ScholarIQanswers from OpenAlex & ORCID
Patrick Sleiman
ResearcherPublications, citations & collaboration network
Patrick Sleiman is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Patrick Sleiman have?
ScholarIQindexed works
Patrick Sleiman has 226 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Patrick Sleiman have?
ScholarIQcitation count
Patrick Sleiman has 19,016 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Patrick Sleiman?
ScholarIQh-index
Patrick Sleiman has an h-index of 60 in OpenAlex.
What is the i10-index of Patrick Sleiman?
ScholarIQi10-index
Patrick Sleiman has an i10-index of 139 in OpenAlex.
What is the ORCID of Patrick Sleiman?
ScholarIQorcid
The ORCID for Patrick Sleiman is on the source record.
What is the OpenAlex record for Patrick Sleiman?
ScholarIQopenalex
The OpenAlex for Patrick Sleiman is on the source record.
What are the most-cited papers on Patrick Sleiman?
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
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
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
Klaus Bønnelykke, Patrick Sleiman, Kasper Nielsen, Eskil Kreiner‐Møller, Josep M. Mercader, Danielle Belgrave, Herman T. den Dekker, Anders Husby, Astrid Sevelsted, Grissel Faura-Tellez, Li Juel Mortensen, Lavinia Paternoster, Richard Flaaten, Anne Mølgaard, David E. Smart, Philip Francis Thomsen, Morten Arendt Rasmussen, Sílvia Bonàs‐Guarch, Claus Holst, Ellen A. Nøhr, Rachita Yadav, Michael March, Thomas Blicher, Peter M. Lackie, Vincent W. V. Jaddoe, Angela Simpson, John W. Holloway, Liesbeth Duijts, Adnan Čustović, Donna E. Davies, David Torrents, Ramneek Gupta, Mads V. Hollegaard, David M. Hougaard, Håkon Håkonarson, Hans Bisgaard
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
A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci
Jonathan P. Bradfield, Hui‐Qi Qu, Kai Wang, Haitao Zhang, Patrick Sleiman, Cecilia E. Kim, Frank Mentch, Haijun Qiu, Joseph Glessner, Kelly Thomas, Edward C. Frackelton, Rosetta Chiavacci, Marcin Imieliński, Dimitri Monos, Rahul Pandey, Marina Bakay, Struan F.A. Grant, Constantin Polychronakos, Håkon Håkonarson