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Gudrun Rappold

ResearcherPublications, citations & collaboration network

Gudrun Rappold is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Gudrun Rappold have?

ScholarIQindexed works

Gudrun Rappold has 563 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Gudrun Rappold have?

ScholarIQcitation count

Gudrun Rappold has 17,422 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Gudrun Rappold?

ScholarIQh-index

Gudrun Rappold has an h-index of 66 in OpenAlex.

What is the i10-index of Gudrun Rappold?

ScholarIQi10-index

Gudrun Rappold has an i10-index of 199 in OpenAlex.

What is the ORCID of Gudrun Rappold?

ScholarIQorcid

The ORCID for Gudrun Rappold is on the source record.

What is the OpenAlex record for Gudrun Rappold?

ScholarIQopenalex

The OpenAlex for Gudrun Rappold is on the source record.

What are the most-cited papers on Gudrun Rappold?

ScholarIQmost cited works
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Rieß, Christian T. Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B. Ekici, Alexander M. Zink, Andreas Rump, Christa Meisinger, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Rieß, Thomas Meitinger, André Reis, Tim M. Strom
The Lancet. 20121,076 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

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