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Daoud Sie
Daoud Sie
Human Genetics, Amsterdam UMC
Verified email at amsterdamumc.nl
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Cited by
Cited by
Year
Nontemplated nucleotide additions distinguish the small RNA composition in cells from exosomes
D Koppers-Lalic, M Hackenberg, IV Bijnsdorp, MAJ van Eijndhoven, ...
Cell reports 8 (6), 1649-1658, 2014
6062014
MicroRNA sequence and expression analysis in breast tumors by deep sequencing
TA Farazi, HM Horlings, JJ Ten Hoeve, A Mihailovic, H Halfwerk, ...
Cancer research 71 (13), 4443-4453, 2011
4202011
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly
I Scheinin, D Sie, H Bengtsson, MA Van De Wiel, AB Olshen, ...
Genome research 24 (12), 2022-2032, 2014
4162014
Copy number signatures and mutational processes in ovarian carcinoma
G Macintyre, TE Goranova, D De Silva, D Ennis, AM Piskorz, M Eldridge, ...
Nature genetics 50 (9), 1262-1270, 2018
3712018
One naive T cell, multiple fates in CD8+ T cell differentiation
C Gerlach, JW Van Heijst, E Swart, D Sie, N Armstrong, RM Kerkhoven, ...
Journal of Experimental Medicine 207 (6), 1235-1246, 2010
2842010
Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping
PJP De Vree, E De Wit, M Yilmaz, M Van De Heijning, P Klous, ...
Nature biotechnology 32 (10), 1019-1025, 2014
2642014
Large-scale mutagenesis in p19ARF-and p53-deficient mice identifies cancer genes and their collaborative networks
AG Uren, J Kool, K Matentzoglu, J de Ridder, J Mattison, M van Uitert, ...
Cell 133 (4), 727-741, 2008
2072008
Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
H Holstege, W Pfeiffer, D Sie, M Hulsman, TJ Nicholas, CC Lee, T Ross, ...
Genome research 24 (5), 733-742, 2014
2032014
Recruitment of antigen-specific CD8+ T cells in response to infection is markedly efficient
JWJ van Heijst, C Gerlach, E Swart, D Sie, C Nunes-Alves, RM Kerkhoven, ...
Science 325 (5945), 1265-1269, 2009
1682009
Dissecting T cell lineage relationships by cellular barcoding
K Schepers, E Swart, JWJ van Heijst, C Gerlach, M Castrucci, D Sie, ...
The Journal of experimental medicine 205 (10), 2309-2318, 2008
1462008
Search for a gene expression signature of breast cancer local recurrence in young women
N Servant, MA Bollet, H Halfwerk, K Bleakley, B Kreike, L Jacob, D Sie, ...
Clinical Cancer Research 18 (6), 1704-1715, 2012
852012
HELLP babies link a novel lincRNA to the trophoblast cell cycle
M Van Dijk, HK Thulluru, J Mulders, OJ Michel, A Poutsma, S Windhorst, ...
The Journal of clinical investigation 122 (11), 4003-4011, 2012
832012
Consensus molecular subtype classification of colorectal adenomas
MA Komor, LJW Bosch, G Bounova, AS Bolijn, PM Delis‐van Diemen, ...
The Journal of pathology 246 (3), 266-276, 2018
772018
Diagnosis of fanconi anemia: mutation analysis by next-generation sequencing
N Ameziane, D Sie, S Dentro, Y Ariyurek, L Kerkhoven, H Joenje, ...
Anemia 2012, 2012
712012
Non-classic EGFR mutations in a cohort of Dutch EGFR-mutated NSCLC patients and outcomes following EGFR-TKI treatment
JL Kuiper, SMS Hashemi, E Thunnissen, PJF Snijders, K Grünberg, ...
British journal of cancer 115 (12), 1504-1512, 2016
692016
No evidence for active human papillomavirus (HPV) in fields surrounding HPV‐positive oropharyngeal tumors
MM Rietbergen, BJM Braakhuis, N Moukhtari, E Bloemena, A Brink, D Sie, ...
Journal of oral pathology & medicine 43 (2), 137-142, 2014
68*2014
MiR expression profiles of paired primary colorectal cancer and metastases by next-generation sequencing
M Neerincx, DLS Sie, MA Van De Wiel, NCT Van Grieken, JD Burggraaf, ...
Oncogenesis 4 (10), e170-e170, 2015
672015
ACE: absolute copy number estimation from low-coverage whole-genome sequencing data
JB Poell, M Mendeville, D Sie, A Brink, RH Brakenhoff, B Ylstra
Bioinformatics 35 (16), 2847-2849, 2019
652019
Volatile anesthetics modulate gene expression in breast and brain tumor cells
JM Huitink, M Heimerikxs, M Nieuwland, SA Loer, W Brugman, A Velds, ...
Anesthesia & Analgesia 111 (6), 1411-1415, 2010
652010
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
H Holstege, M Hulsman, C Charbonnier, B Grenier-Boley, O Quenez, ...
Nature genetics 54 (12), 1786-1794, 2022
572022
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