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Tobias M. Boeckers

ResearcherPublications, citations & collaboration network

Tobias M. Boeckers is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Tobias M. Boeckers have?

ScholarIQindexed works

Tobias M. Boeckers has 290 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Tobias M. Boeckers have?

ScholarIQcitation count

Tobias M. Boeckers has 16,849 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Tobias M. Boeckers?

ScholarIQh-index

Tobias M. Boeckers has an h-index of 69 in OpenAlex.

What is the i10-index of Tobias M. Boeckers?

ScholarIQi10-index

Tobias M. Boeckers has an i10-index of 193 in OpenAlex.

What is the ORCID of Tobias M. Boeckers?

ScholarIQorcid

The ORCID for Tobias M. Boeckers is on the source record.

What is the OpenAlex record for Tobias M. Boeckers?

ScholarIQopenalex

The OpenAlex for Tobias M. Boeckers is on the source record.

What are the most-cited papers on Tobias M. Boeckers?

ScholarIQmost cited works
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Christelle M. Durand, Catalina Betancur, Tobias M. Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Råstam, I. Carina Gillberg, Henrik Anckarsäter, Eili Sponheim, Hany Goubran‐Botros, Richard Delorme, Nadia Chabane, Marie‐Christine Mouren‐Siméoni, P. De Mas, Éric Bieth, Bernadette Rogé, Delphine Héron, Lydie Bürglen, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron
Nature Genetics. 20061,619 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
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
Claire S. Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kévin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M. Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Råstam, I. Carina Gillberg, Gudrun Rappold, Richard Holt, Anthony P. Monaco, Elena Maestrini, Pilar Galán, Delphine Héron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron
PLoS Genetics. 2014672 CitationsOPEN ACCESS
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Råstam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Béatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David Collier, Patrick Bolton, Andreas G. Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Délepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron
PLoS Genetics. 2012446 CitationsOPEN ACCESS
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation
Marcel Naumann, Arun Pal, Anand Goswami, Xenia Lojewski, Julia Japtok, Anne Vehlow, Maximilian Naujock, René Günther, Mengmeng Jin, Nancy Stanslowsky, Peter Reinhardt, Jared Sterneckert, Marie Frickenhaus, Francisco Pan‐Montojo, Erik Storkebaum, Ina Poser, Axel Freischmidt, Jochen H. Weishaupt, Karlheinz Holzmann, Dirk Troost, Albert C. Ludolph, Tobias M. Boeckers, Stefan Liebau, Susanne Petri, Nils Cordes, Anthony A. Hyman, Florian Wegner, Stephan W. Grill, Joachim Weis, Alexander Storch, Andreas Hermann
Nature Communications. 2018292 CitationsOPEN ACCESS

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