B. E. Madsen

发表

A simple way to evaluate self-designed probes for tumor specific Multiplex Ligation-dependent Probe Amplification (MLPA)

L. Hansen, J. Overgaard, E. Wiechec, 2010, BMC Research Notes.

A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

S. Browning, B. Madsen, B. E. Madsen, 2009, PLoS genetics.

A periodic pattern of SNPs in the human genome.

C. Wiuf, P. Villesen, B. Madsen, 2007, Genome research.

The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population

T. Ørntoft, C. Andersen, A. Tjønneland, 2008, BMC Medical Genetics.

Short Tandem Repeats in Human Exons: A Target for Disease Mutations

Carsten Wiuf, Palle Villesen, C. Wiuf, 2008, BMC Genomics.

Germline Mutation in RNASEL Predicts Increased Risk of Head and Neck, Uterine Cervix and Breast Cancer

Carsten Wiuf, Jens Overgaard, Marianne Nordsmark, 2008, PloS one.

Conflicting results in SNP genotype assessment.

C. Wiuf, L. Hansen, B. Madsen, 2007, BioTechniques.

Short tandem repeats and genetic variation.

C. Wiuf, P. Villesen, B. Madsen, 2010, Methods in molecular biology.

Tandem Repeats and Genetic Variation

C. Wiuf, P. Villesen, B. Madsen, 2010 .