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Donders Institute for Brain,
Cognition and Behaviour,
Department of Molecular Developmental Biology,
Donders Institute for Brain, Cognition and Behaviour
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The cluster variation method for efficient linkage analysis on extended pedigrees.
BMC bioinformatics Mar, 2006 | Pubmed ID: 16723002
Haplotype inference in general pedigrees using the cluster variation method.
Genetics Oct, 2007 | Pubmed ID: 17660564
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
Dindel: accurate indel calls from short-read data.
Genome research Jun, 2011 | Pubmed ID: 20980555
The variant call format and VCFtools.
Bioinformatics (Oxford, England) Aug, 2011 | Pubmed ID: 21653522
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.
Nature genetics Jul, 2011 | Pubmed ID: 21765411
A systematic survey of loss-of-function variants in human protein-coding genes.
Science (New York, N.Y.) Feb, 2012 | Pubmed ID: 22344438
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
Seventy-five genetic loci influencing the human red blood cell.
Nature Dec, 2012 | Pubmed ID: 23222517
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.
Genome research May, 2013 | Pubmed ID: 23478400
SMIM1 underlies the Vel blood group and influences red blood cell traits.
Nature genetics May, 2013 | Pubmed ID: 23563608
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci.
Genome research Jul, 2013 | Pubmed ID: 23570689
New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome.
Current opinion in genetics & development Jun, 2013 | Pubmed ID: 23602329
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
Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.
Genome biology Aug, 2015 | Pubmed ID: 26235224
Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.
Genome biology Feb, 2016 | Pubmed ID: 26850229
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Cell Nov, 2016 | Pubmed ID: 27863251
Radboud University
Radboudumc
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
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