Pelin Akan Sahlén
Pelin Akan Sahlén
Royal Institute of Technology
Bestätigte E-Mail-Adresse bei scilifelab.se
Titel
Zitiert von
Zitiert von
Jahr
Visualization and analysis of gene expression in tissue sections by spatial transcriptomics
PL Ståhl, F Salmén, S Vickovic, A Lundmark, JF Navarro, J Magnusson, ...
Science 353 (6294), 78-82, 2016
7322016
Small-world communication of residues and significance for protein dynamics
AR Atilgan, P Akan, C Baysal
Biophysical journal 86 (1), 85-91, 2004
3512004
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus
CG Bell, S Finer, CM Lindgren, GA Wilson, VK Rakyan, AE Teschendorff, ...
PloS one 5 (11), e14040, 2010
2962010
Genome-wide mapping of promoter-anchored interactions with close to single-enhancer resolution
P Sahlén, I Abdullayev, D Ramsköld, L Matskova, N Rilakovic, B Lötstedt, ...
Genome biology 16 (1), 1-13, 2015
1152015
DNA sequence and structural properties as predictors of human and mouse promoters
P Akan, P Deloukas
Gene 410 (1), 165-176, 2008
412008
SNP allele frequency estimation in DNA pools and variance components analysis
K Downes, BJ Barratt, P Akan, SJ Bumpstead, SD Taylor, DG Clayton, ...
Biotechniques 36 (5), 840-845, 2004
412004
Comprehensive analysis of the genome transcriptome and proteome landscapes of three tumor cell lines
P Akan, A Alexeyenko, PI Costea, L Hedberg, BW Solnestam, S Lundin, ...
Genome medicine 4 (11), 1-13, 2012
402012
TagGD: fast and accurate software for DNA Tag generation and demultiplexing
PI Costea, J Lundeberg, P Akan
PLoS One 8 (3), e57521, 2013
382013
Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q
I Prokopenko, E Zeggini, RL Hanson, BD Mitchell, NW Rayner, P Akan, ...
Diabetes 58 (7), 1704-1709, 2009
312009
Multiplex PCB-based electrochemical detection of cancer biomarkers using MLPA-barcode approach
JLA Sánchez, OYF Henry, H Joda, BW Solnestam, L Kvastad, ...
Biosensors and Bioelectronics 82, 224-232, 2016
302016
Interpretation, stratification and evidence for sequence variants affecting mRNA splicing in complete human genome sequences
BC Shirley, EJ Mucaki, T Whitehead, PI Costea, P Akan, PK Rogan
Genomics, proteomics & bioinformatics 11 (2), 77-85, 2013
282013
Comparison of total and cytoplasmic mRNA reveals global regulation by nuclear retention and miRNAs
BW Solnestam, H Stranneheim, J Hällman, M Käller, E Lundberg, ...
BMC genomics 13 (1), 1-9, 2012
282012
HiCapTools: a software suite for probe design and proximity detection for targeted chromosome conformation capture applications
A Anil, R Spalinskas, Ö Åkerborg, P Sahlén
Bioinformatics 34 (4), 675-677, 2018
162018
The BAF and PRC2 complex subunits Dpf2 and Eed antagonistically converge on Tbx3 to control ESC differentiation
W Zhang, C Chronis, X Chen, H Zhang, R Spalinskas, M Pardo, L Chen, ...
Cell stem cell 24 (1), 138-152. e8, 2019
132019
Nanopore arrays in a silicon membrane for parallel single-molecule detection: DNA translocation
M Zhang, T Schmidt, A Jemt, P Sahlén, I Sychugov, J Lundeberg, ...
Nanotechnology 26 (31), 314002, 2015
122015
Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases
M Cavalli, N Baltzer, HM Umer, J Grau, I Lemnian, G Pan, O Wallerman, ...
Scientific reports 9 (1), 1-14, 2019
102019
Electrochemical genetic profiling of single cancer cells
JL Acero Sanchez, H Joda, OYF Henry, BW Solnestam, L Kvastad, ...
Analytical chemistry 89 (6), 3378-3385, 2017
102017
Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing data
M Hu, Q Ayub, JA Guerra-Assunçao, Q Long, Z Ning, N Huang, ...
Human genetics 131 (5), 665-674, 2012
102012
High-resolution regulatory maps connect vascular risk variants to disease-related pathways
Ö Åkerborg, R Spalinskas, S Pradhananga, A Anil, P Höjer, FA Poujade, ...
Circulation: Genomic and Precision Medicine 12 (3), e002353, 2019
82019
Comparison of variant calls from whole genome and whole exome sequencing data using matched samples
N Björn, S Pradhananga, B Sigurgeirsson, J Lundeberg, H Gréen, ...
Journal of Next Generation Sequencing & Applications 5 (1), 1-8, 2018
62018
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