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Rita M. Cantor

ResearcherPublications, citations & collaboration network

Rita M. Cantor is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Rita M. Cantor have?

ScholarIQindexed works

Rita M. Cantor has 164 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Rita M. Cantor have?

ScholarIQcitation count

Rita M. Cantor has 35,452 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Rita M. Cantor?

ScholarIQh-index

Rita M. Cantor has an h-index of 68 in OpenAlex.

What is the i10-index of Rita M. Cantor?

ScholarIQi10-index

Rita M. Cantor has an i10-index of 114 in OpenAlex.

What is the OpenAlex record for Rita M. Cantor?

ScholarIQopenalex

The OpenAlex for Rita M. Cantor is on the source record.

What are the most-cited papers on Rita M. Cantor?

ScholarIQmost cited works
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan Sanders, Xin He, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Kaitlin E. Samocha, A. Ercüment Çiçek, Michael T. Murtha, Vanessa H. Bal, Somer Bishop, Shan Dong, Arthur P. Goldberg, Jinlu Cai, John F. Keaney, Lambertus Klei, Jeffrey D. Mandell, Daniel Moreno‐De‐Luca, Christopher S. Poultney, Elise Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y. Su, Nicole A. Teran, Michael F. Walker, Donna M. Werling, Arthur L. Beaudet, Rita M. Cantor, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, Catherine Lord, Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State
Neuron. 20151,561 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
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State
Neuron. 20111,300 CitationsOPEN ACCESS
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bućan, Joseph Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imieliński, Jonathan P. Bradfield, Patrick Sleiman, Cecilia E. Kim, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Håkon Håkonarson
Nature. 2009975 CitationsOPEN ACCESS
Identification of common variants associated with human hippocampal and intracranial volumes
the Alzheimer's Disease Neuroimaging Initiative (ADNI), Jason L. Stein, Saguenay Youth Study Group (SYS), Sarah E. Medland, Alejandro Arias Vásquez, Derrek P. Hibar, Rudy E Senstad, Anderson M. Winkler, Roberto Toro, Katja Appel, Richard Barteček, Ørjan Bergmann, Manon Bernard, Andrew Brown, Dara M. Cannon, M. Mallar Chakravarty, Andrea Christoforou, Martin Domín, O. Grimm, Marisa O. Hollinshead, Avram J. Holmes, Georg Homuth, Jouke‐Jan Hottenga, Camilla Langan, Lorna M. Lopez, Narelle K. Hansell, Kristy Hwang, Sungeun Kim, Gonzalo Laje, Phil H. Lee, Xinmin Liu, Eva Loth, Anbarasu Lourdusamy, Morten Mattingsdal, Sebastian Mohnke, Susana Muñoz Maniega, Kwangsik Nho, Allison C. Nugent, Carol O’Brien, Martina Papmeyer, Benno Pütz, Adaikalavan Ramasamy, Jerod M. Rasmussen, Mark Rijpkema, Shannon L. Risacher, J. Cooper Roddey, Emma J. Rose, Mina Ryten, Li Shen, Emma Sprooten, Eric Strengman, Alexander Teumer, Daniah Trabzuni, Jessica A. Turner, Kristel van Eijk, Theo G.M. van Erp, Marie‐José van Tol, Katharina Wittfeld, Christiane Wolf, Saskia Woudstra, André Alemán, Saud Alhusaini, Laura Almasy, Elisabeth B. Binder, David G. Brohawn, Rita M. Cantor, Melanie A. Carless, Aiden Corvin, Michael Czisch, Joanne E. Curran, Gail Davies, Marcio Almeida, Norman Delanty, Chantal Depondt, Ravi Duggirala, Thomas D. Dyer, Susanne Erk, Jesen Fagerness, Peter T. Fox, Nelson B Freimer, Michael Gill, Harald H.H. Göring, Donald J. Hagler, David Hoehn, Florian Holsboer, Martine Hoogman, Norbert Hosten, Neda Jahanshad, Matthew P. Johnson, Dalia Kasperavičiūtė, Jack W. Kent, Peter Kochunov, Jack L. Lancaster, Stephen M. Lawrie, David C. Liewald, René C.W. Mandl, Mar Matarín, Manuel Mattheisen, Eva Meisenzahl, Ingrid Melle
Nature Genetics. 2012663 CitationsOPEN ACCESS

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