Gerding WM - Search Results

1

Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.

Kropatsch R, Petrasch-Parwez E, Seelow D, Schlichting A, Gerding WM, Akkad DA, Epplen JT, Dekomien G. Kropatsch R, et al. Among authors: gerding wm. Mol Cell Probes. 2010 Dec;24(6):357-63. doi: 10.1016/j.mcp.2010.07.007. Epub 2010 Aug 4. Mol Cell Probes. 2010. PMID: 20691256

2

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.

Dekomien G, Vollrath C, Petrasch-Parwez E, Boevé MH, Akkad DA, Gerding WM, Epplen JT. Dekomien G, et al. Among authors: gerding wm. Neurogenetics. 2010 May;11(2):163-74. doi: 10.1007/s10048-009-0223-z. Epub 2009 Sep 24. Neurogenetics. 2010. PMID: 19777273

3

Tracing the origin of 'blue Weimaraner' dogs by molecular genetics.

Gerding WM, Schreiber S, Dekomien G, Epplen JT. Gerding WM, et al. J Anim Breed Genet. 2011 Apr;128(2):153-60. doi: 10.1111/j.1439-0388.2010.00888.x. Epub 2010 Sep 22. J Anim Breed Genet. 2011. PMID: 21385230

4

Ccdc66 null mutation causes retinal degeneration and dysfunction.

Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, Rülicke T, Ibrahim S, Epplen JT, Petrasch-Parwez E. Gerding WM, et al. Hum Mol Genet. 2011 Sep 15;20(18):3620-31. doi: 10.1093/hmg/ddr282. Epub 2011 Jun 16. Hum Mol Genet. 2011. PMID: 21680557

5

Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position.

Gerding WM, Koetting J, Rey LP, Bibas Bonet H, Abdala ME, Mazzeo A, Mostacciuolo ML, Arning L, Carrero-Valenzuela R. Gerding WM, et al. Mol Cell Probes. 2013 Jun-Aug;27(3-4):118-21. doi: 10.1016/j.mcp.2013.01.002. Epub 2013 Feb 4. Mol Cell Probes. 2013. PMID: 23384994

6

Spotted Weimaraner dog due to de novo KIT mutation.

Gerding WM, Akkad DA, Epplen JT. Gerding WM, et al. Anim Genet. 2013 Aug;44(5):605-6. doi: 10.1111/age.12056. Epub 2013 May 9. Anim Genet. 2013. PMID: 23659249 No abstract available.

7

SOX9 duplication linked to intersex in deer.

Kropatsch R, Dekomien G, Akkad DA, Gerding WM, Petrasch-Parwez E, Young ND, Altmüller J, Nürnberg P, Gasser RB, Epplen JT. Kropatsch R, et al. Among authors: gerding wm. PLoS One. 2013 Sep 6;8(9):e73734. doi: 10.1371/journal.pone.0073734. eCollection 2013. PLoS One. 2013. PMID: 24040047 Free PMC article.

8

Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs.

Akkad DA, Gerding WM, Gasser RB, Epplen JT. Akkad DA, et al. Among authors: gerding wm. Canine Genet Epidemiol. 2015 Apr 18;2:5. doi: 10.1186/s40575-015-0018-5. eCollection 2015. Canine Genet Epidemiol. 2015. PMID: 26401333 Free PMC article.

9

Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults.

Ocklenburg S, Arning L, Gerding WM, Hengstler JG, Epplen JT, Güntürkün O, Beste C, Akkad DA. Ocklenburg S, et al. Among authors: gerding wm. Mol Neurobiol. 2016 Nov;53(9):6355-6361. doi: 10.1007/s12035-015-9534-2. Epub 2015 Nov 16. Mol Neurobiol. 2016. PMID: 26572639

10

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

Kastner S, Thiemann IJ, Dekomien G, Petrasch-Parwez E, Schreiber S, Akkad DA, Gerding WM, Hoffjan S, Günes S, Günes S, Bagci H, Epplen JT. Kastner S, et al. Among authors: gerding wm. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8045-53. doi: 10.1167/iovs.15-17473. Invest Ophthalmol Vis Sci. 2015. PMID: 26720455

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