Foo Jia Nee

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Aung, T., Ozaki, M., Lee, M. C., Schlötzer-Schrehardt, U., Thorleifsson, G., Mizoguchi, T., Igo, R. P., Haripriya, A., Williams, S. E., Astakhov, Y. S., Orr, A. C., Burdon, K. P., Nakano, S., Mori, K., Abu-Amero, K., Hauser, M., Li, Z., Prakadeeswari, G., Bailey, J. N. C. & Cherecheanu, A. P. & 269 others, Kang, J. H., Nelson, S., Hayashi, K., Manabe, S. I., Kazama, S., Zarnowski, T., Inoue, K., Irkec, M., Coca-Prados, M., Sugiyama, K., Järvelä, I., Schlottmann, P., Lerner, S. F., Lamari, H., Nilgün, Y., Bikbov, M., Park, K. H., Cha, S. C., Yamashiro, K., Zenteno, J. C., Jonas, J. B., Kumar, R. S., Perera, S. A., Chan, A. S. Y., Kobakhidze, N., George, R., Vijaya, L., Do, T., Edward, D. P., De Juan Marcos, L., Pakravan, M., Moghimi, S., Ideta, R., Bach-Holm, D., Kappelgaard, P., Wirostko, B., Thomas, S., Gaston, D., Bedard, K., Greer, W. L., Yang, Z., Chen, X., Huang, L., Sang, J., Jia, H., Jia, L., Qiao, C., Zhang, H., Liu, X., Zhao, B., Wang, Y. X., Xu, L., Leruez, S., Reynier, P., Chichua, G., Tabagari, S., Uebe, S., Zenkel, M., Berner, D., Mossböck, G., Weisschuh, N., Hoja, U., Welge-Luessen, U. C., Mardin, C., Founti, P., Chatzikyriakidou, A., Pappas, T., Anastasopoulos, E., Lambropoulos, A., Ghosh, A., Shetty, R., Porporato, N., Saravanan, V., Venkatesh, R., Shivkumar, C., Kalpana, N., Sarangapani, S., Kanavi, M. R., Beni, A. N., Yazdani, S., Lashay, A., Naderifar, H., Khatibi, N., Fea, A., Lavia, C., Dallorto, L., Rolle, T., Frezzotti, P., Paoli, D., Salvi, E., Manunta, P., Mori, Y., Miyata, K., Higashide, T., Chihara, E., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Ohashi, T., Sakurai, T., Sugimoto, T., Chuman, H., Aihara, M., Inatani, M., Miyake, M., Gotoh, N., Matsuda, F., Yoshimura, N., Ikeda, Y., Ueno, M., Sotozono, C., Jeoung, J. W., Sagong, M., Park, K. H., Ahn, J., Cruz-Aguilar, M., Ezzouhairi, S. M., Rafei, A., Chong, Y. F., Ng, X. Y., Goh, S. R., Chen, Y., Yong, V. H. K., Khan, M. I., Olawoye, O. O., Ashaye, A. O., Ugbede, I., Onakoya, A., Kizor-Akaraiwe, N., Teekhasaenee, C., Suwan, Y., Supakontanasan, W., Okeke, S., Uche, N. J., Asimadu, I., Ayub, H., Akhtar, F., Kosior-Jarecka, E., Lukasik, U., Lischinsky, I., Castro, V., Grossmann, R. P., Megevand, G. S., Roy, S., Dervan, E., Silke, E., Rao, A., Sahay, P., Fornero, P., Cuello, O., Sivori, D., Zompa, T., Mills, R. A., Souzeau, E., Mitchell, P., Wang, J. J., Hewitt, A. W., Coote, M., Crowston, J. G., Astakhov, S. Y., Akopov, E. L., Emelyanov, A., Vysochinskaya, V., Kazakbaeva, G., Fayzrakhmanov, R., Al-Obeidan, S. A., Owaidhah, O., Aljasim, L. A., Chowbay, B., Foo, J. N., Soh, R. Q., Sim, K. S., Xie, Z., Cheong, A. W. O., Mok, S. Q., Soo, H. M., Chen, X. Y., Peh, S. Q., Heng, K. K., Husain, R., Ho, S. L., Hillmer, A. M., Cheng, C. Y., Escudero-Domínguez, F. A., González-Sarmiento, R., Martinon-Torres, F., Salas, A., Pathanapitoon, K., Hansapinyo, L., Wanichwecharugruang, B., Kitnarong, N., Sakuntabhai, A., Nguyn, H. X., Nguyn, G. T. T., Nguyn, T. V., Zenz, W., Binder, A., Klobassa, D. S., Hibberd, M. L., Davila, S., Herms, S., Nöthen, M. M., Moebus, S., Rautenbach, R. M., Ziskind, A., Carmichael, T. R., Ramsay, M., Álvarez, L., García, M., González-Iglesias, H., Rodríguez-Calvo, P. P., Cueto, L. F. V., Oguz, Ç., Tamcelik, N., Atalay, E., Batu, B., Aktas, D., Kaslm, B., Wilson, M. R., Coleman, A. L., Liu, Y., Challa, P., Herndon, L., Kuchtey, R. W., Kuchtey, J., Curtin, K., Chaya, C. J., Crandall, A., Zangwill, L. M., Wong, T. Y., Nakano, M., Kinoshita, S., Den Hollander, A. I., Vesti, E., Fingert, J. H., Lee, R. K., Sit, A. J., Shingleton, B. J., Wang, N., Cusi, D., Qamar, R., Kraft, P., Pericak-Vance, M. A., Raychaudhuri, S., Heegaard, S., Kivelä, T., Reis, A., Kruse, F. E., Weinreb, R. N., Pasquale, L. R., Haines, J. L., Thorsteinsdottir, U., Jonasson, F., Allingham, R. R., Milea, D., Ritch, R., Kubota, T., Tashiro, K., Vithana, E. N., Micheal, S., Topouzis, F., Craig, J. E., Dubina, M., Sundaresan, P., Stefansson, K., Wiggs, J. L., Pasutto, F. & Khor, C. C., Jul 1 2017, In: Nature Genetics. 49, 7, p. 993-1004 12 p.

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118 Citations (Scopus)

Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study in multiple populations

International NKTCL Working Group, Feb 2020, In: The Lancet Oncology. 21, 2, p. 306-316 11 p.

