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Yo-Tsen Liu (劉祐岑)

Yo-Tsen Liu(劉祐岑)

簡介

學歷
  1. 臺灣大學醫學系畢業
  2. 英國倫敦學院大學神經學研究所(UCL Institute of Neurology, Queen Square, London, U.K.)博士
經歷 現職: - 迄今 臺北榮總神經內科癲癇科之主治醫師
醫療專長
  1. 癲癇
  2. 巴金森氏症
  3. 動作障礙疾病
  4. 神經遺傳疾病

著作

得獎紀錄

1. 2014 Award of the best paper of 19th Taiwan Neurology Society Congress, Taiwan. 2014台灣神經學年會最佳論文
2. 2010~2012 Winner of Studying Abroad Scholarship, Ministry of Education, Executive Yuan, Taiwan. 2010~2012教育部公費留學獎學金得主

Awards and Honors

1. Taiwan presentative speaker of East Asia Neurology Forum (EANF)2014
2. Award of the best paper of 19th Taiwan Neurology Society Congress, Taiwan.
3. 2015第18屆國家生技醫療品質獎【特色醫療組銅獎】:臺北榮總癲癇手術團隊: 超越巔峰

Focus

1. Clinical and genetics of epilepsy
2. Clinical and genetics of paroxysmal movement disorders
3. Clinical and genetics of neurodegenerative diseases  

Selected Publications

1. Defects of mutant DNMT1 are linked to a spectrum of neurological disorders. Baets J, Duan X, Wu Y, Smith G, Seeley W, Mademan I, McGrath NM, Beade NC, Khoury J, Botuyan M, Mer G, Worrell GA, Hojo K, DeLeon J, Laura M, *Liu YT, Senderek JP, Weis J, Van den Bergh P, Merrill SL, Reilly MM, Houlden H, Grossman M, Scherer S, De Jonghe P, Dyck PJ, Klein CJ. Brain. 2015 Feb 11. [Epub ahead of print]

2. A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function. 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, and Lee YC. Neurology. 2014 Sep 2;83(10):903-12. Epub 2014 Aug 6.

3. Extended phenotypic spectrum of KIF5A mutations: from spastic paraplegia to axonal neuropathy. *Liu YT, Laurá M, Hersheson J, Horga A, Jaunmuktane Z, Brandner S, Pittman A, Hughes D, Polke J, Sweeney MG, Proukakis C,  Janssen JC, Auer-Grumbach M, Zuchner S, Shields K, Reilly MM, and Houlden H. Neurology. 2014 Jul 9;83(1):1-8, Epub 2014 Jul 9.

4. Autosomal-recessive cerebellar ataxia caused by a novel ADCK3mutation that elongates the protein: clinical, genetic and biochemical characterisation. *Liu YT, Hersheson J, Plagnol V, Fawcett K, Duberley KE, Preza E, Hargreaves IP, Chalasani A, Laurá M, Wood NW, Reilly MM, Houlden H.J Neurol Neurosurg Psychiatry. 2014 May;85(5):493-8. Epub 2013 Nov 11.

5. Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy. Tucci A,*Liu YT, Preza E, Pitceathly RD, Chalasani A, Plagnol V, Land JM, Trabzuni D, Ryten M; on behalf of UKBEC, Jaunmuktane Z, Reilly MM, Brandner S, Hargreaves I, Hardy J, Singleton AB, Abramov AY, Houlden H. J Neurol Neurosurg Psychiatry. 2014 May;85(5):486-92.

6. Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2. Gonzalez M, McLaughlin H, Houlden H, Guo M, *Liu YT, Hadjivassilious M, Speziani F, Yang XL, Antonellis A, Reilly MM, Züchner S; Inherited Neuropathy Consortium. J Neurol Neurosurg Psychiatry. 2013 Nov;84(11):1247-9.

7. Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2. Murphy SM, Ernst D, Wei Y, Laurà M, *Liu YT, Polke J, Blake J, Winer J, Houlden H, Hornemann T, Reilly MM. Neurology. 2013 Jun 4;80(23):2106-11.

8. Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. Murphy SM, Laura M, Fawcett K, Pandraud A, *Liu YT, Davidson GL, Rossor AM, Polke JM, Castleman V, Manji H, Lunn MP, Bull K, Ramdharry G, Davis M, Blake JC, Houlden H, Reilly MM. J Neurol Neurosurg Psychiatry. 2012 Jul;83(7):706-10.

9. Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression. *Liu YT, Lee YC, Yang CC, Chen ML, Lin KP. J Neurol Sci. 2008 Apr 15;267(1-2):91-9.

10. A novel ABCD1 gene mutation in a Chinese-Taiwanese patient with adrenomyeloneuropathy. *Liu YT, Lin KH, Soong BW, Liao KK, Lin KP. Pediatr Neurol. 2007 May;36(5):348-50