| The human transcriptome map: clustering of highly expressed genes in chromosomal domains H Caron, B Schaik, M Mee, F Baas, G Riggins, P Sluis, MC Hermus, ... Science 291 (5507), 1289-1292, 2001 | 964 | 2001 |
| Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014 | 716 | 2014 |
| Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ... Nature genetics 51 (5), 804-814, 2019 | 466 | 2019 |
| The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes R Versteeg, BDC van Schaik, MF van Batenburg, M Roos, R Monajemi, ... Genome research 13 (9), 1998-2004, 2003 | 443 | 2003 |
| Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome JKJ Van Houdt, BA Nowakowska, SB Sousa, BDC Van Schaik, ... Nature genetics 44 (4), 445-449, 2012 | 278 | 2012 |
| Inflamed target tissue provides a specific niche for highly expanded T-cell clones in early human autoimmune disease PL Klarenbeek, MJH De Hair, ME Doorenspleet, BDC Van Schaik, ... Annals of the rheumatic diseases 71 (6), 1088-1093, 2012 | 165 | 2012 |
| Human T-cell memory consists mainly of unexpanded clones PL Klarenbeek, PP Tak, BDC van Schaik, AH Zwinderman, ME Jakobs, ... Immunology letters 133 (1), 42-48, 2010 | 164 | 2010 |
| Deep sequencing of antiviral T-cell responses to HCMV and EBV in humans reveals a stable repertoire that is maintained for many years PL Klarenbeek, EBM Remmerswaal, IJM Ten Berge, ME Doorenspleet, ... Public Library of Science 8 (9), e1002889, 2012 | 140 | 2012 |
| Rheumatoid arthritis synovial tissue harbours dominant B-cell and plasma-cell clones associated with autoreactivity ME Doorenspleet, PL Klarenbeek, MJH de Hair, BDC van Schaik, ... Annals of the rheumatic diseases 73 (4), 756-762, 2014 | 137 | 2014 |
| 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 |
| Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits S Vogelezang, JP Bradfield, TS Ahluwalia, JA Curtin, TA Lakka, N Grarup, ... PLoS genetics 16 (10), e1008718, 2020 | 117 | 2020 |
| A high-quality human reference panel reveals the complexity and distribution of genomic structural variants JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ... Nature communications 7 (1), 1-10, 2016 | 105 | 2016 |
| A sensitive assay for virus discovery in respiratory clinical samples M de Vries, M Deijs, M Canuti, BDC van Schaik, NR Faria, ... PLoS One 6 (1), e16118, 2011 | 103 | 2011 |
| 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 |
| The MEIS1 oncogene is highly expressed in neuroblastoma and amplified in cell line IMR32 N Spieker, P van Sluis, M Beitsma, K Boon, BDC van Schaik, ... Genomics 71 (2), 214-221, 2001 | 91 | 2001 |
| A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity JP Bradfield, S Vogelezang, JF Felix, A Chesi, Ø Helgeland, M Horikoshi, ... Human molecular genetics 28 (19), 3327-3338, 2019 | 88 | 2019 |
| SGCE isoform characterization and expression in human brain: implications for myoclonus–dystonia pathogenesis? K Ritz, BD Van Schaik, ME Jakobs, AH Van Kampen, E Aronica, ... European journal of human genetics 19 (4), 438-444, 2011 | 87 | 2011 |
| USAGE: a web-based approach towards the analysis of SAGE data AHC van Kampen, BDC van Schaik, E Pauws, EMC Michiels, JM Ruijter, ... Bioinformatics 16 (10), 899-905, 2000 | 73 | 2000 |
| 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 |
| Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly A Kim, C Savary, C Dubourg, W Carré, C Mouden, H Hamdi-Roze, ... Brain 142 (1), 35-49, 2019 | 48 | 2019 |
Antoine van KampenProfessor of Medical Bioinformatics, University of Amsterdam在 amc.uva.nl 的电子邮件经过验证
