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Peter Lichtner

ResearcherPublications, citations & collaboration network

Peter Lichtner is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Peter Lichtner have?

ScholarIQindexed works

Peter Lichtner has 280 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Peter Lichtner have?

ScholarIQcitation count

Peter Lichtner has 44,405 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Peter Lichtner?

ScholarIQh-index

Peter Lichtner has an h-index of 85 in OpenAlex.

What is the i10-index of Peter Lichtner?

ScholarIQi10-index

Peter Lichtner has an i10-index of 192 in OpenAlex.

What is the ORCID of Peter Lichtner?

ScholarIQorcid

The ORCID for Peter Lichtner is on the source record.

What is the OpenAlex record for Peter Lichtner?

ScholarIQopenalex

The OpenAlex for Peter Lichtner is on the source record.

What are the most-cited papers on Peter Lichtner?

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
Neuron. 20043,071 CitationsOPEN ACCESS
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou, kConFab Investigators, Australian Ovarian Cancer Study Group, The GENICA (Gene Environment Interaction and Breast Cancer in Germany) Network, Per Hall, Anna González‐Neira, Maya Ghoussaini, Joe Dennis, Roger L. Milne, Marjanka K. Schmidt, Jenny Chang‐Claude, Stig E. Bojesen, Manjeet K. Bolla, Qin Wang, Ed Dicks, Andrew Lee, Clare Turnbull, Nazneen Rahman, Olivia Fletcher, Julian Peto, Lorna J. Gibson, Isabel dos‐Santos‐Silva, Heli Nevanlinna, Taru Muranen, Kristiina Aittomäki, Carl Blomqvist, Kamila Czene, Astrid Irwanto, Jianjun Liu, Quinten Waisfisz, Hanne Meijers‐Heijboer, Muriel A. Adank, Rob B. van der Luijt, Rebecca Hein, Norbert Dahmen, L. Beckman, Alfons Meindl, Rita K. Schmutzler, Bertram Müller‐Myhsok, Peter Lichtner, John L. Hopper, Melissa C. Southey, Enes Makalic, Daniel F. Schmidt, André G. Uitterlinden, Albert Hofman, David J. Hunter, Stephen J. Chanock, Daniel Vincent, François Bacot, Daniel C. Tessier, Sander Canisius, Lodewyk F.A. Wessels, Christopher A. Haiman, Mitul Shah, Robert Luben, Judith Brown, Craig Luccarini, Nils Schoof, Keith Humphreys, Jingmei Li, Børge G. Nordestgaard, Sune F. Nielsen, Henrik Flyger, Fergus J. Couch, Xianshu Wang, Celine M. Vachon, Kristen N. Stevens, Diether Lambrechts, Matthieu Moisse, Robert Paridaens, Marie‐Rose Christiaens, Anja Rudolph, Stefan Nickels, Dieter Flesch‐Janys, Nichola Johnson, Zoe Aitken, Kirsimari Aaltonen, Tuomas Heikkinen, Annegien Broeks, Laura J. van’t Veer, C. Ellen van der Schoot, Pascal Guénel, Thérèse Truong, Pierre Laurent‐Puig, F. Ménégaux, Frederik Marmé, Andreas Schneeweiß, Christof Sohn, Barbara Burwinkel, M. Pilar Zamora, José Ignacio Arias Pérez, Guillermo Pita, M. Rosario Alonso, Angela Cox, Ian W. Brock, Simon S. Cross, Malcolm Reed, Elinor J. Sawyer, Ian Tomlinson
Nature Genetics. 20131,106 CitationsOPEN ACCESS
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
Elisabeth B. Binder, Daria Salyakina, Peter Lichtner, Gabriele M. Wochnik, Marcus Ising, Benno Pütz, Sergi Papiol, Shaun R. Seaman, Susanne Lucae, Martin Kohli, Thomas Nickel, Heike Künzel, B Fuchs, Matthias Majer, Andrea Pfennig, Nikola Kern, Jürgen Brunner, S. Modell, Thomas C. Baghai, Tobias Deiml, Peter Zill, Brigitta Bondy, Rainer Rupprecht, Thomas Messer, Oliver Köhnlein, Heike Dabitz, Tanja Brückl, Nina Müller, Hildegard Pfister, Roselind Lieb, Jakob C. Mueller, Elin Lõhmussaar, Tim M. Strom, Thomas Bettecken, Thomas Meitinger, Manfred Uhr, Theo Rein, Florian Holsboer, Bertram Müller‐Myhsok
Nature Genetics. 2004985 Citations
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
The American Journal of Human Genetics. 2011908 CitationsOPEN ACCESS
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Véronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt, Susana Pinto, Rayomond Press, Stéphanie Millecamps, Nicolas Molko, E Bernard, Claude Desnuelle, Marie‐Hélène Soriani, Johannes Dorst, Elisabeth Graf, Ulrika Nordström, Marisa S. Feiler, Stefan Putz, Tobias M. Boeckers, Thomas Meyer, Andrea Sylvia Winkler, Juliane Winkelman, Mamede de Carvalho, Dietmar Rudolf Thal, Markus Otto, Thomas Brännström, Alexander E. Volk, Petri Kursula, Karin M. Danzer, Peter Lichtner, Ivan Đikić, Thomas Meitinger, Albert C. Ludolph, Tim M. Strom, Peter M. Andersen, Jochen H. Weishaupt
Nature Neuroscience. 2015787 CitationsOPEN ACCESS

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