Browsing by Author Foo, J.N.

Showing results 1 to 9 of 9
Issue DateTitleAuthor(s)
2017A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathySeco, C.Z; Castells-Noba 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.; 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.
11-Jul-2013Coding variants at hexa-allelic amino acid 13 of HLA-DRB1 explain independent SNP associations with follicular lymphoma riskFoo, 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.; Liu, J. 
Apr-2014DNAJ mutations are rare in Chinese Parkinson's disease patients and controlsFoo, J.N.; Liany, H.; Tan, L.C.; Au, W.-L.; Prakash, K.-M.; Liu, J.; Tan, E.-K. 
2-Aug-2012Genetic variants in ER cofactor genes and endometrial cancer riskLi, 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.
Jul-2013Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese populationTan, 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.; Ng, S.B.; Zeng, Y.-X.; Khor, C.C. ; Lin, D.; Seow, A.L.H. ; Jia, W.-H.; Liu, J. 
6-Aug-2013Identification of a novel risk variant in the FUS gene in essential tremorWu, 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. 
Jul-2013Next-generation sequencing diagnostics for neurological diseases/disorders: From a clinical perspectiveFoo, J.N.; Liu, J.; Tan, E.-K. 
May-2013The association between rare large duplication of 16p11.2 and schizophrenia in the Singaporean Chinese populationZheng, 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-2012Validation of GWAS loci for atopic dermatitis in a Singapore chinese populationAndiappan, 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.