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1
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

von Linnér, R. ; Biroli, P. ; Kong, E. ; et al.

Nature Genetics
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2
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

von Taskesen E ; Mishra A ; van der Sluis S ; et al.

Schlagworte: Multidisciplinary
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3
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

von Taskesen, E ; Mishra, A ; van der Sluis, S ; et al.

Scientific Reports, vol 8, iss 1

Schlagworte: 31 Biological Sciences (for-2020); 42 Health Sciences (for-2020); 3105 Genetics (for-2020); Frontotemporal Dementia (FTD) (rcdc); Alzheimer's Disease Related Dementias (ADRD) (rcdc); Dementia (rcdc); Neurodegenerative (rcdc); Rare Diseases (rcdc); Brain Disorders (rcdc); Neurosciences (rcdc); Genetics (rcdc); Aging (rcdc); Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc); ALS (rcdc); Acquired Cognitive Impairment (rcdc); 2.1 Biological and endogenous factors (hrcs-rac); Neurological (hrcs-hc); International FTD-Genomics Consortium
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4
An epigenome-wide association study meta-analysis of educational attainment

von Karlsson Linnér, R ; Marioni, R E ; Rietveld, C A ; et al.

Karlsson Linnér, R, Marioni, R E, Rietveld, C A, Simpkin, A J, Davies, N M, Watanabe, K, Armstrong, N J, Auro, K, Baumbach, C, Bonder, M J, Buchwald, J, Fiorito, G, Ismail, K, Iurato, S, Joensuu, A, Karell, P, Kasela, S, Lahti, J, McRae, A F, Mandaviya, P R, Seppälä, I, Wang, Y, Baglietto, L, Binder, E B, Harris, S E, Hodge, A M, Horvath, S, Hurme, M, Johannesson, M, Latvala, A, Mather, K A, Medland, S E, Metspalu, A, Milani, L, Milne, R L, Pattie, A, Pedersen, N L, Peters, A, Polidoro, S, Räikkönen, K, Severi, G, Starr, ....

Schlagworte: Journal Article; /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being; name=SDG 3 - Good Health and Well-being
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5
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

von Taskesen,E. ; Mishra,A. ; van der Sluis,Sophie ; et al.

Schlagworte: General; Journal Article
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6
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS.

von Taskesen, E ; Mishra, A ; van der Sluis, S ; et al.

Schlagworte: 31 Biological Sciences; 3105 Genetics; Alzheimer's Disease Related Dementias (ADRD); Alzheimer's Disease; Genetics; ALS; Brain Disorders; Neurodegenerative; Biotechnology; Neurosciences; Dementia; Frontotemporal Dementia (FTD); Aging; Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD); Human Genome; Acquired Cognitive Impairment; Clinical Research; Rare Diseases; Prevention; 2.1 Biological and endogenous factors; Neurological
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7
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

von Taskesen, E. ; Mishra, A. ; van der Sluis, S. ; et al.

2045-2322 ; Scientific reports

Schlagworte: Biology; Human medicine
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8
An epigenome-wide association study meta-analysis of educational attainment

von Linner, R. ; Marioni, R. ; Rietveld, C. ; et al.

MOLECULAR PSYCHIATRY
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9
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.

von Hammerschlag, A.R. ; Stringer, S. ; De Leeuw, C.A. ; et al.

Hammerschlag, A R, Stringer, S, De Leeuw, C A, Sniekers, S, Taskesen, E, Watanabe, K, Blanken, T F, Dekker, K, Te Lindert, B H W, Wassing, R, Jonsdottir, I, Thorleifsson, G, Stefansson, H, Gislason, T, Berger, K, Schormair, B, Wellman, J, Winkelmann, J, Stefansson, K, Oexle, K, van Someren, E J W & Posthuma, D 2017, 'Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.', Nature Genetics, vol. 49, pp. 1584-1592. https://doi.org/10.1038/ng1017-1558c
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10
2D Representation of Transcriptomes by t-SNE Exposes Relatedness between Human Tissues

von Taskesen, E. (author) ; Reinders, M.J.T. (author)

Schlagworte: OA-Fund TU Delft
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11
Frequent loss of RAF kinase inhibitor protein expression in acute myeloid leukemia

von Zebisch, A ; Wölfler, A ; Fried, I ; et al.

Leukemia. 26(8):1842-1849
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12
Hydrothermal behavior of hybrid magnetite nanofluid flowing in a pipe under bi-directional magnetic field with different wave types

von Tekir, M. ; Gedik, E. ; Arslan, K. ; et al.

