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G. T. Spijker · SciRah

Researcher profile · Semantic Scholar

G. T. Spijker

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G. T. Spijker — researcher profile on SciRah

h-index: 6
Works: 13
Citations: 137

Most-cited papers

Mapping of a susceptibility gene for multiple sclerosis to the 51 kb interval between G511525 and D6S1666 using a new method of haplotype sharing analysis
M. Boon, I. Nolte, M. Bruinenberg, G. T. Spijker +8 more
2001Neurogenetics41 citations
Semantic Scholar
Simulation studies of detection of a complex disease in a partially isolated population.
D. Levinson, A. Kirby, Stephen Slepner, I. Nolte +2 more
2001American journal of medical genetics38 citations Open access
Semantic Scholar
Anaphylaxis caused by topical application of a sunscreen containing benzophenone‐3
G. T. Spijker, M. Schuttelaar, L. Barkema, A. Velders +1 more
2008Contact Dermatitis25 citations Open access
Semantic Scholar
Association testing by haplotype-sharing methods applicable to whole-genome analysis
I. Nolte, A. D. De Vries, G. T. Spijker, R. Jansen +3 more
2007BMC Proceedings15 citations Open access
Semantic Scholar
A factorial experiment for optimizing the PCR conditions in routine genotyping
M. Niens, G. T. Spijker, A. Diepstra, G. T. Te Meerman
2005Biotechnology and applied biochemistry11 citations
Semantic Scholar
Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained ‐ Permutation Approach
G. T. Spijker, I. Nolte, R. Jansen, G. Te Meerman
2005Annals of Human Genetics6 citations Open access
Semantic Scholar
Efficiency control in large-scale genotyping using analysis of variance
G. T. Spijker, M. Bruinenberg, G. T. Te Meerman
2005Applied Biochemistry and Biotechnology1 citations
Semantic Scholar
Finding causal variants for complex genetic disease
G. T. Spijker
20070 citations
Semantic Scholar
Finding causal variants for complex genetic disease : the contribution of statistical methodology to fine-mapping and assay optimization
G. T. Spijker
20070 citations
Semantic Scholar
Cross Haplotype Sharing Statistic : Haplotype length based method for whole genome association testing
A. D. De Vries, I. Nolte, G. T. Spijker, D. Brinza +2 more
20060 citations
Semantic Scholar
A new method for mapping genes based on haplotype sharing.
Nolte, G. T. Spijker, G. T. Te Meerman
20000 citations
Semantic Scholar
A comparison of the power of haplotype sharing analysis and two locus association analysis for fine-mapping of genes contributing to complex genetic disease.
G. T. Spijker, I. Nolte, G. Meerman
19990 citations
Semantic Scholar
Refinement of the genetic mapping of the hemochromatosis gene by use of haplotype sharing analysis, and application of this method to Multiple Sclerosis
G. Meerman, I. Nolte, G. T. Spijker
19990 citations
Semantic Scholar

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I. Nolte — researcher profile on SciRah
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