Foo Jia Nee

2019

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)

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

Open Access

3 Citations (Scopus)

Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression

Deng, X., Xiao, B., Allen, J. C., Ng, E., Foo, J. N., Lo, Y. L., Tan, L. C. S. & Tan, E. K., Feb 27 2019, In: Journal of Medical Genetics. 56, 11, p. 765-768 4 p.

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

Open Access

7 Citations (Scopus)

2018

Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

Wong, X. F. C. C., Denil, S. L. I. J., Foo, J. N., Chen, H., Tay, A. S. L., Haines, R. L., Tang, M. B. Y., McLean, W. H. I., Sandilands, A., Smith, F. J. D., Lane, E. B., Liu, J. & Common, J. E. A., Feb 2018, In: Journal of Allergy and Clinical Immunology. 141, 2, p. 814-816 3 p.

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

Open Access

40 Citations (Scopus)

ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis

Chourabi, M., Liew, M. S., Lim, S., H'mida-Ben Brahim, D., Boussofara, L., Dai, L., Wong, P. M., Foo, J. N., Sriha, B., Robinson, K. S., Denil, S., Common, J. E., Mamaï, O., Ben Khalifa, Y., Bollen, M., Liu, J., Denguezli, M., Bonnard, C., Saad, A. & Reversade, B., Feb 2018, In: Journal of Investigative Dermatology. 138, 2, p. 291-300 10 p.

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

Open Access

27 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)

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

Kausar, M., Siddiqi, S., Yaqoob, M., Mansoor, S., Makitie, O., Mir, A., Khor, C. C., Foo, J. N. & Anees, M., Nov 17 2018, In: Journal of Biomedical Science. 25, 1, 82.

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

Open Access

12 Citations (Scopus)

Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells

Wang, Y., Liu, K. I., Sutrisnoh, N. A. B., Srinivasan, H., Zhang, J., Li, J., Zhang, F., Lalith, C. R. J., Xing, H., Shanmugam, R., Foo, J. N., Yeo, H. T., Ooi, K. H., Bleckwehl, T., Par, Y. Y. R., Lee, S. M., Ismail, N. N. B., Sanwari, N. A. B., Lee, S. T. V. & Lew, J. & 1 others, Tan, M. H., May 29 2018, In: Genome Biology. 19, 1, 62.

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

Open Access

67 Citations (Scopus)

Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement

Ng, A. S. L., Tan, Y. J., Yi, Z., Tandiono, M., Chew, E., Dominguez, J., Macas, M., Ng, E., Hameed, S., Ting, S., Tan, E. K., Foo, J. N. & Kandiah, N., Aug 2018, In: Neurobiology of Aging. 68, p. 160.e15-160.e19

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

Open Access

17 Citations (Scopus)

2017

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

Seco, C. Z., Castells-Nobau, A., Joo, S. H., Schraders, M., Foo, J. N., Van Der Voet, M., Velan, S. S., Nijhof, B., Oostrik, J., De Vrieze, E., Katana, R., Mansoor, A., Huynen, M., Szklarczyk, R., Oti, M., Tranebjarg, L., Van Wijk, E., Scheffer-De Gooyert, J. M., Siddique, S. & Baets, J. & 10 others, De Jonghe, P., Kazmi, S. A. R., Sadananthan, S. A., Van De Warrenburg, B. P., Khor, C. C., Göpfert, M. C., Qamar, R., Schenck, A., Kremer, H. & Siddiqi, S., Feb 1 2017, In: DMM Disease Models and Mechanisms. 10, 2, p. 105-118 14 p.

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

Open Access

20 Citations (Scopus)

Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

Telomeres Mendelian Randomization Collaboration, May 1 2017, In: JAMA Oncology. 3, 5, p. 636-651 16 p.

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

Open Access

407 Citations (Scopus)

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.

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

Open Access

118 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.

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

Open Access

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.

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

Open Access

95 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)

Possible interaction between cigarette smoking and HLA-DRB1 variation in the risk of follicular lymphoma

Baecklund, F., Foo, J. N., Askling, J., Eloranta, S., Glimelius, I., Liu, J., Hjalgrim, H., Rosenquist, R., Padyukov, L. & Smedby, K. E., Apr 15 2017, In: American Journal of Epidemiology. 185, 8, p. 681-687 7 p.

