Kees Albers
Kees Albers
Andere namenCornelis A Albers
Scenic Biotech
Geverifieerd e-mailadres voor scenicbiotech.com
Geciteerd door
Geciteerd door
A global reference for human genetic variation
AGR 1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison ...
Nature, 2015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061-1073, 2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Genetic drivers of epigenetic and transcriptional variation in human immune cells
L Chen, B Ge, FP Casale, L Vasquez, T Kwan, D Garrido-Martín, S Watt, ...
Cell 167 (5), 1398-1414. e24, 2016
Dindel: accurate indel calls from short-read data
CA Albers, G Lunter, DG MacArthur, G McVean, WH Ouwehand, R Durbin
Genome research 21 (6), 961-973, 2011
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
CA Albers, DS Paul, H Schulze, K Freson, JC Stephens, PA Smethurst, ...
Nature genetics 44 (4), 435-439, 2012
Seventy-five genetic loci influencing the human red blood cell
P van der Harst, W Zhang, IM Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
CA Albers, A Cvejic, R Favier, EE Bouwmans, MC Alessi, P Bertone, ...
Nature genetics 43 (8), 735-737, 2011
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
SB Montgomery, DL Goode, E Kvikstad, CA Albers, ZD Zhang, XJ Mu, ...
Genome research 23 (5), 749-761, 2013
Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays
M Frega, SHC van Gestel, K Linda, J van der Raadt, J Keller, ...
JoVE (Journal of Visualized Experiments), e54900-e54900, 2017
Approximate inference and constrained optimization
T Heskes, K Albers, B Kappen
Proceedings of the Nineteenth conference on Uncertainty in Artificial …, 2002
SMIM1 underlies the Vel blood group and influences red blood cell traits
A Cvejic, L Haer-Wigman, JC Stephens, M Kostadima, PA Smethurst, ...
Nature genetics 45 (5), 542-545, 2013
Dynamics of gene silencing during X inactivation using allele-specific RNA-seq
H Marks, HHD Kerstens, TS Barakat, E Splinter, RAM Dirks, G van Mierlo, ...
Genome biology 16 (1), 1-20, 2015
New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome
CA Albers, R Newbury-Ecob, WH Ouwehand, C Ghevaert
Current opinion in genetics & development 23 (3), 316-323, 2013
Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci
DS Paul, CA Albers, A Rendon, K Voss, J Stephens, P van der Harst, ...
Genome research 23 (7), 1130-1141, 2013
ONECUT transcription factors induce neuronal characteristics and remodel chromatin accessibility
J van der Raadt, SHC van Gestel, N Nadif Kasri, CA Albers
Nucleic acids research, 2019
Estimation of heritability of different outcomes for genetic studies of TNFi response in patients with rheumatoid arthritis
MU Mirkov, L Janss, SH Vermeulen, MAFJ van de Laar, PLCM van Riel, ...
Annals of the rheumatic diseases, annrheumdis-2014-205541, 2014
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