S Niemann

Summary

Publications

  1. ncbi 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. ncbi 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 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 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 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. ncbi 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 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 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 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. ncbi 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 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 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 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. ncbi 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 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 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...