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198 results for Van+Broeckhoven,+Christine

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Select record 41
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The Use of Biomarkers and Genetic Screening to Diagnose Frontotemporal Dementia: Evidence and Clinical Implications
Author / Creator:Gossye, Helena ; Van Broeckhoven, Christine ; Engelborghs, Sebastiaan
Publisher:Switzerland: Frontiers Research Foundation
Journal title:Frontiers in neuroscience, 2019-08, Vol.13, p.757-757
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NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION
Author / Creator:De Roeck, Arne ; De Coster, Wouter ; Bossaerts, Liene ; Cacace, Rita ; De Pooter, Tim ; Van Dongen, Jasper ; D'Hert, Svenn ; De Rijk, Peter ; Strazisar, Mojca ; Van Broeckhoven, Christine ; Sleegers, Kristel
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2019-11, Vol.20 (1), p.239-239, Article 239
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The genetics and neuropathology of frontotemporal lobar degeneration
Author / Creator:Sieben, Anne ; Van Langenhove, Tim ; Engelborghs, Sebastiaan ; Martin, Jean-Jacques ; Boon, Paul ; Cras, Patrick ; De Deyn, Peter-Paul ; Santens, Patrick ; Van Broeckhoven, Christine ; Cruts, Marc
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Acta neuropathologica, 2012-09, Vol.124 (3), p.353-372
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Digenic progressive external ophthalmoplegia in a sporadic patient: Recessive mutations in POLG and C10orf2/Twinkle
Author / Creator:Goethem, Gert Van ; Löfgren, Ann ; Dermaut, Bart ; Ceuterick, Chantal ; Martin, Jean-Jacques ; Broeckhoven, Christine Van
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2003-08, Vol.22 (2), p.175-176
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Select record 45
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Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases
Author / Creator:Perrone, Federica ; Cacace, Rita ; van der Zee, Julie ; Van Broeckhoven, Christine
Publisher:England: BioMed Central Ltd
Journal title:Genome medicine, 2021-04, Vol.13 (1), p.59-59, Article 59
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Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis
Author / Creator:Götzl, Julia K. ; Mori, Kohji ; Damme, Markus ; Fellerer, Katrin ; Tahirovic, Sabina ; Kleinberger, Gernot ; Janssens, Jonathan ; van der Zee, Julie ; Lang, Christina M. ; Kremmer, Elisabeth ; Martin, Jean-Jacques ; Engelborghs, Sebastiaan ; Kretzschmar, Hans A. ; Arzberger, Thomas ; Van Broeckhoven, Christine ; Haass, Christian ; Capell, Anja
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2014-06, Vol.127 (6), p.845-860
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Select record 47
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease
Author / Creator:De Roeck, Arne ; Duchateau, Lena ; Van Dongen, Jasper ; Cacace, Rita ; Bjerke, Maria ; Van den Bossche, Tobi ; Cras, Patrick ; Vandenberghe, Rik ; De Deyn, Peter P. ; Engelborghs, Sebastiaan ; Van Broeckhoven, Christine ; Sleegers, Kristel
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2018-06, Vol.135 (6), p.827-837
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Major affective disorders and schizophrenia: a common molecular signature?
Author / Creator:Bogaert, Ann Van Den ; Del-Favero, Jurgen ; Broeckhoven, Christine Van
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2006-09, Vol.27 (9), p.833-853
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IPSC-Derived Neuronal Cultures Carrying the Alzheimer's Disease Associated TREM2 R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network
Author / Creator:Martins, Soraia ; Müller-Schiffmann, Andreas ; Erichsen, Lars ; Bohndorf, Martina ; Wruck, Wasco ; Sleegers, Kristel ; Van Broeckhoven, Christine ; Korth, Carsten ; Adjaye, James
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2020-06, Vol.21 (12), p.4516
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Select record 50
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Mechanisms of Granulin Deficiency: Lessons from Cellular and Animal Models
Author / Creator:Kleinberger, Gernot ; Capell, Anja ; Haass, Christian ; Van Broeckhoven, Christine
Publisher:New York: Humana Press Inc
Journal title:Molecular neurobiology, 2013-02, Vol.47 (1), p.337-360
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Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation
Author / Creator:Neumann, Alexander ; Küçükali, Fahri ; Bos, Isabelle ; Vos, Stephanie J. B. ; Engelborghs, Sebastiaan ; De Pooter, Tim ; Joris, Geert ; De Rijk, Peter ; De Roeck, Ellen ; Tsolaki, Magda ; Verhey, Frans ; Martinez-Lage, Pablo ; Tainta, Mikel ; Frisoni, Giovanni ; Blin, Oliver ; Richardson, Jill ; Bordet, Régis ; Scheltens, Philip ; Popp, Julius ; Peyratout, Gwendoline ; Johannsen, Peter ; Frölich, Lutz ; Vandenberghe, Rik ; Freund-Levi, Yvonne ; Streffer, Johannes ; Lovestone, Simon ; Legido-Quigley, Cristina ; ten Kate, Mara ; Barkhof, Frederik ; Strazisar, Mojca ; Zetterberg, Henrik ; Bertram, Lars ; Visser, Pieter Jelle ; van Broeckhoven, Christine ; Sleegers, Kristel
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2022-04, Vol.27 (4), p.1990-1999
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Select record 52
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Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth
Author / Creator:Schmid, Bettina ; Hruscha, Alexander ; Hogl, Sebastian ; Banzhaf-Strathmann, Julia ; Strecker, Katrin ; van der Zee, Julie ; Teucke, Mathias ; Eimer, Stefan ; Hegermann, Jan ; Kittelmann, Maike ; Kremmer, Elisabeth ; Cruts, Marc ; Solchenberger, Barbara ; Hasenkamp, Laura ; van Bebber, Frauke ; Van Broeckhoven, Christine ; Edbauer, Dieter ; Lichtenthaler, Stefan F. ; Haass, Christian
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2013-03, Vol.110 (13), p.4986-4991
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Select record 53
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Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration
Author / Creator:Sieben, Anne ; Van Langenhove, Tim ; Vermeiren, Yannick ; Gossye, Helena ; Praet, Marleen ; Vanhauwaert, Dimitri ; Cousaert, Céline ; Engelborghs, Sebastiaan ; Raedt, Robrecht ; Boon, Paul ; Santens, Patrick ; De Deyn, Peter Paul ; Bracke, Ken R ; De Meulemeester, Katia ; Van Broeckhoven, Christine ; Martin, Jean-Jacques ; Bjerke, Maria
Publisher:England: Oxford University Press
