Kristel Sleegers


AuthID: R-00F-K5H

Publicações a aguardarem confirmação

1
TITLE: Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
AUTHORS: Luo, Jiao; Thomassen, Jesper Qvist; Bellenguez, Celine; Grenier Boley, Benjamin; de Rojas, Itziar; Castillo, Atahualpa; Parveen, Kayenat; Kuecuekali, Fahri; Nicolas, Aude; Peters, Oliver; Schneider, Anja; Dichgans, Martin; Rujescu, Dan; Scherbaum, Norbert; Juergen, Deckert; Riedel Heller, Steffi; Hausner, Lucrezia; Porcel, Laura Molina; Duezel, Emrah; Grimmer, Timo; Wiltfang, Jens; Heilmann Heimbach, Stefanie; Moebus, Susanne; Tegos, Thomas; Scarmeas, Nikolaos; Clarimon, Jordi; Moreno, Fermin; Perez Tur, Jordi; Bullido, Maria J.; Pastor, Pau; Sanchez Valle, Raquel; Alvarez, Victoria; Boada, Merce; Garcia Gonzalez, Pablo; Puerta, Raquel; Mir, Pablo; Real, Luis M.; Pinol Ripoll, Gerard; Garcia Alberca, Jose Maria; Royo, Jose Luis; Rodriguez Rodriguez, Eloy; Soininen, Hilkka; Kuulasmaa, Teemu; de Mendonca, Alexandre; Mehrabian, Shima; Hort, Jakub; Vyhnalek, Martin; van der Lee, Sven; Graff, Caroline; Papenberg, Goran; Giedraitis, Vilmantas; Boland, Anne; Bacq Daian, Delphine; Deleuze, Jean Francois; Nicolas, Gael; Dufouil, Carole; Pasquier, Florence; Hanon, Olivier; Debette, Stephanie; Gruenblatt, Edna; Popp, Julius; Benussi, Luisa; Galimberti, Daniela; Arosio, Beatrice; Mecocci, Patrizia; Solfrizzi, Vincenzo; Parnetti, Lucilla; Squassina, Alessio; Tremolizzo, Lucio; Borroni, Barbara; Nacmias, Benedetta; Sorbi, Sandro; Caffarra, Paolo; Seripa, Davide; Rainero, Innocenzo; Daniele, Antonio; Masullo, Carlo; Spalletta, Gianfranco; Williams, Julie; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick; Magda, Tsolaki; Rossi, Giacomina; Sanchez Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Andreassen, Ole A.; Hiltunen, Mikko; Van Duijn, Cornelia; Sims, Rebecca; van der Flier, Wiesje; Ruiz, Agustin; Ramirez, Alfredo; Lambert, Jean Charles; Frikke Schmidt, Ruth; ...More
PUBLISHED: 2023, SOURCE: JAMA NETWORK OPEN, VOLUME: 6, ISSUE: 5
INDEXED IN: Scopus WOS
2
TITLE: Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
AUTHORS: Jan Verheijen; Julie van der Zee; Ilse Gijselinck; Tobi Van den Bossche; Lubina Dillen; Bavo Heeman; Estrella Gomez Tortosa; Albert Llado; Raquel Sanchez Valle; Caroline Graff; Pau Pastor; Maria A Pastor; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Jordi Clarimon; Alexandre de Mendonca; Ellen Gelpi; Magda Tsolaki; Janine Diehl Schmid; Benedetta Nacmias; Maria Rosario Almeida; Barbara Borroni; Radoslav Matej; Agustin Ruiz; Sebastiaan Engelborghs; Rik Vandenberghe; Peter P De Deyn; Marc Cruts; Christine Van Broeckhoven; Kristel Sleegers; ...More
PUBLISHED: 2018, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 62
INDEXED IN: WOS
3
TITLE: Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease  Full Text
AUTHORS: de Roeck, A; van Den Bossche, T; van der Zee, J; Verheijen, J; de Coster, W; van Dongen, J; Dillen, L; Baradaran Heravi, Y; Heeman, B; Sanchez Valle, R; Lladó, A; Nacmias, B; Sorbi, S; Gelpi, E; Grau Rivera, O; Gómez Tortosa, E; Pastor, P; Ortega Cubero, S; Pastor, MA; Graff, C; Thonberg, H; Benussi, L; Ghidoni, R; Binetti, G; de Mendonça, A; Martins, M; Borroni, B; Padovani, A; Almeida, MR; Santana, I; Diehl Schmid, J; Alexopoulos, P; Clarimon, J; Lleó, A; Fortea, J; Tsolaki, M; Koutroumani, M; Matěj, R; Rohan, Z; de Deyn, P; Engelborghs, S; Cras, P; van Broeckhoven, C; Sleegers, K; Bessi, V; Bagnoli, S; Do Couto, FS; Verdelho, A; Fratiglioni, L; Padovani, A; Rohan, Z; Razquin, C; Lorenzo, E; Iglesias, E; Seijo Martínez, M; Rene, R; Gascon, J; Campdelacreu, J; Blesa, R; ...More
PUBLISHED: 2017, SOURCE: ACTA NEUROPATHOLOGICA, VOLUME: 134, ISSUE: 3
INDEXED IN: Scopus WOS
4
TITLE: A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease  Full Text
