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Barbera DC van Schaik
Barbera DC van Schaik
Bioinformatics Laboratory, EDS, Amsterdam UMC
Verified email at amsterdamumc.nl - Homepage
Title
Cited by
Cited by
Year
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
9592001
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Nature genetics 46 (8), 818-825, 2014
7062014
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
4472019
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
4412003
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
2742012
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
1642010
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
1622012
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
1392012
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
1382014
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
1212014
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
1062020
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
1042016
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
1002011
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
972015
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
912001
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
872011
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
832019
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
732000
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
512015
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
462019
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