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Catalina Betancur

ResearcherPublications, citations & collaboration network

Catalina Betancur is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Catalina Betancur have?

ScholarIQindexed works

Catalina Betancur has 150 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Catalina Betancur have?

ScholarIQcitation count

Catalina Betancur has 29,474 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Catalina Betancur?

ScholarIQh-index

Catalina Betancur has an h-index of 57 in OpenAlex.

What is the i10-index of Catalina Betancur?

ScholarIQi10-index

Catalina Betancur has an i10-index of 114 in OpenAlex.

What is the ORCID of Catalina Betancur?

ScholarIQorcid

The ORCID for Catalina Betancur is on the source record.

What is the OpenAlex record for Catalina Betancur?

ScholarIQopenalex

The OpenAlex for Catalina Betancur is on the source record.

What are the most-cited papers on Catalina Betancur?

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
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Péter Szatmári, Ann Thompson, Ping G. Tepper, Andrew D. Paterson, Xiaoqing Liu, Jennifer Skaug, Lars Feuk, Qian Cheng, Christian R Marshall, Stephen W. Scherer, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Lili Senman, John B. Vincent, Susan E. Bryson, Marshall B. Jones, Veronica J. Vieland, Christopher W. Bartlett, La Vonne Mangin, Rhinda Goedken, Alberto M. Segre, Margaret A. Pericak‐Vance, Michael L. Cuccaro, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Marion Leboyer, Thomas Bourgeron, Christopher Gillberg, Joseph D. Buxbaum, Kenneth L. Davis, Eric Hollander, Jeremy M. Silverman, Joachim Hallmayer, Linda Lotspeich, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Thomas H. Wassink, Kacie J. Meyer, Val C. Sheffield, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, Stan F. Nelson, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Clara Lajonchere, Janet Miller, David H. Ledbetter, Christa Lese‐Martin, Carol A Samango-Sprouse, Sarah Spence, Matthew W. State, Fred R. Volkmar, Rudolph E. Tanzi, Hilary Coon, William M. McMahon, Géraldine Dawson, Jeff Munson, Annette Estes, Bernie Devlin, Lambertus Klei, Nancy J. Minshew, Pamela Flodman, Moyra Smith, M. Anne Spence, Elena Korvatska, Gerard D. Schellenberg, Chang-En Yu, Patricia M. Rodier, Chris Stodgell, Ellen M. Wijsman, Bernadette Rogé, Carine Mantoulan, Kerstin Wittemeyer, Annemarie Poustka, Bärbel Felder, Sabine M. Klauck, Claudia Schuster, Fritz Poustka, Sven Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, Gabi Schmötzer, John Tsiantis, Katerina Papanikolaou, Elena Maestrini, Elena Bacchelli, Francesca Blasi, Simona Carone, Claudio Toma, Hermán van Engeland, Maretha Jonge, Chantal Kemner
Nature Genetics. 20071,419 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
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt
Nature Genetics. 2022640 CitationsOPEN ACCESS
Abnormal melatonin synthesis in autism spectrum disorders
Jonas Melke, Hany Goubran Botros, Pauline Chaste, Catalina Betancur, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Ola Ståhlberg, I. Carina Gillberg, Richard Delorme, Nadia Chabane, MC Mouren-Siméoni, Fabien Fauchereau, Christelle M. Durand, Fabien Le Chevalier, Xavier Drouot, Corinne Collet, J.M. Launay, Marion Leboyer, C Gillberg, Thomas Bourgeron, and the PARIS study
Molecular Psychiatry. 2007526 CitationsOPEN ACCESS

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