AUTHORS: Jan Verheijen; Tobi Van den Bossche; Julie van der Zee; Sebastiaan Engelborghs; Raquel Sanchez Valle; Albert Llado; Caroline Graff; Hakan Thonberg; Pau Pastor; Sara Ortega Cubero; Maria A Pastor; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Jordi Clarimon; Alberto Lleo; Juan Fortea; Alexandre de Mendonca; Madalena Martins; Oriol Grau Rivera; Ellen Gelpi; Karolien Bettens; Ligia Mateiu; Lubina Dillen; Patrick Cras; Peter P De Deyn; Christine Van Broeckhoven; Kristel Sleegers; ...More
PUBLISHED: 2016, SOURCE: ACTA NEUROPATHOLOGICA, VOLUME: 132, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
5
TITLE: Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study  Full Text
AUTHORS: Elise Cuyvers; Julie van der Zee; Karolien Bettens; Sebastiaan Engelborghs; Mathieu Vandenbulcke; Caroline Robberecht; Lubina Dillen; Celine Merlin; Nathalie Geerts; Caroline Graff; Hakan Thonberg; Huei Hsin Chiang; Pau Pastor; Sara Ortega Cubero; Maria A Pastor; Janine Diehl Schmid; Panagiotis Alexopoulos; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Benedetta Nacmias; Sandro Sorbi; Raquel Sanchez Valle; Albert Llado; Ellen Gelpi; Maria Rosario Almeida; Isabel Santana; Jordi Clarimon; Alberto Lleo; Juan Fortea; Alexandre de Mendonca; Madalena Martins; Barbara Borroni; Alessandro Padovani; Radoslav Matej; Zdenek Rohan; Agustin Ruiz; Giovanni B Frisoni; Gian Maria Fabrizi; Rik Vandenberghe; Peter P De Deyn; Christine Van Broeckhoven; Kristel Sleegers; ...More
PUBLISHED: 2015, SOURCE: NEUROBIOLOGY OF AGING, VOLUME: 36, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
6
TITLE: Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort. HUMAN MUTATION  Full Text
AUTHORS: Rita Cacace; Tobi Van den Bossche; Sebastiaan Engelborghs; Nathalie Geerts; Annelies Laureys; Lubina Dillen; Caroline Graff; Hakan Thonberg; Huei Hsin Chiang; Pau Pastor; Sara Ortega Cubero; Maria A Pastor; Janine Diehl Schmid; Panagiotis Alexopoulos; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Benedetta Nacmias; Sandro Sorbi; Raquel Sanchez Valle; Albert Llado; Ellen Gelpi; Maria Rosario Almeida; Isabel Santana; Magda Tsolaki; Maria Koutroumani; Jordi Clarimon; Alberto Lleo; Juan Fortea; Alexandre de Mendonca; Madalena Martins; Barbara Borroni; Alessandro Padovani; Radoslav Matej; Zdenek Rohan; Mathieu Vandenbulcke; Rik Vandenberghe; Peter P De Deyn; Patrick Cras; Julie van der Zee; Kristel Sleegers; Christine Van Broeckhoven; ...More
PUBLISHED: 2015, SOURCE: HUMAN MUTATION, VOLUME: 36, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef
7
TITLE: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration  Full Text
AUTHORS: Julie van der Zee; Tim Van Langenhove; Gabor G Kovacs; Lubina Dillen; William Deschamps; Sebastiaan Engelborghs; Radoslav Matej; Mathieu Vandenbulcke; Anne Sieben; Bart Dermaut; Katrien Smets; Philip Van Damme; Celine Merlin; Annelies Laureys; Marleen Van Den Broeck; Maria Mattheijssens; Karin Peeters; Luisa Benussi; Giuliano Binetti; Roberta Ghidoni; Barbara Borroni; Alessandro Padovani; Silvana Archetti; Pau Pastor; Cristina Razquin; Sara Ortega Cubero; Isabel Hernandez; Merce Boada; Agustin Ruiz; Alexandre de Mendonca; Gabriel Miltenberger Miltenyi; Frederico Simoes do Couto; Sandro Sorbi; Benedetta Nacmias; Silvia Bagnoli; Caroline Graff; Huei Hsin Chiang; Hakan Thonberg; Robert Perneczky; Janine Diehl Schmid; Panagiotis Alexopoulos; Giovanni B Frisoni; Christian Bonvicini; Matthis Synofzik; Walter Maetzler; Jennifer Muller vom Hagen; Ludger Schoels; Tobias B Haack; Tim M Strom; Holger Prokisch; Oriol Dols Icardo; Jordi Clarimon; Alberto Lleo; Isabel Santana; Maria Rosario Almeida; Beatriz Santiago; Michael T Heneka; Frank Jessen; Alfredo Ramirez; Raquel Sanchez Valle; Albert Llado; Ellen Gelpi; Stayko Sarafov; Ivailo Tournev; Albena Jordanova; Eva Parobkova; Gian Maria Fabrizi; Silvia Testi; Eric Salmon; Thomas Stroebel; Patrick Santens; Wim Robberecht; Peter De Jonghe; Jean Jacques Martin; Patrick Cras; Rik Vandenberghe; Peter Paul De Deyn; Marc Cruts; Kristel Sleegers; Christine Van Broeckhoven; ...More
PUBLISHED: 2014, SOURCE: ACTA NEUROPATHOLOGICA, VOLUME: 128, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef

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