S Niemann

Summary

Publications

  1. ncbi request reprint Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele
    S Niemann
    RIKEN MIT Neuroscience Research Center, The Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA
    Neurology 70:666-76. 2008
  2. pmc Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect
    S Niemann
    Institute of Human Genetics, Justus Liebig University, Giessen, Germany
    J Neurol Neurosurg Psychiatry 75:1186-8. 2004
  3. ncbi request reprint Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    S Niemann
    Institut fur Humangenetik, Justus Liebig Universitat, Giessen, Germany
    Nat Genet 26:268-70. 2000
  4. ncbi request reprint Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
    S Niemann
    , , Giessen, Germany
    Am J Med Genet 98:32-6. 2001
  5. ncbi request reprint ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in xq13.1
    D Nolte
    Institut fur Humangenetik, Justus Liebig Universitat, Giessen, Germany
    Neurogenetics 3:207-13. 2001
  6. pmc Mycobacterium africanum subtype II is associated with two distinct genotypes and is a major cause of human tuberculosis in Kampala, Uganda
    S Niemann
    National Reference Center for Mycobacteria, Research Center Borstel, Borstel, Germany
    J Clin Microbiol 40:3398-405. 2002
  7. ncbi request reprint The Beijing genotype is emerging among multidrug-resistant Mycobacterium tuberculosis strains from Germany
    T Kubica
    Forschungszentrum Borstel, National Reference Center for Mycobacteria, Borstel, Germany
    Int J Tuberc Lung Dis 8:1107-13. 2004
  8. ncbi request reprint Rifampicin and isoniazid resistance mutations in Mycobacterium tuberculosis strains isolated from patients in Kazakhstan
    D Hillemann
    National Reference Center for Mycobacteria, Forschungszentrum Borstel, Borstel, Germany
    Int J Tuberc Lung Dis 9:1161-7. 2005

Collaborators

Detail Information

Publications8

  1. ncbi request reprint Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele
    S Niemann
    RIKEN MIT Neuroscience Research Center, The Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA
    Neurology 70:666-76. 2008
    ..We tested whether genetic dysfunction of GRIN3B is implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS)...
  2. pmc Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect
    S Niemann
    Institute of Human Genetics, Justus Liebig University, Giessen, Germany
    J Neurol Neurosurg Psychiatry 75:1186-8. 2004
    ..Genotyping with markers from the SOD1 locus revealed a common haplotype and shared allelic characteristics in these patients. These findings suggest that the R115G mutation in the German population originates from a common founder...
  3. ncbi request reprint Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    S Niemann
    Institut fur Humangenetik, Justus Liebig Universitat, Giessen, Germany
    Nat Genet 26:268-70. 2000
    ..Between 10% and 50% of cases are familial and are transmitted as autosomal dominant traits with incomplete and age-dependent penetrance...
  4. ncbi request reprint Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
    S Niemann
    , , Giessen, Germany
    Am J Med Genet 98:32-6. 2001
    ..25 at 1q21-q23 (marker D1S2675); 2) haplotype analysis was most consistent for 1q21-q23 markers; and 3) the locus was excluded from more than 97% of the genome using a total of 381 highly polymorphic markers...
  5. ncbi request reprint ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in xq13.1
    D Nolte
    Institut fur Humangenetik, Justus Liebig Universitat, Giessen, Germany
    Neurogenetics 3:207-13. 2001
    ....
  6. pmc Mycobacterium africanum subtype II is associated with two distinct genotypes and is a major cause of human tuberculosis in Kampala, Uganda
    S Niemann
    National Reference Center for Mycobacteria, Research Center Borstel, Borstel, Germany
    J Clin Microbiol 40:3398-405. 2002
    ..tuberculosis complex. We conclude that M. africanum subtype II is the main cause of human tuberculosis in Kampala, Uganda...
  7. ncbi request reprint The Beijing genotype is emerging among multidrug-resistant Mycobacterium tuberculosis strains from Germany
    T Kubica
    Forschungszentrum Borstel, National Reference Center for Mycobacteria, Borstel, Germany
    Int J Tuberc Lung Dis 8:1107-13. 2004
    ..Germany, 1995 to 2001...
  8. ncbi request reprint Rifampicin and isoniazid resistance mutations in Mycobacterium tuberculosis strains isolated from patients in Kazakhstan
    D Hillemann
    National Reference Center for Mycobacteria, Forschungszentrum Borstel, Borstel, Germany
    Int J Tuberc Lung Dis 9:1161-7. 2005
    ..To analyse possible associations of specific mutations conferring rifampicin (RMP) and isoniazid (INH) resistance with Beijing and non Beijing genotype strains of Mycobacterium tuberculosis from Kazakhstan...