Edwin J C G van den Oord

发表

Optimization of two-stage genetic designs where data are combined using an accurate and efficient approximation for Pearson's statistic.

József Bukszár, Edwin J C G van den Oord, 2006, Biometrics.

MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples.

Daniel Adkins, Patrick F Sullivan, Christina M Hultman, 2012, Epigenomics.

Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.

Hans-Jürgen Möller, József Bukszár, Po-Hsiu Kuo, 2008, Archives of general psychiatry.

Multivariate adaptive regression splines: a powerful method for detecting disease–risk relationship differences among subgroups

Edwin J C G van den Oord, E. J. van den Oord, L. Eaves, 2006, Statistics in medicine.

Twins and the study of rater (dis)agreement.

Meike Bartels, Dorret I Boomsma, James J Hudziak, 2007, Psychological methods.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults.

Guimin Gao, Patrick F Sullivan, Wenan Chen, 2014, JAMA psychiatry.

Accurate and efficient power calculations for 2 × m tables in unmatched case‐control designs

József Bukszár, Edwin J C G van den Oord, E. J. van den Oord, 2006, Statistics in medicine.

False discoveries and models for gene discovery.

Patrick F Sullivan, Edwin J C G van den Oord, P. Sullivan, 2003, Trends in genetics : TIG.

(1)H nuclear magnetic resonance metabolomics analysis identifies novel urinary biomarkers for lung function.

Madhukar S. Dasika, Joel G Pounds, Bradley Todd Webb, 2010, Journal of proteome research.