Works matching AU Van Broeckhoven, Christine

Results: 291

Associating Alzheimer's disease pathology with its cerebrospinal fluid biomarkers.

Published in:

2022

By:

Bridel, Claire;
Somers, Charisse;
Sieben, Anne;
Rozemuller, Annemieke;
Niemantsverdriet, Ellis;
Struyfs, Hanne;
Vermeiren, Yannick;
Broeckhoven, Christine Van;
Deyn, Peter P De;
Bjerke, Maria;
Nagels, Guy;
Teunissen, Charlotte E;
Engelborghs, Sebastiaan;
Van Broeckhoven, Christine;
De Deyn, Peter P

Publication type:

journal article

Age and the association between apolipoprotein E genotype and Alzheimer disease: A cerebrospinal fluid biomarker-based case-control study.

Published in:

2020

By:

Saddiki, Hana;
Fayosse, Aurore;
Cognat, Emmanuel;
Sabia, Séverine;
Engelborghs, Sebastiaan;
Wallon, David;
Alexopoulos, Panagiotis;
Blennow, Kaj;
Zetterberg, Henrik;
Parnetti, Lucilla;
Zerr, Inga;
Hermann, Peter;
Gabelle, Audrey;
Boada, Mercè;
Orellana, Adelina;
de Rojas, Itziar;
Lilamand, Matthieu;
Bjerke, Maria;
Van Broeckhoven, Christine;
Farotti, Lucia

Publication type:

journal article

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

Published in:

Genome Biology, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s13059-019-1856-3

By:

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

Publication type:

Article

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

Published in:

2019

By:

Palaima, Paulius;
Chamova, Teodora;
Jander, Sebastian;
Mitev, Vanyo;
Van Broeckhoven, Christine;
Tournev, Ivailo;
Peeters, Kristien;
Jordanova, Albena

Publication type:

journal article

Studying TLR9 loss‐of‐function in iPSC of patients with deleterious mutation.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.082641

By:

Cacace, Rita;
Frydas, Alexandros;
van Broeckhoven, Christine

Publication type:

Article

Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.

Published in:

Movement Disorders, 2012, v. 27, n. 11, p. 1451, doi. 10.1002/mds.25147

By:

Theuns, Jessie;
Crosiers, David;
Debaene, Luc;
Nuytemans, Karen;
Meeus, Bram;
Sleegers, Kristel;
Goossens, Dirk;
Corsmit, Ellen;
Elinck, Ellen;
Peeters, Karin;
Mattheijssens, Maria;
Pickut, Barbara;
Del-Favero, Jurgen;
Engelborghs, Sebastiaan;
De Deyn, Peter Paul;
Cras, Patrick;
Van Broeckhoven, Christine

Publication type:

Article

Neurodegenerative parkinsonism and progressive external ophthalmoplegia with a Twinkle mutation.

Published in:

Movement Disorders, 2009, v. 24, n. 2, p. 308, doi. 10.1002/mds.22198

By:

Vandenberghe, Wim;
Van Laere, Koen;
Debruyne, Frederik;
Van Broeckhoven, Christine;
Van Goethem, Gert

Publication type:

Article

Motor-neuron disease: Rogue gene in the family.

Published in:

Nature, 2009, v. 458, n. 7237, p. 415, doi. 10.1038/458415a

By:

Sleegers, Kristel;
Van Broeckhoven, Christine

Publication type:

Article

Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor.

Published in:

Biomedicines, 2022, v. 10, n. 1, p. 20, doi. 10.3390/biomedicines10010020

By:

Abondio, Paolo;
Sarno, Stefania;
Giuliani, Cristina;
Laganà, Valentina;
Maletta, Raffaele;
Bernardi, Livia;
Bruno, Francesco;
Colao, Rosanna;
Puccio, Gianfranco;
Frangipane, Francesca;
Borroni, Barbara;
Van Broeckhoven, Christine;
Luiselli, Donata;
Bruni, Amalia

Publication type:

Article

Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia.