Schlagworte: Alternating magnetic field; Forced convection; Hybrid nanofluid; Laminar flow; Wave type
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13
An integrated approach of gene expression and DNA-methylation profiles of WNT signaling genes uncovers novel prognostic markers in Acute Myeloid Leukemia

von Taskesen, E. (author) ; Staal, F.J.T. (author) ; Reinders, M.J.T. (author)

Schlagworte: data integration; gene expression; DNA-methylation; prognostic markers; Acute Myeloid Leukemia; Wingless-Int (WNT); OA-Fund TU Delft
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14
The value of allogeneic and autologous hematopoietic stem cell transplantation in prognostically favorable acute myeloid leukemia with double mutant CEBPA

von Schlenk, R F ; Taskesen, E ; van Norden, Y ; et al.

Schlenk, R F; Taskesen, E; van Norden, Y; Krauter, J; Ganser, A; Bullinger, L; Gaidzik, V I; Paschka, P; Corbacioglu, A; Göhring, G; Kündgen, A; Held, G; Götze, K; Vellenga, E; Kuball, J; Schanz, U; Passweg, J; Pabst, Thomas; Maertens, J; Ossenkoppele, G J; Delwel, R; Döhner, H; Cornelissen, J J; Döhner, K; Löwenberg, B (2013). The value of allogeneic and autologous hematopoietic stem cell transplantation in prognostically favorable acute myeloid leukemia with double mutant CEBPA. Blood, 9(122):1576-1582.

Schlagworte: Clinic for Oncology and Hematology; 610 Medicine & health
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15
Hypergeometric analysis of tiling-array and sequence data: Detection and interpretation of peaks

von Taskesen, E. (author) ; Hoogeboezem, R. (author) ; Delwel, R. (author) ; et al.

Schlagworte: bioinformatics; NGS analysis; ChIP-Seq; peak detection; OA-Fund TU Delft
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16
An epigenome-wide association study meta-analysis of educational attainment

von Linner RK ; Marioni RE ; Rietveld CA ; et al.
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17
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

von Karlsson Linnér, Richard ; Kalnapenkis, A ; Kasela, S ; et al.

Schlagworte: general risk tolerance; risky behaviors; genes; brain tissues
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18
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.

von Karlsson Linnér, R ; Biroli, P ; Kong, E ; et al.

ftleicester

Schlagworte: Behavior; Case-Control Studies; Female; Genetic Loci; Genetic Predisposition to Disease; Genetics; Behavioral; Genome-Wide Association Study; Genotype; Humans; Male; Polymorphism; Single Nucleotide; psy; info
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19
Pan-cancer subtyping in a 2D-map shows substructures that are driven by specific combinations of molecular characteristics (vol 6, 24949, 2016)

von Taskesen, E. ; Huisman, S.M.H. ; Mahfouz, A. ; et al.

Scientific Reports
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20
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS.

von Taskesen, E ; Mishra, A ; van der Sluis, S ; et al.

Schlagworte: International FTD-Genomics Consortium; Article
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21
Genome-wide association meta- Analysis of 78,308 individuals identifies new loci and genes influencing human intelligence

von Sniekers, S. (Suzanne) ; Stringer, S. (Sven) ; Watanabe, K. (Kyoko) ; et al.

Nature Genetics vol. 49 no. 7, pp. 1107-1112
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22
Genome-wide association analyses of risk tolerance and risky behaviors in over one million individuals identify hundreds of loci and shared genetic influences

von Linnér, R. ; Biroli, P. ; Kong, E. ; et al.

HCEO Working Paper Series
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23
High Levels of Canonical Wnt Signaling Lead to Loss of Stemness and Increased Differentiation in Hematopoietic Stem Cells

von Famili, F ; Brugman, MH ; Taskesen, E ; et al.

Famili, F, Brugman, MH, Taskesen, E, Naber, BEA, Fodde, R & Staal, FJT 2016, 'High Levels of Canonical Wnt Signaling Lead to Loss of Stemness and Increased Differentiation in Hematopoietic Stem Cells', Stem Cell Reports, vol. 6, no. 5, pp. 652-659. https://doi.org/10.1016/j.stemcr.2016.04.009

Schlagworte: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM032401; name=EMC MM-03-24-01
- Zum Volltext in PubMed Central
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24
Pan-cancer subtyping in a 2D-map shows substructures that are driven by specific combinations of molecular characteristics

von Taskesen, E. ; Huisman, S.M.H. ; Mahfouz, A. ; et al.

Scientific Reports
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25
An integrated approach of gene expression and DNA-methylation profiles of WNT signaling genes uncovers novel prognostic markers in Acute Myeloid Leukemia

von Taskesen, E. ; Staal, F.J.T. ; Reinders, M.J.T.

BMC Bioinformatics
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