ScholarIQanswers from OpenAlex & ORCID
Jean‐François Deleuze
ResearcherPublications, citations & collaboration network
Jean‐François Deleuze is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Jean‐François Deleuze have?
ScholarIQindexed works
Jean‐François Deleuze has 651 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Jean‐François Deleuze have?
ScholarIQcitation count
Jean‐François Deleuze has 25,864 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Jean‐François Deleuze?
ScholarIQh-index
Jean‐François Deleuze has an h-index of 77 in OpenAlex.
What is the i10-index of Jean‐François Deleuze?
ScholarIQi10-index
Jean‐François Deleuze has an i10-index of 285 in OpenAlex.
What is the ORCID of Jean‐François Deleuze?
ScholarIQorcid
The ORCID for Jean‐François Deleuze is on the source record.
What is the OpenAlex record for Jean‐François Deleuze?
ScholarIQopenalex
The OpenAlex for Jean‐François Deleuze is on the source record.
What are the most-cited papers on Jean‐François Deleuze?
ScholarIQmost cited works
Analysis of shared heritability in common disorders of the brain
Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Raymond K. Walters, José Brás, Laramie E. Duncan, Valentina Escott‐Price, Guido J. Falcone, Padhraig Gormley, Rainer Malik, Nikolaos A. Patsopoulos, Stephan Ripke, Zhi Wei, Dongmei Yu, Phil H. Lee, Patrick Turley, Benjamin Grenier‐Boley, Vincent Chouraki, Yoichiro Kamatani, Claudine Berr, Luc Letenneur, Didier Hannequin, Philippe Amouyel, Anne Boland, Jean‐François Deleuze, Emmanuelle Duron, Badri N. Vardarajan, Christiane Reitz, Alison Goate, Matthew J. Huentelman, M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Felix Graßmann, Sebanti Sengupta, Jennifer L. Bragg‐Gresham, Kathryn P. Burdon, Scott J. Hebbring, Cindy Wen, Mathias Gorski, Ivana K. Kim, David Cho, Donald J. Zack, Eric H. Souied, Hendrik P. N. Scholl, Elisa Bala, Kristine E Lee, David J. Hunter, Rebecca J. Sardell, Paul Mitchell, Joanna E. Merriam, Valentina Cipriani, Joshua Hoffman, Tina Schick, Yara Lechanteur, Robyn H. Guymer, Matthew P. Johnson, Yingda Jiang, Chloë M. Stanton, Gabriëlle H.S. Buitendijk, Xiaowei Zhan, Alan Kwong, Alexis Boleda, Matthew Brooks, Linn Gieser, Rinki Ratnapriya, Kari Branham, Johanna R. Foerster, John R. Heckenlively, Mohammad Othman, Brendan J. Vote, Helena H. Liang, Emmanuelle Souzeau, Ian L. McAllister, Timothy Isaacs, Janette M. Hall, Stewart Lake, David A. Mackey, Ian J. Constable, Jamie E. Craig, Terrie Kitchner, Zhenglin Yang, Zhiguang Su, Hongrong Luo, Daniel Chen, Hong Ouyang, Ken Flagg, Danni Lin, Guanping Mao, Henry Ferreyra, Klaus Stark, Claudia N. von Strachwitz, Armin Wolf, Caroline Brandl, Guenther Rudolph, Matthias Olden, Margaux A. Morrison, Denise J. Morgan, Matthew Schu, Jeeyun Ahn, Giuliana Silvestri, Evangelia E. Tsironi, Kyu Hyung Park, Lindsay A. Farrer, Anton Orlin, Alexander J. Brucker, Mingyao Li, Christine A. Curcio, Saddek Mohand‐Saïd, José‐Alain Sahel, Isabelle Audo, Mustapha Benchaboune, Angela J. Cree, Christina Rennie, Srinivas Goverdhan, Michelle Grunin, Shira Hagbi-Levi, Peter A. Campochiaro, Nicholas Katsanis, Frank G. Holz, Frédéric Blond, Hélène Blanché, Jean‐François Deleuze, Robert P. Igo, Barbara Truitt, Neal S. Peachey, Stacy M. Meuer, Chelsea E. Myers, Emily Moore, Ronald Klein
Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids
Nicolas Alcala, Noémie Leblay, Alice‐Agnes Gabriel, Lise Mangiante, David Hervás, Théo Giffon, Anne-Sophie Sertier, Anthony Ferrari, Jules L. Derks, A. Ghantous, Tiffany M. Delhomme, Amélie Chabrier, Cyrille Cuenin, Behnoush Abedi‐Ardekani, Anne Boland, Robert Olaso, Vincent Meyer, Janine Altmüller, Florence Le Calvez‐Kelm, Geoffroy Durand, Catherine Voegele, Sandrine Boyault, Laura Moonen, Nicole Lemaître, P. Lorimier, Anne‐Claire Toffart, Alex Soltermann, Joachim H. Clement, Joerg Saenger, John K. Field, Marie Brevet, Cécile Blanc‐Fournier, Françoise Galateau-Sallé, Nolwenn Le Stang, Prudence A. Russell, Gavin Wright, Gabriella Sozzi, Ugo Pastorino, Stéphanie Lacomme, J Vignaud, Véronique Hofman, Paul Hofman, Odd Terje Brustugun, Marius Lund‐Iversen, Vincent de Montpréville, Lucia Anna Muscarella, Paolo Graziano, Helmut Popper, Jelena Stojšić, Jean‐François Deleuze, Zdenko Herceg, Alain Viari, Peter Nüernberg, Giuseppe Pelosi, Anne‐Marie C. Dingemans, Massimo Milione, Luca Roz, L. Brcic, Marco Volante, Mauro Papotti, Christophe Caux, Juan Sandoval, Héctor Hernández‐Vargas, Élisabeth Brambilla, E.J.M. Speel, Nicolas Girard, Sylvie Lantuéjoul, James McKay, Matthieu Foll, Lynnette Fernandez‐Cuesta
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
Céline Bellenguez, Camille Charbonnier, Benjamin Grenier‐Boley, Olivier Quenez, Kilan Le Guennec, Gaël Nicolas, Ganesh Chauhan, David Wallon, Stéphane Rousseau, Anne Richard, Anne Boland, Guillaume Bourque, Hans Markus Münter, Robert Olaso, Vincent Meyer, Adeline Rollin‐Sillaire, Florence Pasquier, Luc Letenneur, Richard Redon, Jean‐François Dartigues, Christophe Tzourio, Thierry Frébourg, Mark Lathrop, Jean‐François Deleuze, Didier Hannequin, Emmanuelle Génin, Philippe Amouyel, Stéphanie Debette, Jean‐Charles Lambert, Dominique Campion, Didier Hannequin, Dominique Campion, David Wallon, Olivier Martinaud, Aline Zaréa, Gaël Nicolas, Adeline Rollin‐Sillaire, Stéphanie Bombois, Marie‐Anne Mackowiak, Vincent Deramecourt, Florence Pasquier, Agnès Michon, Isabelle Le Ber, Bruno Dubois, Olivier Godefroy, Frédérique Etcharry‐Bouyx, Valérie Chauviré, Ludivine Chamard, Eric Berger, Éloi Magnin, Jean‐François Dartigues, Sophie Auriacombe, François Tison, Vincent de la Sayette, Dominique Castan, Elsa Dionet, François Sellal, Olivier Rouaud, Christel Thauvin, Olivier Moreaud, Mathilde Sauvée, Maïté Formaglio, Hélène Mollion, Isabelle Roullet‐Solignac, Alain Vighetto, Bernard Croisile, Mira Didic, Olivier Félician, Lejla Koric, Mathieu Ceccaldi, Audrey Gabelle, Cécilia Marelli, Pierre Labauge, Thérèse Jonveaux, Martine Vercelletto, Claire Boutoleau‐Bretonnière, Giovanni Castelnovo, Claire Paquet, Julien Dumurgier, Jacques Hugon, Foucauld De Boisgueheneuc, Serge Belliard, Serge Bakchine, Marie Sarazin, Marie‐Odile Barrellon, Bernard Laurent, Frédéric Blanc, Jérémie Pariente, Snejana Jurici