Kraaij, Robert
Erasmus MC · McGill University and Génome Québec Innovation Centre
7 papers on CoChatORCID 0000-0003-0416-999X
Most cited papers
- Verified
Large-scale association analyses identify host factors influencing human gut microbiome composition
Kurilshikov, A., Medina-Gomez, C., Bacigalupe, R., Radjabzadeh, D., Wang, J., Demirkan, A., Le Roy, C. I., Raygoza Garay, J. A., Finnicum, C. T., Liu, X., et al. (2021) · Nature Genetics
Gut microbiota and healthGenetic Associations and Epidemiology
Cited by 1,786
- Verified
Quantifying prion disease penetrance using large population control cohorts
Minikel, E. V., Vallabh, S. M., Lek, M., Estrada, K., Samocha, K. E., Sathirapongsasuti, J. F., McLean, C. Y., Tung, J. Y., Yu, L. P. C., Gambetti, P., et al. (2016) · Science Translational Medicine
Prion Diseases and Protein MisfoldingGenomics and Rare Diseases
Cited by 442
- Verified
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
Robak, L. A., Jansen, I. E., van Rooij, J., Uitterlinden, A. G., Kraaij, R., Jankovic, J., Heutink, P., Shulman, J. M., International Parkinson’s Disease Genomics Consortium (IPDGC), Nalls, M. A., et al. (2017) · Brain
Lysosomal Storage Disorders ResearchParkinson's Disease Mechanisms and Treatments
Cited by 433
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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Holstege, H., Hulsman, M., Charbonnier, C., Grenier-Boley, B., Quenez, O., Grozeva, D., van Rooij, J. G. J., Sims, R., Ahmad, S., Amin, N., et al. (2022) · Nature Genetics
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 226
- Verified
Uncompromised 10-year survival of oldest old carrying somatic mutations in DNMT3A and TET2
van den Akker, E. B., Pitts, S. J., Deelen, J., Moed, M. H., Potluri, S., van Rooij, J., Suchiman, H. E. D., Lakenberg, N., de Dijcker, W. J., Uitterlinden, A. G., et al. (2016) · Blood
Acute Myeloid Leukemia ResearchCancer Genomics and Diagnostics
Cited by 49
- Verified
A rare missense variant in RCL1 segregates with depression in extended families.
Amin, N., de Vrij, F. M. S., Baghdadi, M., Brouwer, R. W. W., van Rooij, J. G. J., Jovanova, O., Uitterlinden, A. G., Hofman, A., Janssen, H. L. A., Darwish Murad, S., et al. (2018) · Molecular Psychiatry
Genetic Associations and EpidemiologyTreatment of Major Depression
Cited by 37
- Verified
A microbiome study to explore the gut-skin axis in hidradenitis suppurativa
Lam, S. Y., Radjabzadeh, D., Eppinga, H., Nossent, Y. R. A., van der Zee, H. H., Kraaij, R., Konstantinov, S. R., Fuhler, G. M., Prens, E. P., Thio, H. B., et al. (2021) · Journal of Dermatological Science
Hidradenitis Suppurativa and TreatmentsGut microbiota and health
Cited by 36
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