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

Open Access

10 Citations (Scopus)

Screening for TMEM230 mutations in young-onset Parkinson's disease

Ma, D., Foo, J. N., Yulin Ng, E., Zhao, Y., Liu, J. J. & Tan, E. K., Oct 2017, In: Neurobiology of Aging. 58, p. 239.e9-239.e10

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

7 Citations (Scopus)

2016

An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma

Cui, Q., Feng, Q. S., Mo, H. Y., Sun, J., Xia, Y. F., Zhang, H., Foo, J. N., Guo, Y. M., Chen, L. Z., Li, M., Liu, W. S., Xu, M., Zhou, G., He, F., Yu, X., Jia, W. H., Liu, J., Zeng, Y. X. & Bei, J. X., Aug 15 2016, In: Human Molecular Genetics. 25, 16, p. 3626-3634 9 p.

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

Open Access

43 Citations (Scopus)

A synonymous variant in IL10RA affects RNA splicing in paediatric patients with refractory inflammatory bowel disease

Oh, S. H., Baek, J., Liany, H., Foo, J. N., Kim, K. M., Yang, S. C. O., Liu, J. & Song, K., Nov 2016, In: Journal of Crohn's and Colitis. 10, 11, p. 1366-1371 6 p.

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

Open Access

27 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.

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

Open Access

79 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.

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

147 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)

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)

2015

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Aung, T., Ozaki, M., Mizoguchi, T., Allingham, R. R., Li, Z., Haripriya, A., Nakano, S., Uebe, S., Harder, J. M., Chan, A. S. Y., Lee, M. C., Burdon, K. P., Astakhov, Y. S., Abu-Amero, K. K., Zenteno, J. C., Nilgün, Y., Zarnowski, T., Pakravan, M., Safieh, L. A. & Jia, L. & 141 others, Wang, Y. X., Williams, S., Paoli, D., Schlottmann, P. G., Huang, L., Sim, K. S., Foo, J. N., Nakano, M., Ikeda, Y., Kumar, R. S., Ueno, M., Manabe, S. I., Hayashi, K., Kazama, S., Ideta, R., Mori, Y., Miyata, K., Sugiyama, K., Higashide, T., Chihara, E., Inoue, K., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Aihara, M., Ohashi, T., Sakurai, T., Sugimoto, T., Chuman, H., Matsuda, F., Yamashiro, K., Gotoh, N., Miyake, M., Astakhov, S. Y., Osman, E. A., Al-Obeidan, S. A., Owaidhah, O., Al-Jasim, L., Shahwan, S. A., Fogarty, R. A., Leo, P., Yetkin, Y., Ouz, Ç., Kanavi, M. R., Beni, A. N., Yazdani, S., Akopov, E. L., Toh, K. Y., Howell, G. R., Orr, A. C., Goh, Y., Meah, W. Y., Peh, S. Q., Kosior-Jarecka, E., Lukasik, U., Krumbiegel, M., Vithana, E. N., Wong, T. Y., Liu, Y., Koch, A. E. A., Challa, P., Rautenbach, R. M., Mackey, D. A., Hewitt, A. W., Mitchell, P., Wang, J. J., Ziskind, A., Carmichael, T., Ramakrishnan, R., Narendran, K., Venkatesh, R., Vijayan, S., Zhao, P., Chen, X., Guadarrama-Vallejo, D., Cheng, C. Y., Perera, S. A., Husain, R., Ho, S. L., Welge-Luessen, U. C., Mardin, C., Schloetzer-Schrehardt, U., Hillmer, A. M., Herms, S., Moebus, S., Nöthen, M. M., Weisschuh, N., Shetty, R., Ghosh, A., Teo, Y. Y., Brown, M. A., Lischinsky, I., Crowston, J. G., Coote, M., Zhao, B., Sang, J., Zhang, N., You, Q., Vysochinskaya, V., Founti, P., Chatzikyriakidou, A., Lambropoulos, A., Anastasopoulos, E., Coleman, A. L., Wilson, M. R., Rhee, D. J., Kang, J. H., May-Bolchakova, I., Heegaard, S., Mori, K., Alward, W. L. M., Jonas, J. B., Xu, L., Liebmann, J. M., Chowbay, B., Schaeffeler, E., Schwab, M., Lerner, F., Wang, N., Yang, Z., Frezzotti, P., Kinoshita, S., Fingert, J. H., Inatani, M., Tashiro, K., Reis, A., Edward, D. P., Pasquale, L. R., Kubota, T., Wiggs, J. L., Pasutto, F., Topouzis, F., Dubina, M., Craig, J. E., Yoshimura, N., Sundaresan, P., John, S. W. M., Ritch, R., Hauser, M. A. & Khor, C. C., Apr 28 2015, In: Nature Genetics. 47, 4, p. 387-392 6 p.

