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Fredrik Vannberg - Publications

Affiliations: 
Biology Georgia Institute of Technology, Atlanta, GA 
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25 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
2018 Talundzic E, Ravishankar S, Kelly J, Patel D, Plucinski M, Schmedes S, Ljolje D, Clemons B, Madison-Antenucci S, Arguin PM, Lucchi N, Vannberg F, Udhayakumar V. A next-generation sequencing and bioinformatics protocol for Malaria drug Resistance marker Surveillance (MaRS). Antimicrobial Agents and Chemotherapy. PMID 29439965 DOI: 10.1128/Aac.02474-17  0.307
2017 Audano P, Ravishankar S, Vannberg F. Mapping-free variant calling using haplotype reconstruction from k-mer frequencies. Bioinformatics (Oxford, England). PMID 29186321 DOI: 10.1093/bioinformatics/btx753  0.672
2017 Srinivasan S, Su M, Ravishankar S, Moore J, Head P, Dixon JB, Vannberg F. TLR-exosomes exhibit distinct kinetics and effector function. Scientific Reports. 7: 41623. PMID 28290538 DOI: 10.1038/Srep41623  0.681
2016 Srinivasan S, Vannberg FO, Dixon JB. Lymphatic transport of exosomes as a rapid route of information dissemination to the lymph node. Scientific Reports. 6: 24436. PMID 27087234 DOI: 10.1038/Srep24436  0.658
2014 Audano P, Vannberg F. KAnalyze: a fast versatile pipelined k-mer toolkit. Bioinformatics (Oxford, England). 30: 2070-2. PMID 24642064 DOI: 10.1093/Bioinformatics/Btu152  0.651
2013 McLaren PJ, Coulonges C, Ripke S, van den Berg L, Buchbinder S, Carrington M, Cossarizza A, Dalmau J, Deeks SG, Delaneau O, De Luca A, Goedert JJ, Haas D, Herbeck JT, Kathiresan S, ... ... Vannberg F, et al. Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. Plos Pathogens. 9: e1003515. PMID 23935489 DOI: 10.1371/Journal.Ppat.1003515  0.343
2013 Grossman SR, Andersen KG, Shlyakhter I, Tabrizi S, Winnicki S, Yen A, Park DJ, Griesemer D, Karlsson EK, Wong SH, Cabili M, Adegbola RA, Bamezai RN, Hill AV, Vannberg FO, et al. Identifying recent adaptations in large-scale genomic data. Cell. 152: 703-13. PMID 23415221 DOI: 10.1016/J.Cell.2013.01.035  0.441
2012 Thye T, Owusu-Dabo E, Vannberg FO, van Crevel R, Curtis J, Sahiratmadja E, Balabanova Y, Ehmen C, Muntau B, Ruge G, Sievertsen J, Gyapong J, Nikolayevskyy V, Hill PC, Sirugo G, et al. Common variants at 11p13 are associated with susceptibility to tuberculosis. Nature Genetics. 44: 257-9. PMID 22306650 DOI: 10.1038/Ng.1080  0.415
2011 Vannberg FO, Chapman SJ, Hill AV. Human genetic susceptibility to intracellular pathogens. Immunological Reviews. 240: 105-16. PMID 21349089 DOI: 10.1111/j.1600-065X.2010.00996.x  0.437
2011 Fairfax BP, Davenport EE, Makino S, Hill AV, Vannberg FO, Knight JC. A common haplotype of the TNF receptor 2 gene modulates endotoxin tolerance. Journal of Immunology (Baltimore, Md. : 1950). 186: 3058-65. PMID 21282507 DOI: 10.4049/Jimmunol.1001791  0.381
2010 Chapman SJ, Khor CC, Vannberg FO, Rautanen A, Walley A, Segal S, Moore CE, Davies RJ, Day NP, Peshu N, Crook DW, Berkley JA, Williams TN, Scott JA, Hill AV. Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association study. Critical Care (London, England). 14: R227. PMID 21171993 DOI: 10.1186/cc9377  0.403
2010 Kubarenko AV, Ranjan S, Rautanen A, Mills TC, Wong S, Vannberg F, Neumaier M, Bekeredjian-Ding I, Hill AV, Ahmad-Nejad P, Weber AN. A naturally occurring variant in human TLR9, P99L, is associated with loss of CpG oligonucleotide responsiveness. The Journal of Biological Chemistry. 285: 36486-94. PMID 20843814 DOI: 10.1074/jbc.M110.117200  0.446
