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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Thomas Sander

Department of Neurology

University Hospital Charité

Campus Virchow Clinic

Humboldt University of Berlin

Germany

[email]@aol.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Neurology, University Hospital Charité, Campus Virchow Clinic, Humboldt University of Berlin, Germany. 1999 - 2003
  • Department of Neurology, Humboldt University Berlin, University Hospital Charité, Germany. 1999 - 2000

References

  1. Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12. Sander, T., Windemuth, C., Schulz, H., Saar, K., Gennaro, E., Riggio, C., Bianchi, A., Zara, F., Rudolf, G., Picard, F., Bulteau, C., Kaminska, A., Cieuta, C., Prud'homme, J.F., Dulac, O., Bate, L., Robinson, R., Gardiner, R.M., Covanis, A., de Haan, G.J., Janssen, G.A., van Erp, M.G., Boezeman, E.H., Lindhout, D., Heils, A., Nürnberg, P., Janz, D. Epilepsia (2003) [Pubmed]
  2. Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy. Sander, T., Toliat, M.R., Heils, A., Becker, C., Nürnberg, P. Epilepsy Res. (2002) [Pubmed]
  3. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1. Sander, T., Windemuth, C., Schulz, H., Saar, K., Gennaro, E., Bianchi, A., Zara, F., Bulteau, C., Kaminska, A., Ville, D., Cieuta, C., Prud'homme, J.F., Dulac, O., Bate, L., Gardiner, R.M., de Haan, G.J., Janssen, G.A., Witte, J., Halley, D.J., Lindhout, D., Wienker, T.F., Janz, D. Am. J. Med. Genet. (2002) [Pubmed]
  4. Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy. Sander, T., Berlin, W., Gscheidel, N., Wendel, B., Janz, D., Hoehe, M.R. Epilepsy Res. (2000) [Pubmed]
  5. Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy. Sander, T., Berlin, W., Ostapowicz, A., Samochowiec, J., Gscheidel, N., Hoehe, M.R. Epilepsy Res. (2000) [Pubmed]
  6. Genetic variation of the glutamate transporter EAAT2 gene and vulnerability to alcohol dependence. Sander, T., Ostapowicz, A., Samochowiec, J., Smolka, M., Winterer, G., Schmidt, L.G. Psychiatr. Genet. (2000) [Pubmed]
  7. Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy. Sander, T., Schölz, L., Janz, D., Epplen, J.T., Riess, O. Epilepsy Res. (1999) [Pubmed]
  8. Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14. Sander, T., Schulz, H., Vieira-Saeker, A.M., Bianchi, A., Sailer, U., Bauer, G., Scaramelli, A., Wienker, T.F., Saar, K., Reis, A., Janz, D., Epplen, J.T., Riess, O. Am. J. Med. Genet. (1999) [Pubmed]
  9. Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy. Sander, T., Peters, C., Kämmer, G., Samochowiec, J., Zirra, M., Mischke, D., Ziegler, A., Kaupmann, K., Bettler, B., Epplen, J.T., Riess, O. Am. J. Med. Genet. (1999) [Pubmed]
  10. Association analysis of exonic variants of the gene encoding the GABAB receptor and alcohol dependence. Sander, T., Samochowiec, J., Ladehoff, M., Smolka, M., Peters, C., Riess, O., Rommelspacher, H., Schmidt, L.G. Psychiatr. Genet. (1999) [Pubmed]
  11. Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy. Sander, T., Syagailo, Y., Samochowiec, J., Okladnova, O., Lesch, K.P., Janz, D. Epilepsy Res. (1999) [Pubmed]
 
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