Published in:

Neuropathology, 2016, v. 36, n. 1, p. 27, doi. 10.1111/neup.12233

By:

Kovacs, Gabor G.;
Zee, Julie;
Hort, Jakub;
Kristoferitsch, Wolfgang;
Leitha, Thomas;
Höftberger, Romana;
Ströbel, Thomas;
Van Broeckhoven, Christine;
Matej, Radoslav

Publication type:

Article

Investigation of the role of miRNA variants in neurodegenerative brain diseases.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1506169

By:

Frydas, Alexandros;
Cacace, Rita;
van der Zee, Julie;
Van Broeckhoven, Christine;
Wauters, Eline

Publication type:

Article

SNPbox: web-based high-throughput primer design from gene to genome.

Published in:

Nucleic Acids Research, 2004, v. 32, n. suppl 2, p. w170, doi. 10.1093/nar/gkh369

By:

Weckx, Stefan;
De Rijk, Peter;
Van Broeckhoven, Christine;
Del-Favero, Jurgen

Publication type:

Article

Twinkle and POLG defects enhance age‐dependent accumulation of mutations in the control region of mtDNA.

Published in:

Nucleic Acids Research, 2004, v. 32, n. 10, p. 3053, doi. 10.1093/nar/gkh634

By:

Wanrooij, Sjoerd;
Luoma, Petri;
van Goethem, Gert;
van Broeckhoven, Christine;
Suomalainen, Anu;
Spelbrink, Johannes N.

Publication type:

Article

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 4, p. 471, doi. 10.1038/sj.ejhg.5201986

By:

Nuytemans, Karen;
Rademakers, Rosa;
Theuns, Jessie;
Pals, Philippe;
Engelborghs, Sebastiaan;
Pickut, Barbara;
de Pooter, Tim;
Peeters, Karin;
Mattheijssens, Maria;
Van den Broeck, Marleen;
Cras, Patrick;
De Deyn, Peter Paul;
van Broeckhoven, Christine

Publication type:

Article

Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 5, p. 389, doi. 10.1038/sj.ejhg.5201161

By:

Croes, Esther A.;
Alizadeh, Behrooz Z.;
Bertoli-Avella, Aida M.;
Rademaker, Tessa;
Vergeer-Drop, Jeannette;
Dermaut, Bart;
Houwing-Duistermaat, Jeanine J.;
Wientjens, Dorothee P. W. M.;
Hofman, Albert;
Van Broeckhoven, Christine;
van Duijn, Cornelia M.

Publication type:

Article

Parametric and nonparametric genome scan analyses for human handedness.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 10, p. 779, doi. 10.1038/sj.ejhg.5201048

By:

Agtmael, Tom Van;
Forrest, Susan M.;
Del-Favero, Jurgen;
Van Broeckhoven, Christine;
Williamson, Robert

Publication type:

Article

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 7, p. 547, doi. 10.1038/sj.ejhg.5201002

By:

Van Goethem, Gert;
Schwartz, Marianne;
Lofgren, Ann;
Dermaut, Bart;
Van Broeckhoven, Christine;
Vissing, John

Publication type:

Article

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 276, doi. 10.1038/sj.ejhg.5200803

By:

Del-Favero, Jurgen;
Van Gestel, Sofie;
Borglum, Anders D.;
Muir, Walter;
Ewald, Henrik;
Mors, Ole;
Ivezic, Sladana;
Oruc, Lilijana;
Adolfsson, Rolf;
Blackwood, Douglas;
Kruse, Torben;
Mendlewicz, Julien;
Schalling, Martin;
Van Broeckhoven, Christine

Publication type:

Article

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 8, p. 646, doi. 10.1038/sj.ejhg.5200686

By:

Ismailov, Shoukhrat M;
Fedotov, Valeriy P;
Dadali, Elena L;
Polyakov, Alexander V;
Van Broeckhoven, Christine;
Ivanov, Vladimir I;
De Jonghe, Peter;
Timmerman, Vincent;
Evgrafov, Oleg V

Publication type:

Article

No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200469

By:

Goossens, Dirk;
Villafuerte, Sandra;
Tissir, Fadel;
Van Gestel, Sofie;
Claes, Stephan;
Souery, Daniel;
Massat, Isabelle;
Van den Bossche, Dirk;
Van Zand, Karel;
Mendlewicz, Julien;
Van Broeckhoven, Christine;
Del-Favero, Jurgen

Publication type:

Article

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 8, p. 920, doi. 10.1038/sj.ejhg.5200384

By:

Meuleman, Jan;
Kuhlenbäumer, Gregor;
Schirmacher, Anja;
Wehnert, Manfred;
De Jonghe, Peter;
De Vriendt, Els;
Young, Peter;
Airaksinen, Eila;
Pou-Serradell, Adolfo;
Prats, José-Maria;
Ringelstein, Bernd;
Stögbauer, Florian;
Van Broeckhoven, Christine;
Timmerman, Vincent

Publication type:

Article

Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 7, p. 801, doi. 10.1038/sj.ejhg.5200373

By:

Duijn, Cornelia M van;
Cruts, Marc;
Theuns, Jessie;
Van Gassen, Geert;
Backhovens, Hubert;
van den Broeck, Marleen;
Wehnert, Anita;
Serneels, Sally;
Hofman, Albert;
Van Broeckhoven, Christine

Publication type:

Article

Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 4, p. 427, doi. 10.1038/sj.ejhg.5200318

By:

Verheyen, Geert R;
Villafuerte, Sandra M;
Del-Favero, Jurgen;
Souery, Daniel;
Mendlewicz, Julien;
Van Broeckhoven, Christine;
Raeymaekers, Peter

Publication type:

Article

The Use of Biomarkers and Genetic Screening to Diagnose Frontotemporal Dementia: Evidence and Clinical Implications.

Published in:

Frontiers in Neuroscience, 2019, p. 1, doi. 10.3389/fnins.2019.00757

By:

Gossye, Helena;
Van Broeckhoven, Christine;
Engelborghs, Sebastiaan

Publication type:

Article

Current Insights into Molecular Mechanisms of Alzheimer Disease and Their Implications for Therapeutic Approaches.

Published in:

Neurodegenerative Diseases, 2007, v. 4, n. 5, p. 349, doi. 10.1159/000105156

By:

van Broeck, Bianca;
van Broeckhoven, Christine;
Kumar-Singh, Samir

Publication type:

Article

Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions: A Molecular Genetic Update.

Published in:

Neurodegenerative Diseases, 2007, v. 4, n. 2/3, p. 227, doi. 10.1159/000101847

By:

van der Zee, Julie;
Gijselinck, Ilse;
Pirici, Daniel;
Kumar-Singh, Samir;
Cruts, Marc;
Van Broeckhoven, Christine

Publication type:

Article

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.

Published in:

Nature Genetics, 2008, v. 40, n. 12, p. 1402, doi. 10.1038/ng.251

By:

Aulchenko, Yurii S.;
Hoppenbrouwers, Ilse A.;
Ramagopalan, Sreeram V.;
Broer, Linda;
Jafari, Naghmeh;
Hillert, Jan;
Link, Jenny;
Lundström, Wangko;
Greiner, Eva;
Dessa Sadovnick, A;
Goossens, Dirk;
Van Broeckhoven, Christine;
Del-Favero, Jurgen;
Ebers, George C.;
Oostra, Ben A.;
van Duijn, Cornelia M.;
Hintzen, Rogier Q.

Publication type:

Article

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.

Published in:

Nature Genetics, 2008, v. 40, n. 1, p. 29, doi. 10.1038/ng.2007.52

By:

van Es, Michael A.;
van Vught, Paul W. J.;
Blauw, Hylke M.;
Franke, Lude;
Saris, Christiaan G. J.;
Van Den Bosch, Ludo;
de Jong, Sonja W.;
de Jong, Vianney;
Baas, Frank;
van't Slot, Ruben;
Lemmens, Robin;
Schelhaas, Helenius J.;
Birve, Anna;
Sleegers, Kristel;
Van Broeckhoven, Christine;
Schymick, Jennifer C.;
Traynor, Bryan J.;
Wokke, John H. J.;
Wijmenga, Cisca;
Robberecht, Wim

Publication type:

Article

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.

