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

بواسطة Foo, J.N., Liu, J., Tan, E.-K.
منشور في 2014

CHCHD2 and Parkinson's disease

بواسطة Foo J.N., Liu J., Tan E.-K.
منشور في 2018

Whole-genome and whole-exome sequencing in neurological diseases

بواسطة Foo J.-N., Liu J.-J., Tan E.-K.
منشور في 2018

Identifying genes in parkinson disease: State of the art

بواسطة Chew E.G.Y., Foo J.N., Tan E.-K.
منشور في 2018

Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases

بواسطة Foo J.N., Zhao Y., Liu J., Tan E.-K.
منشور في 2018

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

بواسطة Bonassi, A., Cataldo, I., Tandiono, M., Foo, J. N., Lepri, B., Esposito, Gianluca
منشور في 2021

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

بواسطة Foo J.N., Lee J., Tan L.C., Liu J., Tan E.-K.
منشور في 2018

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

بواسطة Chao Y.X., Ng E.Y., Foo J.N., Liu J., Zhao Y., Tan E.-K.
منشور في 2018

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

بواسطة Ma D., Foo J.N., Yulin Ng E., Zhao Y., Liu J.-J., Tan E.K.
منشور في 2018

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

بواسطة Foo J.N., Tan L.C., Au W.-L., Prakash K.-M., Liu J., Tan E.-K.
منشور في 2018

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

بواسطة Foo, J.N., Liany, H., Tan, L.C., Au, W.-L., Prakash, K.-M., Liu, J., Tan, E.-K.
منشور في 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

بواسطة Ajmal, M, Mir, A, Wahid, S, Khor, C.C, Foo, J.N, Siddiqi, S, Kauser, M, Malik, S.A, Nasir, M
منشور في 2020

Analysis of EIF4G1 in Parkinson's disease among Asians

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

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

بواسطة 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.
منشور في 2014

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

بواسطة 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.
منشور في 2014

Clinical/scientific notes

بواسطة 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.
منشور في 2014

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

بواسطة 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.
منشور في 2018

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

بواسطة 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.
منشور في 2014

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

بواسطة 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.
منشور في 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

بواسطة 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.
منشور في 2018