Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
NanoPack: visualizing and processing long-read sequencing data
20181.7k citationsWouter De Coster, Svenn D’Hert et al.Bioinformaticsprofile →
The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
2013928 citationsKristin Rentzsch, Marc Cruts et al.profile →
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene
1992568 citationsCornelia M. van Duijn, Patrick Cras et al.profile →
Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins
2013362 citationsIlse Gijselinck, Kristin Rentzsch et al.profile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of Marc Cruts'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 Marc Cruts with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc Cruts more than expected).
This network shows the impact of papers produced by Marc Cruts. 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 Marc Cruts. The network helps show where Marc Cruts may publish in the future.
Co-authorship network of co-authors of Marc Cruts
This figure shows the co-authorship network connecting the top 25 collaborators of Marc Cruts.
A scholar is included among the top collaborators of Marc Cruts 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 Marc Cruts. Marc Cruts is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Coster, Wouter De, Svenn D’Hert, Darrin T. Schultz, Marc Cruts, & Christine Van Broeckhoven. (2018). NanoPack: visualizing and processing long-read sequencing data. Bioinformatics. 34(15). 2666–2669.1729 indexed citations breakdown →
2.
Philtjens, Stéphanie, Sara Van Mossevelde, Julie van der Zee, et al.. (2016). Unraveling the genetic role of SORT1 in the Belgian frontotemporal dementia population. Journal of Neurochemistry. 138. 310–311.1 indexed citations
Dickerson, Bradford C., John R. Hodges, Paul McMonagle, et al.. (2015). Hodges' Frontotemporal Dementia. Cambridge University Press eBooks.11 indexed citations
6.
Cruts, Marc, Sebastiaan Engelborghs, Julie van der Zee, & Christine Van Broeckhoven. (2015). C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. VUBIR (Vrije Universiteit Brussel). 1–26.12 indexed citations
Gijselinck, Ilse, Kristel Sleegers, Sebastiaan Engelborghs, et al.. (2007). Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Ghent University Academic Bibliography (Ghent University).3 indexed citations
11.
Lind, J., Martin Ingvar, Jonas Persson, Marc Cruts, & Lars‐Göran Nilsson. (2006). Parietal cortex activation predicts longitudinal memory decline in APOE ε4 carriers.. Neuroreport. 1683–1686.2 indexed citations
12.
Broeckhoven, Christine Van, et al.. (2004). The molecular genetics of early-onset Alzheimer's disease. Ghent University Academic Bibliography (Ghent University).2 indexed citations
Dermaut, Bart, Jessie Theuns, Marleen Van den Broeck, et al.. (2002). Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample. Ghent University Academic Bibliography (Ghent University).1 indexed citations
15.
Cruts, Marc, Bart Dermaut, Samir Kumar‐Singh, et al.. (2002). Novel German APP V715A mutation associated with presenile Alzheimer's disease. Neurobiology of Aging. 23(1).5 indexed citations
16.
Theuns, Jessie, Samir Kumar‐Singh, Bart Dermaut, et al.. (2002). In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing. Neurobiology of Aging. 23(1).1 indexed citations
17.
Rademakers, R., Marc Cruts, Bart Dermaut, et al.. (2002). Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cm interval. Neurobiology of Aging. 23(1).17 indexed citations
18.
Cruts, Marc, Bart Dermaut, R. Rademakers, et al.. (2001). Amyloid beta-secretase gene (BACE) is neither mutated nor associated with early-onset Alzheimers disease. Ghent University Academic Bibliography (Ghent University).1 indexed citations
19.
Cruts, Marc, C. De Jonghe, Carolyn Tysoe, et al.. (1999). Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion. The American Journal of Human Genetics. 65(4).10 indexed citations
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.