Latest papers

Widespread genomic divergence during sympatric speciation.

QTL detection by multi-parent linkage mapping in oil palm (Elaeis guineensis Jacq.).

Linkage and association study of discoidin domain receptor 1 as a novel susceptibility gene for childhood IgA nephropathy.

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.

Suggestive evidence on chromosomes 2 and 19 for HTR1A-independent linkage of genes to major depression.

Genotypic linkages of VP4, VP6, VP7, NSP4, NSP5 genes of rotaviruses circulating among children with acute gastroenteritis in Thailand.

Variance component methods for analysis of complex phenotypes.

Quantitative trait loci for resistance to Pyrenophora tritici-repentis race 1 in a Chinese wheat.

Molecular mapping and candidate gene identification of the Rf2 gene for pollen fertility restoration in sorghum [Sorghum bicolor (L.) Moench].

Quantitative trait loci in the Ogle/TAM O-301 oat mapping population controlling resistance to Puccinia coronata in the field.

Fine mapping of a resistance gene to bacterial leaf pustule in soybean.

Potentials and limits of pairwise kinship analysis using autosomal short tandem repeat loci.

A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse.

Confirmation and generalization of an alcohol-dependence locus on chromosome 10q.

Genomic microstructure and differential expression of the genes encoding UDP-glucose:sinapate glucosyltransferase (UGT84A9) in oilseed rape (Brassica napus).

Genes, genetics, and Class III malocclusion.

Mutation and the evolution of recombination.

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase.

Copy number variation, chromosome rearrangement, and their association with recombination during avian evolution.

Comprehensive genetic and mutation analysis of familial dementia with Lewy bodies linked to 2q35-q36.