Bonin M - Search Results

1

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes.

Dufke C, Schlipf N, Schüle R, Bonin M, Auer-Grumbach M, Stevanin G, Depienne C, Kassubek J, Klebe S, Klimpe S, Klopstock T, Otto S, Poths S, Seibel A, Stolze H, Gal A, Schöls L, Bauer P. Dufke C, et al. Among authors: bonin m. Neurogenetics. 2012 Aug;13(3):215-27. doi: 10.1007/s10048-012-0329-6. Epub 2012 May 3. Neurogenetics. 2012. PMID: 22552817

2

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.

Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L. Schüle R, et al. Among authors: bonin m. Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8. Neurology. 2009. PMID: 19357379

3

Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.

Bauer P, Winner B, Schüle R, Bauer C, Häfele V, Hehr U, Bonin M, Walter M, Karle K, Ringer TM, Riess O, Winkler J, Schöls L. Bauer P, et al. Among authors: bonin m. Neurogenetics. 2009 Feb;10(1):43-8. doi: 10.1007/s10048-008-0144-2. Epub 2008 Sep 12. Neurogenetics. 2009. PMID: 18787847

4

Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.

Hehr U, Bauer P, Winner B, Schule R, Olmez A, Koehler W, Uyanik G, Engel A, Lenz D, Seibel A, Hehr A, Ploetz S, Gamez J, Rolfs A, Weis J, Ringer TM, Bonin M, Schuierer G, Marienhagen J, Bogdahn U, Weber BH, Topaloglu H, Schols L, Riess O, Winkler J. Hehr U, et al. Among authors: bonin m. Ann Neurol. 2007 Dec;62(6):656-65. doi: 10.1002/ana.21310. Ann Neurol. 2007. PMID: 18067136

5

RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player.

Häbig K, Walter M, Poths S, Riess O, Bonin M. Häbig K, et al. Among authors: bonin m. Neurogenetics. 2008 May;9(2):83-94. doi: 10.1007/s10048-007-0114-0. Epub 2007 Dec 21. Neurogenetics. 2008. PMID: 18097693

6

Utilization of AFFX spike-in control probes to monitor sample identity throughout Affymetrix GeneChip Array processing.

Walter M, Honegger A, Schweizer R, Poths S, Bonin M. Walter M, et al. Among authors: bonin m. Biotechniques. 2010 May;48(5):371-8. doi: 10.2144/000113421. Biotechniques. 2010. PMID: 20569210 Free article.

7

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein.

Kuhn M, Haebig K, Bonin M, Ninkina N, Buchman VL, Poths S, Riess O. Kuhn M, et al. Among authors: bonin m. Neurogenetics. 2007 Apr;8(2):71-81. doi: 10.1007/s10048-007-0079-z. Epub 2007 Feb 22. Neurogenetics. 2007. PMID: 17318638 Free PMC article.

8

High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.

Schroeder C, Walter M, Berg D, Leitner P, Bauer P, Kohl Z, Winkler J, Riess O, Bonin M. Schroeder C, et al. Among authors: bonin m. J Mol Diagn. 2008 May;10(3):217-24. doi: 10.2353/jmoldx.2008.070100. Epub 2008 Apr 10. J Mol Diagn. 2008. PMID: 18403612 Free PMC article.

9

Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features.

Synofzik M, Beetz C, Bauer C, Bonin M, Sanchez-Ferrero E, Schmitz-Hübsch T, Wüllner U, Nägele T, Riess O, Schöls L, Bauer P. Synofzik M, et al. Among authors: bonin m. J Med Genet. 2011 Jun;48(6):407-12. doi: 10.1136/jmg.2010.087023. Epub 2011 Mar 1. J Med Genet. 2011. PMID: 21367767

10

UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays.

Schroeder C, Sturm M, Dufke A, Mau-Holzmann U, Eggermann T, Poths S, Riess O, Bonin M. Schroeder C, et al. Among authors: bonin m. Bioinformatics. 2013 Jun 15;29(12):1562-4. doi: 10.1093/bioinformatics/btt174. Epub 2013 Apr 14. Bioinformatics. 2013. PMID: 23589652

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