Foo Jia Nee

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

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)

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)

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)

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)

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 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 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 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 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 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 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)

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)

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)

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)

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 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)

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.

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

Open Access

52 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

Open Access

163 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.

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

Open Access

36 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.

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

Open Access

26 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

96 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)

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.

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

Open Access

88 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)

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.

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

Open Access

76 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.

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

8 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 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)

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)

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 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.

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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 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)

Generation of Human PSC-Derived Kidney Organoids with Patterned Nephron Segments and a De Novo Vascular Network

Low, J. H., Li, P., Chew, E. G. Y., Zhou, B., Suzuki, K., Zhang, T., Lian, M. M., Liu, M., Aizawa, E., Rodriguez Esteban, C., Yong, K. S. M., Chen, Q., Campistol, J. M., Fang, M., Khor, C. C., Foo, J. N., Izpisua Belmonte, J. C. & Xia, Y., Sept 5 2019, In: Cell Stem Cell. 25, 3, p. 373-387.e9

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251 Citations (Scopus)

Gene–Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time

Neoh, M. J. Y., Setoh, P., Bizzego, A., Tandiono, M., Foo, J. N., Lee, A., Bornstein, M. H. & Esposito, G., Jun 9 2022, In: Frontiers in Psychology. 13, 873676.

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3 Citations (Scopus)

Expanding the DARS phenotype: Late-adult onset myelopathy and leukoencephalopathy

Tan, A. H., Ng, A. S. L., Ramli, N. M., Lim, W. K., Cheah, P. L., Teo, J. X., Kuan, J. L., Tan, Y. J., Lim, J. L., Chew, E. G. Y., Foo, J. N., Goh, K. J., Tan, E. K. & Lim, S. Y., 2023, In: Neurology Asia. 28, 1, p. 185-189 5 p.

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Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease risk

Chew, E. G. Y., Liu, Z., Li, Z., Chung, S. J., Lian, M. M., Tandiono, M., Heng, Y. J., Ng, E. Y., Tan, L. C. S., Chng, W. L., Tan, T. J., Peh, E. K. L., Ho, Y. S., Chen, X. Y., Lim, E. Y. T., Chang, C. H., Leong, J. J., Peh, T. X., Chan, L. L. & Chao, Y. & 30 others, Au, W. L., Prakash, K. M., Lim, J. L., Tay, Y. W., Mok, V., Chan, A. Y. Y., Lin, J. J., Jeon, B. S., Song, K., Tham, C. C., Pang, C. P., Ahn, J., Park, K. H., Wiggs, J. L., Aung, T., Tan, A. H., Ahmad Annuar, A., Makarious, M. B., Blauwendraat, C., Nalls, M. A., Robak, L. A., Alcalay, R. N., Gan-Or, Z., Reynolds, R., Lim, S. Y., Xia, Y., Khor, C. C., Tan, E. K., Wang, Z. & Foo, J. N., 2024, (Accepted/In press) In: Nature Aging.

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

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2 Citations (Scopus)

Evaluation of novel Parkinson's disease candidate genes in the Chinese population

Chew, E. G. Y., Liany, H., Tan, L. C. S., Au, W. L., Prakash, K. M., Annuar, A. A., Chan, A. Y. Y., Lim, S. Y., Mok, V., Chung, S. J., Song, K., Liu, J., Foo, J. N. & Tan, E. K., Feb 2019, In: Neurobiology of Aging. 74, p. 235.e1-235.e4

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5 Citations (Scopus)

Erratum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome (Nature Genetics (2015) 47 (387-392))

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., Oaiuz, 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., May 27 2015, In: Nature Genetics. 47, 6, p. 689 1 p.

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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.

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27 Citations (Scopus)

Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levels

Murray, A., Gough, G., Cindrić, A., Vučković, F., Koschut, D., Borelli, V., Petrović, D. J., Bekavac, A., Plećaš, A., Hribljan, V., Brunmeir, R., Jurić, J., Pučić-Baković, M., Slana, A., Deriš, H., Frkatović, A., Groet, J., O'Brien, N. L., Chen, H. Y. & Yeap, Y. J. & 25 others, Delom, F., Havlicek, S., Gammon, L., Hamburg, S., Startin, C., D'Souza, H., Mitrečić, D., Kero, M., Odak, L., Krušlin, B., Krsnik, Ž., Kostović, I., Foo, J. N., Loh, Y. H., Dunn, N. R., de la Luna, S., Spector, T., Barišić, I., Thomas, M. S. C., Strydom, A., Franceschi, C., Lauc, G., Krištić, J., Alić, I. & Nižetić, D., Aug 2023, In: EBioMedicine. 94, 104692.

