Sinke, R.J.
University Medical Center Groningen · University of Groningen
3 papers on CoChatORCID 0000-0002-0497-4780
Most cited papers
- Verified
A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q
Bakker, S. C., Meulen, E. M. V. D., Buitelaar, J. K., Sandkuijl, L. A., Pauls, D. L., Monsuur, A. J., Slot, R. V. ‘., Minderaa, R. B., Gunning, W. B., Pearson, P. L., et al. (2003) · The American Journal of Human Genetics
Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology
Cited by 257
- Verified
Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis
Deelen, P., van Dam, S., Herkert, J. C., Karjalainen, J. M., Brugge, H., Abbott, K. M., van Diemen, C. C., van der Zwaag, P. A., Gerkes, E. H., Zonneveld-Huijssoon, E., et al. (2019) · Nature Communications
Genomics and Rare DiseasesBioinformatics and Genomic Networks
Cited by 138
- Verified
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1
Miyake, N., Wolf, N. I., Cayami, F. K., Crawford, J., Bley, A., Bulas, D., Conant, A., Bent, S. J., Gripp, K. W., Hahn, A., et al. (2017) · neurogenetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 48
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