Irene Pichler

18.4k total citations
45 papers, 1.2k citations indexed

About

Irene Pichler is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Irene Pichler has authored 45 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Neurology, 21 papers in Molecular Biology and 16 papers in Cellular and Molecular Neuroscience. Recurrent topics in Irene Pichler's work include Parkinson's Disease Mechanisms and Treatments (23 papers), Genetic Neurodegenerative Diseases (8 papers) and Restless Legs Syndrome Research (7 papers). Irene Pichler is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (23 papers), Genetic Neurodegenerative Diseases (8 papers) and Restless Legs Syndrome Research (7 papers). Irene Pichler collaborates with scholars based in Italy, Germany and United States. Irene Pichler's co-authors include Peter P. Pramstaller, Andrew A. Hicks, Alessandra Zanon, Thomas Meitinger, Christine Klein, Fabio Marroni, Alessandro De Grandi, Cláudia B. Volpato, Fabiola Del Greco M and Christine Schwienbacher and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Irene Pichler

45 papers receiving 1.2k citations

Peers

Countries citing papers authored by Irene Pichler

Since Specialization

Citations

This map shows the geographic impact of Irene Pichler's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Irene Pichler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irene Pichler more than expected).

Fields of papers citing papers by Irene Pichler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Irene Pichler. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Irene Pichler. The network helps show where Irene Pichler may publish in the future.

Co-authorship network of co-authors of Irene Pichler

This figure shows the co-authorship network connecting the top 25 collaborators of Irene Pichler. A scholar is included among the top collaborators of Irene Pichler based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Irene Pichler. Irene Pichler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2 2024 ·Journal of Translational Medicine ·Alessandra Zanon, Marianna Guida, Alexandros Α. Lavdas, Corrado Corti, (unknown), Alessandro Negro, Peter P. Pramstaller, Francisco S. Domingues, Andrew A. Hicks, Irene Pichler	1
2	Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers 2023 ·npj Parkinson s Disease ·(unknown), Alessandra Zanon, (unknown), Alexandros Α. Lavdas, (unknown), Sylvie Delcambre, Fabiola Del Greco M, Christine Klein, Anne Grünewald, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler	12
3	A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson’s disease by highlighting the use of cybrid models 2022 ·Cellular and Molecular Life Sciences ·Martin Lang, Anne Grünewald, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler	2
4	Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture 2021 ·Frontiers in Cell and Developmental Biology ·(unknown), Giovanna Gentile, (unknown), (unknown), Alexandros Α. Lavdas, Emanuela Kerschbamer, Christian X. Weichenberger, Marcelo D. Rosato‐Siri, Simona Casarosa, Luciano Conti, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler, Alessandra Zanon	20
5	Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls 2021 ·Parkinsonism & Related Disorders ·Jannik Prasuhn, Max Borsche, Andrew A. Hicks, Martin Gögele, (unknown), (unknown), Irene Pichler, (unknown), (unknown), Meike Kasten, Deborah Mascalzoni, Christine Klein, Peter P. Pramstaller, Norbert Brüggemann	8
6	Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort 2021 ·Frontiers in Neurology ·(unknown), (unknown), Martin Gögele, Max Borsche, David Emmert, Christian Fuchsberger, (unknown), Vladimir Vuković, Christine Klein, Peter P. Pramstaller, Irene Pichler, Andrew A. Hicks	22
7	Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson’s Disease 2020 ·Frontiers in Neuroscience ·(unknown), Giovanna Gentile, (unknown), Andrew A. Hicks, Peter P. Pramstaller, Alessandra Zanon, Martin Lévesque, Irene Pichler	43
8	Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene 2019 ·Stem Cell Research ·Alessandra Zanon, (unknown), (unknown), Cláudia B. Volpato, Anne Picard, Chiara Cantaloni, (unknown), Rosamaria Silipigni, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler	4
9	The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1 2018 ·Frontiers in Molecular Neuroscience ·María Dolores Pérez‐Carrión, Francesca Pischedda, Alice Biosa, Isabella Russo, Letizia Straniero, Laura Civiero, Marianna Guida, Christian Johannes Gloeckner, Nicola Ticozzi, Cinzia Tiloca, Claudio Mariani, Gianni Pezzoli, Stefano Duga, Irene Pichler, Lifeng Pan, John E. Landers, Elisa Greggio, Michael W. Hess, Stefano Goldwurm, Giovanni Piccoli	32
10	SLP-2: a potential new target for improving mitochondrial function in Parkinson's disease 2017 ·Neural Regeneration Research ·Irene Pichler, Alessandra Zanon, Andrew A. Hicks, Peter P. Pramstaller	6
11	Profiling of Parkin-Binding Partners Using Tandem Affinity Purification 2013 ·PLoS ONE ·Alessandra Zanon, Aleksandar Raković, Hagen Blankenburg, Nadezhda T. Doncheva, Christine Schwienbacher, Alice Serafin, Adrian Alexa, Christian X. Weichenberger, Mario Albrecht, Christine Klein, Andrew A. Hicks, Peter P. Pramstaller, Francisco S. Domingues, Irene Pichler	50
12	Exome sequencing in a family with restless legs syndrome 2012 ·Movement Disorders ·Anne Weißbach, (unknown), Norbert Brüggemann, Alexander Schmidt, Meike Kasten, Irene Pichler, Hiltrud Muhle, Ebba Lohmann, Thora Lohnau, E. Schwinger, Johann Hagenah, Ulrich Stephani, Peter P. Pramstaller, Christine Klein, Katja Lohmann	17
13	Fine-Mapping of Restless Legs Locus 4 (RLS4) Identifies a Haplotype over the SPATS2L and KCTD18 Genes 2012 ·Journal of Molecular Neuroscience ·Irene Pichler, Christine Schwienbacher, Alessandra Zanon, Christian Fuchsberger, Alice Serafin, Maurizio Facheris, Fabio Marroni, Cristian Pattaro, Yiping Shen, Christian Tellgren‐Roth, Ulf Gyllensten, James F. Gusella, Andrew A. Hicks, Peter P. Pramstaller	8
14	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 2011 ·Human Molecular Genetics ·Fabiola Del Greco M, Cristian Pattaro, Andreas Luchner, Irene Pichler, Thomas W. Winkler, Andrew A. Hicks, Christian Fuchsberger, André Franke, Scott A. Melville, Annette Peters, H.‐Erich Wichmann, Stefan Schreiber, Iris M. Heid, Michael Krawczak, Cosetta Minelli, Christian J. Wiedermann, Peter P. Pramstaller	38
15	CLOCK Gene Variants Associate with Sleep Duration in Two Independent Populations 2010 ·Biological Psychiatry ·Karla V. Allebrandt, Maris Teder‐Laving, Mahmut Akyol, Irene Pichler, Bertram Müller-Myhsok, Peter P. Pramstaller, Martha Merrow, Thomas Meitinger, (unknown), Till Roenneberg	110
16	Exclusion of linkage to chromosome 14q in a large South Tyrolean family with idiopathic basal ganglia calcification (IBGC) 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Cláudia B. Volpato, Alessandro De Grandi, (unknown), Irene Pichler, (unknown), (unknown), (unknown), Peter P. Pramstaller	8
17	The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives 2007 ·BMC Medical Genetics ·Cristian Pattaro, Fabio Marroni, (unknown), Deborah Mascalzoni, Irene Pichler, Cláudia B. Volpato, (unknown), Alessandro De Grandi, (unknown), (unknown), Christian Fuchsberger, Martin Gögele, (unknown), (unknown), Стефан Стефанов, Florian D. Vogl, Christian J. Wiedermann, Thomas Meitinger, Peter P. Pramstaller	42
18	Restless legs syndrome: an update on genetics and future perspectives 2007 ·Clinical Genetics ·Irene Pichler, Andrew A. Hicks, Peter P. Pramstaller	26
19	Genetic Structure in Contemporary South Tyrolean Isolated Populations Revealed by Analysis of Y-Chromosome, mtDNA, and Alu Polymorphisms 2006 ·Human Biology ·Irene Pichler, Jakob C. Mueller, Стефан Стефанов, Alessandro De Grandi, Cláudia B. Volpato, (unknown), Agnes Mayr, (unknown), Franz Ploner, Thomas Meitinger, Peter P. Pramstaller	20
20	Population Isolates in South Tyrol and Their Value for Genetic Dissection of Complex Diseases 2006 ·Annals of Human Genetics ·Fabio Marroni, Irene Pichler, Alessandro De Grandi, Cláudia B. Volpato, Florian D. Vogl, (unknown), Joan E. Bailey‐Wilson, Peter P. Pramstaller	13

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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