Research output: Contribution to journal › Article › peer-review

56 Citations (Scopus)

Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study

Li, Z., Xia, Y., Feng, L. N., Chen, J. R., Li, H. M., Cui, J., Cai, Q. Q., Sim, K. S., Nairismägi, M. L., Laurensia, Y., Meah, W. Y., Liu, W. S., Guo, Y. M., Chen, L. Z., Feng, Q. S., Pang, C. P., Chen, L. J., Chew, S. H., Ebstein, R. P. & Foo, J. N. & 26 others, Liu, J., Ha, J., Khoo, L. P., Chin, S. T., Zeng, Y. X., Aung, T., Chowbay, B., Diong, C. P., Zhang, F., Liu, Y. H., Tang, T., Tao, M., Quek, R., Mohamad, F., Tan, S. Y., Teh, B. T., Ng, S. B., Chng, W. J., Ong, C. K., Okada, Y., Raychaudhuri, S., Lim, S. T., Tan, W., Peng, R. J., Khor, C. C. & Bei, J. X., Sept 1 2016, In: The Lancet Oncology. 17, 9, p. 1240-1247 8 p.

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79 Citations (Scopus)

Genetic susceptibility of diffuse large B-cell lymphoma: a meta genome-wide association study in Asian population: LYMPHOMA

Cui, Q., Tan, W., Song, B., Peng, R. J., Wang, L., Dorajoo, R., Ng, K. P., Lin, G. W., Au, W. Y., Liang, R. H. S., Khor, C. C., Zhang, Q. L., FOO, J. N., Li, S. P., Zhang, F. R., Zhang, X. J., Yu, X. Q., Lan, Q., Chanock, S. & Jia, W. H. & 7 others, Lim, S. T., Li, W. Y., Rothman, N., Bei, J. X., Liu, J., Lin, D. & Liu, J. J., 2024, (Accepted/In press) In: Leukemia. 1826.

Research output: Contribution to journal › Article › peer-review

Genetic variants in ER cofactor genes and endometrial cancer risk

Li, Y., Low, H. Q., Foo, J. N., Darabi, H., Einarsdöttir, K., Humphreys, K., Spurdle, A., Easton, D. F., Thompson, D. J., Dunning, A. M., Pharoah, P. D. P., Czene, K., Chia, K. S., Hall, P. & Liu, J., Aug 2 2012, In: PLoS One. 7, 8, e42445.

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5 Citations (Scopus)

Genome-Wide Analysis of Protein-Coding Variants in Leprosy

Liu, H., Wang, Z., Li, Y., Yu, G., Fu, X., Wang, C., Liu, W., Yu, Y., Bao, F., Irwanto, A., Liu, J., Chu, T., Andiappan, A. K., Maurer-Stroh, S., Limviphuvadh, V., Wang, H., Mi, Z., Sun, Y., Sun, L. & Wang, L. & 30 others, Wang, C., You, J., Li, J., Foo, J. N., Liany, H., Meah, W. Y., Niu, G., Yue, Z., Zhao, Q., Wang, N., Yu, M., Yu, W., Cheng, X., Khor, C. C., Sim, K. S., Aung, T., Wang, N., Wang, D., Shi, L., Ning, Y., Zheng, Z., Yang, R., Li, J., Yang, J., Yan, L., Shen, J., Zhang, G., Chen, S., Liu, J. & Zhang, F., Dec 2017, In: Journal of Investigative Dermatology. 137, 12, p. 2544-2551 8 p.

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39 Citations (Scopus)

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Lu, Y., Vitart, V., Burdon, K. P., Khor, C. C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A. W., Koehn, D., Hysi, P. G., Ramdas, W. D., Zeller, T., Vithana, E. N., Cornes, B. K., Tay, W. T., Tai, E. S., Cheng, C. Y., Liu, J., Foo, J. N., Saw, S. M. & Thorleifsson, G. & 70 others, Stefansson, K., Dimasi, D. P., Mills, R. A., Mountain, J., Ang, W., Hoehn, R., Verhoeven, V. J. M., Grus, F., Wolfs, R., Castagne, R., Lackner, K. J., Springelkamp, H., Yang, J., Jonasson, F., Leung, D. Y. L., Chen, L. J., Tham, C. C. Y., Rudan, I., Vatavuk, Z., Hayward, C., Gibson, J., Cree, A. J., MacLeod, A., Ennis, S., Polasek, O., Campbell, H., Wilson, J. F., Viswanathan, A. C., Fleck, B., Li, X., Siscovick, D., Taylor, K. D., Rotter, J. I., Yazar, S., Ulmer, M., Li, J., Yaspan, B. L., Ozel, A. B., Richards, J. E., Moroi, S. E., Haines, J. L., Kang, J. H., Pasquale, L. R., Allingham, R. R., Ashley-Koch, A., Mitchell, P., Wang, J. J., Wright, A. F., Pennell, C., Spector, T. D., Young, T. L., Klaver, C. C. W., Martin, N. G., Montgomery, G. W., Anderson, M. G., Aung, T., Willoughby, C. E., Wiggs, J. L., Pang, C. P., Thorsteinsdottir, U., Lotery, A. J., Hammond, C. J., Van Duijn, C. M., Hauser, M. A., Rabinowitz, Y. S., Pfeiffer, N., MacKey, D. A., Craig, J. E., MacGregor, S. & Wong, T. Y., Feb 1 2013, In: Nature Genetics. 45, 2, p. 155-163 9 p.

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245 Citations (Scopus)

Genome-Wide Association Analysis of Protein-Coding Variants in IgA Nephropathy

Li, M., Wang, Y. N., Wang, L., Meah, W. Y., Shi, D. C., Heng, K. K., Wang, L., Khor, C. C., Bei, J. X., Cheng, C. Y., Aung, T., Liao, Y. H., Chen, Q. K., Gu, J. R., Kong, Y. Z., Lee, J., Chong, S. A., Subramaniam, M., Foo, J. N. & Cai, F. T. & 16 others, Jiang, G. R., Xu, G., Wan, J. X., Chen, M. H., Yin, P. R., Dong, X. Q., Feng, S. Z., Tang, X. Q., Zhong, Z., Tan, E. K., Chen, N., Zhang, H., Liu, Z. H., Tai, E. S., Liu, J. J. & Yu, X. Q., Nov 1 2023, In: Journal of the American Society of Nephrology : JASN. 34, 11, p. 1900-1913 14 p.