Published in:

Nature Genetics, 2004, v. 36, n. 6, p. 597, doi. 10.1038/ng1328

By:

Irobi, Joy;
Van Impe, Katrien;
Seeman, Pavel;
Jordanova, Albena;
Dierick, Ines;
Verpoorten, Nathalie;
Michalik, Andrej;
De Vriendt, Els;
Jacobs, An;
Van Gerwen, Veerle;
Vennekens, Krist'l;
Mazanec, Radim;
Tournev, Ivailo;
Hilton-Jones, David;
Talbot, Kevin;
Kremensky, Ivo;
Van Den Bosch, Ludo;
Robberecht, Wim;
Vandekerckhove, Joël;
Van Broeckhoven, Christine

Publication type:

Article

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.

Published in:

Nature Genetics, 2001, v. 28, n. 3, p. 211, doi. 10.1038/90034

By:

Van Goethem, Gert;
Dermaut, Bart;
Löfgren, Ann;
Martin, Jean-Jacques;
Van Broeckhoven, Christine

Publication type:

Article

Of giant axons and curly hair.

Published in:

Nature Genetics, 2000, v. 26, n. 3, p. 254, doi. 10.1038/81521

By:

Timmerman, Vincent;
De Jonghe, Peter;
Van Broeckhoven, Christine

Publication type:

Article

Why female crested tits copulate repeatedly with the same partner: evidence for the mate assessment hypothesis

Published in:

Behavioral Ecology, 1997, v. 8, n. 1, p. 87, doi. 10.1093/beheco/8.1.87

By:

Lens, Luc;
Dhondt, Andre A.;
Van Broeckhoven, Christine;
Van Dongen, Stefan;
Van den Broeck, Marleen

Publication type:

Article

Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.

Published in:

Journal of the Peripheral Nervous System, 2002, v. 7, n. 2, p. 87, doi. 10.1046/j.1529-8027.2002.02014.x

By:

Irobi, Joy;
Nelis, Eva;
Verhoeven, Kristien;
De Vriendt, Els;
Dierick, Ines;
De Jonghe, Peter;
Van Broeckhoven, Christine;
Timmerman, Vincent

Publication type:

Article

Course of objective memory impairment in non-demented subjects attending a memory clinic and predictors of outcome.

Published in:

International Journal of Geriatric Psychiatry, 2000, v. 15, n. 4, p. 363, doi. 10.1002/(SICI)1099-1166(200004)15:4<363::AID-GPS129>3.0.CO;2-4

By:

Visser, Pieter Jelle;
Verhey, Frans R. J.;
Ponds, Rudolf W. H. M.;
Cruts, Marc;
Van Broeckhoven, Christine L.;
Jolles, Jellemer

Publication type:

Article

Phenotypic Variation of Autosomal-Dominant Corticobasal Degeneration.

Published in:

European Neurology, 2012, v. 67, n. 3, p. 142, doi. 10.1159/000334731

By:

Jung, Hans H.;
Bremer, Juliane;
Streffer, Johannes;
Virdee, Kanwar;
Spillantini, Maria Grazia;
Crowther, R. Anthony;
Brugger, Peter;
Van Broeckhoven, Christine;
Aguzzi, Adriano;
Tolnay, Markus

Publication type:

Article

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

Published in:

Molecular Neurodegeneration, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13024-015-0024-9

By:

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

Publication type:

Article

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 Gene.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13633, doi. 10.3390/ijms222413633

By:

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

Publication type:

Article

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

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 12, p. 4516, doi. 10.3390/ijms21124516

By:

Martins, Soraia;
Müller-Schiffmann, Andreas;
Erichsen, Lars;
Bohndorf, Martina;
Wruck, Wasco;
Sleegers, Kristel;
Van Broeckhoven, Christine;
Korth, Carsten;
Adjaye, James

Publication type:

Article

Cyclin-dependent kinase 5 is associated with risk for Alzheimer’s disease in a Dutch population-based study.

Published in:

Journal of Neurology, 2008, v. 255, n. 5, p. 655, doi. 10.1007/s00415-008-0770-5

By:

Arias-Vásquez, Alejandro;
Aulchenko, Yurii S.;
Isaacs, Aaron;
Van Oosterhout, Andy;
Sleegers, Kristel;
Hofman, Albert;
Van Broeckhoven, Christine;
Oostra, Ben A.;
Breteler, Monique;
Van Duijn, Cornelia M.

Publication type:

Article

Novel PSEN1 Mutation in a Bulgarian Patient With Very Early-Onset Alzheimer's Disease, Spastic Paraparesis, and Extrapyramidal Signs.

Published in:

2009

By:

Traykov, Latchezar Dintchov;
Mehrabian, Shima;
Van den Broeck, Marleen;
Raycheva, Margarita Radoslavova;
Cruts, Marc;
Jordanova, Albena Kirilova;
Van Broeckhoven, Christine

Publication type:

Case Study

Mutation (variation) databases and registries: a rationale for coordination of efforts.

Published in:

2011

By:

Auerbach, Arleen D.;
Burn, John;
Cassiman, Jean-Jacques;
Claustres, Mireille;
Cotton, Richard G. H.;
Cutting, Garry;
den Dunnen, Johan T.;
El-Ruby, Mona;
Vargas, Aida Falcon;
Greenblatt, Marc S.;
Macrae, Finlay;
Matsubara, Yoichi;
Rimoin, David L.;
Vihinen, Mauno;
Van Broeckhoven, Christine

Publication type:

Letter

Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.

Published in:

Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0441-9

By:

Thonberg, Håkan;
Huei-Hsin Chiang;
Lilius, Lena;
Forsell, Charlotte;
Lindström, Anna-Karin;
Johansson, Charlotte;
Björkström, Jenny;
Thordardottir, Steinunn;
Sleegers, Kristel;
Van Broeckhoven, Christine;
Rönnbäck, Annica;
Graff, Caroline

Publication type:

Article

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies.

Published in:

Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0195-1

By:

Goossens, Joery;
Vanmechelen, Eugeen;
Trojanowski, John Q.;
Lee, Virginia M. Y.;
Van Broeckhoven, Christine;
van der Zee, Julie;
Engelborghs, Sebastiaan

Publication type:

Article

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies.

Published in:

Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0195-1

By:

Goossens, Joery;
Vanmechelen, Eugeen;
Trojanowski, John Q.;
Lee, Virginia M. Y.;
Van Broeckhoven, Christine;
van der Zee, Julie;
Engelborghs, Sebastiaan

Publication type:

Article

Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 1, p. 70, doi. 10.3109/17482968.2012.690418

By:

Chester, Catarina;
de Carvalho, Mamede;
Miltenberger, Gabriel;
Pereira, Sónia;
Dillen, Lubina;
van der Zee, Julie;
van Broeckhoven, Christine;
de Mendonça, Alexandre

Publication type:

Article

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 2, p. 313, doi. 10.1093/hmg/ddm309

By:

van der Zee, Julie;
Urwin, Hazel;
Engelborghs, Sebastiaan;
Bruyland, Marc;
Vandenberghe, Rik;
Dermaut, Bart;
De Pooter, Tim;
Peeters, Karin;
Santens, Patrick;
De Deyn, Peter P.;
Fisher, Elizabeth M.;
Collinge, John;
Isaacs, Adrian M.;
Van Broeckhoven, Christine

Publication type:

Article

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 13, p. 1753, doi. 10.1093/hmg/ddi182

By:

Cruts, Marc;
Rademakers, Rosa;
Gijselinck, Ilse;
van der Zee, Julie;
Dermaut, Bart;
de Pooter, Tim;
de Rijk, Peter;
Del-Favero, Jurgen;
van Broeckhoven, Christine

Publication type:

Article

Alzheimer-associated C allele of the promoter polymorphism −22C>T causes a critical neuron-specific decrease of presenilin 1 expression.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 8, p. 869, doi. 10.1093/hmg/ddg098

By:

Theuns, Jessie;
Remacle, Jacques;
Killick, Richard;
Corsmit, Ellen;
Vennekens, Krist'l;
Huylebroeck, Danny;
Cruts, Marc;
Broeckhoven, Christine Van

Publication type:

Article

Pathogenesis of polyglutamine disorders: aggregation revisited.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 2, p. 173, doi. 10.1093/hmg/ddg295

By:

Michalik, Andrej;
Van Broeckhoven, Christine

Publication type:

Article

Pathogenesis of polyglutamine disorders: aggregation revisited.

Published in:

Human Molecular Genetics, 2003, v. 12, n. suppl_2, p. R173, doi. 10.1093/hmg/ddg295

By:

Michalik, Andrej;
Van Broeckhoven, Christine

Publication type:

Article