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Barbara Stranger - Publications

Affiliations: 
University of Chicago, Chicago, IL 
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36/101 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
2024 Pividori M, Sadeeq S, Krishnan A, Stranger BE, Gignoux CR. Uncovering hidden gene-trait patterns through biclustering analysis of the UK Biobank. Biorxiv : the Preprint Server For Biology. PMID 39605717 DOI: 10.1101/2024.11.08.622657  0.381
2024 Strom NI, Gerring ZF, Galimberti M, Yu D, Halvorsen MW, Abdellaoui A, Rodriguez-Fontenla C, Sealock JM, Bigdeli T, Coleman JR, Mahjani B, Thorp JG, Bey K, Burton CL, Luykx JJ, ... ... Stranger BE, et al. Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci. Medrxiv : the Preprint Server For Health Sciences. PMID 38712091 DOI: 10.1101/2024.03.13.24304161  0.323
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  0.355
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  0.34
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 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  0.363
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  0.399
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  0.359
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  0.323
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  0.369
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  0.368
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  0.396
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  0.339
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  0.312
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  0.362
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  0.353
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  0.367
2013 Raj T, Kuchroo M, Replogle JM, Raychaudhuri S, Stranger BE, De Jager PL. Common risk alleles for inflammatory diseases are targets of recent positive selection. American Journal of Human Genetics. 92: 517-29. PMID 23522783 DOI: 10.1016/J.Ajhg.2013.03.001  0.304
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  0.34
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  0.346
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  0.34
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  0.432
2010 Yang TP, Beazley C, Montgomery SB, Dimas AS, Gutierrez-Arcelus M, Stranger BE, Deloukas P, Dermitzakis ET. Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies. Bioinformatics (Oxford, England). 26: 2474-6. PMID 20702402 DOI: 10.1093/bioinformatics/btq452  0.303
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  0.333
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  0.36
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  0.382
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  0.344
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  0.347
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  0.389
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  0.368
2006 Dermitzakis ET, Stranger BE. Genetic variation in human gene expression. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 503-8. PMID 16783632 DOI: 10.1007/s00335-006-0005-y  0.342
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  0.382
2005 Stranger BE, Dermitzakis ET. The genetics of regulatory variation in the human genome. Human Genomics. 2: 126-31. PMID 16004727  0.377
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  0.342
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  0.605
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  0.456
Low-probability matches (unlikely to be authored by this person)
