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Rosetta Chiavacci

ResearcherPublications, citations & collaboration network

Rosetta Chiavacci is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Rosetta Chiavacci have?

ScholarIQindexed works

Rosetta Chiavacci has 101 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Rosetta Chiavacci have?

ScholarIQcitation count

Rosetta Chiavacci has 16,332 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Rosetta Chiavacci?

ScholarIQh-index

Rosetta Chiavacci has an h-index of 54 in OpenAlex.

What is the i10-index of Rosetta Chiavacci?

ScholarIQi10-index

Rosetta Chiavacci has an i10-index of 70 in OpenAlex.

What is the OpenAlex record for Rosetta Chiavacci?

ScholarIQopenalex

The OpenAlex for Rosetta Chiavacci is on the source record.

What are the most-cited papers on Rosetta Chiavacci?

ScholarIQmost cited works
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Joseph Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James H. Flory, F. George Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Håkon Håkonarson
Nature. 20091,448 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
Common variants at five new loci associated with early-onset inflammatory bowel disease
Marcin Imieliński, Robert N. Baldassano, Anne M. Griffiths, Richard K. Russell, Vito Annese, Marla Dubinsky, Subra Kugathasan, Jonathan P. Bradfield, Thomas D. Walters, Patrick Sleiman, Cecilia E Kim, Aleixo M. Muise, Kai Wang, Joseph Glessner, Shehzad A. Saeed, Haitao Zhang, Edward C. Frackelton, Cuiping Hou, James H. Flory, George Otieno, Rosetta Chiavacci, Robert W. Grundmeier, Massimo Castro, Anna Latiano, Bruno Dallapiccola, Joanne M. Stempak, Debra Abrams, Kent D. Taylor, Dermot McGovern, Melvin B. Heyman, George D. Ferry, Barbara S. Kirschner, Jessica Lee, Jonah Essers, Richard J. Grand, Michael C. Stephens, Arie Levine, David A. Piccoli, Johan Van Limbergen, Salvatore Cucchiara, Dimitri Monos, Stephen L. Guthery, Lee A. Denson, David C. Wilson, Struan F.A. Grant, Mark J. Daly, Mark S. Silverberg, Jack Satsangi, Håkon Håkonarson
Nature Genetics. 2009488 CitationsOPEN ACCESS
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
Josephine Elia, Joseph Glessner, Kai Wang, Nagahide Takahashi, Corina Shtir, Dexter Hadley, Patrick Sleiman, Haitao Zhang, Cecilia E Kim, Reid Robison, Gholson J. Lyon, James H. Flory, Jonathan P. Bradfield, Marcin Imieliński, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Takeshi Sakurai, Cara Rabin, Frank A. Middleton, Kelly Thomas, Maria Garris, Frank Mentch, Christine M. Freitag, Hans‐Christoph Steinhausen, Alexandre A. Todorov, Andreas Reif, Aribert Rothenberger, Barbara Franke, Eric Mick, Herbert Roeyers, Jan K. Buitelaar, Klaus‐Peter Lesch, Tobias Banaschewski, Richard P. Ebstein, Fernando Mulas, Robert D. Oades, Joseph A. Sergeant, Edmund Sonuga‐Barke, Tobias Renner, Marcel Romanos, Jasmin Romanos, Andreas Warnke, Susanne Walitza, Jobst Meyer, Haukur Pálmason, Christiane Seitz, Sandra K. Loo, Susan L. Smalley, Joseph Biederman, Lindsey Kent, Philip Asherson, Richard Anney, J. William Gaynor, Philip Shaw, Marcella Devoto, Peter S. White, Struan F.A. Grant, Joseph D. Buxbaum, Judith L. Rapoport, Nigel M Williams, Stanley F. Nelson, Stephen V. Faraone, Håkon Håkonarson
Nature Genetics. 2011408 CitationsOPEN ACCESS
Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
Gail P. Jarvik, Laura M. Amendola, Jonathan S. Berg, Kyle B. Brothers, Ellen Wright Clayton, Wendy K. Chung, Barbara J. Evans, James P. Evans, Stephanie M. Fullerton, Carlos J. Gallego, Nanibaa’ A. Garrison, Stacy W. Gray, Ingrid A. Holm, Iftikhar J. Kullo, Lisa Soleymani Lehmann, Cathy McCarty, Cynthia A. Prows, Heidi L. Rehm, Richard R. Sharp, Joseph K. Salama, Saskia C. Sanderson, Sara L. Van Driest, Marc S. Williams, Susan M. Wolf, Wendy A. Wolf, Wylie Burke, John B. Harley, Melanie F. Myers, Bahram Namjou, Sander Vinks, John J. Connolly, Brendan J. Keating, Glenn S. Gerhard, Agnes S. Sundaresan, Gerard Tromp, David R. Crosslin, Kathy Leppig, Cathy Wicklund, Christopher G. Chute, John Lynch, Mariza de Andrade, John A. Heit, Jen McCormick, Murray H. Brilliant, Terrie Kitchner, Marylyn D. Ritchie, Erwin P. Böttinger, Inga Peter, Stephen D. Persell, Laura J. Rasmussen‐Torvik, Tracy L. McGregor, Dan M. Roden, Armand H. Matheny Antommaria, Rosetta Chiavacci, Andy Faucett, David H. Ledbetter, Janet L. Williams, Andrea L. Hartzler, Carolyn R. Rohrer Vitek, Norm Frost, Kadija Ferryman, Carol R. Horowitz, Rosamond Rhodes, Randi E. Zinberg, Sharon Aufox, Vivian Pan, Rochelle M. Long, Erin M. Ramos, Jackie Odgis, Anastasia L. Wise, Sara Chandros Hull, Jonathan D. Gitlin, Robert C. Green, Danielle R. Metterville, Amy L. McGuire, Sek Won Kong, Sue Trinidad, David L. Veenstra, Myra I. Roche, Debra Skinner, Kelly Raspberry, Julianne O’Daniel, William H. Parsons, Christine M. Eng, Susan G. Hilsenbeck, Dean Karavite, Laura K. Conlin, Nancy B. Spinner, Ian D. Krantz, Marni J. Falk, Avni Santani, Elizabeth T. DeChene, Matthew C. Dulik, Barbara A. Bernhardt, Scott M. Schuetze, Jessica N. Everett, Michele C. Gornick, Ben Wilfond, Holly K. Tabor, Amy A. Lemke
The American Journal of Human Genetics. 2014378 CitationsOPEN ACCESS

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