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Foo Jia Nee

Asst Prof

Calculated based on number of publications stored in Pure and citations from Scopus
Calculated based on number of publications stored in Pure and citations from Scopus
Calculated based on number of publications stored in Pure and citations from Scopus
20082024

Research activity per year

Search results

  • 2020

    Oxytocin receptor gene polymorphisms and early parental bonding interact in shaping instagram social behavior

    Bonassi, A., Cataldo, I., Gabrieli, G., Foo, J. N., Lepri, B. & Esposito, G., Oct 1 2020, In: International Journal of Environmental Research and Public Health. 17, 19, p. 1-20 20 p., 7232.

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

    Open Access
    14 Citations (Scopus)

  • Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort

    Chen, Z., Xu, Z., Cheng, Q., Tan, Y. J., Ong, H. L., Zhao, Y., Lim, W. K., Teo, J. X., Foo, J. N., Lee, H. Y., Tan, J. M. M., Hang, L., Yu, W. Y., Ting, S. K. S., Tan, E. K., Lim, T. C. C. & Ng, A. S. L., Sept 1 2020, In: Clinical Genetics. 98, 3, p. 274-281 8 p.

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

    34 Citations (Scopus)

  • The Parkinson's Disease Genome-Wide Association Study Locus Browser

    the International Parkinson's Disease Genomics Consortium (IPDGC), Nov 2020, In: Movement Disorders. 35, 11, p. 2056-2067 12 p.

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

    Open Access
    64 Citations (Scopus)
  • 2019

    A novel homozygous frameshift variant in XYLT2 causes spondyloocular syndrome in a consanguineous Pakistani family

    Kausar, M., Chew, E. G. Y., Ullah, H., Anees, M., Khor, C. C., Foo, J. N., Makitie, O. & Siddiqi, S., 2019, In: Frontiers in Genetics. 10, MAR, 144.

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

    Open Access
    13 Citations (Scopus)

  • A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families

    Sadia, Foo, J. N., Khor, C. C., Jelani, M. & Ali, G., Sept 1 2019, In: Journal of Gene Medicine. 21, 9, e3113.

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

    Open Access
    2 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)

  • 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

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

    Open Access
    5 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

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

    Open Access
    259 Citations (Scopus)

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

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

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

    13 Citations (Scopus)

  • 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
    127 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
    8 Citations (Scopus)

  • Polycystic kidney disease: new knowledge and future promises

    Foo, J. N. & Xia, Y., Jun 2019, In: Current Opinion in Genetics and Development. 56, p. 69-75 7 p.

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

    Open Access
    4 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
    41 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
    13 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
    68 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
    411 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
    120 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
    96 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
    44 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
    28 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
    80 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

    149 Citations (Scopus)

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

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

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

    Open Access
    9 Citations (Scopus)

  • 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
    105 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
    30 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
    115 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)
  • 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)
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