Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy

Por Dekomien, Gabriele, Epplen, Jörg Thomas
Publicado em 2002

Clinical utility gene card for: Huntington's disease

Por Saft, Carsten, Leavitt, Blair R, Epplen, Jörg T
Publicado em 2014

Variation in genes encoding eosinophil granule proteins in atopic dermatitis patients from Germany

Por Parwez, Qumar, Stemmler, Susanne, Epplen, Jörg T, Hoffjan, Sabine
Publicado em 2008

Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis

Por Wieczorek, Stefan, Knaup, Silvia, Gross, Wolfgang L., Epplen, Jörg T.
Publicado em 2009

MAN1B1 Mutation Leads to a Recognizable Phenotype: A Case Report and Future Prospects

Por Hoffjan, Sabine, Epplen, Jörg T., Reis, André, Abou Jamra, Rami
Publicado no Mol Syndromol (2015)

Long-term fitness consequences of female extra-pair matings in a socially monogamous passerine.

Por Schmoll, Tim, Dietrich, Verena, Winkel, Wolfgang, Epplen, Jörg T, Lubjuhn, Thomas
Publicado em 2003

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)

Por Arning, Larissa, Kraus, Peter H, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado em 2005

Genomic NGFB variation and multiple sclerosis in a case control study

Por Akkad, Denis A, Kruse, Niels, Arning, Larissa, Gold, Ralf, Epplen, Jörg T
Publicado em 2008

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

Por Akkad, Denis A, Gerding, Wanda M, Gasser, Robin B, Epplen, Jörg T
Publicado no Canine Genet Epidemiol (2015)

ApoE polymorphisms in narcolepsy

Por Gencik, Martin, Dahmen, Norbert, Wieczorek, Stefan, Kasten, Meike, Gencikova, Alexandra, Epplen, Jorg T
Publicado em 2001

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

Por Arning, Larissa, Jagiello, Peter, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado em 2004

Novel KIF7 Mutation in a Tunisian Boy with Acrocallosal Syndrome: Case Report and Review of the Literature

Por Ibisler, Aysegül, Hehr, Ute, Barth, Andre, Koch, Margarete, Epplen, Jörg T., Hoffjan, Sabine
Publicado no Mol Syndromol (2015)

Genome-wide profiling of S/MAR-based replicon contact sites

Por Hagedorn, Claudia, Gogol-Döring, Andreas, Schreiber, Sabrina, Epplen, Jörg T., Lipps, Hans J.
Publicado no Nucleic Acids Res (2017)

Haplotype-defined linkage region for gPRA in Schapendoes dogs

Por Lippmann, Tanja, Jonkisz, Anna, Dobosz, Tadeusz, Petrasch-Parwez, Elisabeth, Epplen, Jörg T., Dekomien, Gabriele
Publicado em 2007

Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization

Por Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Publicado em 2013

A Novel ECM1 Splice Site Mutation in Lipoid Proteinosis: Case Report plus Review of the Literature

Por Rey, Linda K., Kohlhase, Jürgen, Möllenhoff, Katrin, Dekomien, Gabriele, Epplen, Jörg T., Hoffjan, Sabine
Publicado no Mol Syndromol (2016)

Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes

Por Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T., Arning, Larissa
Publicado no BMC Neurol (2018)

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

Por Hansen, Wiebke, Saft, Carsten, Andrich, Jürgen, Müller, Thomas, Wieczorek, Stefan, Epplen, Jörg T, Arning, Larissa
Publicado em 2005

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

Por Engelfried, Kathrin, Vorgerd, Matthias, Hagedorn, Michaela, Haas, Gerhard, Gilles, Jürgen, Epplen, Jörg T, Meins, Moritz
Publicado em 2006

Complex genetic predisposition in adult and juvenile rheumatoid arthritis

Por Oppermann Joachim, Klein Wolfram, Böschow Gundula, Drynda Susanne, Miterski Bianca, Kekow Jörn, Epplen Jörg Thomas
Publicado em 2004-02-01