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Volumn 71, Issue 5, 2012, Pages 390-391

Genomic tics in tourette syndrome

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE HISTIDINE TRIAD PROTEIN; HISTAMINE;

EID: 84858725515     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2011.12.017     Document Type: Note
Times cited : (1)

References (9)
  • 1
    • 81755183108 scopus 로고    scopus 로고
    • Relative burden of large CNVs on a range of neurodevelopmental phenotypes
    • S. Girirajan, Z. Brkanac, B.P. Coe, C. Baker, L. Vives, T.H. Vu Relative burden of large CNVs on a range of neurodevelopmental phenotypes PLoS Genet 7 2011 e1002334
    • (2011) PLoS Genet , vol.7 , pp. 1002334
    • Girirajan, S.1    Brkanac, Z.2    Coe, B.P.3    Baker, C.4    Vives, L.5    Vu, T.H.6
  • 2
    • 79958074870 scopus 로고    scopus 로고
    • Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
    • S.J. Sanders, A.G. Ercan-Sencicek, V. Hus, R. Luo, M.T. Murtha, D. Moreno-De-Luca Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism Neuron 70 2011 863 885
    • (2011) Neuron , vol.70 , pp. 863-885
    • Sanders, S.J.1    Ercan-Sencicek, A.G.2    Hus, V.3    Luo, R.4    Murtha, M.T.5    Moreno-De-Luca, D.6
  • 3
    • 51649107017 scopus 로고    scopus 로고
    • Rare chromosomal deletions and duplications increase risk of schizophrenia
    • International Schizophrenia Consortium
    • International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia Nature 455 2008 237 241
    • (2008) Nature , vol.455 , pp. 237-241
  • 4
    • 77956628767 scopus 로고    scopus 로고
    • Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
    • H.C. Mefford, H. Muhle, P. Ostertag, S. von Spiczak, K. Buysse, C. Baker, A. Franke Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies PLoS Genet 6 2010 e1000962
    • (2010) PLoS Genet , vol.6 , pp. 1000962
    • Mefford, H.C.1    Muhle, H.2    Ostertag, P.3    Von Spiczak, S.4    Buysse, K.5    Baker, C.6    Franke, A.7
  • 6
    • 42649125261 scopus 로고    scopus 로고
    • Familial deletion within NLGN4 associated with autism and Tourette syndrome
    • DOI 10.1038/sj.ejhg.5202006, PII 5202006
    • A. Lawson-Yuen, J.S. Saldivar, S. Sommer, J. Picker Familial deletion within NLGN4 associated with autism and Tourette syndrome Eur J Hum Genet 16 2008 614 618 (Pubitemid 351594128)
    • (2008) European Journal of Human Genetics , vol.16 , Issue.5 , pp. 614-618
    • Lawson-Yuen, A.1    Saldivar, J.-S.2    Sommer, S.3    Picker, J.4
  • 8
    • 84856716148 scopus 로고    scopus 로고
    • Increasing histamine neurotransmission in Gilles de la Tourette syndrome
    • [published online ahead of print July 22] 10.1007/s00415-011-6171-1
    • A. Hartmann, Y. Worbe, I. Arnulf Increasing histamine neurotransmission in Gilles de la Tourette syndrome [published online ahead of print July 22] J Neurol 2011 10.1007/s00415-011-6171-1
    • (2011) J Neurol
    • Hartmann, A.1    Worbe, Y.2    Arnulf, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.