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Joseph Maranville

TitlePostdoctoral Fellow
InstitutionUniversity of Chicago
DepartmentMedicine
AddressChicago IL 60637
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Kurki MI, Karjalainen J, Palta P, Kristiansson K, Donner KM, Reeve MP, Laivuori H, Aavikko M, Kaunisto MA, Loukola A, Lahtela E, Mattsson H, Della Briotta Parolo P, Lehisto AA, Kanai M, Mars N, Kiiskinen T, Heyne HO, Veerapen K, Zhou W, Ruotsalainen S, Hiekkalinna T, Koskelainen S, Paajanen T, Llorens V, Gracia-Tabuenca J, Siirtola H, Reis K, Elnahas AG, Sun B, Foley CN, Alasoo K, Arvas M, Auro K, Biswas S, Bizaki-Vallaskangas A, Carpen O, Chen CY, Dada OA, Ding Z, Ehm MG, Eklund K, Finucane H, Ganna A, Ghazal A, Graham RR, Green EM, Hakanen A, Hautalahti M, Hiltunen M, Hinttala R, Hovatta I, Hu X, Huertas-Vazquez A, Huilaja L, Hunkapiller J, Jacob H, Jensen JN, Joensuu H, John S, Julkunen V, Jung M, Junttila J, Kaarniranta K, Kajanne R, Kallio L, Kaprio J, FinnGen, Kerimov N, Kettunen J, Kilpi T, Klinger K, Kosma VM, Kurra V, Laisk T, Lawless N, Liu A, Longerich S, Malarstig A, Mannermaa A, Maranville J, Matakidou A, Meretoja T, Mozaffari SV, Niemi MEK, Niemi M, Niiranen T, O Donnell CJ, Obeidat ME, Okafo G, Ollila HM, Palotie T, Partanen J, Paul DS, Pelkonen M, Pendergrass RK, Platt A, Pulford D, Punkka E, Pussinen P, Raghavan N, Rahimov F, Rajpal D, Renaud NA, Riley-Gillis B, Rodosthenous R, Saarentaus E, Salminen A, Salminen E, Salomaa V, Schleutker J, Serpi R, Shen HY, Siegel R, Silander K, Siltanen S, Soini S, Soininen H, Sul JH, Tachmazidou I, Tasanen K, Tienari P, Toppila-Salmi S, Tukiainen T, Tuomi T, Turunen JA, Ulirsch JC, Vaura F, Virolainen P, Waring J, Waterworth D, Yang R, Nelis M, Reigo A, Metspalu A, Milani L, Fox C, Havulinna AS, Perola M, Ripatti S, Jalanko A, Laitinen T, Plenge R, McCarthy M, Runz H, Daly MJ, Palotie A, Sipilä TP, Laiho P, Rämö J, Rüeger S, Lemmelä S, Pärn K, Aalto-Setälä K, Färkkilä M, Hedman ÅK, Kähönen M, Kälviäinen R, Kilpeläinen E, Kuopio T, Laukkanen J, Mägi R, Mäkelä J, Mäkitie A, Palomäki A, Petrovski S, Pitkäranta A, Esko T, Mäkelä TP. FinnGen provides genetic insights from a well-phenotyped isolated population. Nature. 2023 01; 613(7944):508-518. PMID: 36653562; PMCID: PMC9849126.
      Citations: 914     Fields:    Translation:Humans
    2. Caliskan M, Brown CD, Maranville JC. A catalog of GWAS fine-mapping efforts in autoimmune disease. Am J Hum Genet. 2021 04 01; 108(4):549-563. PMID: 33798443; PMCID: PMC8059376.
      Citations: 20     Fields:    Translation:Humans
    3. Zheng J, Haberland V, Baird D, Walker V, Haycock PC, Hurle MR, Gutteridge A, Erola P, Liu Y, Luo S, Robinson J, Richardson TG, Staley JR, Elsworth B, Burgess S, Sun BB, Danesh J, Runz H, Maranville JC, Martin HM, Yarmolinsky J, Laurin C, Holmes MV, Liu JZ, Estrada K, Santos R, McCarthy L, Waterworth D, Nelson MR, Smith GD, Butterworth AS, Hemani G, Scott RA, Gaunt TR. Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases. Nat Genet. 2020 10; 52(10):1122-1131. PMID: 32895551; PMCID: PMC7610464.
