ScholarIQanswers from OpenAlex & ORCID
Karolien Bettens
ResearcherPublications, citations & collaboration network
Karolien Bettens is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Karolien Bettens have?
ScholarIQindexed works
Karolien Bettens has 61 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Karolien Bettens have?
ScholarIQcitation count
Karolien Bettens has 18,077 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Karolien Bettens?
ScholarIQh-index
Karolien Bettens has an h-index of 30 in OpenAlex.
What is the i10-index of Karolien Bettens?
ScholarIQi10-index
Karolien Bettens has an i10-index of 36 in OpenAlex.
What is the OpenAlex record for Karolien Bettens?
ScholarIQopenalex
The OpenAlex for Karolien Bettens is on the source record.
What are the most-cited papers on Karolien Bettens?
ScholarIQmost cited works
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold, Richard Abraham, Paul Hollingworth, Rebecca Sims, Amy Gerrish, Marian L. Hamshere, Jaspreet Singh Pahwa, Valentina Moskvina, Kimberley Dowzell, Amy L. Williams, Nicola Jones, Charlene Thomas, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle Brown, Peter Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Reinhard Heun, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John S.K. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H‐Erich Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter Holmans, Michael O‘Donovan, Michael J. Owen, Julie Williams
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
the European Alzheimer's Disease Initiative Investigators, Jean‐Charles Lambert, Simon Heath, Gaël Even, Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zélénika, María J. Bullido, Béatrice Tavernier, Luc Letenneur, Karolien Bettens, Claudine Berr, Florence Pasquier, Nathalie Fiévet, Pascale Barberger‐Gateau, Sebastiaan Engelborghs, Peter Paul De Deyn, Ignacio Mateo, A. Franck, Seppo Helisalmi, Elisa Porcellini, Olivier Hanon, Marian M. de Pancorbo, Corinne Lendon, Carole Dufouil, Céline Jaillard, Thierry Léveillard, Victoria Álvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Paola Piccardi, Giorgio Annoni, Davide Seripa, Daniela Galimberti, Didier Hannequin, Federico Licastro, Hilkka Soininen, Karen Ritchie, Hélène Blanché, Jean‐François Dartigues, Christophe Tzourio, Marta Gut, Christine Van Broeckhoven, Annick Alpérovitch, Mark Lathrop, Philippe Amouyel
APOE and Alzheimer disease: a major gene with semi-dominant inheritance
Emmanuelle Génin, Didier Hannequin, David Wallon, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, María J. Bullido, Sebastiaan Engelborghs, Peter Paul De Deyn, Claudine Berr, Florence Pasquier, Bruno Dubois, Gloria Tognoni, Nathalie Fiévet, Nathalie Brouwers, Karolien Bettens, Beatrice Arosio, Eliécer Coto, Maria Del Zompo, Ignacio Mateo, Jacques Epelbaum, Ana Frank, Seppo Helisalmi, Elisa Porcellini, Alberto Pilotto, Paola Forti, Raffaele Ferri, Elio Scarpini, Gabriele Siciliano, Vincenzo Solfrizzi, Sandro Sorbi, Gianfranco Spalletta, Fernando Valdivieso, Saila Vepsäläinen, Victoria Álvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Olivier Hanon, Paola Piccardi, G Annoni, Davide Seripa, Daniela Galimberti, Federico Licastro, Hilkka Soininen, Dartigues Jf, M. Ilyas Kamboh, Christine Van Broeckhoven, Jean‐Charles Lambert, Philippe Amouyel, Dominique Campion
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Stéphanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson, Sebastiaan Engelborghs, Anne Sieben, Peter De Jonghe, Rik Vandenberghe, Patrick Santens, Jan De Bleecker, Githa Maes, Veerle Bäumer, Lubina Dillen, Geert Joris, Ivy Cuijt, Ellen Corsmit, Ellen Elinck, Jasper Van Dongen, Steven Vermeulen, Marleen Van den Broeck, C Vaerenberg, Maria Mattheijssens, Karin Peeters, Wim Robberecht, Patrick Cras, Jean‐Jacques Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven