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

per Zanon, Alessandra, Hicks, Andrew A., Pramstaller, Peter P., Pichler, Irene
Publicat a Neural Regen Res (2017)

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

per Zanon, Alessandra, Pramstaller, Peter P., Hicks, Andrew A., Pichler, Irene
Publicat a Parkinsons Dis (2018)

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

per Facheris, Maurizio F, Hicks, Andrew A, Pramstaller, Peter P, Pichler, Irene
Publicat 2010

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

per Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole
Publicat 2010

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

per Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole
Publicat 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

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

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

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

Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson’s Disease

per Gilmozzi, Valentina, Gentile, Giovanna, Castelo Rueda, Maria Paulina, Hicks, Andrew A., Pramstaller, Peter P., Zanon, Alessandra, Lévesque, Martin, Pichler, Irene
Publicat a Front Neurosci (2020)

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

per 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
Publicat a Int J Mol Sci (2019)

Profiling of Parkin-Binding Partners Using Tandem Affinity Purification

per 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
Publicat 2013

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

per 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
Publicat a Am J Med Genet B Neuropsychiatr Genet (2015)

Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations

per 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
Publicat 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

per 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.
Publicat 2011

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

per 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
Publicat a 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

per 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
Publicat a Hum Mol Genet (2019)

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

per 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
Publicat 2013

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

per 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
Publicat 2013

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

per 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
Publicat a Front Mol Neurosci (2018)

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

per 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
Publicat 2007

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

per 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
Publicat 2009