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8 Citations (Scopus)

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

Lowe, J. K., Maller, J. B., Pe'er, I., Neale, B. M., Salit, J., Kenny, E. E., Shea, J. L., Burkhardt, R., Smith, J. G., Ji, W., Noel, M., Jia, N. F., Blundell, M. L., Skilling, V., Garcia, L., Sullivan, M. L., Lee, H. E., Labek, A., Ferdowsian, H. & Auerbach, S. B. & 7 others, Lifton, R. P., Newton-Cheh, C., Breslow, J. L., Stoffel, M., Daly, M. J., Altshuler, D. M. & Friedman, J. M., Feb 2009, In: PLoS Genetics. 5, 2, e1000365.

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76 Citations (Scopus)

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

Khor, C. C., Do, T., Jia, H., Nakano, M., George, R., Abu-Amero, K., Duvesh, R., Chen, L. J., Li, Z., Nongpiur, M. E., Perera, S. A., Qiao, C., Wong, H. T., Sakai, H., De Melo, M. B., Lee, M. C., SChan, A., Azhany, Y., Dao, T. L. H. & Ikeda, Y. & 209 others, Perez-Grossmann, R. A., Zarnowski, T., Day, A. C., Jonas, J. B., Tam, P. O. S., Tran, T. A., Ayub, H., Akhtar, F., Micheal, S., Chew, P. T. K., Aljasim, L. A., Dada, T., Luu, T. T., Awadalla, M. S., Kitnarong, N., Wanichwecharungruang, B., Aung, Y. Y., Mohamed-Noor, J., Vijayan, S., Sarangapani, S., Husain, R., Jap, A., Baskaran, M., Goh, D., Su, D. H., Wang, H., Yong, V. K., Yip, L. W., Trinh, T. B., Makornwattana, M., Nguyen, T. T., Leuenberger, E. U., Park, K. H., Wiyogo, W. A., SKumar, R., Tello, C., Kurimoto, Y., Thapa, S. S., Pathanapitoon, K., Salmon, J. F., Sohn, Y. H., Fea, A., Ozaki, M., Lai, J. S. M., Tantisevi, V., Khaing, C. C., Mizoguchi, T., Nakano, S., Kim, C. Y., Tang, G., Fan, S., Wu, R., Meng, H., Nguyen, T. T. G., Tran, T. D., Ueno, M., Martinez, J. M., Ramli, N., Aung, Y. M., Reyes, R. D., Vernon, S. A., Fang, S. K., Xie, Z., Chen, X. Y., Foo, J. N., Sim, K. S., Wong, T. T., Quek, D. T., Venkatesh, R., Kavitha, S., Krishnadas, S. R., Soumittra, N., Shantha, B., Lim, B. A., Ogle, J., Vasconcellos, J. P. C., Costa, V. P., Abe, R. Y., De Souza, B. B., Sng, C. C., Aquino, M. C., Kosior-Jarecka, E., Fong, G. B., Tamanaja, V. C., Fujita, R., Jiang, Y., Waseem, N., Low, S., Pham, H. N., Al-Shahwan, S., Craven, E., Khan, M. I., Dada, R., Mohanty, K., Faiq, M. A., WHewitt, A., Burdon, K. P., Gan, E. H., Prutthipongsit, A., Patthanathamrongkasem, T., TCatacutan, M. A., Felarca, I. R., SLiao, C., Rusmayani, E., Istiantoro, V. W., Consolandi, G., Pignata, G., Lavia, C., Rojanapongpun, P., Mangkornkanokpong, L., Chansangpetch, S., Chan, J. C. H., Choy, B. N. K., Shum, J. W. H., Than, H. M., Oo, K. T., Han, A. T., Yong, V. H., Ng, X. Y., Goh, S. R., Chong, Y. F., Hibberd, M. L., Seielstad, M., Png, E., Dunstan, S. J., Van Vinh Chau, N., Bei, J., Zeng, Y. X., Karkey, A., Basnyat, B., Pasutto, F., Paoli, D., Frezzotti, P., Wang, J. J., Mitchell, P., Fingert, J. H., Allingham, R. R., Hauser, M. A., Lim, S. T., Chew, S. H., Ebstein, R. P., Sakuntabhai, A., Park, K. H., Ahn, J., Boland, G., Snippe, H., Stead, R., Quino, R., Zaw, S. N., Lukasik, U., Shetty, R., Zahari, M., Bae, H. W., Oo, N. L., Kubota, T., Manassakorn, A., Ho, W. L., Dallorto, L., Hwang, Y. H., Kiire, C. A., Kuroda, M., Djamal, Z. E., Peregrino, J. I. M., Ghosh, A., Jeoung, J. W., Hoan, T. S., Srisamran, N., Sandragasu, T., Set, S. H., Doan, V. H., Bhattacharya, S. S., Ho, C. L., Tan, D. T., Sihota, R., Loon, S. C., Mori, K., Kinoshita, S., Den Hollander, A. I., Qamar, R., Wang, Y. X., Teo, Y. Y., Tai, E. S., Hartleben-Matkin, C., Lozano-Giral, D., Saw, S. M., Cheng, C. Y., Czenteno, J., Pang, C. P., Bui, H. T. T., Hee, O., Craig, J. E., Edward, D. P., Yonahara, M., Neto, J. M., Guevara-Fujita, M. L., Xu, L., Ritch, R., Liza-Sharmini, A. T., Wong, T. Y., Al-Obeidan, S., Do, N. H., Sundaresan, P., Tham, C. C., Foster, P. J., Vijaya, L., Tashiro, K., Vithana, E. N., Wang, N. & Aung, T., May 1 2016, In: Nature Genetics. 48, 5, p. 556-562 7 p.