Journal title:Journal of neuropathology and experimental neurology, 2021-04, Vol.80 (4), p.313-324
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Select record 54
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Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gen...
Author / Creator:Benussi, Luisa ; Longobardi, Antonio ; Kocoglu, Cemile ; Carrara, Matteo ; Bellini, Sonia ; Ferrari, Clarissa ; Nicsanu, Roland ; Saraceno, Claudia ; Bonvicini, Cristian ; Fostinelli, Silvia ; Zanardini, Roberta ; Catania, Marcella ; Moisse, Matthieu ; Van Damme, Philip ; Di Fede, Giuseppe ; Binetti, Giuliano ; Van Broeckhoven, Christine ; van der Zee, Julie ; Ghidoni, Roberta
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2021-12, Vol.22 (24), p.13633
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Select record 55
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Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusion
Author / Creator:Bossaerts, Liene ; Hendrickx Van de Craen, Elisabeth ; Cacace, Rita ; Asselbergh, Bob ; Van Broeckhoven, Christine
Publisher:England: BioMed Central Ltd
Journal title:Acta neuropathologica communications, 2022-03, Vol.10 (1), p.43-43, Article 43
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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
Author / Creator:Cacace, Rita ; Heeman, Bavo ; Van Mossevelde, Sara ; De Roeck, Arne ; Hoogmartens, Julie ; De Rijk, Peter ; Gossye, Helena ; De Vos, Kristof ; De Coster, Wouter ; Strazisar, Mojca ; De Baets, Greet ; Schymkowitz, Joost ; Rousseau, Frederic ; Geerts, Nathalie ; De Pooter, Tim ; Peeters, Karin ; Sieben, Anne ; Martin, Jean-Jacques ; Engelborghs, Sebastiaan ; Salmon, Eric ; Santens, Patrick ; Vandenberghe, Rik ; Cras, Patrick ; P. De Deyn, Peter ; C. van Swieten, John ; M. van Duijn, Cornelia ; van der Zee, Julie ; Sleegers, Kristel ; Van Broeckhoven, Christine
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2019-06, Vol.137 (6), p.901-918
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Select record 57
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A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS
Author / Creator:Lehmer, Carina ; Schludi, Martin H ; Ransom, Linnea ; Greiling, Johanna ; Junghänel, Michaela ; Exner, Nicole ; Riemenschneider, Henrick ; van der Zee, Julie ; Van Broeckhoven, Christine ; Weydt, Patrick ; Heneka, Michael T ; Edbauer, Dieter
Publisher:London: Nature Publishing Group UK
Journal title:EMBO molecular medicine, 2018-06, Vol.10 (6), p.1-n/a
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Select record 58
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Peripheral myelin protein 2 - a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy
Author / Creator:Palaima, Paulius ; Chamova, Teodora ; Jander, Sebastian ; Mitev, Vanyo ; Van Broeckhoven, Christine ; Tournev, Ivailo ; Peeters, Kristien ; Jordanova, Albena
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2019-08, Vol.14 (1), p.197-197, Article 197
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Select record 59
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Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice
Author / Creator:Janssens, Jonathan ; Wils, Hans ; Kleinberger, Gernot ; Joris, Geert ; Cuijt, Ivy ; Ceuterick-de Groote, Chantal ; Van Broeckhoven, Christine ; Kumar-Singh, Samir
Publisher:Boston: Springer US
Journal title:Molecular neurobiology, 2013-08, Vol.48 (1), p.22-35
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Select record 60
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Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations
Author / Creator:Bettens, Karolien ; Vermeulen, Steven ; Van Cauwenberghe, Caroline ; Heeman, Bavo ; Asselbergh, Bob ; Robberecht, Caroline ; Engelborghs, Sebastiaan ; Vandenbulcke, Mathieu ; Vandenberghe, Rik ; De Deyn, Peter Paul ; Cruts, Marc ; Van Broeckhoven, Christine ; Sleegers, Kristel
Publisher:England: BioMed Central Ltd
Journal title:Molecular neurodegeneration, 2015-07, Vol.10 (1), p.30-30, Article 30
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The Use of Biomarkers and Genetic Screening to Diagnose Frontotemporal Dementia: Evidence and Clinical Implications

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NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION

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The genetics and neuropathology of frontotemporal lobar degeneration

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Digenic progressive external ophthalmoplegia in a sporadic patient: Recessive mutations in POLG and C10orf2/Twinkle

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Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

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Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease

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Major affective disorders and schizophrenia: a common molecular signature?

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IPSC-Derived Neuronal Cultures Carrying the Alzheimer's Disease Associated TREM2 R47H Variant Enables the Construction of an Aβ-Induced Gene Regulatory Network

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Mechanisms of Granulin Deficiency: Lessons from Cellular and Animal Models

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Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation

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Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth

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Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration

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Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gen...

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Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusion

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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

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A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS

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Peripheral myelin protein 2 - a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy

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Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice

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Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations

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