ScholarIQanswers from OpenAlex & ORCID
Alexander Zimprich
ResearcherPublications, citations & collaboration network
Alexander Zimprich is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Alexander Zimprich have?
ScholarIQindexed works
Alexander Zimprich has 171 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Alexander Zimprich have?
ScholarIQcitation count
Alexander Zimprich has 16,123 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Alexander Zimprich?
ScholarIQh-index
Alexander Zimprich has an h-index of 53 in OpenAlex.
What is the i10-index of Alexander Zimprich?
ScholarIQi10-index
Alexander Zimprich has an i10-index of 107 in OpenAlex.
What is the ORCID of Alexander Zimprich?
ScholarIQorcid
The ORCID for Alexander Zimprich is on the source record.
What is the OpenAlex record for Alexander Zimprich?
ScholarIQopenalex
The OpenAlex for Alexander Zimprich is on the source record.
What are the most-cited papers on Alexander Zimprich?
ScholarIQmost cited works
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew J. Farrer, Sarah Lincoln, Jennifer M. Kachergus, Mary Hulihan, Ryan J. Uitti, Donald B. Calne, A. Jon Stoessl, Ronald F. Pfeiffer, Nadja Patenge, Iria Carballo‐Carbajal, P. Vieregge, Friedrich Asmus, Bertram Müller‐Myhsok, Dennis W. Dickson, Thomas Meitinger, Tim M. Strom, Zbigniew K. Wszołek, Thomas Gasser
A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal, Elisabeth Graf, Sebastian Eck, Marc N. Offman, Dietrich Haubenberger, Sabine Spielberger, Eva C. Schulte, Peter Lichtner, Shaila C. Rössle, Norman Klopp, Elisabeth Wolf, Klaus Seppi, Walter Pirker, Stefan Presslauer, Brit Mollenhauer, Regina Katzenschlager, Thomas Foki, Christoph Hotzy, Eva M. Reinthaler, Ashot S. Harutyunyan, Róbert Královics, Annette Peters, Fritz Zimprich, Thomas Brücke, Werner Poewe, Eduard Auff, Claudia Trenkwalder, Burkhard Rost, Gerhard Ransmayr, Juliane Winkelmann, Thomas Meitinger, Tim M. Strom
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Barbara Schormair, David Kemlink, Darina Roeske, Gertrud Eckstein, Lan Xiong, Peter Lichtner, Stephan Ripke, Claudia Trenkwalder, Alexander Zimprich, Karin Stiasny‐Kolster, Wolfgang H. Oertel, Cornelius G. Bachmann, Walter Paulus, Birgit Högl, Birgit Frauscher, Viola Gschliesser, Werner Poewe, Ines Peglau, Pavel Vodička, Jana Vávrová, Karel Šonka, Soňa Nevšímalová, Jacques Montplaisir, Gustavo Turecki, Guy A. Rouleau, Christian Gieger, Thomas Illig, H‐Erich Wichmann, Florian Holsboer, Bertram Müller‐Myhsok, Thomas Meitinger, Juliane Winkelmann
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Paul Cannon, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Nicholas Eriksson, Teresa Filshtein, Alison Fitch, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Julie M. Granka, Alejandro Hernandez, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Alan Kwong, Keng‐Han Lin, Bianca A. Llamas, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Priyanka Nandakumar, Dominique T. Nguyen, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Alexandra Reynoso, Madeleine Schloetter, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Qiaojuan Jane Su, Susana A. Tat, Christophe Toukam Tchakouté, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Corinna D. Wong, Hirotaka Iwaki, Julie Lake, Caroline Warly Solsberg, Hampton L. Leonard, Mary B. Makarious, Eng‐King Tan, Andrew Singleton, Sara Bandrés‐Ciga, Alastair J. Noyce, the Global Parkinson’s Genetics Program (GP2), Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, M. Leonor Bustamante, Patricio Olguı́n, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan
Variant in the sequence of the LINGO1 gene confers risk of essential tremor
Hreinn Stefánsson, Stacy Steinberg, Hjörvar Pétursson, Ómar Gústafsson, Iris H Gudjonsdottir, Guðrún A. Jónsdóttir, Stefan Palsson, Thorlákur Jónsson, Jona Saemundsdottir, Gyða Björnsdóttir, Yvonne Böttcher, Theodora Thorlacius, Dietrich Haubenberger, Alexander Zimprich, Eduard Auff, Christoph Hotzy, Claudia Testa, Lisa A Miyatake, Ami Rosen, Kristleifur Kristleifsson, David B. Rye, Friedrich Asmus, Lüdger Schöls, Martin Dichgans, Finnbogi Jakobsson, John Benedikz, Unnur Þorsteinsdóttir, Jeffrey R. Gulcher, Augustine Kong, Kāri Stefánsson