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Barbara Stranger - Publications

Affiliations: 
2002  
Website:
http://www.igsb.org/labs/barbara-stranger
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32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Huang Y, Shan Y, Zhang W, Lee AM, Li F, Stranger BE, Huang RS. Deciphering genetic causes for sex differences in human health through drug metabolism and transporter genes. Nature Communications. 14: 175. PMID 36635277 DOI: 10.1038/s41467-023-35808-6  0.338
2020 Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, ... Stranger BE, et al. The impact of sex on gene expression across human tissues. Science (New York, N.Y.). 369. PMID 32913072 DOI: 10.1126/Science.Aba3066  0.321
2019 Khramtsova E, Martin J, Goleva S, Stranger B, Davis L. SHARED SEX-DEPENDENT GENETIC EFFECTS ACROSS NEUROPSYCHIATRIC AND BEHAVIORAL TRAITS European Neuropsychopharmacology. 29: S56-S57. DOI: 10.1016/J.Euroneuro.2019.07.118  0.346
2019 Martin J, Khramtsova E, Stranger B, Davis L. EXAMINING SEX DIFFERENCES IN SHARED ETIOLOGY ACROSS NEUROPSYCHIATRIC AND BEHAVIORAL TRAITS European Neuropsychopharmacology. 29: S1032-S1033. DOI: 10.1016/J.Euroneuro.2018.07.026  0.301
2019 Stranger B, Blokland G, Davis L. THE ROLE OF SEX IN THE GENETICS AND GENOMICS OF NEUROPSYCHIATRIC TRAITS European Neuropsychopharmacology. 29: S1031-S1032. DOI: 10.1016/J.Euroneuro.2018.07.024  0.368
2019 Khramtsova E, Davis L, Stranger B. SEX-STRATIFIED ANALYSIS OF OBSESSIVE-COMPULSIVE DISORDER REVEALS MINOR DIFFERENCES IN GENETIC ARCHITECTURE European Neuropsychopharmacology. 29: S860. DOI: 10.1016/J.Euroneuro.2017.08.142  0.403
2019 Davis L, Beiter E, Khramtsova E, Van Der Merwe C, Chimusa E, Simonti C, Stein D, Capra J, Knowles J, Straub P, Hucks D, Stranger B. Polygenic Adaptation Underlies Evolution of Brain Structures and Behavioral Traits European Neuropsychopharmacology. 29: S755-S756. DOI: 10.1016/J.Euroneuro.2017.06.102  0.353
2018 Khramtsova EA, Heldman R, Derks EM, Yu D, Davis LK, Stranger BE. Sex differences in the genetic architecture of obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30456828 DOI: 10.1002/Ajmg.B.32687  0.327
2018 Ye CJ, Chen J, Villani AC, Gate RE, Subramaniam M, Bhangale T, Lee MN, Raj T, Raychowdhury R, Li W, Rogel N, Simmons S, Imboywa SH, Chipendo PI, McCabe C, ... Stranger BE, et al. Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of transcripts under balancing selection. Genome Research. PMID 30446528 DOI: 10.1101/Gr.240390.118  0.341
2016 Stranger BE. 0413 Genotypes to phenotypes: Lessons from functional variation in the human genome and transcriptome Journal of Animal Science. 94: 200-200. DOI: 10.2527/Jam2016-0413  0.354
2016 Aplebaum MA, Jha A, Chlenski A, Mariani C, Kao C, Nelson M, Hernandez K, Salwen H, Dobratic M, White K, Stranger B, Cohn SL. Abstract A01: Evaluation of hypoxia adaptation in neuroblastoma identifies reproducible transcriptional and phenotypic responses Cancer Research. 76. DOI: 10.1158/1538-7445.Pedca15-A01  0.353
2015 Croteau-Chonka DC, Rogers AJ, Raj T, McGeachie MJ, Qiu W, Ziniti JP, Stubbs BJ, Liang L, Martinez FD, Strunk RC, Lemanske RF, Liu AH, Stranger BE, Carey VJ, Raby BA. Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. Plos One. 10: e0140758. PMID 26474488 DOI: 10.1371/Journal.Pone.0140758  0.317
2015 Trynka G, Westra HJ, Slowikowski K, Hu X, Xu H, Stranger BE, Klein RJ, Han B, Raychaudhuri S. Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci. American Journal of Human Genetics. 97: 139-52. PMID 26140449 DOI: 10.1016/J.Ajhg.2015.05.016  0.301
2014 Li Q, Stram A, Chen C, Kar S, Gayther S, Pharoah P, Haiman C, Stranger B, Kraft P, Freedman ML. Expression QTL-based analyses reveal candidate causal genes and loci across five tumor types. Human Molecular Genetics. 23: 5294-302. PMID 24907074 DOI: 10.1093/Hmg/Ddu228  0.333
2013 Stranger BE, Raj T. Genetics of human gene expression. Current Opinion in Genetics & Development. 23: 627-34. PMID 24238872 DOI: 10.1016/j.gde.2013.10.004  0.329
2013 Gokcumen O, Zhu Q, Mulder LC, Iskow RC, Austermann C, Scharer CD, Raj T, Boss JM, Sunyaev S, Price A, Stranger B, Simon V, Lee C. Balancing selection on a regulatory region exhibiting ancient variation that predates human-neandertal divergence. Plos Genetics. 9: e1003404. PMID 23593015 DOI: 10.1371/Journal.Pgen.1003404  0.358
