Christine Van Broeckhoven

30PUBLICATIONS
285CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Archaeology of Asia, Africa and the Americas
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Publications (30)

|Sep 03, 2024
The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer's disease.

Anne Mette G Jensen, Jan Raska, Petr Fojtik

|Jul 11, 2023
Mutated Toll-like receptor 9 increases Alzheimer's disease risk by compromising innate immunity protection.

Rita Cacace, Lujia Zhou, Elisabeth Hendrickx Van de Craen

|Sep 29, 2022
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.

Helena Gossye, Sara Van Mossevelde, Anne Sieben

|Apr 05, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementias.

Céline Bellenguez, Fahri Küçükali, Iris E Jansen

|Mar 25, 2022
Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology.

Evelien Van Schoor, Mathieu Vandenbulcke, Valérie Bercier

|Feb 17, 2022
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation.

Alexander Neumann, Fahri Küçükali, Isabelle Bos

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Frequent Collaborators

8 joint publications

Kristel Sleegers

7 joint publications

Magda Tsolaki

6 joint publications

Sven J van der Lee

6 joint publications

Florence Pasquier