., Smedby, Karin E., Skibola, Christine F.

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A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families von Sadia, Foo, Jia Nee, Khor, Chiea Chuen, Jelani, Musharraf, Ali, Ghazanfar

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A meta-analysis of genome-wide association studies of follicular lymphoma von Skibola, Christine F, Conde, Lucia, Foo, Jia-Nee, Riby, Jacques, Humphreys, Keith, Sillé, Fenna C M, Darabi, Hatef, Sanchez, Sylvia, Hjalgrim, Henrik, Liu, Jianjun, Bracci, Paige M, Smedby, Karin E

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A 3D Fiber‐Hydrogel Based Non‐Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury von Zhang, Na, Lin, Junquan, Lin, Vincent Po Hen, Milbreta, Ulla, Chin, Jiah Shin, Chew, Elaine Guo Yan, Lian, Michelle Mulan, Foo, Jia Nee, Zhang, Kunyu, Wu, Wutian, Chew, Sing Yian

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A comprehensive association analysis of homocysteine metabolic pathway genes in Singaporean Chinese with ischemic stroke von Low, Hui-Qi, Chen, Christopher P L H, Kasiman, Katherine, Thalamuthu, Anbupalam, Ng, Seok-Shin, Foo, Jia-Nee, Chang, Hui-Meng, Wong, Meng-Cheong, Tai, E-Shyong, Liu, Jianjun

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Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus? von Lázaro‐Figueroa, Alejandra, Hernández‐Medrano, Ana Jimena, Ramírez‐Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres‐Ciga, Sara, Periñan, Maria Teresa

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Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia von Ng, Adeline Su Lyn, Tan, Ai Huey, Tan, Yi Jayne, Lim, Jia Lun, Lian, Michelle Mulan, Dy Closas, Alfand Marl, Ahmad‐Annuar, Azlina, Viswanathan, Shanthi, Chia, Yuen Kang, Foo, Jia Nee, Lim, Weng Khong, Tan, Eng‐King, Lim, Shen‐Yang

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Trans‐Ethnic Fine‐Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease von Naito, Tatsuhiko, Satake, Wataru, Ogawa, Kotaro, Suzuki, Ken, Hirata, Jun, Foo, Jia Nee, Tan, Eng‐King, Toda, Tatsushi, Okada, Yukinori

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Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells von Wang, Yuanming, Liu, Kaiwen Ivy, Sutrisnoh, Norfala-Aliah Binte, Srinivasan, Harini, Zhang, Junyi, Li, Jia, Zhang, Fan, Lalith, Charles Richard John, Xing, Heyun, Shanmugam, Raghuvaran, Foo, Jia Nee, Yeo, Hwee Ting, Ooi, Kean Hean, Bleckwehl, Tore, Par, Yi Yun Rachel, Lee, Shi Mun, Ismail, Nur Nadiah Binte, Sanwari, Nur Aidah Binti, Lee, Si Ting Vanessa, Lew, Jan, Tan, Meng How

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NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long‐Term Follow‐up von Ng, Adeline S. L., Lim, Weng Khong, Xu, Zheyu, Ong, Helen L., Tan, Yi Jayne, Sim, Wei Ying, Ng, Ebonne Y. L., Teo, Jing Xian, Foo, Jia Nee, Lim, Tchoyoson C. C., Yu, Wai‐Yung, Chan, Ling‐Ling, Lee, Hwei‐Yee, Chen, Zhiyong, Lim, Ee‐Wei, Ting, Simon K. S., Prakash, Kumar M., Tan, Louis C. S., Yi, Zhao, Tan, Eng‐King

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