2012 Stranger BE, De Jager PL. Coordinating GWAS results with gene expression in a systems immunologic paradigm in autoimmunity. Current Opinion in Immunology. 24: 544-51. PMID 23040211 DOI: 10.1016/j.coi.2012.09.002  0.299
2017 Brynedal B, Choi J, Raj T, Bjornson R, Stranger BE, Neale BM, Voight BF, Cotsapas C. Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation. American Journal of Human Genetics. PMID 28285767 DOI: 10.1016/J.Ajhg.2017.02.004  0.299
2015 Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B. Accurate and fast multiple-testing correction in eQTL studies. American Journal of Human Genetics. 96: 857-68. PMID 26027500 DOI: 10.1016/J.Ajhg.2015.04.012  0.298
2008 Dimas AS, Stranger BE, Beazley C, Finn RD, Ingle CE, Forrest MS, Ritchie ME, Deloukas P, Tavaré S, Dermitzakis ET. Modifier effects between regulatory and protein-coding variation. Plos Genetics. 4: e1000244. PMID 18974877 DOI: 10.1371/Journal.Pgen.1000244  0.296
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  0.293
2012 Raj T, Shulman JM, Keenan BT, Chibnik LB, Evans DA, Bennett DA, Stranger BE, De Jager PL. Alzheimer disease susceptibility loci: evidence for a protein network under natural selection. American Journal of Human Genetics. 90: 720-6. PMID 22482808 DOI: 10.1016/J.Ajhg.2012.02.022  0.29
2016 Applebaum MA, Jha AR, Kao C, Hernandez KM, DeWane G, Salwen HR, Chlenski A, Dobratic M, Mariani CJ, Godley LA, Prabhakar N, White K, Stranger BE, Cohn SL. Integrative genomics reveals hypoxia inducible genes that are associated with a poor prognosis in neuroblastoma patients. Oncotarget. PMID 27765905 DOI: 10.18632/Oncotarget.12713  0.29
2015 Gamazon ER, Stranger BE. The impact of human copy number variation on gene expression. Briefings in Functional Genomics. 14: 352-7. PMID 25922366 DOI: 10.1093/bfgp/elv017  0.281
2020 Shi X, Radhakrishnan S, Wen J, Chen JY, Chen J, Lam BA, Mills RE, Stranger BE, Lee C, Setlur SR. Association of CNVs with methylation variation. Npj Genomic Medicine. 5: 41. PMID 34556651 DOI: 10.1038/s41525-020-00145-w  0.281
2020 Shi X, Radhakrishnan S, Wen J, Chen JY, Chen J, Lam BA, Mills RE, Stranger BE, Lee C, Setlur SR. Association of CNVs with methylation variation. Npj Genomic Medicine. 5: 41. PMID 33062306 DOI: 10.1038/s41525-020-00145-w  0.281
2014 Raj T, Replogle JM, Ryan K, Chibnik L, Ye J, Mostafavi S, Lee M, Rothamel K, McCabe C, Korff AV, Bradshaw EM, Evans D, Bennett D, Benoist C, Stranger B, et al. Expression Qtl Analysis From Primary Immune Cells Identifies Novel Regulatory Effects Underlying Alzheimer'S Disease Susceptibility Alzheimers & Dementia. 10: 216. DOI: 10.1016/J.Jalz.2014.04.290  0.273
2014 Ferraro A, D'Alise AM, Raj T, Asinovski N, Phillips R, Ergun A, Replogle JM, Bernier A, Laffel L, Stranger BE, De Jager PL, Mathis D, Benoist C. Interindividual variation in human T regulatory cells. Proceedings of the National Academy of Sciences of the United States of America. 111: E1111-20. PMID 24610777 DOI: 10.1073/Pnas.1401343111  0.27
2006 Stranger BE, Dermitzakis ET. From DNA to RNA to disease and back: the 'central dogma' of regulatory disease variation. Human Genomics. 2: 383-90. PMID 16848976  0.269
2014 Hu X, Kim H, Raj T, Brennan PJ, Trynka G, Teslovich N, Slowikowski K, Chen WM, Onengut S, Baecher-Allan C, De Jager PL, Rich SS, Stranger BE, Brenner MB, Raychaudhuri S. Regulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cells. Plos Genetics. 10: e1004404. PMID 24968232 DOI: 10.1371/Journal.Pgen.1004404  0.267
2021 Martin J, Khramtsova EA, Goleva SB, Blokland GAM, Traglia M, Walters RK, Hübel C, Coleman JRI, Breen G, Børglum AD, Demontis D, Grove J, Werge T, Bralten J, Bulik CM, ... ... Stranger BE, et al. Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits. Biological Psychiatry. PMID 33648717 DOI: 10.1016/j.biopsych.2020.12.024  0.264
