Christoffer Nellåker
Christoffer Nellåker
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Mouse genomic variation and its effect on phenotypes and gene regulation
TM Keane, L Goodstadt, P Danecek, MA White, K Wong, B Yalcin, ...
Nature 477 (7364), 289-294, 2011
The RNA-editing enzyme ADAR1 controls innate immune responses to RNA
NM Mannion, SM Greenwood, R Young, S Cox, J Brindle, D Read, ...
Cell reports 9 (4), 1482-1494, 2014
Sequence-based characterization of structural variation in the mouse genome
B Yalcin, K Wong, A Agam, M Goodson, TM Keane, X Gan, C Nellåker, ...
Nature 477 (7364), 326-329, 2011
High levels of RNA-editing site conservation amongst 15 laboratory mouse strains
P Danecek, C Nellåker, RE McIntyre, JE Buendia-Buendia, S Bumpstead, ...
Genome biology 13 (4), 1-12, 2012
The genomic landscape shaped by selection on transposable elements across 18 mouse strains
C Nellåker, TM Keane, B Yalcin, K Wong, A Agam, TG Belgard, J Flint, ...
Genome biology 13 (6), R45, 2012
Transactivation of elements in the human endogenous retrovirus W family by viral infection
C Nellåker, Y Yao, L Jones-Brando, F Mallet, RH Yolken, H Karlsson
Retrovirology 3 (1), 1-11, 2006
Evaluation of minor groove binding probe and Taqman probe PCR assays: Influence of mismatches and template complexity on quantification
Y Yao, C Nellåker, H Karlsson
Molecular and cellular probes 20 (5), 311-316, 2006
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
M Ansari, G Poke, Q Ferry, K Williamson, R Aldridge, AM Meynert, ...
Journal of medical genetics 51 (10), 659-668, 2014
Diagnostically relevant facial gestalt information from ordinary photos
Q Ferry, J Steinberg, C Webber, DR FitzPatrick, CP Ponting, A Zisserman, ...
Elife 3, e02020, 2014
Elevated levels of human endogenous retrovirus‐W transcripts in blood cells from patients with first episode schizophrenia
Y Yao, J Schröder, C Nellåker, C Bottmer, S Bachmann, RH Yolken, ...
Genes, Brain and Behavior 7 (1), 103-112, 2008
Turning a blind eye: Explicit removal of biases and variation from deep neural network embeddings
M Alvi, A Zisserman, C Nellåker
Proceedings of the European Conference on Computer Vision (ECCV), 0-0, 2018
Transcriptional derepression of the ERVWE1 locus following influenza A virus infection
F Li, C Nellåker, S Sabunciyan, RH Yolken, L Jones-Brando, ...
Journal of virology 88 (8), 4328-4337, 2014
A systematic evaluation of expression of HERV-W elements; influence of genomic context, viral structure and orientation
F Li, C Nellåker, RH Yolken, H Karlsson
Bmc Genomics 12 (1), 22, 2011
Clinical and molecular consequences of disease-associated de novo mutations in SATB2
H Bengani, M Handley, M Alvi, R Ibitoye, M Lees, SA Lynch, W Lam, ...
Genetics in Medicine 19 (8), 900-908, 2017
Molecular Beacon–Based Temperature Control and Automated Analyses for Improved Resolution of Melting Temperature Analysis Using SYBR I Green Chemistry
C Nellaker, U Wallgren, H Karlsson
Clinical chemistry 53 (1), 98-103, 2007
Rapid turnover of functional sequence in human and other genomes
CP Ponting, C Nellåker, S Meader
Annual review of genomics and human genetics 12, 275-299, 2011
Expression profiling of repetitive elements by melting temperature analysis: variation in HERV-W gag expression across human individuals and tissues
C Nellåker, F Li, F Uhrzander, J Tyrcha, H Karlsson
Bmc Genomics 10 (1), 532, 2009
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
MRF Reijnders, R Janowski, M Alvi, JE Self, TJ Van Essen, M Vreeburg, ...
Journal of medical genetics 55 (2), 104-113, 2018
Influenza A virus transactivates the mouse envelope gene encoding syncytin B and its regulator, glial cells missing 1
L Asp, C Nellåker, H Karlsson
Journal of neurovirology 13 (1), 29-37, 2007
De Novo and inherited loss-of-function variants in TLK2: clinical and genotype-phenotype evaluation of a distinct neurodevelopmental disorder
MRF Reijnders, KA Miller, M Alvi, JAC Goos, MM Lees, A De Burca, ...
The American Journal of Human Genetics 102 (6), 1195-1203, 2018
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