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

Open Access

104 Citations (Scopus)

A common variant near TGFBR3 is associated with primary open angle glaucoma

Li, Z., Allingham, R. R., Nakano, M., Jia, L., Chen, Y., Ikeda, Y., Mani, B., Chen, L. J., Kee, C., Garway-Heath, D. F., Sripriya, S., Fuse, N., Abu-Amero, K. K., Huang, C., Namburi, P., Burdon, K., Perera, S. A., Gharahkhani, P., Lin, Y. & Ueno, M. & 91 others, Ozaki, M., Mizoguchi, T., Krishnadas, S. R., Osman, E. A., Lee, M. C., Chan, A. S. Y., Tajudin, L. S. A., Do, T., Goncalves, A., Reynier, P., Zhang, H., Bourne, R., Goh, D., Broadway, D., Husain, R., Negi, A. K., Su, D. H., Ho, C. L., Blanco, A. A., Leung, C. K. S., Wong, T. T., Yakub, A., Liu, Y., Nongpiur, M. E., Han, J. C., Hon, D. N., Shantha, B., Zhao, B., Sang, J., Zhang, N. H., Sato, R., Yoshii, K., Panda-Jonas, S., Ashley Koch, A. E., Herndon, L. W., Moroi, S. E., Challa, P., Foo, J. N., Bei, J. X., Zeng, Y. X., Simmons, C. P., Bich Chau, T. N., Sharmila, P. F., Chew, M., Lim, B., Tam, P. O. S., Chua, E., Ng, X. Y., Yong, V. H. K., Chong, Y. F., Meah, W. Y., Vijayan, S., Seongsoo, S., Xu, W., Teo, Y. Y., Cooke Bailey, J. N., Kang, J. H., Haines, J. L., Cheng, C. Y., Saw, S. M., Tai, E. S., Richards, J. E., Ritch, R., Gaasterland, D. E., Pasquale, L. R., Liu, J., Jonas, J. B., Milea, D., George, R., Al-Obeidan, S. A., Mori, K., Macgregor, S., Hewitt, A. W., Girkin, C. A., Zhang, M., Sundaresan, P., Vijaya, L., Mackey, D. A., Wong, T. Y., Craig, J. E., Sun, X., Kinoshita, S., Wiggs, J. L., Khor, C. C., Yang, Z., Pang, C. P., Wang, N., Hauser, M. A., Tashiro, K., Aung, T. & Vithana, E. N., Jul 1 2015, In: Human Molecular Genetics. 24, 13, p. 3880-3892 13 p.

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

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96 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.

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

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163 Citations (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)

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

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126 Citations (Scopus)

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol

Sadananda, S. N., Foo, J. N., Toh, M. T., Cermakova, L., Trigueros-Motos, L., Chan, T., Liany, H., Collins, J. A., Gerami, S., Singaraja, R. R., Hayden, M. R., Francis, G. A., Frohlich, J., Khor, C. C. & Brunham, L. R., Oct 1 2015, In: Journal of Lipid Research. 56, 10, p. 1993-2001 9 p.