2014 Lee MN, Ye C, Villani AC, Raj T, Li W, Eisenhaure TM, Imboywa SH, Chipendo PI, Ran FA, Slowikowski K, Ward LD, Raddassi K, McCabe C, Lee MH, Frohlich IY, ... ... Stranger BE, et al. Common genetic variants modulate pathogen-sensing responses in human dendritic cells. Science (New York, N.Y.). 343: 1246980. PMID 24604203 DOI: 10.1126/Science.1246980  0.261
2012 Brown KH, Dobrinski KP, Lee AS, Gokcumen O, Mills RE, Shi X, Chong WW, Chen JY, Yoo P, David S, Peterson SM, Raj T, Choy KW, Stranger BE, Williamson RE, et al. Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis. Proceedings of the National Academy of Sciences of the United States of America. 109: 529-34. PMID 22203992 DOI: 10.1073/Pnas.1112163109  0.261
2014 Okada Y, Wu D, Trynka G, Raj T, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Yoshida S, Graham RR, Manoharan A, Ortmann W, Bhangale T, Denny JC, ... ... Stranger BE, et al. Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature. 506: 376-81. PMID 24390342 DOI: 10.1038/Nature12873  0.258
2020 Tilot AK, Khramtsova EA, Liang D, Grasby KL, Jahanshad N, Painter J, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, ... Stranger BE, et al. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cerebral Cortex (New York, N.Y. : 1991). PMID 33290510 DOI: 10.1093/cercor/bhaa327  0.257
2007 Bird CP, Stranger BE, Liu M, Thomas DJ, Ingle CE, Beazley C, Miller W, Hurles ME, Dermitzakis ET. Fast-evolving noncoding sequences in the human genome. Genome Biology. 8: R118. PMID 17578567 DOI: 10.1186/Gb-2007-8-6-R118  0.256
2015 De Jager PL, Hacohen N, Mathis D, Regev A, Stranger BE, Benoist C. ImmVar project: Insights and design considerations for future studies of "healthy" immune variation. Seminars in Immunology. 27: 51-7. PMID 25819567 DOI: 10.1016/J.Smim.2015.03.003  0.252
2023 Khramtsova EA, Wilson MA, Martin J, Winham SJ, He KY, Davis LK, Stranger BE. Quality control and analytic best practices for testing genetic models of sex differences in large populations. Cell. 186: 2044-2061. PMID 37172561 DOI: 10.1016/j.cell.2023.04.014  0.251
2013 Raj T, Chibnik L, McCabe C, Stranger B, Barnes LL, Weir D, Mayeux R, Foroud T, Bennett D, Hall KS, Murrell J, Evans D, De Jager P. O4-01-03: Genome-wide association study and admixture mapping of age-related cognitive decline in African-Americans Alzheimer's & Dementia. 9: P678-P679. DOI: 10.1016/J.Jalz.2013.04.336  0.247
2013 Patsopoulos NA, Barcellos LF, Hintzen RQ, Schaefer C, van Duijn CM, Noble JA, Raj T, Gourraud PA, Stranger BE, Oksenberg J, Olsson T, Taylor BV, Sawcer S, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. Plos Genetics. 9: e1003926. PMID 24278027 DOI: 10.1371/Journal.Pgen.1003926  0.243
2017 Manolio TA, Fowler DM, Starita LM, Haendel MA, MacArthur DG, Biesecker LG, Worthey E, Chisholm RL, Green ED, Jacob HJ, McLeod HL, Roden D, Rodriguez LL, Williams MS, Cooper GM, ... ... Stranger BE, et al. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 169: 6-12. PMID 28340351 DOI: 10.1016/J.Cell.2017.03.005  0.237
2019 Stranger B, Oliva M, Gamazon E, Reverter F, Wucher V, Balliu B, Dumitrascu B, Parsana P, Payne A, Jo B, Montgomery S, Battle A, Ardlie K, Guigo R, Engelhardt B. SEX DIFFERENCES AT THE MOLECULAR LEVEL: LESSONS FROM THE HUMAN TRANSCRIPTOME European Neuropsychopharmacology. 29: S1034. DOI: 10.1016/J.Euroneuro.2018.07.028  0.233
2020 Kim-Hellmuth S, Aguet F, Oliva M, Muñoz-Aguirre M, Kasela S, Wucher V, Castel SE, Hamel AR, Viñuela A, Roberts AL, Mangul S, Wen X, Wang G, Barbeira AN, Garrido-Martín D, ... ... Stranger BE, et al. Cell type-specific genetic regulation of gene expression across human tissues. Science (New York, N.Y.). 369. PMID 32913075 DOI: 10.1126/Science.Aaz8528  0.233
