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

nork Dekomien Gabriele, Epplen Joerg T
Argitaratua 2003-07-01

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

nork Dekomien, Gabriele, Epplen, Joerg T
Argitaratua 2003

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

nork Schlang, Katharina J, Arning, Larissa, Epplen, Joerg T, Stemmler, Susanne
Argitaratua 2008

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

nork Miterski, Bianca, Sindern, Eckhart, Haupts, Michael, Schimrigk, Sebastian, Epplen, Joerg T
Argitaratua 2002

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

nork Szyld, Paweł, Jagiello, Peter, Csernok, Elena, Gross, Wolfgang L, Epplen, Joerg T
Argitaratua 2006

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

nork Schmoll, Tim, Schurr, Frank M., Winkel, Wolfgang, Epplen, Joerg T., Lubjuhn, Thomas
Argitaratua 2008

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

nork Stemmler, Susanne, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Epplen, Joerg T, Hoffjan, Sabine
Argitaratua izan da BMC Dermatol (2014)

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

nork Bernhardt, Christiane, Schwan, Anne-Marie, Kraus, Peter, Epplen, Joerg Thomas, Kunstmann, Erdmute
Argitaratua 2009

Association study with Wegener granulomatosis of the human phospholipase Cγ2 gene

nork Jagiello, Peter, Wieczorek, Stefan, Yu, Philipp, Csernok, Elena, Gross, Wolfgang L, Epplen, Joerg T
Argitaratua 2005

Association of toll-interacting protein gene polymorphisms with atopic dermatitis

nork Schimming, Tobias T, Parwez, Qumar, Petrasch-Parwez, Elisabeth, Nothnagel, Michael, Epplen, Joerg T, Hoffjan, Sabine
Argitaratua 2007

HNPCC: Six new pathogenic mutations

nork Kunstmann, Erdmute, Vieland, Judith, Brasch, Frank E, Hahn, Stephan A, Epplen, Joerg T, Schulmann, Karsten, Schmiegel, Wolff
Argitaratua 2004

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

nork Schlitter, Anna Melissa, Kurz, Martin, Larsen, Jan P, Woitalla, Dirk, Mueller, Thomas, Epplen, Joerg T, Dekomien, Gabriele
Argitaratua 2005

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

nork Hoffjan, Sabine, Waldmüller, Stephan, Blankenfeldt, Wulf, Kötting, Judith, Gehle, Petra, Binner, Priska, Epplen, Joerg T, Scheffold, Thomas
Argitaratua 2011

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

nork Dusanic, Maja, Dekomien, Gabriele, Lücke, Thomas, Vorgerd, Matthias, Weis, Joachim, Epplen, Joerg T., Köhler, Cornelia, Hoffjan, Sabine
Argitaratua izan da Mol Syndromol (2018)

mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis

nork 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.
Argitaratua 2008

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

nork 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
Argitaratua izan da G3 (Bethesda) (2016)

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

nork 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
Argitaratua 2013