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

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27 Citations (Scopus)

2014

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

Li, J., Lindström, L. S., Foo, J. N., Rafiq, S., Schmidt, M. K., Pharoah, P. D. P., Michailidou, K., Dennis, J., Bolla, M. K., Wang, Q., Van'T Veer, L. J., Cornelissen, S., Rutgers, E., Southey, M. C., Apicella, C., Dite, G. S., Hopper, J. L., Fasching, P. A., Haeberle, L. & Ekici, A. B. & 83 others, Beckmann, M. W., Blomqvist, C., Muranen, T. A., Aittomäki, K., Lindblom, A., Margolin, S., Mannermaa, A., Kosma, V. M., Hartikainen, J. M., Kataja, V., Chenevix-Trench, G., Investigators, K., Phillips, K. A., McLachlan, S. A., Lambrechts, D., Thienpont, B., Smeets, A., Wildiers, H., Chang-Claude, J., Flesch-Janys, D., Seibold, P., Rudolph, A., Giles, G. G., Baglietto, L., Severi, G., Haiman, C. A., Henderson, B. E., Schumacher, F., Le Marchand, L., Kristensen, V., Alnæs, G. I. G., Borresen-Dale, A. L., Nord, S., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, I. L., Knight, J. A., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, R., Seynaeve, C., Hooning, M., Kriege, M., Hollestelle, A., Van Den Ouweland, A., Li, Y., Hamann, U., Torres, D., Ulmer, H. U., Rüdiger, T., Shen, C. Y., Hsiung, C. N., Wu, P. E., Chen, S. T., Teo, S. H., Taib, N. A. M., Har Yip, C., Fuang Ho, G., Matsuo, K., Ito, H., Iwata, H., Tajima, K., Kang, D., Choi, J. Y., Park, S. K., Yoo, K. Y., Maishman, T., Tapper, W. J., Dunning, A., Shah, M., Luben, R., Brown, J., Chuen Khor, C., Eccles, D. M., Nevanlinna, H., Easton, D., Humphreys, K., Liu, J., Hall, P. & Czene, K., Jun 17 2014, In: Nature Communications. 5, 4051.

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

Open Access

16 Citations (Scopus)

A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival

Baecklund, F., Foo, J. N., Bracci, P., Darabi, H., Karlsson, R., Hjalgrim, H., Rosenquist, R., Adami, H. O., Glimelius, B., Melbye, M., Conde, L., Liu, J., Humphreys, K., Skibola, C. F. & Smedby, K. E., Oct 8 2014, In: BMC Medical Genetics. 15, 1, 113.

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

Open Access

16 Citations (Scopus)

Analysis of non-synonymous-coding variants of parkinson's disease-related pathogenic and susceptibility genes in East Asian populations

Foo, J. N., Tan, L. C., Liany, H., Koh, T. H., Irwan, I. D., Ng, Y. Y., Ahmad-Annuar, A., Au, W. L., Aung, T., Chan, A. Y. Y., Chong, S. A., Chung, S. J., Jung, Y., Khor, C. C., Kim, J., Lee, J., Lim, S. Y., Mok, V., Prakash, K. M. & Song, K. & 5 others, Tai, E. S., Vithana, E. N., Wong, T. Y., Tan, E. K. & Liu, J., Jul 2014, In: Human Molecular Genetics. 23, 14, p. 3891-3897 7 p., ddu086.

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27 Citations (Scopus)

A novel splice-site mutation in ALS establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias

Siddiqi, S., Foo, J. N., Vu, A., Azim, S., Silver, D. L., Mansoor, A., Tay, S. K. H., Abbasi, S., Hashmi, A. H., Janjua, J., Khalid, S., Tai, E. S., Yeo, G. W. & Khor, C. C., Dec 4 2014, In: PLoS One. 9, 12, e113258.

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

Open Access

19 Citations (Scopus)

Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations

Tan, L. C. S., Methawasin, K., Teng, E. W. L., Ng, A. R. J., Seah, S. H., Au, W. L., Liu, J. J., Foo, J. N., Zhao, Y. & Tan, E. K., Apr 2014, In: European Journal of Neurology. 21, 4, p. 674-678 5 p.

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

32 Citations (Scopus)

Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data

Li, Y., Foo, J. N., Liany, H., Low, H. Q. & Liu, J., Jun 17 2014, In: BMC Proceedings. 8, S29.

