Andrich J - Search Results

1

No association between polymorphisms in the BDNF gene and age at onset in Huntington disease.

Mai M, Akkad AD, Wieczorek S, Saft C, Andrich J, Kraus PH, Epplen JT, Arning L. Mai M, et al. Among authors: andrich j. BMC Med Genet. 2006 Nov 10;7:79. doi: 10.1186/1471-2350-7-79. BMC Med Genet. 2006. PMID: 17096834 Free PMC article.

2

Glutathione S-Transferase Omega 1 variation does not influence age at onset of Huntington's disease.

Arning L, Jagiello P, Wieczorek S, Saft C, Andrich J, Epplen JT. Arning L, et al. Among authors: andrich j. BMC Med Genet. 2004 Mar 24;5:7. doi: 10.1186/1471-2350-5-7. BMC Med Genet. 2004. PMID: 15040808 Free PMC article.

3

NR2A and NR2B receptor gene variations modify age at onset in Huntington disease.

Arning L, Kraus PH, Valentin S, Saft C, Andrich J, Epplen JT. Arning L, et al. Among authors: andrich j. Neurogenetics. 2005 Feb;6(1):25-8. doi: 10.1007/s10048-004-0198-8. Epub 2004 Nov 17. Neurogenetics. 2005. PMID: 15742215

4

Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD).

Arning L, Kraus PH, Saft C, Andrich J, Epplen JT. Arning L, et al. Among authors: andrich j. BMC Med Genet. 2005 Oct 3;6:35. doi: 10.1186/1471-2350-6-35. BMC Med Genet. 2005. PMID: 16202123 Free PMC article.

5

Failure to confirm influence of methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease.

Hansen W, Saft C, Andrich J, Müller T, Wieczorek S, Epplen JT, Arning L. Hansen W, et al. Among authors: andrich j. J Negat Results Biomed. 2005 Dec 22;4:12. doi: 10.1186/1477-5751-4-12. J Negat Results Biomed. 2005. PMID: 16372906 Free PMC article.

6

NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.

Arning L, Saft C, Wieczorek S, Andrich J, Kraus PH, Epplen JT. Arning L, et al. Among authors: andrich j. Hum Genet. 2007 Sep;122(2):175-82. doi: 10.1007/s00439-007-0393-4. Epub 2007 Jun 14. Hum Genet. 2007. PMID: 17569088

7

Huntington's disease as caused by 34 CAG repeats.

Andrich J, Arning L, Wieczorek S, Kraus PH, Gold R, Saft C. Andrich J, et al. Mov Disord. 2008 Apr 30;23(6):879-81. doi: 10.1002/mds.21958. Mov Disord. 2008. PMID: 18307262

8

ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease.

Arning L, Monté D, Hansen W, Wieczorek S, Jagiello P, Akkad DA, Andrich J, Kraus PH, Saft C, Epplen JT. Arning L, et al. Among authors: andrich j. J Mol Med (Berl). 2008 Apr;86(4):485-90. doi: 10.1007/s00109-007-0299-6. Epub 2008 Mar 8. J Mol Med (Berl). 2008. PMID: 18327563

9

PGC-1alpha as modifier of onset age in Huntington disease.

Taherzadeh-Fard E, Saft C, Andrich J, Wieczorek S, Arning L. Taherzadeh-Fard E, et al. Among authors: andrich j. Mol Neurodegener. 2009 Feb 6;4:10. doi: 10.1186/1750-1326-4-10. Mol Neurodegener. 2009. PMID: 19200361 Free PMC article.

10

Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease.

Arning L, Haghikia A, Taherzadeh-Fard E, Saft C, Andrich J, Pula B, Höxtermann S, Wieczorek S, Akkad DA, Perrech M, Gold R, Epplen JT, Chan A. Arning L, et al. Among authors: andrich j. J Mol Med (Berl). 2010 Apr;88(4):431-6. doi: 10.1007/s00109-010-0589-2. Epub 2010 Jan 29. J Mol Med (Berl). 2010. PMID: 20108082

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