2019 Hernandez W, Danahey K, Pei X, Yeo KJ, Leung E, Volchenboum SL, Ratain MJ, Meltzer DO, Stranger BE, Perera MA, O'Donnell PH. Pharmacogenomic genotypes define genetic ancestry in patients and enable population-specific genomic implementation. The Pharmacogenomics Journal. PMID 31506565 DOI: 10.1038/S41397-019-0095-Z  0.232
2014 Raj T, Rothamel K, Mostafavi S, Ye C, Lee MN, Replogle JM, Feng T, Lee M, Asinovski N, Frohlich I, Imboywa S, Von Korff A, Okada Y, Patsopoulos NA, Davis S, ... ... Stranger BE, et al. Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes. Science (New York, N.Y.). 344: 519-23. PMID 24786080 DOI: 10.1126/Science.1249547  0.231
2010 Prescott NJ, Dominy KM, Kubo M, Lewis CM, Fisher SA, Redon R, Huang N, Stranger BE, Blaszczyk K, Hudspith B, Parkes G, Hosono N, Yamazaki K, Onnie CM, Forbes A, et al. Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease. Human Molecular Genetics. 19: 1828-39. PMID 20106866 DOI: 10.1093/hmg/ddq041  0.23
2018 Khramtsova EA, Davis LK, Stranger BE. The role of sex in the genomics of human complex traits. Nature Reviews. Genetics. PMID 30581192 DOI: 10.1038/S41576-018-0083-1  0.228
2014 Gamazon ER, Stranger BE. Genomics of alternative splicing: evolution, development and pathophysiology. Human Genetics. 133: 679-87. PMID 24378600 DOI: 10.1007/s00439-013-1411-3  0.222
2020 Skol AD, Jung SC, Sokovic AM, Chen S, Fazal S, Sosina O, Borkar PP, Lin A, Sverdlov M, Cao D, Swaroop A, Bebu I, Stranger BE, Grassi MA. Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes. Elife. 9. PMID 33164750 DOI: 10.7554/eLife.59980  0.221
2015 Peters MJ, Joehanes R, Pilling LC, Schurmann C, Conneely KN, Powell J, Reinmaa E, Sutphin GL, Zhernakova A, Schramm K, Wilson YA, Kobes S, Tukiainen T, Ramos YF, ... ... Stranger BE, et al. The transcriptional landscape of age in human peripheral blood. Nature Communications. 6: 8570. PMID 26490707 DOI: 10.1038/Ncomms9570  0.221
2019 Goleva S, Khramtsova E, Martin J, Stranger B, Davis L. A STUDY OF OVER 2 MILLION INDIVIDUALS FROM THE VANDERBILT UNIVERSITY MEDICAL CENTER REVEALS SEX- AND AGE-DEPENDENT COMORBIDITY PATTERNS IN PSYCHIATRIC DISORDERS European Neuropsychopharmacology. 29: S57-S58. DOI: 10.1016/J.Euroneuro.2019.07.119  0.22
2013 Li Q, Seo JH, Stranger B, McKenna A, Pe'er I, Laframboise T, Brown M, Tyekucheva S, Freedman ML. Integrative eQTL-based analyses reveal the biology of breast cancer risk loci. Cell. 152: 633-41. PMID 23374354 DOI: 10.1016/J.Cell.2012.12.034  0.22
2017 Hungate EA, Applebaum MA, Skol AD, Vaksman Z, Diamond M, McDaniel L, Volchenboum SL, Stranger BE, Maris JM, Diskin SJ, Onel K, Cohn SL. Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma. Journal of the National Cancer Institute. 109. PMID 29117357 DOI: 10.1093/Jnci/Djx093  0.215
2014 Ye CJ, Feng T, Kwon HK, Raj T, Wilson MT, Asinovski N, McCabe C, Lee MH, Frohlich I, Paik HI, Zaitlen N, Hacohen N, Stranger B, De Jager P, Mathis D, et al. Intersection of population variation and autoimmunity genetics in human T cell activation. Science (New York, N.Y.). 345: 1254665. PMID 25214635 DOI: 10.1126/Science.1254665  0.215
2008 Johnston CM, Lovell FL, Leongamornlert DA, Stranger BE, Dermitzakis ET, Ross MT. Large-scale population study of human cell lines indicates that dosage compensation is virtually complete. Plos Genetics. 4: e9. PMID 18208332 DOI: 10.1371/journal.pgen.0040009  0.215
2007 Birney E, Stamatoyannopoulos JA, Dutta A, Guigó R, Gingeras TR, Margulies EH, Weng Z, Snyder M, Dermitzakis ET, Thurman RE, Kuehn MS, Taylor CM, Neph S, Koch CM, ... ... Stranger BE, et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 447: 799-816. PMID 17571346 DOI: 10.1038/Nature05874  0.212
