| A global reference for human genetic variation AGR 1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison ... Nature, 2015 | 15939 | 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 | 13986 | 2011 |
| A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061-1073, 2010 | 8912 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56-65, 2012 | 8535 | 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 | 1415 | 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 | 735 | 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 | 700 | 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 | 562 | 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 | 476 | 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 | 391 | 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 | 333 | 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 | 281 | 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 | 175 | 2017 |
| 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 | 141 | 2013 |
| Approximate inference and constrained optimization T Heskes, K Albers, B Kappen Proceedings of the Nineteenth conference on Uncertainty in Artificial …, 2002 | 140* | 2002 |
| 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 | 133 | 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 | 110 | 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 | 51 | 2019 |
| 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 | 48 | 2013 |
| 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 | 31 | 2014 |
Gerton LunterFull Professor, Groningen UniversityGeverifieerd e-mailadres voor umcg.nl