2012 Dimas AS, Nica AC, Montgomery SB, Stranger BE, Raj T, Buil A, Giger T, Lappalainen T, Gutierrez-Arcelus M, McCarthy MI, Dermitzakis ET. Sex-biased genetic effects on gene regulation in humans. Genome Research. 22: 2368-75. PMID 22960374 DOI: 10.1101/gr.134981.111  0.323
2012 Stranger BE, Montgomery SB, Dimas AS, Parts L, Stegle O, Ingle CE, Sekowska M, Smith GD, Evans D, Gutierrez-Arcelus M, Price A, Raj T, Nisbett J, Nica AC, Beazley C, et al. Patterns of cis regulatory variation in diverse human populations. Plos Genetics. 8: e1002639. PMID 22532805 DOI: 10.1371/Journal.Pgen.1002639  0.328
2011 Stranger BE, Stahl EA, Raj T. Progress and promise of genome-wide association studies for human complex trait genetics. Genetics. 187: 367-83. PMID 21115973 DOI: 10.1534/Genetics.110.120907  0.325
2011 Raj T, Shulman J, Chibnik L, Keenan B, Stranger B, Evans D, Bennett D, Jager PD. Alzheimer’s Disease Susceptibility Loci: Evidence for Natural Selection and Altered Gene Expression Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.506  0.392
2010 Nica AC, Montgomery SB, Dimas AS, Stranger BE, Beazley C, Barroso I, Dermitzakis ET. Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations. Plos Genetics. 6: e1000895. PMID 20369022 DOI: 10.1371/journal.pgen.1000895  0.325
2009 Dimas AS, Deutsch S, Stranger BE, Montgomery SB, Borel C, Attar-Cohen H, Ingle C, Beazley C, Gutierrez Arcelus M, Sekowska M, Gagnebin M, Nisbett J, Deloukas P, Dermitzakis ET, Antonarakis SE. Common regulatory variation impacts gene expression in a cell type-dependent manner. Science (New York, N.Y.). 325: 1246-50. PMID 19644074 DOI: 10.1126/science.1174148  0.327
2009 Kudaravalli S, Veyrieras JB, Stranger BE, Dermitzakis ET, Pritchard JK. Gene expression levels are a target of recent natural selection in the human genome. Molecular Biology and Evolution. 26: 649-58. PMID 19091723 DOI: 10.1093/Molbev/Msn289  0.346
2007 Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... Stranger BE, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250  0.321
2007 Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... Stranger BE, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258  0.327
2007 Stranger BE, Nica AC, Forrest MS, Dimas A, Bird CP, Beazley C, Ingle CE, Dunning M, Flicek P, Koller D, Montgomery S, Tavaré S, Deloukas P, Dermitzakis ET. Population genomics of human gene expression. Nature Genetics. 39: 1217-24. PMID 17873874 DOI: 10.1038/Ng2142  0.361
2007 Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Thorne N, Redon R, Bird CP, de Grassi A, Lee C, Tyler-Smith C, Carter N, Scherer SW, Tavaré S, Deloukas P, et al. Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science (New York, N.Y.). 315: 848-53. PMID 17289997 DOI: 10.1126/Science.1136678  0.36
2005 Stranger BE, Forrest MS, Clark AG, Minichiello MJ, Deutsch S, Lyle R, Hunt S, Kahl B, Antonarakis SE, Tavaré S, Deloukas P, Dermitzakis ET. Genome-wide associations of gene expression variation in humans. Plos Genetics. 1: e78. PMID 16362079 DOI: 10.1371/Journal.Pgen.0010078  0.359
2005 Stranger BE, Dermitzakis ET. The genetics of regulatory variation in the human genome. Human Genomics. 2: 126-31. PMID 16004727  0.341
2005 Stranger BE, Mitchell-Olds T. Nucleotide variation at the myrosinase-encoding locus, TGG1, and quantitative myrosinase enzyme activity variation in Arabidopsis thaliana. Molecular Ecology. 14: 295-309. PMID 15643972 DOI: 10.1111/J.1365-294X.2004.02403.X  0.546
2004 Ramos-Onsins SE, Stranger BE, Mitchell-Olds T, Aguadé M. Multilocus analysis of variation and speciation in the closely related species Arabidopsis halleri and A. lyrata. Genetics. 166: 373-88. PMID 15020431 DOI: 10.1534/Genetics.166.1.373  0.569
2002 Kuittinen H, Aguadé M, Charlesworth D, Haan ADE, Lauga B, Mitchell-Olds T, Oikarinen S, Ramos-Onsins S, Stranger B, Van Tienderen P, Savolainen O. Primers for 22 candidate genes for ecological adaptations in Brassicaceae Molecular Ecology Notes. 2: 258-262. DOI: 10.1046/J.1471-8286.2002.00210.X  0.575
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