Barbara Stranger
Barbara Stranger
Associate Professor of Pharmacology, Northwestern Feinberg School of Medicine
Verified email at
Cited by
Cited by
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
ENCODE Project Consortium
nature 447 (7146), 799, 2007
Relative impact of nucleotide and copy number variation on gene expression phenotypes
BE Stranger, MS Forrest, M Dunning, CE Ingle, C Beazley, N Thorne, ...
Science 315 (5813), 848-853, 2007
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Y Okada, D Wu, G Trynka, T Raj, C Terao, K Ikari, Y Kochi, K Ohmura, ...
Nature 506 (7488), 376-381, 2014
Genetic effects on gene expression across human tissues
GTEx Consortium
Nature 550 (7675), 204-213, 2017
Population genomics of human gene expression
BE Stranger, AC Nica, MS Forrest, A Dimas, CP Bird, C Beazley, CE Ingle, ...
Nature genetics 39 (10), 1217-1224, 2007
A haplotype map of the human genome
D Altshuler, P Donnelly, International HapMap Consortium
Nature 437 (7063), nature04226, 2005
Common regulatory variation impacts gene expression in a cell type–dependent manner
AS Dimas, S Deutsch, BE Stranger, SB Montgomery, C Borel, ...
Science 325 (5945), 1246-1250, 2009
Progress and promise of genome-wide association studies for human complex trait genetics
BE Stranger, EA Stahl, T Raj
Genetics 187 (2), 367-383, 2011
Genome-wide associations of gene expression variation in humans
BE Stranger, MS Forrest, AG Clark, MJ Minichiello, S Deutsch, R Lyle, ...
PLoS Genet 1 (6), e78, 2005
Patterns of cis regulatory variation in diverse human populations
BE Stranger, SB Montgomery, AS Dimas, L Parts, O Stegle, CE Ingle, ...
PLoS Genet 8 (4), e1002639, 2012
Chromatin marks identify critical cell types for fine mapping complex trait variants
G Trynka, C Sandor, B Han, H Xu, BE Stranger, XS Liu, S Raychaudhuri
Nature genetics 45 (2), 124-130, 2013
Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations
AC Nica, SB Montgomery, AS Dimas, BE Stranger, C Beazley, I Barroso, ...
PLoS Genet 6 (4), e1000895, 2010
Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes
T Raj, K Rothamel, S Mostafavi, C Ye, MN Lee, JM Replogle, T Feng, ...
Science 344 (6183), 519-523, 2014
Common genetic variants modulate pathogen-sensing responses in human dendritic cells
MN Lee, C Ye, AC Villani, T Raj, W Li, TM Eisenhaure, SH Imboywa, ...
Science 343 (6175), 2014
Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies
TP Yang, C Beazley, SB Montgomery, AS Dimas, M Gutierrez-Arcelus, ...
Bioinformatics 26 (19), 2474-2476, 2010
Integrative eQTL-based analyses reveal the biology of breast cancer risk loci
Q Li, JH Seo, B Stranger, A McKenna, I Pe’er, T LaFramboise, M Brown, ...
Cell 152 (3), 633-641, 2013
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects
NA Patsopoulos, LF Barcellos, RQ Hintzen, C Schaefer, CM Van Duijn, ...
PLoS Genet 9 (11), e1003926, 2013
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