      Citations: 222     Fields:    Translation:Humans
    4. Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, Giri A, Sieber KB, Qiu C, Kirsten H, Tin A, Chu AY, Bansal N, Feitosa MF, Wang L, Chai JF, Cocca M, Gorski M, Hoppmann A, Horn K, Li M, Marten J, Nutile T, Sedaghat S, Sveinbjornsson G, Tayo BO, van der Most PJ, Xu Y, Yu Z, Gerstner L, Bakker SJL, Baptista D, Biggs ML, Boerwinkle E, Brenner H, Burkhardt R, Carroll RJ, Chee ML, Chee ML, Chen M, Cheng CY, Cook JP, Coresh J, Danesh J, de Borst MH, de Vries APJ, Degenhardt F, Dittrich K, Divers J, Ehret G, Endlich K, Felix JF, Franco OH, Franke A, Freedman BI, Freitag-Wolf S, Gansevoort RT, Giedraitis V, Grundner-Culemann F, Gudbjartsson DF, Gudnason V, Hamet P, Harris TB, Holm H, Foo VHX, Hwang SJ, Ikram MA, Ingelsson E, Jaddoe VWV, Jakobsdottir J, Josyula NS, Jung B, Khor CC, Kiess W, Kovacs P, Kramer H, Kronenberg F, Lange LA, Langefeld CD, Lee JJ, Lieb W, Lim SC, Lind L, Lindgren CM, Liu J, Loeffler M, Mahajan A, Maranville JC, McMullen B, Meitinger T, Miliku K, Mook-Kanamori DO, Mychaleckyj JC, Nauck M, Nikus K, Ning B, Noordam R, Connell JO, Olafsson I, Palmer ND, Peters A, Podgornaia AI, Poulain T, Rabelink TJ, Raffield LM, Reilly DF, Rettig R, Rheinberger M, Rice KM, Rivadeneira F, Runz H, Ryan KA, Sabanayagam C, Saum KU, Shaffer CM, Shi Y, Smith AV, Stumvoll M, Sun BB, Szymczak S, Tai ES, Tan NYQ, Taylor KD, Teren A, Tham YC, Thiery J, Thio CHL, Thomsen H, Thorsteinsdottir U, Tremblay J, van der Harst P, Verweij N, Vogelezang S, Waldenberger M, Wang C, Wilson OD, Wong C, Wong TY, Yang Q, Yasuda M, Akilesh S, Devuyst O, Edwards TL, Ho K, Morris AP, Parsa A, Pendergrass SA, Psaty BM, Rotter JI, Stefansson K, Wilson JG, Susztak K, Snieder H, Heid IM, Scholz M, Butterworth AS, Hung AM, Fuchsberger C, Noce D, Ärnlöv J, Corre T, De Grandi A, de Mutsert R, Eckardt KU, Gögele M, Hicks AA, Kähönen M, Koenig W, Körner A, Krämer BK, Lehtimäki T, Lyytikäinen LP, Mascalzoni D, Meisinger C, Müller-Nurasyid M, Ponte B, Pramstaller PP, Schöttker B, Strauch K, Tönjes A, Uitterlinden AG, Völker U, Bochud M, Böger CA, Pattaro C, Köttgen A. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nat Commun. 2019 09 11; 10(1):4130. PMID: 31511532; PMCID: PMC6739370.
      Citations: 109     Fields:    Translation:HumansAnimals
    5. Tian C, Franklin CS, Alanne-Kinnunen M, March M, Spencer CCA, Vangjeli C, Weale ME, Mattsson H, Sleiman PMA, Reilly DF, McElwee J, Maranville JC, Chatterjee AK, Bhandari A, Nguyen KH, Estrada K, Reeve MP, Hutz J, Bing N, John S, MacArthur DG, Salomaa V, Ripatti S, Hakonarson H, Daly MJ, Palotie A, Hinds DA, Donnelly P, Fox CS, Day-Williams AG, Plenge RM, Runz H, Diogo D, Kilpeläinen E. Phenome-wide association studies across large population cohorts support drug target validation. Nat Commun. 2018 10 16; 9(1):4285. PMID: 30327483; PMCID: PMC6191429.
      Citations: 80     Fields:    Translation:Humans
    6. Yao C, Chen G, Song C, Keefe J, Mendelson M, Huan T, Sun BB, Maranville JC, Wu H, Ho JE, Courchesne P, Lyass A, Larson MG, Graumann J, Johnson AD, Danesh J, Runz H, Hwang SJ, Liu C, Butterworth AS, Suhre K, Levy D, Laser A, Gieger C. Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. Nat Commun. 2018 08 15; 9(1):3268. PMID: 30111768; PMCID: PMC6093935.
      Citations: 172     Fields:    Translation:HumansCells
    7. Kariuki SN, Maranville JC, Baxter SS, Jeong C, Nakagome S, Hrusch CL, Witonsky DB, Sperling AI, Di Rienzo A. Mapping Variation in Cellular and Transcriptional Response to 1,25-Dihydroxyvitamin D3 in Peripheral Blood Mononuclear Cells. PLoS One. 2016; 11(7):e0159779. PMID: 27454520; PMCID: PMC4959717.
