Analysis of <it>PDE6D </it>and <it>PDE6G </it>genes for generalised progressive retinal atrophy (gPRA) mutations in dogs

מאת Dekomien Gabriele, Epplen Joerg T
יצא לאור 2003-07-01

Analysis of PDE6D and PDE6G genes for generalised progressive retinal atrophy (gPRA) mutations in dogs

מאת Dekomien, Gabriele, Epplen, Joerg T
יצא לאור 2003

Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)

מאת Schlang, Katharina J, Arning, Larissa, Epplen, Joerg T, Stemmler, Susanne
יצא לאור 2008

PTPRC (CD45) is not associated with multiple sclerosis in a large cohort of German patients

מאת Miterski, Bianca, Sindern, Eckhart, Haupts, Michael, Schimrigk, Sebastian, Epplen, Joerg T
יצא לאור 2002

On the Wegener granulomatosis associated region on chromosome 6p21.3

מאת Szyld, Paweł, Jagiello, Peter, Csernok, Elena, Gross, Wolfgang L, Epplen, Joerg T
יצא לאור 2006

Lifespan, lifetime reproductive performance and paternity loss of within-pair and extra-pair offspring in the coal tit Periparus ater

מאת Schmoll, Tim, Schurr, Frank M., Winkel, Wolfgang, Epplen, Joerg T., Lubjuhn, Thomas
יצא לאור 2008

Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case–control cohort

מאת Stemmler, Susanne, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Epplen, Joerg T, Hoffjan, Sabine
הוצא לאור ב BMC Dermatol (2014)

Decreasing uptake of predictive testing for Huntington's disease in a German centre: 12 years' experience (1993–2004)

מאת Bernhardt, Christiane, Schwan, Anne-Marie, Kraus, Peter, Epplen, Joerg Thomas, Kunstmann, Erdmute
יצא לאור 2009

Association study with Wegener granulomatosis of the human phospholipase Cγ2 gene

מאת Jagiello, Peter, Wieczorek, Stefan, Yu, Philipp, Csernok, Elena, Gross, Wolfgang L, Epplen, Joerg T
יצא לאור 2005

Association of toll-interacting protein gene polymorphisms with atopic dermatitis

מאת Schimming, Tobias T, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Nothnagel, Michael, Epplen, Joerg T, Hoffjan, Sabine
יצא לאור 2007

HNPCC: Six new pathogenic mutations

מאת Kunstmann, Erdmute, Vieland, Judith, Brasch, Frank E, Hahn, Stephan A, Epplen, Joerg T, Schulmann, Karsten, Schmiegel, Wolff
יצא לאור 2004

Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations

מאת Schlitter, Anna Melissa, Kurz, Martin, Larsen, Jan P, Woitalla, Dirk, Mueller, Thomas, Epplen, Joerg T, Dekomien, Gabriele
יצא לאור 2005

Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections

מאת Hoffjan, Sabine, Waldmüller, Stephan, Blankenfeldt, Wulf, Kötting, Judith, Gehle, Petra, Binner, Priska, Epplen, Joerg T, Scheffold, Thomas
יצא לאור 2011

Novel Nonsense Mutation in SLC39A13 Initially Presenting as Myopathy: Case Report and Review of the Literature

מאת Dusanic, Maja, Dekomien, Gabriele, Lücke, Thomas, Vorgerd, Matthias, Weis, Joachim, Epplen, Joerg T., Köhler, Cornelia, Hoffjan, Sabine
הוצא לאור ב Mol Syndromol (2018)

mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis

מאת Yu, Xinhua, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A., Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I., Mørk, Sverre J., Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G., Myhr, Kjell-Morten, Epplen, Joerg T., Saarela, Janna, Ibrahim, Saleh M.
יצא לאור 2008

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

מאת Sadovnick, A. Dessa, Traboulsee, Anthony L., Bernales, Cecily Q., Ross, Jay P., Forwell, Amanda L., Yee, Irene M., Guillot-Noel, Lena, Fontaine, Bertrand, Cournu-Rebeix, Isabelle, Alcina, Antonio, Fedetz, Maria, Izquierdo, Guillermo, Matesanz, Fuencisla, Hilven, Kelly, Dubois, Bénédicte, Goris, An, Astobiza, Ianire, Alloza, Iraide, Antigüedad, Alfredo, Vandenbroeck, Koen, Akkad, Denis A., Aktas, Orhan, Blaschke, Paul, Buttmann, Mathias, Chan, Andrew, Epplen, Joerg T., Gerdes, Lisa-Ann, Kroner, Antje, Kubisch, Christian, Kümpfel, Tania, Lohse, Peter, Rieckmann, Peter, Zettl, Uwe K., Zipp, Frauke, Bertram, Lars, Lill, Christina M, Fernandez, Oscar, Urbaneja, Patricia, Leyva, Laura, Alvarez-Cermeño, Jose Carlos, Arroyo, Rafael, Garagorri, Aroa M., García-Martínez, Angel, Villar, Luisa M., Urcelay, Elena, Malhotra, Sunny, Montalban, Xavier, Comabella, Manuel, Berger, Thomas, Fazekas, Franz, Reindl, Markus, Schmied, Mascha C., Zimprich, Alexander, Vilariño-Güell, Carles
הוצא לאור ב G3 (Bethesda) (2016)

MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

מאת Lill, Christina M., Schjeide, Brit-Maren M., Graetz, Christiane, Ban, Maria, Alcina, Antonio, Ortiz, Miguel A., Pérez, Jennifer, Damotte, Vincent, Booth, David, Lopez de Lapuente, Aitzkoa, Broer, Linda, Schilling, Marcel, Akkad, Denis A., Aktas, Orhan, Alloza, Iraide, Antigüedad, Alfredo, Arroyo, Rafa, Blaschke, Paul, Buttmann, Mathias, Chan, Andrew, Compston, Alastair, Cournu-Rebeix, Isabelle, Dörner, Thomas, Epplen, Joerg T., Fernández, Óscar, Gerdes, Lisa-Ann, Guillot-Noël, Léna, Hartung, Hans-Peter, Hoffjan, Sabine, Izquierdo, Guillermo, Kemppinen, Anu, Kroner, Antje, Kubisch, Christian, Kümpfel, Tania, Li, Shu-Chen, Lindenberger, Ulman, Lohse, Peter, Lubetzki, Catherine, Luessi, Felix, Malhotra, Sunny, Mescheriakova, Julia, Montalban, Xavier, Papeix, Caroline, Paredes, Lidia F., Rieckmann, Peter, Steinhagen-Thiessen, Elisabeth, Winkelmann, Alexander, Zettl, Uwe K., Hintzen, Rogier, Vandenbroeck, Koen, Stewart, Graeme, Fontaine, Bertrand, Comabella, Manuel, Urcelay, Elena, Matesanz, Fuencisla, Sawcer, Stephen, Bertram, Lars, Zipp, Frauke
יצא לאור 2013