Cornelis A. Albers Donders Institute for Brain, Cognition and Behaviour Radboud University Biography Publications Institution JoVE Articles Cornelis A. Albers has not added a biography. If you are Cornelis A. Albers and would like to personalize this page please email our Author Liaison for assistance. Publications Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells Cell. Nov, 2016 | Pubmed ID: 27863251 Erratum To: Dynamics of Gene Silencing During X Inactivation Using Allele-specific RNA-seq Genome Biology. Feb, 2016 | Pubmed ID: 26850229 Dynamics of Gene Silencing During X Inactivation Using Allele-specific RNA-seq Genome Biology. Aug, 2015 | Pubmed ID: 26235224 Estimation of Heritability of Different Outcomes for Genetic Studies of TNFi Response in Patients with Rheumatoid Arthritis Annals of the Rheumatic Diseases. Dec, 2015 | Pubmed ID: 25114059 New Insights into the Genetic Basis of TAR (thrombocytopenia-absent Radii) Syndrome Current Opinion in Genetics & Development. Jun, 2013 | Pubmed ID: 23602329 Maps of Open Chromatin Highlight Cell Type-restricted Patterns of Regulatory Sequence Variation at Hematological Trait Loci Genome Research. Jul, 2013 | Pubmed ID: 23570689 SMIM1 Underlies the Vel Blood Group and Influences Red Blood Cell Traits Nature Genetics. May, 2013 | Pubmed ID: 23563608 The Origin, Evolution, and Functional Impact of Short Insertion-deletion Variants Identified in 179 Human Genomes Genome Research. May, 2013 | Pubmed ID: 23478400 Seventy-five Genetic Loci Influencing the Human Red Blood Cell Nature. Dec, 2012 | Pubmed ID: 23222517 Compound Inheritance of a Low-frequency Regulatory SNP and a Rare Null Mutation in Exon-junction Complex Subunit RBM8A Causes TAR Syndrome Nature Genetics. Feb, 2012 | Pubmed ID: 22366785 A Systematic Survey of Loss-of-function Variants in Human Protein-coding Genes Science (New York, N.Y.). Feb, 2012 | Pubmed ID: 22344438 Exome Sequencing Identifies NBEAL2 As the Causative Gene for Gray Platelet Syndrome Nature Genetics. Jul, 2011 | Pubmed ID: 21765411 The Variant Call Format and VCFtools Bioinformatics (Oxford, England). Aug, 2011 | Pubmed ID: 21653522 Dindel: Accurate Indel Calls from Short-read Data Genome Research. Jun, 2011 | Pubmed ID: 20980555 Multipoint Approximations of Identity-by-descent Probabilities for Accurate Linkage Analysis of Distantly Related Individuals American Journal of Human Genetics. Mar, 2008 | Pubmed ID: 18319071 Modeling Linkage Disequilibrium in Exact Linkage Computations: a Comparison of First-order Markov Approaches and the Clustered-markers Approach BMC Proceedings. 2007 | Pubmed ID: 18466504 Haplotype Inference in General Pedigrees Using the Cluster Variation Method Genetics. Oct, 2007 | Pubmed ID: 17660564 The Cluster Variation Method for Efficient Linkage Analysis on Extended Pedigrees BMC Bioinformatics. Mar, 2006 | Pubmed ID: 16723002 Rapid neuronal Differensiering av Induced Pluripotent stamceller for måling Network Aktivitet på Micro-elektrode Arrays Monica Frega*1,2, Sebastianus H. C. van Gestel*3, Katrin Linda2,3, Jori van der Raadt3, Jason Keller1,2, Jon-Ruben Van Rhijn1,2, Dirk Schubert1,2, Cornelis A. Albers2,3,4, Nael Nadif Kasri1,2,3 1Department of Cognitive Neurosciences, Radboudumc, 2Donders Institute for Brain, Cognition and Behaviour, Radboud University, 3Department of Human Genetics, Radboudumc, 4Department of Molecular Developmental Biology, Radboud University JoVE 54900 Developmental Biology
Rapid neuronal Differensiering av Induced Pluripotent stamceller for måling Network Aktivitet på Micro-elektrode Arrays Monica Frega*1,2, Sebastianus H. C. van Gestel*3, Katrin Linda2,3, Jori van der Raadt3, Jason Keller1,2, Jon-Ruben Van Rhijn1,2, Dirk Schubert1,2, Cornelis A. Albers2,3,4, Nael Nadif Kasri1,2,3 1Department of Cognitive Neurosciences, Radboudumc, 2Donders Institute for Brain, Cognition and Behaviour, Radboud University, 3Department of Human Genetics, Radboudumc, 4Department of Molecular Developmental Biology, Radboud University JoVE 54900 Developmental Biology