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10 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

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21 Citations (Scopus)

Destabilization of β Cell FIT2 by saturated fatty acids alter lipid droplet numbers and contribute to ER stress and diabetes

Zheng, X., Ho, Q. W. C., Chua, M., Stelmashenko, O., Yeo, X. Y., Muralidharan, S., Torta, F., Chew, E. G. Y., Lian, M. M., Foo, J. N., Jung, S., Wong, S. H., Tan, N. S., Tong, N., Rutter, G. A., Wenk, M. R., Silver, D. L., Berggren, P. O. & Ali, Y., Mar 15 2022, In: Proceedings of the National Academy of Sciences of the United States of America. 119, 11, e2113074119.

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28 Citations (Scopus)

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Towns, C., Richer, M., Jasaityte, S., Stafford, E. J., Joubert, J., Antar, T., Martinez-Carrasco, A., Makarious, M. B., Casey, B., Vitale, D., Levine, K., Leonard, H., Pantazis, C. B., Screven, L. A., Hernandez, D. G., Wegel, C. E., Solle, J., Nalls, M. A., Blauwendraat, C. & Singleton, A. B. & 224 others, Tan, M. M. X., Iwaki, H., Morris, H. R., 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., Orozco, 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., Kp, D., 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., Cornejo-Olivas, M., Doquenia, M. L., Rosales, R., Vinuela, A., Iakovenko, E., Mubarak, B. A., Umair, M., Tan, E. K., Foo, J. N., 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., Zweier, C., 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., Noyce, A., Schrag, A., Schapira, A., Carroll, C., Bale, C., Grosset, D., Houlden, H., Hardy, J., Mok, K. Y., Rizig, M., Wood, N., Williams, N., Okunoye, O., Lewis, P. A., Kaiyrzhanov, R., Weil, R., Love, S., Stott, S., Jasaitye, S., Dey, S., Obese, V., Espay, A., O’Grady, A., Sobering, A. K., Siddiqi, B., Fiske, B., Jonas, C., Cruchaga, C., 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., Kim, J. 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., Bandres-Ciga, S., Chowdhury, S., Dumanis, S., Lubbe, S., Xie, T., Foroud, T., Beach, T., Sherer, T., Song, Y., Nguyen, D., Nguyen, T. & Atadzhanov, M., Dec 2023, In: npj Parkinson's Disease. 9, 1, 131.

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

Open Access

12 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.

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

Open Access

140 Citations (Scopus)

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

Cheng, C. Y., Yamashiro, K., Chen, L. J., 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., Ong, P. G., 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., Wong, T. Y. & Khor, C. C., Mar 2015, In: Nature Communications. 6, 6817.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

25 Citations (Scopus)

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta (Journal of Biomedical Science (2018) 25 (82) DOI: 10.1186/s12929-018-0481-x)

Kausar, M., Siddiqi, S., Yaqoob, M., Mansoor, S., Makitie, O., Mir, A., Khor, C. C., Foo, J. N. & Anees, M., Apr 28 2019, In: Journal of Biomedical Science. 26, 1, 31.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

1 Citation (Scopus)

Correction: Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain (Molecular Psychiatry, (2021), 26, 10, (5766-5788), 10.1038/s41380-020-0806-5)

LonDownS Consortium, Oct 2021, In: Molecular Psychiatry. 26, 10, p. 5789 1 p.

Research output: Contribution to journal › Comment/debate › peer-review

Open Access

3 Citations (Scopus)

Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population

Wang, Y., Fu, W., Xie, F., Wang, Y., Chu, X., Wang, H., Shen, M., Wang, Y., Wang, Y., Sun, W., Lei, R., Yang, L., Wu, H., Foo, J., Liu, J., Jin, L. & Huang, W., Aug 2010, In: Journal of Human Genetics. 55, 8, p. 490-494 5 p.

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

Open Access

24 Citations (Scopus)

Foo Jia Nee

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