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Genomics|June 26, 2007
Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inferenceIan W Saunders, Jesper Brohede, Garry N Hannan
Genetic Epidemiology|April 20, 2007
A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker dataIan W Saunders, Garry N Hannan, Jesper Brohede, et al.
Nucleic Acids Research|October 4, 2005
PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarraysJesper Brohede, Rob Dunne, James D McKay, et al.
Prenatal Diagnosis|November 13, 2007
Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarrayJillian Cross, Greg Peters, Zhanhe Wu, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer familiesIan W Saunders, Jason Ross, Finlay Macrae, et al.
Clinical Dysmorphology|December 1, 2005
Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual associationKatherine Neas, Greg Peters, Julianne Jackson, et al.
Human Genetics|March 7, 2006
Evolutionary evidence suggests that CpG island-associated Alus are frequently unmethylated in human germlineJesper Brohede, Keith N Rand
Molecular Biology and Evolution|October 8, 2003
Single-molecule analysis of the hypermutable tetranucleotide repeat locus D21S1245 through sperm genotyping: a heterogeneous pattern of mutation but no clear male age effectJesper Brohede, Norman Arnheim, Hans Ellegren
Mutation Research|December 31, 2003
Individual variation in microsatellite mutation rate in barn swallowsJesper Brohede, Anders P Møller, Hans Ellegren
Journal of Neurogenetics|October 6, 2010
A DNA methylation study of the amyloid precursor protein gene in several brain regions from patients with familial Alzheimer diseaseJesper Brohede, Mia Rinde, Bengt Winblad, et al.
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