Karolien Bettens

17.9k total citations
24 papers, 1.4k citations indexed

About

Karolien Bettens is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Karolien Bettens has authored 24 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 10 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Karolien Bettens's work include Alzheimer's disease research and treatments (17 papers), Genetic Associations and Epidemiology (4 papers) and Bioinformatics and Genomic Networks (4 papers). Karolien Bettens is often cited by papers focused on Alzheimer's disease research and treatments (17 papers), Genetic Associations and Epidemiology (4 papers) and Bioinformatics and Genomic Networks (4 papers). Karolien Bettens collaborates with scholars based in Belgium, Netherlands and United States. Karolien Bettens's co-authors include Kristel Sleegers, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter Paul De Deyn, Rik Vandenberghe, Nathalie Brouwers, Maria Mattheijssens, Karin Peeters, Mathieu Vandenbulcke and Caroline Van Cauwenberghe and has published in prestigious journals such as The Lancet Neurology, Human Molecular Genetics and Cerebral Cortex.

In The Last Decade

Karolien Bettens

23 papers receiving 1.4k citations

Peers

Countries citing papers authored by Karolien Bettens

Since Specialization

Citations

This map shows the geographic impact of Karolien Bettens's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Karolien Bettens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karolien Bettens more than expected).

Fields of papers citing papers by Karolien Bettens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karolien Bettens. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Karolien Bettens. The network helps show where Karolien Bettens may publish in the future.

