Onderzoeker
Christine Van Broeckhoven
- Trefwoorden:Geneeskunde
- Disciplines:Translationele wetenschappen, Klinische wetenschappen, Basiswetenschappen
Affiliaties
- Pathologische Biochemie en Fysiologie (Departement)
Lid
Vanaf1 okt 1999 → 30 sep 2003 - Geneeskunde en Farmacie academisch/administratief (Office)
Lid
Vanaf1 okt 1993 → 30 sep 1999
Publicaties
1 - 10 van 77
- Subclinical epileptiform activity in the Alzheimer continuum(2024)
Auteurs: Amber Nous, Laura Seynaeve, Odile Feys, Vincent Wens, Xavier De Tiège, Pieter van Mierlo, Amir G Baroumand, Koenraad Nieboer, Gert-Jan Allemeersch, Shana Mangelschots, et al.
- Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum(2023)
Auteurs: Helena Gossye, Sara Van Mossevelde, Anne Sieben, Maria Bjerke, Elisabeth Hendrickx Van de Craen, Julie Van Der Zee, Peter P De Deyn, Jan De Bleecker, Jan Versijpt, Jenneke Van Den Ende, et al.
Pagina's: 1624-1636 - Associating Alzheimer's disease pathology with its cerebrospinal fluid biomarkers(2022)
Auteurs: Claire Bridel, Charisse Somers, Anne Sieben, Annemieke Rozemuller, Ellis Niemantsverdriet, Hanne Struyfs, Yannick Vermeiren, Christine Van Broeckhoven, Peter P De Deyn, Maria Bjerke, et al.
Pagina's: 4056-4064 - Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers(2022)
Auteurs: Iris E Jansen, Sven J van der Lee, Duber Gomez-Fonseca, Itziar de Rojas, Maria Carolina Dalmasso, Benjamin Grenier-Boley, Anna Zettergren, Aniket Mishra, Muhammad Ali, Victor Andrade, et al.
Pagina's: 821-842 - New insights into the genetic etiology of Alzheimer's disease and related dementias(2022)
Auteurs: Céline Bellenguez, Fahri Küçükali, Iris E Jansen, Luca Kleineidam, Sonia Moreno-Grau, Najaf Amin, Adam C Naj, Rafael Campos-Martin, Benjamin Grenier-Boley, Victor Andrade, et al.
Pagina's: 412-436 - Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease(2021)
Auteurs: Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.
- TMEM106B and CPOX are genetic determinants of cerebrospinal fluid Alzheimer's disease biomarker levels(2021)
Auteurs: Shengjun Hong, Valerija Dobricic, Olena Ohlei, Isabelle Bos, Stephanie J B Vos, Dmitry Prokopenko, Betty M Tijms, Ulf Andreasson, Kaj Blennow, Rik Vandenberghe, et al.
Pagina's: 1628-1640 - Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis(2021)
Auteurs: Julie Van Der Zee, Lubina Dillen, Yalda Baradaran-Heravi, Helena Gossye, Cemile Koçoğlu, Ivy Cuyt, Bart Dermaut, Anne Sieben, Jonathan Baets, Peter De Jonghe, et al.
- Common variants in Alzheimer's disease and risk stratification by polygenic risk scores(2021)
Auteurs: Itziar de Rojas, Sonia Moreno-Grau, Niccolo Tesi, Benjamin Grenier-Boley, Victor Andrade, Iris E Jansen, Nancy L Pedersen, Najada Stringa, Anna Zettergren, Isabel Hernández, et al.
- Hippocampal Sclerosis in Frontotemporal Dementia(2021)
Auteurs: Anne Sieben, Tim Van Langenhove, Yannick Vermeiren, Helena Gossye, Marleen Praet, Dimitri Vanhauwaert, Céline Cousaert, Sebastiaan Engelborghs, Robrecht Raedt, Paul Boon, et al.
Pagina's: 313-324