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147 Citations (Scopus)

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region

Skibola, C. F., Berndt, S. I., Vijai, J., Conde, L., Wang, Z., Yeager, M., De Bakker, P. I. W., Birmann, B. M., Vajdic, C. M., Foo, J. N., Bracci, P. M., Vermeulen, R. C. H., Slager, S. L., De Sanjose, S., Wang, S. S., Linet, M. S., Salles, G., Lan, Q., Severi, G. & Hjalgrim, H. & 92 others, Lightfoot, T., Melbye, M., Gu, J., Ghesquières, H., Link, B. K., Morton, L. M., Holly, E. A., Smith, A., Tinker, L. F., Teras, L. R., Kricker, A., Becker, N., Purdue, M. P., Spinelli, J. J., Zhang, Y., Giles, G. G., Vineis, P., Monnereau, A., Bertrand, K. A., Albanes, D., Zeleniuch-Jacquotte, A., Gabbas, A., Chung, C. C., Burdett, L., Hutchinson, A., Lawrence, C., Montalvan, R., Liang, L., Huang, J., Ma, B., Liu, J., Adami, H. O., Glimelius, B., Ye, Y., Nowakowski, G. S., Dogan, A., Thompson, C. A., Habermann, T. M., Novak, A. J., Liebow, M., Witzig, T. E., Weiner, G. J., Schenk, M., Hartge, P., De Roos, A. J., Cozen, W., Zhi, D., Akers, N. K., Riby, J., Smith, M. T., Lacher, M., Villano, D. J., Maria, A., Roman, E., Kane, E., Jackson, R. D., North, K. E., Diver, W. R., Turner, J., Armstrong, B. K., Benavente, Y., Boffetta, P., Brennan, P., Foretova, L., Maynadie, M., Staines, A., McKay, J., Brooks-Wilson, A. R., Zheng, T., Holford, T. R., Chamosa, S., Kaaks, R., Kelly, R. S., Ohlsson, B., Travis, R. C., Weiderpass, E., Clavel, J., Giovannucci, E., Kraft, P., Virtamo, J., Mazza, P., Cocco, P., Ennas, M. G., Chiu, B. C. H., Fraumeni, J. F., Nieters, A., Offit, K., Wu, X., Cerhan, J. R., Smedby, K. E., Chanock, S. J. & Rothman, N., 2014, In: American Journal of Human Genetics. 95, 4, p. 462-471 10 p.

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88 Citations (Scopus)

Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population

Tan, D. E. K., Foo, J. N., Bei, J. X., Chang, J., Peng, R., Zheng, X., Wei, L., Huang, Y., Lim, W. Y., Li, J., Cui, Q., Chew, S. H., Ebstein, R. P., Kuperan, P., Lim, S. T., Tao, M., Tan, S. H., Wong, A., Wong, G. C. & Tan, S. Y. & 7 others, Ng, S. B., Zeng, Y. X., Khor, C. C., Lin, D., Seow, A. L. H., Jia, W. H. & Liu, J., Jul 2013, In: Nature Genetics. 45, 7, p. 804-807 4 p.

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39 Citations (Scopus)

Genome-wide association study of Parkinson's disease in East Asians

Foo, J. N., Tan, L. C., Irwan, I. D., Au, W. L., Low, H. Q., Prakash, K. M., Ahmad-Annuar, A., Bei, J., Chan, A. Y. Y., Chen, C. M., Chen, Y. C., Chung, S. J., Deng, H., Lim, S. Y., Mok, V., Pang, H., Pei, Z., Peng, R., Shang, H. F. & Song, K. & 22 others, Tan, A. H., Wu, Y. R., Aung, T., Cheng, C. Y., Chew, F. T., Chew, S. H., Chong, S. A., Ebstein, R. P., Lee, J., Saw, S. M., Seow, A., Subramaniam, M., Tai, E. S., Vithana, E. N., Wong, T. Y., Heng, K. K., Meah, W. Y., Khor, C. C., Liu, H., Zhang, F., Liu, J. & Tan, E. K., Jan 1 2017, In: Human Molecular Genetics. 26, 1, p. 226-232 7 p.

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96 Citations (Scopus)

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population

the Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC), Dec 2023, In: npj Parkinson's Disease. 9, 1, 22.

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25 Citations (Scopus)

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria

Liu, H., Li, Y., Hung, K. K. H., Wang, N., Wang, C., Chen, X., Sheng, D., Fu, X., See, K., Foo, J. N., Low, H., Liany, H., Irwan, I. D., Liu, J., Yang, B., Chen, M., Yu, Y., Yu, G., Niu, G. & You, J. & 17 others, Zhou, Y., Ma, S., Wang, T., Yan, X., Goh, B. K., Common, J. E. A., Lane, B. E., Sun, Y., Zhou, G., Lu, X., Wang, Z., Tian, H., Cao, Y., Chen, S., Liu, Q., Liu, J. & Zhang, F., Feb 3 2014, In: PLoS One. 9, 2, e87250.

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36 Citations (Scopus)

Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility

Yin, X., Low, H. Q., Wang, L., Li, Y., Ellinghaus, E., Han, J., Estivill, X., Sun, L., Zuo, X., Shen, C., Zhu, C., Zhang, A., Sanchez, F., Padyukov, L., Catanese, J. J., Krueger, G. G., Duffin, K. C., Mucha, S., Weichenthal, M. & Weidinger, S. & 19 others, Lieb, W., Foo, J. N., Li, Y., Sim, K., Liany, H., Irwan, I., Teo, Y., Theng, C. T. S., Gupta, R., Bowcock, A., De Jager, P. L., Qureshi, A. A., De Bakker, P. I. W., Seielstad, M., Liao, W., Ståhle, M., Franke, A., Zhang, X. & Liu, J., Apr 23 2015, In: Nature Communications. 6, 6916.

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163 Citations (Scopus)

Genome-wide meta-analysis identifies three novel susceptibility loci and reveals ethnic heterogeneity of genetic susceptibility for Iga nephropathy

Li, M., Wang, L., Shi, D. C., Foo, J. N., Zhong, Z., Khor, C. C., Lanzani, C., Citterio, L., Salvi, E., Yin, P. R., Bei, J. X., Wang, L., Liao, Y. H., Chen, J., Chen, Q. K., Xu, G., Jiang, G. R., Wan, J. X., Chen, M. H. & Chen, N. & 5 others, Zhang, H., Zeng, Y. X., Liu, Z. H., Liu, J. J. & Yu, X. Q., Dec 2020, In: Journal of the American Society of Nephrology : JASN. 31, 12, p. 2949-2963 15 p.

