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| Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014 | 715 | 2014 |
| Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 602 | 2016 |
| Genome-wide patterns and properties of de novo mutations in humans LC Francioli, PP Polak, A Koren, A Menelaou, S Chun, I Renkens, ... Nature genetics 47 (7), 822-826, 2015 | 409 | 2015 |
| The Genome of the Netherlands: design, and project goals DI Boomsma, C Wijmenga, EP Slagboom, MA Swertz, LC Karssen, ... European journal of human genetics 22 (2), 221-227, 2014 | 328 | 2014 |
| Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci RC Betz, L Petukhova, S Ripke, H Huang, A Menelaou, S Redler, ... Nature communications 6 (1), 5966, 2015 | 276 | 2015 |
| Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’ P Deelen, A Menelaou, EM Van Leeuwen, A Kanterakis, F Van Dijk, ... European Journal of Human Genetics 22 (11), 1321-1326, 2014 | 123 | 2014 |
| Population-specific genotype imputations using minimac or IMPUTE2 EM Van Leeuwen, A Kanterakis, P Deelen, MV Kattenberg, PE Slagboom, ... Nature protocols 10 (9), 1285-1296, 2015 | 99 | 2015 |
| High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms MI Kurki, EI Gaal, J Kettunen, T Lappalainen, A Menelaou, V Anttila, ... PLoS genetics 10 (1), e1004134, 2014 | 78 | 2014 |
| Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold A Menelaou, J Marchini Bioinformatics 29 (1), 84-91, 2013 | 59 | 2013 |
| Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels EM Van Leeuwen, LC Karssen, J Deelen, A Isaacs, C Medina-Gomez, ... Nature communications 6 (1), 6065, 2015 | 52 | 2015 |
| Genomic and functional overlap between somatic and germline chromosomal rearrangements S van Heesch, M Simonis, MJ van Roosmalen, V Pillalamarri, H Brand, ... Cell reports 9 (6), 2001-2010, 2014 | 30 | 2014 |
| A framework for the detection of de novo mutations in family-based sequencing data LC Francioli, M Cretu-Stancu, KV Garimella, M Fromer, WP Kloosterman, ... European Journal of Human Genetics 25 (2), 227-233, 2017 | 29 | 2017 |
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| Association claims in the sequencing era SL Pulit, M Leusink, A Menelaou, PIW De Bakker Genes 5 (1), 196-213, 2014 | 11 | 2014 |
| The Genome of the Netherlands: design, and project goals A Abdellaoui, K Ye, V Guryev, M Vermaat, F van Dijk, LC Francioli, ... Eur J Hum Genet 22 (2), 221227Browning, 2014 | 3 | 2014 |
| Meta-analysis of genome-wide association studies in alopecia areata resolves HLA associations and reveals two new susceptibility loci S Redler, L Petukhova, S Ripke, H Huang, A Menelaou, T Becker, ... EXPERIMENTAL DERMATOLOGY 24 (3), E17-E17, 2015 | | 2015 |
| Meta-analysis of genome-wide association studies in alopecia areata reveals new susceptibility loci L Petukhova, RC Betz, S Ripke, H Huang, A Menelaou, S Redler, ... JOURNAL OF INVESTIGATIVE DERMATOLOGY 134, S79-S79, 2014 | | 2014 |
| High Risk Population Isolate Reveals Low Frequency Variants Predisposing to MI Kurki, EI Gaál, J Kettunen, T Lappalainen, A Menelaou | | 2014 |
| LD-based SNP and genotype calling from next-generation sequencing reads. A Menelaou University of Oxford, 2012 | | 2012 |
