SLP-2: a potential new target for improving mitochondrial function in Parkinson's disease

Por Zanon, Alessandra, Hicks, Andrew A., Pramstaller, Peter P., Pichler, Irene
Publicado no Neural Regen Res (2017)

Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease Penetrance

Por Zanon, Alessandra, Pramstaller, Peter P., Hicks, Andrew A., Pichler, Irene
Publicado no Parkinsons Dis (2018)

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

Genotyping human ancient mtDNA control and coding region polymorphisms with a multiplexed Single-Base-Extension assay: the singular maternal history of the Tyrolean Iceman

Por Endicott, Phillip, Sanchez, Juan J, Pichler, Irene, Brotherton, Paul, Brooks, Jerome, Egarter-Vigl, Eduard, Cooper, Alan, Pramstaller, Peter
Publicado em 2009

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

Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells

Por Guida, Marianna, Zanon, Alessandra, Montibeller, Luigi, Lavdas, Alexandros A., Ladurner, Judith, Pischedda, Francesca, Rakovic, Aleksandar, Domingues, Francisco S., Piccoli, Giovanni, Klein, Christine, Pramstaller, Peter P., Hicks, Andrew A., Pichler, Irene
Publicado no Int J Mol Sci (2019)

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)

Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations

Por Mueller, Jakob C., Lõhmussaar, Elin, Mägi, Reedik, Remm, Maido, Bettecken, Thomas, Lichtner, Peter, Biskup, Saskia, Illig, Thomas, Pfeufer, Arne, Luedemann, Jan, Schreiber, Stefan, Pramstaller, Peter, Pichler, Irene, Romeo, Giovanni, Gaddi, Anthony, Testa, Alessandra, Wichmann, Heinz-Erich, Metspalu, Andres, Meitinger, Thomas
Publicado em 2005

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

SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and Drosophila

Por Zanon, Alessandra, Kalvakuri, Sreehari, Rakovic, Aleksandar, Foco, Luisa, Guida, Marianna, Schwienbacher, Christine, Serafin, Alice, Rudolph, Franziska, Trilck, Michaela, Grünewald, Anne, Stanslowsky, Nancy, Wegner, Florian, Giorgio, Valentina, Lavdas, Alexandros A., Bodmer, Rolf, Pramstaller, Peter P., Klein, Christine, Hicks, Andrew A., Pichler, Irene, Seibler, Philip
Publicado no Hum Mol Genet (2017)

Corrigendum: SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and Drosophila

Por Zanon, Alessandra, Kalvakuri, Sreehari, Rakovic, Aleksandar, Foco, Luisa, Guida, Marianna, Schwienbacher, Christine, Serafin, Alice, Rudolph, Franziska, Trilck, Michaela, Grünewald, Anne, Stanslowsky, Nancy, Wegner, Florian, Giorgio, Valentina, Lavdas, Alexandros A, Bodmer, Rolf, Pramstaller, Peter P, Klein, Christine, Hicks, Andrew A, Pichler, Irene, Philip, Seibler
Publicado no Hum Mol Genet (2019)

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

Correction: 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

The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1

Por Perez Carrion, Maria, Pischedda, Francesca, Biosa, Alice, Russo, Isabella, Straniero, Letizia, Civiero, Laura, Guida, Marianna, Gloeckner, Christian J., Ticozzi, Nicola, Tiloca, Cinzia, Mariani, Claudio, Pezzoli, Gianni, Duga, Stefano, Pichler, Irene, Pan, Lifeng, Landers, John E., Greggio, Elisa, Hess, Michael W., Goldwurm, Stefano, Piccoli, Giovanni
Publicado no Front Mol Neurosci (2018)

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives

Por Pattaro, Cristian, Marroni, Fabio, Riegler, Alice, Mascalzoni, Deborah, Pichler, Irene, Volpato, Claudia B, Dal Cero, Umberta, De Grandi, Alessandro, Egger, Clemens, Eisendle, Agatha, Fuchsberger, Christian, Gögele, Martin, Pedrotti, Sara, Pinggera, Gerd K, Stefanov, Stefan A, Vogl, Florian D, Wiedermann, Christian J, Meitinger, Thomas, Pramstaller, Peter P
Publicado em 2007

A genome-wide association scan of RR and QT interval duration in three European genetically isolated populations. The EUROSPAN project

Por Marroni, Fabio, Pfeufer, Arne, Aulchenko, Yurii S, Franklin, Christopher S, Isaacs, Aaron, Pichler, Irene, Wild, Sarah H, Oostra, Ben A, Wright, Alan F, Campbell, Harry, Witteman, Jacqueline C, Kääb, Stefan, Hicks, Andrew A, Gyllensten, Ulf, Rudan, Igor, Meitinger, Thomas, Pattaro, Cristian, van Duijn, Cornelia M, Wilson, James F, Pramstaller, Peter P
Publicado em 2009

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

Por Oexle, Konrad, Ried, Janina S., Hicks, Andrew A., Tanaka, Toshiko, Hayward, Caroline, Bruegel, Mathias, Gögele, Martin, Lichtner, Peter, Müller-Myhsok, Bertram, Döring, Angela, Illig, Thomas, Schwienbacher, Christine, Minelli, Cosetta, Pichler, Irene, Fiedler, G. Martin, Thiery, Joachim, Rudan, Igor, Wright, Alan F., Campbell, Harry, Ferrucci, Luigi, Bandinelli, Stefania, Pramstaller, Peter P., Wichmann, H.-Erich, Gieger, Christian, Winkelmann, Juliane, Meitinger, Thomas
Publicado em 2011