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52 Citations (Scopus)

GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers

Li, S., Qian, J., Yang, Y., Zhao, W., Dai, J., Bei, J. X., Foo, J. N., McLaren, P. J., Li, Z., Yang, J., Shen, F., Liu, L., Yang, J., Li, S., Pan, S., Wang, Y., Li, W., Zhai, X., Zhou, B. & Shi, L. & 29 others, Chen, X., Chu, M., Yan, Y., Wang, J., Cheng, S., Shen, J., Jia, W., Liu, J., Yang, J., Wen, Z., Li, A., Zhang, Y., Zhang, G., Luo, X., Qin, H., Chen, M., Wang, H., Jin, L., Lin, D., Shen, H., He, L., de Bakker, P. I. W., Wang, H., Zeng, Y. X., Wu, M., Hu, Z., Shi, Y., Liu, J. & Zhou, W., Jul 2012, In: PLoS Genetics. 8, 7, e1002791.

Research output: Contribution to journal › Article › peer-review

Open Access

182 Citations (Scopus)

GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma

Smedby, K. E., Foo, J. N., Skibola, C. F., Darabi, H., Conde, L., Hjalgrim, H., Kumar, V., Chang, E. T., Rothman, N., Cerhan, J. R., Brooks-Wilson, A. R., Rehnberg, E., Irwan, I. D., Ryder, L. P., Brown, P. N., Bracci, P. M., Agana, L., Riby, J., Cozen, W. & Davis, S. & 32 others, Hartge, P., Morton, L. M., Severson, R. K., Wang, S. S., Slager, S. L., Fredericksen, Z. S., Novak, A. J., Kay, N. E., Habermann, T. M., Armstrong, B., Kricker, A., Milliken, S., Purdue, M. P., Vajdic, C. M., Boyle, P., Lan, Q., Zahm, S. H., Zhang, Y., Zheng, T., Leach, S., Spinelli, J. J., Smith, M. T., Chanock, S. J., Padyukov, L., Alfredsson, L., Klareskog, L., Glimelius, B., Melbye, M., Liu, E. T., Adami, H. O., Humphreys, K. & Liu, J., Apr 2011, In: PLoS Genetics. 7, 4, e1001378.

Research output: Contribution to journal › Article › peer-review

Open Access

91 Citations (Scopus)

GWAS reveal novel IgA nephropathy risk loci

Foo, J. N., Liu, J. & Yu, X. Q., 2015, In: Oncotarget. 6, 18, p. 15738-15739 2 p.

Research output: Contribution to journal › Editorial › peer-review

Open Access

4 Citations (Scopus)

High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystrophy

Chen, Z., Tan, Y. J., Lian, M. M., Tandiono, M., Foo, J. N., Lim, W. K., Kandiah, N., Tan, E. K. & Ng, A. S. L., Feb 1 2021, In: Frontiers in Neurology. 12, 631407.

Research output: Contribution to journal › Article › peer-review

Open Access

7 Citations (Scopus)

HLA-B*13:01 and the dapsone hypersensitivity syndrome

Zhang, F. R., Liu, H., Irwanto, A., Fu, X. A., Li, Y., Yu, G. Q., Yu, Y. X., Chen, M. F., Low, H. Q., Li, J. H., Bao, F. F., Foo, J. N., Bei, J. X., Jia, X. M., Liu, J., Liany, H., Wang, N., Niu, G. Y., Wang, Z. Z. & Shi, B. Q. & 47 others, Tian, H. Q., Liu, H. X., Ma, S. S., Zhou, Y., You, J. B., Yang, Q., Wang, C., Chu, T. S., Liu, D. C., Yu, X. L., Sun, Y. H., Ning, Y., Wei, Z. H., Chen, S. L., Chen, X. C., Zhang, Z. X., Liu, Y. X., Pulit, S. L., Wu, W. B., Zheng, Z. Y., Yang, R. D., Long, H., Liu, Z. S., Wang, J. Q., Li, M., Zhang, L. H., Wang, H., Wang, L. M., Xiao, P., Li, J. L., Huang, Z. M., Huang, J. X., Li, Z., Liu, J., Xiong, L., Yang, J., Wang, X. D., Yu, D. B., Lu, X. M., Zhou, G. Z., Yan, L. B., Shen, J. P., Zhang, G. C., Zeng, Y. X., De Bakker, P. I. W., Chen, S. M. & Liu, J. J., 2013, In: New England Journal of Medicine. 369, 17, p. 1620-1628 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

289 Citations (Scopus)

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

Ajmal, M., Mir, A., Wahid, S., Khor, C. C., Foo, J. N., Siddiqi, S., Kauser, M., Malik, S. A. & Nasir, M., Dec 13 2017, In: BMC Medical Genetics. 18, 1, 148.

Research output: Contribution to journal › Article › peer-review

Open Access

6 Citations (Scopus)

Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome

Ali, G., Sadia, Foo, J. N., Nasir, A., Chang, C. H., Chew, E. G., Latif, Z., Azeem, Z., Ain-Ul-Batool, S., Kazmi, S. A. R., Awan, N. B., Khan, A. H., Rehman, F. U., Khalid, M., Wali, A., Sarwar, S., Akhtar, W., Ahmed Abbasi, A. & Nisar, R., 2021, In: BioMed Research International. 2021, 6626015.

Research output: Contribution to journal › Article › peer-review

Open Access

2 Citations (Scopus)

Identification of a novel risk variant in the FUS gene in essential tremor

Wu, Y. R., Foo, J. N., Tan, L. C. S., Chen, C. M., Prakash, K. M., Chen, Y. C., Bei, J. X., Au, W. L., Chang, C. W., Wong, T. Y., Liu, J. J., Zhao, Y. & Tan, E. K., Aug 6 2013, In: Neurology. 81, 6, p. 541-544 4 p.

Research output: Contribution to journal › Article › peer-review

25 Citations (Scopus)

Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families

Ali, G., Awan, N. B., Sadia, Khawaja, A. W., Foo, J. N., Khor, C. C., Chang, C. H., Chew, E. G. Y., Kiani, F. R. & Jelani, M., May 1 2020, In: Journal of Gene Medicine. 22, 5, e3167.

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

Nigeria Parkinson Disease Research Network, International Parkinson's Disease Genomics Consortium Africa, Black and African American Connections to Parkinson's Disease Study Group, 23andMe Research Team & Global Parkinson's Genetics Program, Nov 2023, In: The Lancet Neurology. 22, 11, p. 1015-1025 11 p.

