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ScholarIQanswers from OpenAlex & ORCID

Peter M. Andersen

ResearcherPublications, citations & collaboration network

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

How many works does Peter M. Andersen have?

ScholarIQindexed works

Peter M. Andersen has 404 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 M. Andersen have?

ScholarIQcitation count

Peter M. Andersen has 29,666 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Peter M. Andersen?

ScholarIQh-index

Peter M. Andersen has an h-index of 93 in OpenAlex.

What is the i10-index of Peter M. Andersen?

ScholarIQi10-index

Peter M. Andersen has an i10-index of 260 in OpenAlex.

What is the ORCID of Peter M. Andersen?

ScholarIQorcid

The ORCID for Peter M. Andersen is on the source record.

What is the OpenAlex record for Peter M. Andersen?

ScholarIQopenalex

The OpenAlex for Peter M. Andersen is on the source record.

What are the most-cited papers on Peter M. Andersen?

ScholarIQmost cited works
EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force
The EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis:, Peter M. Andersen, Sharon Abrahams, Gian Domenico Borasio, Mamede de Carvalho, Adriano Chiò, Philip Van Damme, Orla Hardiman, Katja Kollewe, Karen Morrison, Susanne Petri, Pierre‐François Pradat, Vincenzo Silani, Barbara Tomik, Maria Wasner, Markus Weber
European Journal of Neurology. 20111,107 Citations
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
Diether Lambrechts, Erik Storkebaum, Masafumi Morimoto, Jurgen Del‐Favero, Frederik Desmet, Stefan L. Marklund, Sabine Wyns, Vincent Thijs, Jörgen Andersson, Ingrid van Marion, Ammar Al‐Chalabi, Stéphanie Bornes, Rhiannon Musson, Valerie K. Hansen, L. Beckman, Rolf Adolfsson, Hardev Pall, Hervé Prats, Séverine Vermeire, Paul Rutgeerts, Shigehiro Katayama, Takuya Awata, Nigel Leigh, Loı̈c Lang-Lazdunski, Mieke Dewerchin, Christopher E. Shaw, Lieve Moons, Robert Vlietinck, Karen Morrison, Wim Robberecht, Christine Van Broeckhoven, Désiré Collen, Peter M. Andersen, Peter Carmeliet
Nature Genetics. 2003860 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
Phase 1–2 Trial of Antisense Oligonucleotide Tofersen for <i>SOD1</i> ALS
Jonathan Mill, Merit Cudkowicz, Pamela J. Shaw, Peter M. Andersen, Nazem Atassi, Robert C. Bucelli, Angela Genge, Jonathan D. Glass, Shafeeq Ladha, Albert Ludolph, Nicholas J. Maragakis, Christopher McDermott, Alan Pestronk, John Ravits, François Salachas, Randall Trudell, Philip Van Damme, Lorne Zinman, C. Frank Bennett, Roger Lane, Alfred Sandrock, Heiko Runz, Danielle Graham, Hani Houshyar, Alexander McCampbell, Ivan Nestorov, Ih Chang, Manjit McNeill, Laura Fanning, Stephanie Fradette, Toby A. Ferguson
New England Journal of Medicine. 2020556 CitationsOPEN ACCESS
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kevin P. Kenna, Perry T.C. van Doormaal, Annelot M. Dekker, Nicola Ticozzi, Brendan Kenna, Frank P. Diekstra, Wouter van Rheenen, Kristel R. van Eijk, Ashley R Jones, Pamela Keagle, Aleksey Shatunov, William Sproviero, Bradley Smith, Michael A. van Es, Simon Topp, Aoife Kenna, Jack W. Miller, Claudia Fallini, Cinzia Tiloca, Russell L. McLaughlin, Caroline Vance, Claire Troakes, Claudia Colombrita, Gabriele Mora, Andrea Calvo, Federico Verde, Safa Al‐Sarraj, Andrew King, Daniela Calini, Jacqueline de Belleroche, Frank Baas, Anneke J. van der Kooi, Marianne de Visser, Anneloor L.M.A. ten Asbroek, Peter C. Sapp, Diane McKenna‐Yasek, Meraida Polak, Seneshaw Asress, José Luís Muñoz-Blanco, Tim M. Strom, Thomas Meitinger, Karen Morrison, Giuseppe Lauria, Kelly L. Williams, P. Nigel Leigh, Garth A. Nicholson, Ian P. Blair, Claire S. Leblond, Patrick A. Dion, Guy A. Rouleau, Hardev Pall, Pamela J. Shaw, Martin R. Turner, Kevin Talbot, Franco Taroni, Khrista Boylan, Marka van Blitterswijk, Rosa Rademakers, Jesús Esteban‐Pérez, Alberto García‐Redondo, Phillip Van Damme, Wim Robberecht, Adriano Chiò, Cinzia Gellera, Carsten Drepper, Michael Sendtner, Antonia Ratti, Jonathan D. Glass, Jesús S. Mora, Nazlı Başak, Orla Hardiman, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt, Robert H. Brown, Ammar Al‐Chalabi, Vincenzo Silani, Christopher E. Shaw, Leonard H. van den Berg, Jan H. Veldink, John E. Landers
Nature Genetics. 2016298 CitationsOPEN ACCESS

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