| Year |
Citation |
Score |
| 2019 |
Lai KL, Liao YC, Tsai PC, Hsiao CT, Soong BW, Lee YC. Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia. Parkinsonism & Related Disorders. PMID 31422002 DOI: 10.1016/J.Parkreldis.2019.08.004 |
0.336 |
|
| 2018 |
Tsai PC, Liao YC, Jih KY, Soong BW, Lin KP, Lee YC. Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan. Neurobiology of Aging. PMID 30054183 DOI: 10.1016/J.Neurobiolaging.2018.07.002 |
0.352 |
|
| 2017 |
Tsai PC, Liao YC, Chen PL, Guo YC, Chen YH, Jih KY, Lin KP, Soong BW, Tsai CP, Lee YC. Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis. Neurobiology of Aging. PMID 29102476 DOI: 10.1016/J.Neurobiolaging.2017.09.031 |
0.35 |
|
| 2017 |
Chen YH, Lee YC, Tsai YS, Guo YC, Hsiao CT, Tsai PC, Huang JA, Liao YC, Soong BW. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. Plos One. 12: e0177296. PMID 28481932 DOI: 10.1371/Journal.Pone.0177296 |
0.319 |
|
| 2017 |
Tsai PC, Tsai YS, Soong BW, Huang YH, Wu HT, Chen YH, Lin KP, Liao YC, Lee YC. A novel DNAJB6 mutation causes dominantly-inherited distal-onset myopathy and compromises DNAJB6 function. Clinical Genetics. PMID 28233300 DOI: 10.1111/Cge.13001 |
0.345 |
|
| 2016 |
Tsai PC, Yang DM, Liao YC, Chiu TY, Kuo HC, Su YP, Guo YC, Soong BW, Lin KP, Liu YT, Lee YC. Clinical and biophysical characterization of 19 GJB1 mutations. Annals of Clinical and Translational Neurology. 3: 854-865. PMID 27844031 DOI: 10.1002/Acn3.347 |
0.304 |
|
| 2016 |
Lee YC, Tsai PC, Guo YC, Hsiao CT, Liu GT, Liao YC, Soong BW. Spinocerebellar ataxia type 36 in the Han Chinese. Neurology. Genetics. 2: e68. PMID 27123487 DOI: 10.1212/Nxg.0000000000000068 |
0.31 |
|
| 2016 |
Tsai PC, Liu YC, Lin KP, Liu YT, Liao YC, Hsiao CT, Soong BW, Yip PK, Lee YC. Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of Aging. PMID 26804609 DOI: 10.1016/J.Neurobiolaging.2015.12.022 |
0.35 |
|
| 2015 |
Liao YC, Liu YT, Tsai PC, Chang CC, Huang YH, Soong BW, Lee YC. Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease. Plos One. 10: e0133423. PMID 26244500 DOI: 10.1371/Journal.Pone.0133423 |
0.309 |
|
| 2015 |
Lin KP, Tsai PC, Liao YC, Chen WT, Tsai CP, Soong BW, Lee YC. Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of Aging. 36: 2005.e1-4. PMID 25771394 DOI: 10.1016/J.Neurobiolaging.2015.02.008 |
0.349 |
|
| 2014 |
Hsiao CT, Tsai PC, Liao YC, Lee YC, Soong BW. C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome. Journal of the Neurological Sciences. 347: 322-4. PMID 25467142 DOI: 10.1016/J.Jns.2014.10.042 |
0.339 |
|
| 2014 |
Guo YC, Lin JJ, Liao YC, Tsai PC, Lee YC, Soong BW. Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization. Neurology. 83: 1554-61. PMID 25253745 DOI: 10.1212/Wnl.0000000000000909 |
0.342 |
|
| 2014 |
Tsai PC, Huang YH, Guo YC, Wu HT, Lin KP, Tsai YS, Liao YC, Liu YT, Liu TT, Kao LS, Yet SF, Fann MJ, Soong BW, Lee YC. A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function. Neurology. 83: 903-12. PMID 25098539 DOI: 10.1212/Wnl.0000000000000758 |
0.328 |
|
| 2013 |
Soong BW, Liao YC, Tu PH, Tsai PC, Lee IH, Chung CP, Lee YC. A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain. Journal of the Chinese Medical Association : Jcma. 76: 319-24. PMID 23602593 DOI: 10.1016/J.Jcma.2013.03.002 |
0.343 |
|
| 2013 |
Soong BW, Huang YH, Tsai PC, Huang CC, Pan HC, Lu YC, Chien HJ, Liu TT, Chang MH, Lin KP, Tu PH, Kao LS, Lee YC. Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease. American Journal of Human Genetics. 92: 422-30. PMID 23434117 DOI: 10.1016/J.Ajhg.2013.01.014 |
0.363 |
|
| 2012 |
Tsai PC, Breen M. Array-based comparative genomic hybridization-guided identification of reference genes for normalization of real-time quantitative polymerase chain reaction assay data for lymphomas, histiocytic sarcomas, and osteosarcomas of dogs. American Journal of Veterinary Research. 73: 1335-43. PMID 22924713 DOI: 10.2460/Ajvr.73.9.1335 |
0.539 |
|
| 2012 |
Tsai CP, Soong BW, Tu PH, Lin KP, Fuh JL, Tsai PC, Lu YC, Lee IH, Lee YC. A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan. Neurobiology of Aging. 33: 2232.e11-2232.e18. PMID 22673113 DOI: 10.1016/J.Neurobiolaging.2012.05.002 |
0.315 |
|
| 2009 |
Thomas R, Wang HJ, Tsai PC, Langford CF, Fosmire SP, Jubala CM, Getzy DM, Cutter GR, Modiano JF, Breen M. Influence of genetic background on tumor karyotypes: evidence for breed-associated cytogenetic aberrations in canine appendicular osteosarcoma. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 17: 365-77. PMID 19337847 DOI: 10.1007/S10577-009-9028-Z |
0.509 |
|
| 2009 |
Lin TY, Thomas R, Tsai PC, Breen M, London CA. Generation and characterization of novel canine malignant mast cell line CL1. Veterinary Immunology and Immunopathology. 127: 114-24. PMID 19054577 DOI: 10.1016/J.Vetimm.2008.09.027 |
0.444 |
|
| 2007 |
Thomas R, Duke SE, Bloom SK, Breen TE, Young AC, Feiste E, Seiser EL, Tsai PC, Langford CF, Ellis P, Karlsson EK, Lindblad-Toh K, Breen M. A cytogenetically characterized, genome-anchored 10-Mb BAC set and CGH array for the domestic dog. The Journal of Heredity. 98: 474-84. PMID 17702974 DOI: 10.1093/Jhered/Esm053 |
0.551 |
|
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