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Peter J. Nestor

ResearcherPublications, citations & collaboration network

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

How many works does Peter J. Nestor have?

ScholarIQindexed works

Peter J. Nestor has 226 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 J. Nestor have?

ScholarIQcitation count

Peter J. Nestor has 21,385 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Peter J. Nestor?

ScholarIQh-index

Peter J. Nestor has an h-index of 71 in OpenAlex.

What is the i10-index of Peter J. Nestor?

ScholarIQi10-index

Peter J. Nestor has an i10-index of 133 in OpenAlex.

What is the ORCID of Peter J. Nestor?

ScholarIQorcid

The ORCID for Peter J. Nestor is on the source record.

What is the OpenAlex record for Peter J. Nestor?

ScholarIQopenalex

The OpenAlex for Peter J. Nestor is on the source record.

What are the most-cited papers on Peter J. Nestor?

ScholarIQmost cited works
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Günter U. Höglinger, Gesine Respondek, María Stamelou, Carolin Kurz, Keith A. Josephs, Anthony E. Lang, Brit Mollenhauer, Ulrich Müller, Christer Nilsson, Jennifer L. Whitwell, Thomas Arzberger, Elisabet Englund, Ellen Gelpí, Armin Giese, David J. Irwin, Wassilios G. Meissner, Alexander Pantelyat, Alex Rajput, John C. van Swieten, Claire Troakes, Angelo Antonini, Kailash P. Bhatia, Yvette Bordelon, Yaroslau Compta, Jean‐Christophe Corvol, Carlo Colosimo, Dennis W. Dickson, Richard Dodel, Leslie W. Ferguson, Murray Grossman, Jan Kassubek, Florian Krismer, Johannes Levin, Stefan Lorenzl, Huw R. Morris, Peter J. Nestor, Wolfgang H. Oertel, Werner Poewe, Gil D. Rabinovici, James B. Rowe, Gerard D. Schellenberg, Klaus Seppi, Thilo van Eimeren, Gregor K. Wenning, Adam L. Boxer, Lawrence I. Golbe, Irene Litvan, for the Movement Disorder Society–endorsed PSP Study Group
Movement Disorders. 20172,378 Citations
Consensus classification of posterior cortical atrophy
Sebastian J. Crutch, Jonathan M. Schott, Gil D. Rabinovici, Melissa E. Murray, Julie S. Snowden, Wiesje M. van der Flier, Bradford C. Dickerson, Rik Vandenberghe, Samrah Ahmed, Thomas H. Bak, Bradley F. Boeve, Christopher Butler, Stefano F. Cappa, Mathieu Ceccaldi, Leonardo Cruz de Souza, Bruno Dubois, Olivier Félician, Douglas Galasko, Jonathan Graff‐Radford, Neill R. Graff‐Radford, Patrick R. Hof, Pierre Krolak‐Salmon, Manja Lehmann, Éloi Magnin, Mario F. Mendez, Peter J. Nestor, Chiadi U. Onyike, Victoria S. Pelak, Yolande A.L. Pijnenburg, Silvia Primativo, Martin N. Rossor, Natalie S. Ryan, Philip Scheltens, Timothy J. Shakespeare, Aida Suárez González, David F. Tang‐Wai, Keir Yong, María C. Carrillo, Nick C. Fox
Alzheimer s & Dementia. 2017667 CitationsOPEN ACCESS
Design and first baseline data of the DZNE multicenter observational study on predementia Alzheimer’s disease (DELCODE)
Frank Jessen, Annika Spottke, Henning Boecker, Frederic Brosseron, Katharina Büerger, Cihan Catak, Klaus Fließbach, Christiana Franke, Manuel Fuentes, Michael T. Heneka, Daniel Janowitz, Ingo Kilimann, Christoph Laske, Felix Menne, Peter J. Nestor, Oliver Peters, Josef Priller, Verena Pross, Alfredo Ramı́rez, Anja Schneider, Oliver Speck, Eike Jakob Spruth, Stefan Teipel, Ruth Vukovich, Christine Westerteicher, Jens Wiltfang, Steffen Wolfsgruber, Michael Wagner, Emrah Düzel
Alzheimer s Research & Therapy. 2018262 CitationsOPEN ACCESS
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
Bradley Smith, Simon Topp, Claudia Fallini, Hideki Shibata, Han-Jou Chen, Claire Troakes, Andrew King, Nicola Ticozzi, Kevin P. Kenna, Athina Soragia-Gkazi, Jack W. Miller, Akane Sato, Diana Marques Dias, Maryangel Jeon, Caroline Vance, Chun Hao Wong, Martina de Majo, Wejdan Kattuah, Jacqueline C. Mitchell, Emma L. Scotter, Nicholas Parkin, Peter C. Sapp, Matthew Nolan, Peter J. Nestor, Michael A. Simpson, Michael E. Weale, Monkel Lek, Frank Baas, J. M. Vianney de Jong, Anneloor L.M.A. ten Asbroek, Alberto García‐Redondo, Jesús Esteban‐Pérez, Cinzia Tiloca, Federico Verde, Stefano Duga, Nigel Leigh, Hardev Pall, Karen Morrison, Ammar Al‐Chalabi, Pamela J. Shaw, Janine Kirby, Martin R. Turner, Kevin Talbot, Orla Hardiman, Jonathan D. Glass, Jacqueline de Belleroche, Masatoshi Maki, Stephen E. Moss, Christopher C.J. Miller, Cinzia Gellera, Antonia Ratti, Safa Al‐Sarraj, Robert H. Brown, Vincenzo Silani, John E. Landers, Christopher E. Shaw
Science Translational Medicine. 2017254 CitationsOPEN ACCESS
The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
Bradley Smith, Stephen Newhouse, Aleksey Shatunov, Caroline Vance, Simon Topp, Lauren Johnson, Jack W. Miller, Youn‐Bok Lee, Claire Troakes, Kirsten M. Scott, Ashley Jones, Ian C. Gray, Jamie Wright, Tibor Hortobágyi, Safa Al‐Sarraj, Boris Rogelj, John Powell, Michelle K. Lupton, Simon Lovestone, Peter C. Sapp, Markus Weber, Peter J. Nestor, Helenius J. Schelhaas, Anneloor ALM ten Asbroek, Vincenzo Silani, Cinzia Gellera, Franco Taroni, Nicola Ticozzi, Leonard van den Berg, Jan H. Veldink, Philip Van Damme, Wim Robberecht, Pamela J. Shaw, Janine Kirby, Hardev Pall, Karen Morrison, Alex Morris, Jacqueline de Belleroche, J.M.B.V. de Jong, Frank Baas, Peter M. Andersen, John E. Landers, Robert H. Brown, Michael E. Weale, Ammar Al‐Chalabi, Christopher E. Shaw
European Journal of Human Genetics. 2012232 CitationsOPEN ACCESS

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