Cornelis A. Albers

Donders Institute for Brain, Radboud University

Affiliated withRadboud University Radboudumc

Research Area

Developmental Biology

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 170	2017

Other Publications

Article	Year
The cluster variation method for efficient linkage analysis on extended pedigrees. BMC bioinformatics\| PubMed ID: 16723002	2006
Haplotype inference in general pedigrees using the cluster variation method. Genetics\| PubMed ID: 17660564	2007
Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals. American journal of human genetics\| PubMed ID: 18319071	2008
Modeling linkage disequilibrium in exact linkage computations: a comparison of first-order Markov approaches and the clustered-markers approach. BMC proceedings\| PubMed ID: 18466504	2007
Dindel: accurate indel calls from short-read data. Genome research\| PubMed ID: 20980555	2011
The variant call format and VCFtools. Bioinformatics (Oxford, England)\| PubMed ID: 21653522	2011
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nature genetics\| PubMed ID: 21765411	2011
A systematic survey of loss-of-function variants in human protein-coding genes. Science (New York, N.Y.)\| PubMed ID: 22344438	2012
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nature genetics\| PubMed ID: 22366785	2012
Seventy-five genetic loci influencing the human red blood cell. Nature\| PubMed ID: 23222517	2012
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome research\| PubMed ID: 23478400	2013
SMIM1 underlies the Vel blood group and influences red blood cell traits. Nature genetics\| PubMed ID: 23563608	2013
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci. Genome research\| PubMed ID: 23570689	2013
New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome. Current opinion in genetics & development\| PubMed ID: 23602329	2013
Estimation of heritability of different outcomes for genetic studies of TNFi response in patients with rheumatoid arthritis. Annals of the rheumatic diseases\| PubMed ID: 25114059	2015
Dynamics of gene silencing during X inactivation using allele-specific RNA-seq. Genome biology\| PubMed ID: 26235224	2015
Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq. Genome biology\| PubMed ID: 26850229	2016
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Cell\| PubMed ID: 27863251	2016