ScholarIQanswers from OpenAlex & ORCID
Gerard D. Schellenberg
ResearcherPublications, citations & collaboration network
Gerard D. Schellenberg is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Gerard D. Schellenberg have?
ScholarIQindexed works
Gerard D. Schellenberg has 488 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Gerard D. Schellenberg have?
ScholarIQcitation count
Gerard D. Schellenberg has 41,142 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Gerard D. Schellenberg?
ScholarIQh-index
Gerard D. Schellenberg has an h-index of 92 in OpenAlex.
What is the i10-index of Gerard D. Schellenberg?
ScholarIQi10-index
Gerard D. Schellenberg has an i10-index of 240 in OpenAlex.
What is the ORCID of Gerard D. Schellenberg?
ScholarIQorcid
The ORCID for Gerard D. Schellenberg is on the source record.
What is the OpenAlex record for Gerard D. Schellenberg?
ScholarIQopenalex
The OpenAlex for Gerard D. Schellenberg is on the source record.
What are the most-cited papers on Gerard D. Schellenberg?
ScholarIQmost cited works
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
Ephrat Levy‐Lahad, Wilma Wasco, Parvoneh Poorkaj, Donna Romano, Junko Oshima, Warren H. Pettingell, Chang-En Yu, P. D. Jondro, Stephen D. Schmidt, Kai Wang, Annette C. Crowley, Ying‐Hui Fu, Suzanne Y. Guénette, David J. Galas, Ellen Nemens, Ellen M. Wijsman, Thomas D. Bird, Gerard D. Schellenberg, Rudolph E. Tanzi
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
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
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