2012 Zaitlen N, Pasaniuc B, Patterson N, Pollack S, Voight B, Groop L, Altshuler D, Henderson BE, Kolonel LN, Le Marchand L, Waters K, Haiman CA, Stranger BE, Dermitzakis ET, Kraft P, et al. Analysis of case-control association studies with known risk variants. Bioinformatics (Oxford, England). 28: 1729-37. PMID 22556366 DOI: 10.1093/Bioinformatics/Bts259  0.21
2013 Trynka G, Sandor C, Han B, Xu H, Stranger BE, Liu XS, Raychaudhuri S. Chromatin marks identify critical cell types for fine mapping complex trait variants Nature Genetics. 45: 124-130. PMID 23263488 DOI: 10.1038/Ng.2504  0.208
2007 Marioni JC, Thorne NP, Valsesia A, Fitzgerald T, Redon R, Fiegler H, Andrews TD, Stranger BE, Lynch AG, Dermitzakis ET, Carter NP, Tavaré S, Hurles ME. Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization. Genome Biology. 8: R228. PMID 17961237 DOI: 10.1186/Gb-2007-8-10-R228  0.202
2023 Khramtsova EA, Winham SJ, Davis LK, Stranger BE, Wilson MA. Toward a deeper understanding of gene-by-sex interaction models. Cell Genomics. 3: 100324. PMID 37228751 DOI: 10.1016/j.xgen.2023.100324  0.193
2019 Stone G, Choi A, Oliva M, Gorham J, Heydarpour M, Seidman CE, Seidman JG, Aranki SF, Body SC, Carey VJ, Raby BA, Stranger BE, Muehlschlegel JD. Sex differences in gene expression in response to ischemia in the human left ventricular myocardium. Human Molecular Genetics. PMID 30649309 DOI: 10.1093/hmg/ddz014  0.192
2013 Cui J, Stahl EA, Saevarsdottir S, Miceli C, Diogo D, Trynka G, Raj T, Mirkov MU, Canhao H, Ikari K, Terao C, Okada Y, Wedrén S, Askling J, Yamanaka H, ... ... Stranger BE, et al. Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Plos Genetics. 9: e1003394. PMID 23555300 DOI: 10.1371/Journal.Pgen.1003394  0.177
2014 Raj T, Ryan KJ, Replogle JM, Chibnik LB, Rosenkrantz L, Tang A, Rothamel K, Stranger BE, Bennett DA, Evans DA, De Jager PL, Bradshaw EM. CD33: increased inclusion of exon 2 implicates the Ig V-set domain in Alzheimer's disease susceptibility. Human Molecular Genetics. 23: 2729-36. PMID 24381305 DOI: 10.1093/Hmg/Ddt666  0.169
2019 Davis LK, Stranger BE. The new science of sex differences in neuropsychiatric traits. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 31237066 DOI: 10.1002/ajmg.b.32747  0.168
2019 Khramtsova EA, Davis LK, Stranger BE. Author Correction: The role of sex in the genomics of human complex traits. Nature Reviews. Genetics. PMID 31253947 DOI: 10.1038/S41576-019-0148-9  0.163
2017 Khramtsova EA, Stranger BE. Assocplots: a Python package for static and interactive visualization of multiple-group GWAS results. Bioinformatics (Oxford, England). 33: 432-434. PMID 28172529 DOI: 10.1093/Bioinformatics/Btw641  0.158
2016 Khramtsova EA, Stranger BE. Assocplots: a python package for static and interactive visualization of multiple-group GWAS results. Bioinformatics (Oxford, England). PMID 27742694 DOI: 10.1093/bioinformatics/btw641  0.157
2019 Gal-Oz ST, Maier B, Yoshida H, Seddu K, Elbaz N, Czysz C, Zuk O, Stranger BE, Ner-Gaon H, Shay T. ImmGen report: sexual dimorphism in the immune system transcriptome. Nature Communications. 10: 4295. PMID 31541153 DOI: 10.1038/S41467-019-12348-6  0.155
2017 Raj T, Chibnik LB, McCabe C, Wong A, Replogle JM, Yu L, Gao S, Unverzagt FW, Stranger B, Murrell J, Barnes L, Hendrie HC, Foroud T, Krichevsky A, Bennett DA, et al. Genetic architecture of age-related cognitive decline in African Americans. Neurology. Genetics. 3: e125. PMID 28078323 DOI: 10.1212/Nxg.0000000000000125  0.15
2006 Bird CP, Stranger BE, Dermitzakis ET. Functional variation and evolution of non-coding DNA. Current Opinion in Genetics & Development. 16: 559-64. PMID 17055246 DOI: 10.1016/j.gde.2006.10.003  0.143