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Open Access

2 Citations (Scopus)

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls

Foo, J. N., Liany, H., Tan, L. C., Au, W. L., Prakash, K. M., Liu, J. & Tan, E. K., Apr 2014, In: Neurobiology of Aging. 35, 4, p. 935.e1-935.e2

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

21 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 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)

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.

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43 Citations (Scopus)

Variation at HLA-DRB1 is associated with resistance to enteric fever

Dunstan, S. J., Hue, N. T., Han, B., Li, Z., Tram, T. T. B., Sim, K. S., Parry, C. M., Chinh, N. T., Vinh, H., Lan, N. P. H., Thieu, N. T. V., Vinh, P. V., Koirala, S., Dongol, S., Arjyal, A., Karkey, A., Shilpakar, O., Dolecek, C., Foo, J. N. & Phuong, L. T. & 16 others, Lanh, M. N., Do, T., Aung, T., Hon, D. N., Teo, Y. Y., Hibberd, M. L., Anders, K. L., Okada, Y., Raychaudhuri, S., Simmons, C. P., Baker, S., De Bakker, P. I. W., Basnyat, B., Hien, T. T., Farrar, J. J. & Khor, C. C., Dec 11 2014, In: Nature Genetics. 46, 12, p. 1333-1336 4 p.

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77 Citations (Scopus)

2013

Absence of A673T amyloid-β precursor protein variant in alzheimer's disease and other neurological diseases

Ting, S. K. S., Chong, M. S., Kandiah, N., Hameed, S., Tan, L., Au, W. L., Prakash, K. M., Pavanni, R., Lee, T. S., Foo, J. N., Bei, J. X., Yu, X. Q., Liu, J. J., Zhao, Y., Lee, W. L. & Tan, E. K., Oct 2013, In: Neurobiology of Aging. 34, 10, p. 2441.e7-2441.e8

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24 Citations (Scopus)

Analysis of EIF4G1 in Parkinson's disease among Asians

Zhao, Y., Ho, P., Prakash, K. M., Foo, J. N., Liu, J. J., Au, W. L., Tan, L. C. & Tan, E. K., Apr 2013, In: Neurobiology of Aging. 34, 4, p. 1311.e5-1311.e6

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8 Citations (Scopus)

A rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease

Foo, J. N., Liany, H., Bei, J. X., Yu, X. Q., Liu, J., Au, W. L., Prakash, K. M., Tan, L. C. & Tan, E. K., Dec 2013, In: Neurobiology of Aging. 34, 12, p. 2890.e13-2890.e15

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76 Citations (Scopus)

Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population

Tayebi, N., Ke, T., Foo, J. N., Friedlander, Y., Liu, J. & Heng, C. K., Jun 2013, In: Clinical Biochemistry. 46, 9, p. 755-759 5 p.

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24 Citations (Scopus)

Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma risk

Foo, J. N., Smedby, K. E., Akers, N. K., Berglund, M., Irwan, I. D., Jia, X., Li, Y., Conde, L., Darabi, H., Bracci, P. M., Melbye, M., Adami, H. O., Glimelius, B., Khor, C. C., Hjalgrim, H., Padyukov, L., Humphreys, K., Enblad, G., Skibola, C. F. & De Bakker, P. I. W. & 1 others, Liu, J., Jul 11 2013, In: American Journal of Human Genetics. 93, 1, p. 167-172 6 p.

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26 Citations (Scopus)

Deep whole-genome sequencing of 100 southeast Asian malays

Wong, L. P., Ong, R. T. H., Poh, W. T., Liu, X., Chen, P., Li, R., Lam, K. K. Y., Pillai, N. E., Sim, K. S., Xu, H., Sim, N. L., Teo, S. M., Foo, J. N., Tan, L. W. L., Lim, Y., Koo, S. H., Gan, L. S. H., Cheng, C. Y., Wee, S. & Yap, E. P. H. & 10 others, Ng, P. C., Lim, W. Y., Soong, R., Wenk, M. R., Aung, T., Wong, T. Y., Khor, C. C., Little, P., Chia, K. S. & Teo, Y. Y., Jan 10 2013, In: American Journal of Human Genetics. 92, 1, p. 52-66 15 p.

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140 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 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.

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

39 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 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)

Foo Jia Nee

Research output

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