Research output: Contribution to journal › Article › peer-review

Open Access

60 Citations (Scopus)

Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia

Ng, A. S. L., Tan, A. H., Tan, Y. J., Lim, J. L., Lian, M. M., Dy Closas, A. M., Ahmad-Annuar, A., Viswanathan, S., Chia, Y. K., Foo, J. N., Lim, W. K., Tan, E. K. & Lim, S. Y., 2024, (Accepted/In press) In: Movement Disorders.

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Identification of new susceptibility loci for IgA nephropathy in Han Chinese

Li, M., Foo, J. N., Wang, J. Q., Low, H. Q., Tang, X. Q., Toh, K. Y., Yin, P. R., Khor, C. C., Goh, Y. F., Irwan, I. D., Xu, R. C., Andiappan, A. K., Bei, J. X., Rotzschke, O., Chen, M. H., Cheng, C. Y., Sun, L. D., Jiang, G. R., Wong, T. Y. & Lin, H. L. & 21 others, Aung, T., Liao, Y. H., Saw, S. M., Ye, K., Ebstein, R. P., Chen, Q. K., Shi, W., Chew, S. H., Chen, J., Zhang, F. R., Li, S. P., Xu, G., Tai, E. S., Wang, L., Chen, N., Zhang, X. J., Zeng, Y. X., Zhang, H., Liu, Z. H., Yu, X. Q. & Liu, J. J., Jun 1 2015, In: Nature Communications. 6, 7270.

Research output: Contribution to journal › Article › peer-review

Open Access

113 Citations (Scopus)

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk between Asians and Europeans: A Genome-Wide Association Study

Foo, J. N., Chew, E. G. Y., Chung, S. J., Peng, R., Blauwendraat, C., Nalls, M. A., Mok, K. Y., Satake, W., Toda, T., Chao, Y., Tan, L. C. S., Tandiono, M., Lian, M. M., Ng, E. Y., Prakash, K. M., Au, W. L., Meah, W. Y., Mok, S. Q., Annuar, A. A. & Chan, A. Y. Y. & 25 others, Chen, L., Chen, Y., Jeon, B. S., Jiang, L., Lim, J. L., Lin, J. J., Liu, C., Mao, C., Mok, V., Pei, Z., Shang, H. F., Shi, C. H., Song, K., Tan, A. H., Wu, Y. R., Xu, Y. M., Xu, R., Yan, Y., Yang, J., Zhang, B., Koh, W. P., Lim, S. Y., Khor, C. C., Liu, J. & Tan, E. K., Jun 2020, In: JAMA Neurology. 77, 6, p. 746-754 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

151 Citations (Scopus)

Identifying genes in parkinson disease: State of the art

Chew, E. G. Y., Foo, J. N. & Tan, E. K., May 21 2018, In: Medical Journal of Australia. 208, 9, p. 381-382.e1

Research output: Contribution to journal › Article › peer-review

Open Access

1 Citation (Scopus)

Insights into the Genetic Structure and Diversity of 38 South Asian Indians from Deep Whole-Genome Sequencing

Wong, L. P., Lai, J. K. H., Saw, W. Y., Ong, R. T. H., Cheng, A. Y., Pillai, N. E., Liu, X., Xu, W., Chen, P., Foo, J. N., Tan, L. W. L., Koo, S. H., Soong, R., Wenk, M. R., Lim, W. Y., Khor, C. C., Little, P., Chia, K. S. & Teo, Y. Y., May 2014, In: PLoS Genetics. 10, 5, e1004377.

Research output: Contribution to journal › Article › peer-review

Open Access

43 Citations (Scopus)

Investigation of the predisposing factor of pemphigus and its clinical subtype through a genome-wide association and next generation sequence analysis

Sun, Y., Liu, H., Yang, B., Wang, C., Foo, J. N., Bao, F., Irwanto, A., Yu, G., Fu, X., Wang, Z., You, J., Liu, J., Zhou, G., Liu, J. & Zhang, F., Feb 2019, In: Journal of the European Academy of Dermatology and Venereology. 33, 2, p. 410-415 6 p.

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

the Global Parkinson's Genetics Program (GP2), 2024, (Accepted/In press) In: Movement Disorders.

Research output: Contribution to journal › Letter › peer-review

Open Access

ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians

Chew, E. G. Y., Tan, L. C. S., Au, W. L., Prakash, K. M., Liu, J., Foo, J. N. & Tan, E. K., Feb 2020, In: Neurobiology of Aging. 86, p. 201.e15-201.e17

Research output: Contribution to journal › Article › peer-review

Open Access

5 Citations (Scopus)

Kidney organoid models reveal cilium-autophagy metabolic axis as a therapeutic target for PKD both in vitro and in vivo

Liu, M., Zhang, C., Gong, X., Zhang, T., Lian, M. M., Chew, E. G. Y., Cardilla, A., Suzuki, K., Wang, H., Yuan, Y., Li, Y., Naik, M. Y., Wang, Y., Zhou, B., Soon, W. Z., Aizawa, E., Li, P., Low, J. H., Tandiono, M. & Montagud, E. & 10 others, Moya-Rull, D., Rodriguez Esteban, C., Luque, Y., Fang, M., Khor, C. C., Montserrat, N., Campistol, J. M., Izpisua Belmonte, J. C., Foo, J. N. & Xia, Y., Jan 4 2024, In: Cell Stem Cell. 31, 1, p. 52-70.e8

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)

Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia

Foo, J. N., Lee, J., Tan, L. C., Liu, J. & Tan, E. K., Dec 1 2016, In: Movement Disorders. 31, 12, p. 1924-1925 2 p.

Research output: Contribution to journal › Letter › peer-review

Open Access

9 Citations (Scopus)

Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size

Li, J., Foo, J. N., Schoof, N., Varghese, J. S., Fernandez-Navarro, P., Gierach, G. L., Quek, S. T., Hartman, M., Nord, S., Kristensen, V. N., Pollán, M., Figueroa, J. D., Thompson, D. J., Li, Y., Khor, C. C., Humphreys, K., Liu, J., Czene, K. & Hall, P., 2013, In: Journal of Medical Genetics. 50, 10, p. 666-673 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

12 Citations (Scopus)

Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore

SG10K Consortium, Oct 17 2019, In: Cell. 179, 3, p. 736-749.e15

Research output: Contribution to journal › Article › peer-review

Open Access

124 Citations (Scopus)

Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease

Foo, J. N., Chung, S. J., Tan, L. C., Liany, H., Ryu, H. S., Hong, M., Koh, T. H., Irwan, I. D., Au, W. L., Prakash, K. M., Aung, T., Cheng, C. Y., Chong, S. A., Khor, C. C., Lee, J., Tai, E. S., Vithana, E. N., Wong, T. Y., Song, K. & Liu, J. & 1 others, Tan, E. K., Apr 1 2016, In: Movement Disorders. 31, 4, p. 484-487 4 p.

