Update on the management of restless legs syndrome: existing and emerging treatment options

Por Facheris, Maurizio F, Hicks, Andrew A, Pramstaller, Peter P, Pichler, Irene
Publicado em 2010

Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes

Por Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole
Publicado em 2010

Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes

Por Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole
Publicado em 2010

Mutations in PINK1 and Parkin Impair Ubiquitination of Mitofusins in Human Fibroblasts

Por Rakovic, Aleksandar, Grünewald, Anne, Kottwitz, Jan, Brüggemann, Norbert, Pramstaller, Peter P., Lohmann, Katja, Klein, Christine
Publicado em 2011

Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate

Por Pichler, Irene, Marroni, Fabio, Beu Volpato, Claudia, Gusella, James F., Klein, Christine, Casari, Giorgio, De Grandi, Alessandro, Pramstaller, Peter P.
Publicado em 2006

Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson’s disease blood samples

Por Serafin, Alice, Foco, Luisa, Blankenburg, Hagen, Picard, Anne, Zanigni, Stefano, Zanon, Alessandra, Pramstaller, Peter P, Hicks, Andrew A, Schwienbacher, Christine
Publicado em 2014

Mode of Inheritance and Susceptibility Locus for Restless Legs Syndrome, on Chromosome 12q

Por Kock, Norman, Culjkovic, Biljana, Maniak, Susanna, Schilling, Karla, Müller, Birgitt, Zühlke, Christine, Ozelius, Laurie, Klein, Christine, Pramstaller, Peter P., Kramer, Patricia L.
Publicado em 2002

Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids

Por Meraviglia, Viviana, Zanon, Alessandra, Lavdas, Alexandros A., Schwienbacher, Christine, Silipigni, Rosamaria, Di Segni, Marina, Chen, Huei-Sheng Vincent, Pramstaller, Peter P., Hicks, Andrew A., Rossini, Alessandra
Publicado no J Vis Exp (2015)

Copy Number Variation across European Populations

Por Chen, Wanting, Hayward, Caroline, Wright, Alan F., Hicks, Andrew A., Vitart, Veronique, Knott, Sara, Wild, Sarah H., Pramstaller, Peter P., Wilson, James F., Rudan, Igor, Porteous, David J.
Publicado em 2011

Mutant Parkin Impairs Mitochondrial Function and Morphology in Human Fibroblasts

Por Grünewald, Anne, Voges, Lisa, Rakovic, Aleksandar, Kasten, Meike, Vandebona, Himesha, Hemmelmann, Claudia, Lohmann, Katja, Orolicki, Slobodanka, Ramirez, Alfredo, Schapira, Anthony H. V., Pramstaller, Peter P., Sue, Carolyn M., Klein, Christine
Publicado em 2010

Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia

Por Müller, Birgitt, Hedrich, Katja, Kock, Norman, Dragasevic, Natasa, Svetel, Marina, Garrels, Jennifer, Landt, Olfert, Nitschke, Matthias, Pramstaller, Peter P., Reik, Wolf, Schwinger, Eberhard, Sperner, Jürgen, Ozelius, Laurie, Kostic, Vladimir, Klein, Christine
Publicado em 2002

Profiling of Parkin-Binding Partners Using Tandem Affinity Purification

Por Zanon, Alessandra, Rakovic, Aleksandar, Blankenburg, Hagen, Doncheva, Nadezhda T., Schwienbacher, Christine, Serafin, Alice, Alexa, Adrian, Weichenberger, Christian X., Albrecht, Mario, Klein, Christine, Hicks, Andrew A., Pramstaller, Peter P., Domingues, Francisco S., Pichler, Irene
Publicado em 2013

Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease

Por Ramos, Eliana Marisa, Gillis, Tammy, Mysore, Jayalakshmi S., Lee, Jong‐Min, Gögele, Martin, D'Elia, Yuri, Pichler, Irene, Sequeiros, Jorge, Pramstaller, Peter P., Gusella, James F., MacDonald, Marcy E., Alonso, Isabel
Publicado no Am J Med Genet B Neuropsychiatr Genet (2015)

Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping

Por Nagamine, Yoshitaka, Pong-Wong, Ricardo, Navarro, Pau, Vitart, Veronique, Hayward, Caroline, Rudan, Igor, Campbell, Harry, Wilson, James, Wild, Sarah, Hicks, Andrew A., Pramstaller, Peter P., Hastie, Nicholas, Wright, Alan F., Haley, Chris S.
Publicado em 2012

Heterogeneous susceptibility for uraemic media calcification and concomitant inflammation within the arterial tree

Por Kirsch, Alexander H., Kirsch, Andrijana, Artinger, Katharina, Schabhüttl, Corinna, Goessler, Walter, Klymiuk, Ingeborg, Gülly, Christian, Fritz, Gerald A., Frank, Saša, Wimmer, Roxana, Brodmann, Marianne, Anders, Hans-Joachim, Pramstaller, Peter P., Rosenkranz, Alexander R., Eller, Kathrin, Eller, Philipp
Publicado no Nephrol Dial Transplant (2015)

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13

Por Kemlink, David, Plazzi, Giuseppe, Vetrugno, Roberto, Provini, Federica, Polo, Olli, Stiasny-Kolster, Karin, Oertel, Wolfgang, Nevsimalova, Sona, Sonka, Karel, Högl, Birgit, Frauscher, Birgit, Hadjigeorgiou, Georgios M., Pramstaller, Peter P., Lichtner, Peter, Meitinger, Thomas, Müller-Myshok, Bertram, Winkelmann, Juliane, Montagna, Pasquale
Publicado em 2008

Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster

Por Del Greco M., Fabiola, Pattaro, Cristian, Luchner, Andreas, Pichler, Irene, Winkler, Thomas, Hicks, Andrew A., Fuchsberger, Christian, Franke, Andre, Melville, Scott A., Peters, Annette, Wichmann, H. Erich, Schreiber, Stefan, Heid, Iris M., Krawczak, Michael, Minelli, Cosetta, Wiedermann, Christian J., Pramstaller, Peter P.
Publicado em 2011

Acetylation mediates Cx43 reduction caused by electrical stimulation

Por Meraviglia, Viviana, Azzimato, Valerio, Colussi, Claudia, Florio, Maria Cristina, Binda, Anna, Panariti, Alice, Qanud, Khaled, Suffredini, Silvia, Gennaccaro, Laura, Miragoli, Michele, Barbuti, Andrea, Lampe, Paul D., Gaetano, Carlo, Pramstaller, Peter P., Capogrossi, Maurizio C., Recchia, Fabio A., Pompilio, Giulio, Rivolta, Ilaria, Rossini, Alessandra
Publicado no J Mol Cell Cardiol (2015)

Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates

Por Wei, Wenhua, Hemani, Gibran, Hicks, Andrew A., Vitart, Veronique, Cabrera-Cardenas, Claudia, Navarro, Pau, Huffman, Jennifer, Hayward, Caroline, Knott, Sara A., Rudan, Igor, Pramstaller, Peter P., Wild, Sarah H., Wilson, James F., Campbell, Harry, Dunlop, Malcolm G., Hastie, Nicholas, Wright, Alan F., Haley, Chris S.
Publicado em 2011

Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

Por Pichler, Irene, Del Greco M., Fabiola, Gögele, Martin, Lill, Christina M., Bertram, Lars, Do, Chuong B., Eriksson, Nicholas, Foroud, Tatiana, Myers, Richard H., Nalls, Michael, Keller, Margaux F., Benyamin, Beben, Whitfield, John B., Pramstaller, Peter P., Hicks, Andrew A., Thompson, John R., Minelli, Cosetta
Publicado em 2013