Foo Jia Nee

2008

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Ji, W., Foo, J. N., O'Roak, B. J., Zhao, H., Larson, M. G., Simon, D. B., Newton-Cheh, C., State, M. W., Levy, D. & Lifton, R. P., May 2008, In: Nature Genetics. 40, 5, p. 592-599 8 p.

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

Open Access

685 Citations (Scopus)

2009

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)

2010

Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease

Petersen, K. F., Dufour, S., Hariri, A., Nelson-Williams, C., Foo, J. N., Zhang, X. M., Dziura, J., Lifton, R. P. & Shulman, G. I., Mar 25 2010, In: New England Journal of Medicine. 362, 12, p. 1082-1089 8 p.

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

Open Access

364 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)

2011

A comprehensive association analysis of homocysteine metabolic pathway genes in singaporean Chinese with ischemic stroke

Low, H. Q., Chen, C. P. L. H., Kasiman, K., Thalamuthu, A., Ng, S. S., Foo, J. N., Chang, H. M., Wong, M. C., Tai, E. S. & Liu, J., Sept 15 2011, In: PLoS One. 6, 9, e24757.

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

Open Access

25 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)

2012

A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy

Yu, X. Q., Li, M., Zhang, H., Low, H. Q., Wei, X., Wang, J. Q., Sun, L. D., Sim, K. S., Li, Y., Foo, J. N., Wang, W., Li, Z. J., Yin, X. Y., Tang, X. Q., Fan, L., Chen, J., Li, R. S., Wan, J. X., Liu, Z. S. & Lou, T. Q. & 5 others, Zhu, L., Huang, X. J., Zhang, X. J., Liu, Z. H. & Liu, J. J., Feb 2012, In: Nature Genetics. 44, 2, p. 178-182 5 p.

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

258 Citations (Scopus)

A meta-analysis of genome-wide association studies of follicular lymphoma

Skibola, C. F., Conde, L., Foo, J. N., Riby, J., Humphreys, K., Sillé, F. C. M., Darabi, H., Sanchez, S., Hjalgrim, H., Liu, J., Bracci, P. M. & Smedby, K. E., Oct 1 2012, In: BMC Genomics. 13, 1, 516.

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

Open Access

19 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.

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

Open Access

5 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)

Validation of GWAS loci for atopic dermatitis in a Singapore chinese population

Andiappan, A. K., Foo, J. N., Choy, M. W., Chen, H., Common, J. E. A., Tang, M. B. Y., Van Bever, H. P., Giam, Y. C., Suri, B. K., Ramani, A., Nilkanth, P. P., Lane, E. B., Wang, D. Y., Chew, F. T. & Liu, J., May 2012, In: Journal of Investigative Dermatology. 132, 5, p. 1505-1507 3 p.

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

Open Access

2 Citations (Scopus)

Whole-genome and whole-exome sequencing in neurological diseases

Foo, J. N., Liu, J. J. & Tan, E. K., Sept 2012, In: Nature Reviews Neurology. 8, 9, p. 508-517 10 p.

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

98 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

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

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

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

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

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

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.

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

24 Citations (Scopus)

Clinical/scientific notes

Tan, E. K., Foo, J. N., Tan, L., Au, W. L., Prakash, K. M., Ng, E., Kamran Ikram, M., Wong, T. Y., Liu, J. J. & Zhao, Y., Apr 23 2013, In: Neurology. 80, 17, p. 1618-1619 2 p.

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

36 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.

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

Open Access

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.

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

Open Access

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.

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

Open Access

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)

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)

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)

The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese population

Zheng, X., Bei, J. X., Xu, H., Lee, J., Chong, S. A., Sim, K., Liany, H., Tai, E. S., Liu, T., Foo, J. N., Irwan, I. D., Teo, Y. Y. & Liu, J., May 2013, In: Schizophrenia Research. 146, 1-3, p. 368-369 2 p.

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

9 Citations (Scopus)

X chromosome-wide association study of follicular lymphoma

Conde, L., Foo, J. N., Riby, J., Liu, J., Darabi, H., Hjalgrim, H., Bracci, P. M., Smedby, K. E. & Skibola, C. F., Sept 2013, In: British Journal of Haematology. 162, 6, p. 858-862 5 p.

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

Open Access

5 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.

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

Open Access

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.

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

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.

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

Open Access

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.

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

Open Access

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.

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

Open Access

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.

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

Open Access

77 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

Open Access

96 Citations (Scopus)

CHCHD2 and Parkinson's disease

Foo, J. N., Liu, J. & Tan, E. K., Jul 1 2015, In: The Lancet Neurology. 14, 7, p. 681-682 2 p.

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

Open Access

31 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)

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.

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

Open Access

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)

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)

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)

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)

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)

Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases

Foo, J. N., Zhao, Y., Liu, J. & Tan, E. K., Jul 1 2015, In: Annals of Neurology. 78, 1, p. 152-153 2 p.

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

8 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

Open Access

27 Citations (Scopus)

Foo Jia Nee

Research output

Search results