Research output: Contribution to journal › Article › peer-review

10 Citations (Scopus)

Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry

Lim, S. Y., Tan, A. H., Foo, J. N., Tan, Y. J., Chew, E. G. Y., Annuar, A. A., Closas, A. M. D., Pajo, A., Lim, J. L., Tay, Y. W., Nadhirah, A., Hor, J. W., Toh, T. S., Lit, L. C., Zulkefli, J., Ngim, S. J., Lim, W. K., Morris, H. R., Tan, E. K. & Ng, A. S. L., Apr 2024, In: Journal of Movement Disorders. 17, 2, p. 213-217 5 p.

Research output: Contribution to journal › Article › peer-review

Open Access

3 Citations (Scopus)

Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction

Ai, Z., Li, M., Liu, W., Foo, J. N., Mansouri, O., Yin, P., Zhou, Q., Tang, X., Dong, X., Feng, S., Xu, R., Zhong, Z., Chen, J., Wan, J., Lou, T., Yu, J., Zhou, Q., Fan, J., Mao, H. & Gale, D. & 4 others, Barratt, J., Armour, J. A. L., Liu, J. & Yu, X., Jun 29 2016, In: Science Translational Medicine. 8, 345, 345ra88.

Research output: Contribution to journal › Article › peer-review

Open Access

32 Citations (Scopus)

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease

Chao, Y. X., Ng, E. Y., Foo, J. N., Liu, J., Zhao, Y. & Tan, E. K., Jul 20 2015, In: Neurogenetics. 16, 3, p. 241-242 2 p.

Research output: Contribution to journal › Letter › peer-review

12 Citations (Scopus)

Modulation of instagram number of followings by avoidance in close relationships in young adults under a gene x environment perspective

Bonassi, A., Carollo, A., Cataldo, I., Gabrieli, G., Tandiono, M., Foo, J. N., Lepri, B. & Esposito, G., Jul 2 2021, In: International Journal of Environmental Research and Public Health. 18, 14, 7547.

Research output: Contribution to journal › Article › peer-review

Open Access

2 Citations (Scopus)

Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1∗04 subtypes

EADB, GR at ACE study group, DEGESCO consortium, Demgene, EADI, GERAD & Asian Parkinson’s Disease, Genetics consortium, 2023, In: Proceedings of the National Academy of Sciences of the United States of America. 120, 36, e2302720120.

Research output: Contribution to journal › Article › peer-review

Open Access

16 Citations (Scopus)

Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Kim, J. J., Vitale, D., Otani, D. V., Lian, M. M., Heilbron, K., Aslibekyan, S., Auton, A., Babalola, E., Bell, R. K., Bielenberg, J., Bryc, K., Bullis, E., Cannon, P., Coker, D., Partida, G. C., Dhamija, D., Das, S., Elson, S. L., Eriksson, N. & Filshtein, T. & 279 others, Fitch, A., Fletez-Brant, K., Fontanillas, P., Freyman, W., Granka, J. M., Hernandez, A., Hicks, B., Hinds, D. A., Jewett, E. M., Jiang, Y., Kukar, K., Kwong, A., Lin, K. H., Llamas, B. A., Lowe, M., McCreight, J. C., McIntyre, M. H., Micheletti, S. J., Moreno, M. E., Nandakumar, P., Nguyen, D. T., Noblin, E. S., O’Connell, J., Petrakovitz, A. A., Poznik, G. D., Reynoso, A., Schloetter, M., Schumacher, M., Shastri, A. J., Shelton, J. F., Shi, J., Shringarpure, S., Su, Q. J., Tat, S. A., Tchakouté, C. T., Tran, V., Tung, J. Y., Wang, X., Wang, W., Weldon, C. H., Wilton, P., Wong, C. D., Iwaki, H., Lake, J., Solsberg, C. W., Leonard, H., Makarious, M. B., Tan, E. K., Singleton, A. B., Bandres-Ciga, S., Noyce, A. J., Gatto, E. M., Kauffman, M., Khachatryan, S., Tavadyan, Z., Shepherd, C. E., Hunter, J., Kumar, K., Ellis, M., Rentería, M. E., Koks, S., Zimprich, A., Schumacher-Schuh, A. F., Rieder, C., Awad, P. S., Tumas, V., Camargos, S., Fon, E. A., Monchi, O., Fon, T., Galleguillos, B. P., Miranda, M., Bustamante, M. L., Olguin, P., Chana, P., Tang, B., Shang, H., Guo, J., Chan, P., Luo, W., Arboleda, G., Orozc, J., del Rio, M. J., Hernandez, A., Salama, M., Kamel, W. A., Zewde, Y. Z., Brice, A., Corvol, J. C., Westenberger, A., Illarionova, A., Mollenhauer, B., Klein, C., Vollstedt, E. J., Hopfner, F., Höglinger, G., Madoev, H., Trinh, J., Junker, J., Lohmann, K., Lange, L. M., Sharma, M., Groppa, S., Gasser, T., Fang, Z. H., Akpalu, A., Xiromerisiou, G., Hadjigorgiou, G., Dagklis, I., Tarnanas, I., Stefanis, L., Stamelou, M., Dadiotis, E., Medina, A., Chan, G. H. F., Ip, N., Cheung, N. Y. F., Chan, P., Zhou, X., Kishore, A., Divya, K. P., Pal, P., Kukkle, P. L., Rajan, R., Borgohain, R., Salari, M., Quattrone, A., Valente, E. M., Parnetti, L., Avenali, M., Schirinzi, T., Funayama, M., Hattori, N., Shiraishi, T., Karimova, A., Kaishibayeva, G., Shambetova, C., Krüger, R., Tan, A. H., Ahmad-Annuar, A., Norlinah, M. I., Murad, N. A. A., Azmin, S., Lim, S. Y., Mohamed, W., Tay, Y. W., Martinez-Ramirez, D., Rodriguez-Violante, M., Reyes-Pérez, P., Tserensodnom, B., Ojha, R., Anderson, T. J., Pitcher, T. L., Sanyaolu, A., Okubadejo, N., Ojo, O., Aasly, J. O., Pihlstrøm, L., Tan, M., Ur-Rehman, S., Veliz-Otani, D., Cornejo-Olivas, M., Doquenia, M. L., Rosales, R., Vinuela, A., Iakovenko, E., Mubarak, B. A., Umair, M., Amod, F., Carr, J., Bardien, S., Jeon, B., Kim, Y. J., Cubo, E., Alvarez, I., Hoenicka, J., Beyer, K., Periñan, M. T., Pastor, P., El-Sadig, S., Brolin, K., Zweier, C., Tinkhauser, G., Krack, P., Lin, C. H., Wu, H. C., Kung, P. J., Wu, R. M., Wu, Y., Amouri, R., Sassi, S. B., Başak, A. N., Genc, G., Çakmak, Ö. Ö., Ertan, S., Martínez-Carrasco, A., Schrag, A., Schapira, A., Carroll, C., Bale, C., Grosset, D., Stafford, E. J., Houlden, H., Morris, H. R., Hardy, J., Mok, K. Y., Rizig, M., Wood, N., Williams, N., Okunoye, O., Lewis, P. A., Kaiyrzhanov, R., Weil, R., Love, S., Stott, S., Jasaityte, S., Dey, S., Obese, V., Espay, A., O’Grady, A., Sobering, A. K., Siddiqi, B., Casey, B., Fiske, B., Jonas, C., Cruchaga, C., Pantazis, C. B., Comart, C., Wegel, C., Hall, D., Hernandez, D., Shiamim, E., Riley, E., Faghri, F., Serrano, G. E., Chen, H., Mata, I. F., Sarmiento, I. J. K., Williamson, J., Jankovic, J., Shulman, J., Solle, J. C., Murphy, K., Nuytemans, K., Kieburtz, K., Markopoulou, K., Marek, K., Levine, K. S., Chahine, L. M., Ibanez, L., Screven, L., Ruffrage, L., Shulman, L., Marsili, L., Kuhl, M., Dean, M., Koretsky, M., Puckelwartz, M. J., Inca-Martinez, M., Louie, N., Mencacci, N. E., Albin, R., Alcalay, R., Walker, R., Chowdhury, S., Dumanis, S., Lubbe, S., Xie, T., Foroud, T., Beach, T., Sherer, T., Song, Y., Nguyen, D., Nguyen, T., Atadzhanov, M., Blauwendraat, C., Nalls, M. A., Foo, J. N. & Mata, I., Jan 2024, In: Nature Genetics. 56, 1, p. 27-36 10 p.

