Cornelis A. Albers

The cluster variation method for efficient linkage analysis on extended pedigrees.

Haplotype inference in general pedigrees using the cluster variation method.

Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals.

Modeling linkage disequilibrium in exact linkage computations: a comparison of first-order Markov approaches and the clustered-markers approach.

Dindel: accurate indel calls from short-read data.

The variant call format and VCFtools.

Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.

A systematic survey of loss-of-function variants in human protein-coding genes.

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.

Seventy-five genetic loci influencing the human red blood cell.

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.

SMIM1 underlies the Vel blood group and influences red blood cell traits.

Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.

New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome.

Estimation of heritability of different outcomes for genetic studies of TNFi response in patients with rheumatoid arthritis.

Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.

Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.