2021 Nadel BB, Oliva M, Shou BL, Mitchell K, Ma F, Montoya DJ, Mouton A, Kim-Hellmuth S, Stranger BE, Pellegrini M, Mangul S. Systematic evaluation of transcriptomics-based deconvolution methods and references using thousands of clinical samples. Briefings in Bioinformatics. PMID 34346485 DOI: 10.1093/bib/bbab265  0.137
2016 Wang J, Gamazon ER, Pierce BL, Stranger BE, Im HK, Gibbons RD, Cox NJ, Nicolae DL, Chen LS. Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx. American Journal of Human Genetics. PMID 27040689 DOI: 10.1016/j.ajhg.2016.02.020  0.137
2019 Applebaum MA, Barr EK, Karpus J, Nie J, Zhang Z, Armstrong AE, Uppal S, Sukhanova M, Zhang W, Chlenski A, Salwen HR, Wilkinson E, Dobratic M, Grossman R, Godley LA, ... Stranger BE, et al. 5-Hydroxymethylcytosine Profiles Are Prognostic of Outcome in Neuroblastoma and Reveal Transcriptional Networks That Correlate With Tumor Phenotype. Jco Precision Oncology. 3. PMID 31179414 DOI: 10.1200/PO.18.00402  0.134
2012 Stranger BE, Björkegren J, Dolan ME, Ritchie MD. Systems and genome-wide approaches unite to provide a route to personalized medicine. Genome Medicine. 4: 29. PMID 22494390 DOI: 10.1186/Gm328  0.13
2020 Demanelis K, Jasmine F, Chen LS, Chernoff M, Tong L, Delgado D, Zhang C, Shinkle J, Sabarinathan M, Lin H, Ramirez E, Oliva M, Kim-Hellmuth S, Stranger BE, Lai TP, et al. Determinants of telomere length across human tissues. Science (New York, N.Y.). 369. PMID 32913074 DOI: 10.1126/Science.Aaz6876  0.118
2016 Applebaum MA, Vaksman Z, Lee SM, Hungate EA, Henderson TO, London WB, Pinto N, Volchenboum SL, Park JR, Naranjo A, Hero B, Pearson AD, Stranger BE, Cohn SL, Diskin SJ. Neuroblastoma survivors are at increased risk for second malignancies: A report from the International Neuroblastoma Risk Group Project. European Journal of Cancer (Oxford, England : 1990). 72: 177-185. PMID 28033528 DOI: 10.1016/J.Ejca.2016.11.022  0.112
2019 Applebaum MA, Barr EK, Karpus J, West-Szymanski DC, Oliva M, Sokol EA, Zhang S, Zhang Z, Zhang W, Chlenksi A, Salwen HR, Wilkinson E, Dobratic M, Grossman RL, Godley LA, ... Stranger BE, et al. 5-hydroxymethylcytosine profiles in circulating cell-free DNA associate with disease burden in children with neuroblastoma. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 31852832 DOI: 10.1158/1078-0432.Ccr-19-2829  0.101
2015 Tilburgs T, Crespo ÂC, van der Zwan A, Rybalov B, Raj T, Stranger B, Gardner L, Moffett A, Strominger JL. Human HLA-G+ extravillous trophoblasts: Immune-activating cells that interact with decidual leukocytes. Proceedings of the National Academy of Sciences of the United States of America. 112: 7219-24. PMID 26015573 DOI: 10.1073/Pnas.1507977112  0.091
2023 Català-Senent JF, Andreu Z, Hidalgo MR, Soler-Sáez I, Roig FJ, Yanguas-Casás N, Neva-Alejo A, López-Cerdán A, de la Iglesia-Vayá M, Stranger BE, García-García F. A deep transcriptome meta-analysis reveals sex differences in multiple sclerosis. Neurobiology of Disease. 181: 106113. PMID 37023829 DOI: 10.1016/j.nbd.2023.106113  0.073
2024 Huang Y, Shan Y, Zhang W, Printzis C, Pesce L, Maeser D, Stanhope C, Stranger BE, Huang RS. Sex differences in the molecular profile of adult diffuse glioma are shaped by IDH status and tumor microenvironment. Neuro-Oncology. PMID 39367624 DOI: 10.1093/neuonc/noae207  0.055
2022 Huang Y, Cho HJ, Stranger BE, Huang RS. Sex dimorphism in response to targeted therapy and immunotherapy in non-small cell lung cancer patients: a narrative review. Translational Lung Cancer Research. 11: 920-934. PMID 35693273 DOI: 10.21037/tlcr-21-1013  0.047
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