Research output: Contribution to journal › Article › peer-review

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51 Citations (Scopus)

New insights from a multi-ethnic Asian progressive supranuclear palsy cohort

Lim, S. Y., Dy Closas, A. M. F., Tan, A. H., Lim, J. L., Tan, Y. J., Vijayanathan, Y., Tay, Y. W., Abdul Khalid, R. B., Ng, W. K., Kanesalingam, R., Martinez-Martin, P., Ahmad Annuar, A., Lit, L. C., Foo, J. N., Lim, W. K., Ng, A. S. L. & Tan, E. K., Mar 2023, In: Parkinsonism and Related Disorders. 108, 105296.

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

New loci and coding variants confer risk for age-related macular degeneration in East Asians

Cheng, C. Y., Yamashiro, K., Jia Chen, L., Ahn, J., Huang, L., Huang, L., Cheung, C. M. G., Miyake, M., Cackett, P. D., Yeo, I. Y., Laude, A., Mathur, R., Pang, J., Sim, K. S., Koh, A. H., Chen, P., Lee, S. Y., Wong, D., Chan, C. M. & Loh, B. K. & 84 others, Sun, Y., Davila, S., Nakata, I., Nakanishi, H., Akagi-Kurashige, Y., Gotoh, N., Tsujikawa, A., Matsuda, F., Mori, K., Yoneya, S., Sakurada, Y., Iijima, H., Iida, T., Honda, S., Lai, T. Y. Y., Tam, P. O. S., Chen, H., Tang, S., Ding, X., Wen, F., Lu, F., Zhang, X., Shi, Y., Zhao, P., Zhao, B., Sang, J., Gong, B., Dorajoo, R., Yuan, J. M., Koh, W. P., Van Dam, R. M., Friedlander, Y., Lin, Y., Hibberd, M. L., Foo, J. N., Wang, N., Wong, C. H., Tan, G. S., Park, S. J., Bhargava, M., Gopal, L., Naing, T., Liao, J., Guan Ong, P., Mitchell, P., Zhou, P., Xie, X., Liang, J., Mei, J., Jin, X., Saw, S. M., Ozaki, M., Mizoguchi, T., Kurimoto, Y., Woo, S. J., Chung, H., Yu, H. G., Shin, J. Y., Park, D. H., Kim, I. T., Chang, W., Sagong, M., Lee, S. J., Kim, H. W., Lee, J. E., Li, Y., Liu, J., Teo, Y. Y., Heng, C. K., Lim, T. H., Yang, S. K., Song, K., Vithana, E. N., Aung, T., Bei, J. X., Zeng, Y. X., Tai, E. S., Li, X. X., Yang, Z., Park, K. H., Pang, C. P., Yoshimura, N., Yin Wong, T. & Khor, C. C., Jan 28 2015, In: Nature Communications. 6, 6063.

Research output: Contribution to journal › Article › peer-review

Open Access

126 Citations (Scopus)

Next-generation sequencing diagnostics for neurological diseases/disorders: From a clinical perspective

Foo, J. N., Liu, J. & Tan, E. K., Jul 2013, In: Human Genetics. 132, 7, p. 721-734 14 p.

Research output: Contribution to journal › Review article › peer-review

12 Citations (Scopus)

No association of DNM3 with age of onset in Asian Parkinson's disease

Foo, J. N., Tan, L. C., Au, W. L., Prakash, K. M., Liu, J. & Tan, E. K., May 2019, In: European Journal of Neurology. 26, 5, p. 827-829 3 p.

Research output: Contribution to journal › Article › peer-review

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Foo Jia Nee

Research output

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