2010 Thye T, Vannberg FO, Wong SH, Owusu-Dabo E, Osei I, Gyapong J, Sirugo G, Sisay-Joof F, Enimil A, Chinbuah MA, Floyd S, Warndorff DK, Sichali L, Malema S, Crampin AC, et al. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. Nature Genetics. 42: 739-41. PMID 20694014 DOI: 10.1038/Ng.639  0.401
2010 Wong SH, Gochhait S, Malhotra D, Pettersson FH, Teo YY, Khor CC, Rautanen A, Chapman SJ, Mills TC, Srivastava A, Rudko A, Freidin MB, Puzyrev VP, Ali S, Aggarwal S, ... ... Vannberg FO, et al. Leprosy and the adaptation of human toll-like receptor 1. Plos Pathogens. 6: e1000979. PMID 20617178 DOI: 10.1371/Journal.Ppat.1000979  0.459
2010 Khor CC, Vannberg FO, Chapman SJ, Guo H, Wong SH, Walley AJ, Vukcevic D, Rautanen A, Mills TC, Chang KC, Kam KM, Crampin AC, Ngwira B, Leung CC, Tam CM, et al. CISH and susceptibility to infectious diseases. The New England Journal of Medicine. 362: 2092-101. PMID 20484391 DOI: 10.1056/NEJMoa0905606  0.385
2010 Wong SH, Hill AV, Vannberg FO. Genomewide association study of leprosy. The New England Journal of Medicine. 362: 1446-7; author reply. PMID 20393182 DOI: 10.1056/NEJMc1001451  0.343
2010 Wong SH, Vannberg FO, Spencer AJ, van der Weyden L, Hill AV, Wyllie DH. Comment on "CRTAM confers late-stage activation of CD8+ T cells to regulate retention within lymph node". Journal of Immunology (Baltimore, Md. : 1950). 184: 4052-3. PMID 20368284 DOI: 10.4049/jimmunol.1090017  0.35
2010 Chapman SJ, Vannberg FO, Khor CC, Rautanen A, Maskell NA, Davies CW, Moore CE, Day NP, Crook DW, Davies RJ, Hill AV. Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema. Bmc Medical Genetics. 11: 5. PMID 20078874 DOI: 10.1186/1471-2350-11-5  0.398
2010 Fairfax BP, Vannberg FO, Radhakrishnan J, Hakonarson H, Keating BJ, Hill AV, Knight JC. An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6. Human Molecular Genetics. 19: 720-30. PMID 19942621 DOI: 10.1093/Hmg/Ddp530  0.39
2008 Vannberg FO, Chapman SJ, Khor CC, Tosh K, Floyd S, Jackson-Sillah D, Crampin A, Sichali L, Bah B, Gustafson P, Aaby P, McAdam KP, Bah-Sow O, Lienhardt C, Sirugo G, et al. CD209 genetic polymorphism and tuberculosis disease. Plos One. 3: e1388. PMID 18167547 DOI: 10.1371/journal.pone.0001388  0.376
2007 Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, ... ... Vannberg F, et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nature Genetics. 39: 1329-37. PMID 17952073 DOI: 10.1038/Ng.2007.17  0.476
2007 Chapman SJ, Khor CC, Vannberg FO, Frodsham A, Walley A, Maskell NA, Davies CW, Segal S, Moore CE, Gillespie SH, Denny P, Day NP, Crook DW, Davies RJ, Hill AV. IkappaB genetic polymorphisms and invasive pneumococcal disease. American Journal of Respiratory and Critical Care Medicine. 176: 181-7. PMID 17463416 DOI: 10.1164/rccm.200702-169OC  0.386
2007 Chapman SJ, Vannberg FO, Khor CC, Segal S, Moore CE, Knox K, Day NP, Davies RJ, Crook DW, Hill AV. Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease. Molecular Immunology. 44: 3267-70. PMID 17382393 DOI: 10.1016/j.molimm.2006.04.013  0.402
2007 Khor CC, Chapman SJ, Vannberg FO, Dunne A, Murphy C, Ling EY, Frodsham AJ, Walley AJ, Kyrieleis O, Khan A, Aucan C, Segal S, Moore CE, Knox K, Campbell SJ, et al. A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis. Nature Genetics. 39: 523-8. PMID 17322885 DOI: 10.1038/ng1976  0.456
2006 Chapman SJ, Khor CC, Vannberg FO, Maskell NA, Davies CW, Hedley EL, Segal S, Moore CE, Knox K, Day NP, Gillespie SH, Crook DW, Davies RJ, Hill AV. PTPN22 and invasive bacterial disease. Nature Genetics. 38: 499-500. PMID 16642008 DOI: 10.1038/ng0506-499  0.329
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