Co-authorship network of co-authors of Karolien Bettens

This figure shows the co-authorship network connecting the top 25 collaborators of Karolien Bettens. A scholar is included among the top collaborators of Karolien Bettens based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karolien Bettens. Karolien Bettens is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Validation of a next generation sequencing assay for BRCA1, BRCA2, CHEK2 and PALB2 genetic testing 2020 ·Experimental and Molecular Pathology ·(unknown), (unknown), (unknown), Karolien Bettens, (unknown), Liuh Ling Goh	3
2	Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations 2015 ·Molecular Neurodegeneration ·Karolien Bettens, Steven Vermeulen, Caroline Van Cauwenberghe, Bavo Heeman, Bob Asselbergh, Caroline Robberecht, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, Kristel Sleegers	46
3	A 22‐single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ₄₂ 2015 ·Alzheimer s & Dementia ·Kristel Sleegers, Karolien Bettens, Arne De Roeck, Caroline Van Cauwenberghe, Elise Cuyvers, Jan Verheijen, Hanne Struyfs, Jasper Van Dongen, Steven Vermeulen, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Rik Vandenberghe, Peter Paul De Deyn, Christine Van Broeckhoven	71
4	Functional Changes in the Language Network in Response to Increased Amyloid β Deposition in Cognitively Intact Older Adults 2014 ·Cerebral Cortex ·Katarzyna Adamczuk, (unknown), Natalie Nelissen, Patrick Dupont, Stefan Sunaert, Karolien Bettens, Kristel Sleegers, Christine Van Broeckhoven, Koen Van Laere, Rik Vandenberghe	23
5	O4‐04‐03: HIGH SCORES ON A 22‐GENE RISK SCORE FOR ALZHEIMER'S DEMENTIA CORRELATE WITH EARLIER ONSET AGE AND REDUCED CSF Aβ 2014 ·Alzheimer s & Dementia ·Karolien Bettens, Caroline Van Cauwenberghe, Elise Cuyvers, Jan Verheijen, Arne De Roeck, Jasper Van Dongen, Steven Vermeulen, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Rik Vandenberghe, Peter Paul De Deyn, Christine Van Broeckhoven, Kristel Sleegers	0
6	Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia 2013 ·Neurobiology of Aging ·Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens, Tim Van Langenhove, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, (unknown), Githa Maes, Maria Mattheijssens, Karin Peeters, Patrick Cras, Rik Vandenberghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts, Kristel Sleegers	148
7	Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes 2013 ·Neurobiology of Aging ·Caroline Van Cauwenberghe, Karolien Bettens, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Steven Vermeulen, Rik Vandenberghe, Peter Paul De Deyn, Christine Van Broeckhoven, Kristel Sleegers	21
8	C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment 2013 ·Neurobiology of Aging ·Rita Cacace, Caroline Van Cauwenberghe, Karolien Bettens, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Veerle Bäumer, Lubina Dillen, Maria Mattheijssens, Karin Peeters, Marc Cruts, Rik Vandenberghe, Peter P. De Deyn, Christine Van Broeckhoven, Kristel Sleegers	62
9	Polymorphism of brain derived neurotrophic factor influences β amyloid load in cognitively intact apolipoprotein E ε4 carriers 2013 ·NeuroImage Clinical ·Katarzyna Adamczuk, (unknown), Natalie Nelissen, Kewei Chen, Kristel Sleegers, Karolien Bettens, Christine Van Broeckhoven, Mathieu Vandenbulcke, Pradeep Thiyyagura, Patrick Dupont, Koen Van Laere, Eric M. Reiman, Rik Vandenberghe	49
10	Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk 2012 ·Molecular Neurodegeneration ·Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Jean‐Charles Lambert, Ekaterina Rogaeva, Rik Vandenberghe, Nathalie Le Bastard, Florence Pasquier, Steven Vermeulen, Jasper Van Dongen, Maria Mattheijssens, Karin Peeters, Richard Mayeux, Peter St George‐Hyslop, Philippe Amouyel, Peter Paul De Deyn, Kristel Sleegers, Christine Van Broeckhoven	66
11	Genetic insights in Alzheimer's disease 2012 ·The Lancet Neurology ·Karolien Bettens, Kristel Sleegers, Christine Van Broeckhoven	248
12	Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites 2011 ·Molecular Psychiatry ·Nathalie Brouwers, Caroline Van Cauwenberghe, Sebastiaan Engelborghs, Jean‐Charles Lambert, Karolien Bettens, Nathalie Le Bastard, Florence Pasquier, (unknown), Karin Peeters, Maria Mattheijssens, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Philippe Amouyel, Kristel Sleegers, Christine Van Broeckhoven	163
13	Follow-Up Study of Susceptibility Loci for Alzheimer's Disease and Onset Age Identified by Genome-Wide Association 2010 ·Journal of Alzheimer s Disease ·Karolien Bettens, Nathalie Brouwers, Helen Van Miegroet, Ana Paula Gil, Sebastiaan Engelborghs, Peter Paul De Deyn, Rik Vandenberghe, Christine Van Broeckhoven, Kristel Sleegers	26
14	Current status on Alzheimer disease molecular genetics: from past, to present, to future 2010 ·Human Molecular Genetics ·Karolien Bettens, Kristel Sleegers, Christine Van Broeckhoven	130
15	No association betweenCALHM1and risk for Alzheimer dementia in a Belgian population 2009 ·Human Mutation ·Kristel Sleegers, Nathalie Brouwers, Karolien Bettens, Sebastiaan Engelborghs, Helen Van Miegroet, Peter Paul De Deyn, Christine Van Broeckhoven	17
16	APPandBACE1miRNA genetic variability has no major role in risk for Alzheimer disease 2009 ·Human Mutation ·Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Helen Van Miegroet, Peter Paul De Deyn, Jessie Theuns, Kristel Sleegers, Christine Van Broeckhoven	41
17	Common variation inGRB-associated Binding Protein 2 (GAB2)and increased risk for Alzheimer dementia 2008 ·Human Mutation ·Kristel Sleegers, Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Helen Van Miegroet, Peter Paul De Deyn, Christine Van Broeckhoven	27
18	DNMBP is genetically associated with Alzheimer dementia in the Belgian population 2008 ·Neurobiology of Aging ·Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Tim De Pooter, Peter Paul De Deyn, Kristel Sleegers, Christine Van Broeckhoven	9
19	SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population 2008 ·Human Mutation ·Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Kristel Sleegers	79
20	P3‐202: The neuronal sorting receptor SORL1 is genetically associated with increased risk for late‐onset Alzheimer's disease in the Belgian population 2008 ·Alzheimer s & Dementia ·Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Kristel Sleegers	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact