Next-generation sequencing diagnostics for neurological diseases/disorders: From a clinical perspective

由 Foo, J.N., Liu, J., Tan, E.-K.
出版 2014

CHCHD2 and Parkinson's disease

由 Foo J.N., Liu J., Tan E.-K.
出版 2018

Whole-genome and whole-exome sequencing in neurological diseases

由 Foo J.-N., Liu J.-J., Tan E.-K.
出版 2018

Identifying genes in parkinson disease: State of the art

由 Chew E.G.Y., Foo J.N., Tan E.-K.
出版 2018

Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases

由 Foo J.N., Zhao Y., Liu J., Tan E.-K.
出版 2018

P.112 Effect of early paternal caregiving and genotype rs25531 polymorphisms on the adult relationship with the partner

由 Bonassi, A., Cataldo, I., Tandiono, M., Foo, J. N., Lepri, B., Esposito, Gianluca
出版 2021

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

由 Foo J.N., Lee J., Tan L.C., Liu J., Tan E.-K.
出版 2018

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease

由 Chao Y.X., Ng E.Y., Foo J.N., Liu J., Zhao Y., Tan E.-K.
出版 2018

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

由 Ma D., Foo J.N., Yulin Ng E., Zhao Y., Liu J.-J., Tan E.K.
出版 2018

No association of DNM3 with age of onset in Asian Parkinson's disease

由 Foo J.N., Tan L.C., Au W.-L., Prakash K.-M., Liu J., Tan E.-K.
出版 2018

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

由 Foo, J.N., Liany, H., Tan, L.C., Au, W.-L., Prakash, K.-M., Liu, J., Tan, E.-K.
出版 2014

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

由 Ajmal, M, Mir, A, Wahid, S, Khor, C.C, Foo, J.N, Siddiqi, S, Kauser, M, Malik, S.A, Nasir, M
出版 2020

Analysis of EIF4G1 in Parkinson's disease among Asians

由 Zhao, Y., Ho, P., Prakash, K.-M., Foo, J.-N., Liu, J.-J., Au, W.-L., Tan, L.C., Tan, E.-K.
出版 2014

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

由 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.
出版 2014

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

由 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.
出版 2014

Clinical/scientific notes

由 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.
出版 2014

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

由 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.
出版 2018

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

由 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.
出版 2014

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

由 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.
出版 2018

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

由 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.
出版 2018