      Citations: 9     Fields:    Translation:HumansCells
    8. Huang C, Haritunians T, Okou DT, Cutler DJ, Zwick ME, Taylor KD, Datta LW, Maranville JC, Liu Z, Ellis S, Chopra P, Alexander JS, Baldassano RN, Cross RK, Dassopoulos T, Dhere TA, Duerr RH, Hanson JS, Hou JK, Hussain SZ, Isaacs KL, Kachelries KE, Kader H, Kappelman MD, Katz J, Kellermayer R, Kirschner BS, Kuemmerle JF, Kumar A, Kwon JH, Lazarev M, Mannon P, Moulton DE, Osuntokun BO, Patel A, Rioux JD, Rotter JI, Saeed S, Scherl EJ, Silverberg MS, Silverman A, Targan SR, Valentine JF, Wang MH, Simpson CL, Bridges SL, Kimberly RP, Rich SS, Cho JH, Rienzo AD, Kao LWH, McGovern DPB, Brant SR, Kugathasan S. Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. Gastroenterology. 2015 Nov; 149(6):1575-1586. PMID: 26278503; PMCID: PMC4685036.
      Citations: 36     Fields:    Translation:Humans
    9. Maranville JC, Cox NJ. Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits. Pharmacogenomics J. 2016 08; 16(4):388-92. PMID: 26149738; PMCID: PMC4704992.
      Citations: 38     Fields:    Translation:Humans
    10. Mihelich BL, Maranville JC, Nolley R, Peehl DM, Nonn L. Elevated serum microRNA levels associate with absence of high-grade prostate cancer in a retrospective cohort. PLoS One. 2015; 10(4):e0124245. PMID: 25874774; PMCID: PMC4396984.
      Citations: 35     Fields:    Translation:Humans
    11. Maranville JC, Nanda R, Fleming GF, Skor MN, Di Rienzo A, Conzen SD. Gene expression of peripheral blood cells reveals pathways downstream of glucocorticoid receptor antagonism and nab-paclitaxel treatment. Pharmacogenet Genomics. 2014 Sep; 24(9):451-8. PMID: 25000515; PMCID: PMC4122588.
      Citations:    Fields:    Translation:Humans
    12. Maranville JC, Micic D, Hanauer SB, Di Rienzo A, Kupfer SS. In vitro sensitivity assays and clinical response to glucocorticoids in patients with inflammatory bowel disease. J Crohns Colitis. 2014 Nov; 8(11):1539-47. PMID: 25052346; PMCID: PMC4648270.
      Citations: 7     Fields:    Translation:HumansCells
    13. Maranville JC, Di Rienzo A. Combining genetic and nongenetic biomarkers to realize the promise of pharmacogenomics for inflammatory diseases. Pharmacogenomics. 2014; 15(15):1931-40. PMID: 25495413; PMCID: PMC4291228.
      Citations: 6     Fields:    Translation:Humans
    14. Kupfer SS, Maranville JC, Baxter SS, Huang Y, Di Rienzo A. Comparison of cellular and transcriptional responses to 1,25-dihydroxyvitamin d3 and glucocorticoids in peripheral blood mononuclear cells. PLoS One. 2013; 8(10):e76643. PMID: 24116131; PMCID: PMC3792986.
      Citations: 4     Fields:    Translation:HumansCells
    15. Maranville JC, Baxter SS, Witonsky DB, Chase MA, Di Rienzo A. Genetic mapping with multiple levels of phenotypic information reveals determinants of lymphocyte glucocorticoid sensitivity. Am J Hum Genet. 2013 Oct 03; 93(4):735-43. PMID: 24055111; PMCID: PMC3791266.
      Citations: 20     Fields:    Translation:HumansCells
    16. Luca F, Maranville JC, Richards AL, Witonsky DB, Stephens M, Di Rienzo A. Genetic, functional and molecular features of glucocorticoid receptor binding. PLoS One. 2013; 8(4):e61654. PMID: 23637875; PMCID: PMC3640037.
      Citations: 12     Fields:    Translation:HumansCells
    17. Maranville JC, Luca F, Stephens M, Di Rienzo A. Mapping gene-environment interactions at regulatory polymorphisms: insights into mechanisms of phenotypic variation. Transcription. 2012 Mar-Apr; 3(2):56-62. PMID: 22414753.
      Citations: 7     Fields:    Translation:HumansAnimals
    18. Maranville JC, Baxter SS, Torres JM, Di Rienzo A. Inter-ethnic differences in lymphocyte sensitivity to glucocorticoids reflect variation in transcriptional response. Pharmacogenomics J. 2013 Apr; 13(2):121-9. PMID: 22158329; PMCID: PMC3774530.
      Citations: 20     Fields:    Translation:HumansCells
    19. Maranville JC, Luca F, Richards AL, Wen X, Witonsky DB, Baxter S, Stephens M, Di Rienzo A. Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. PLoS Genet. 2011 Jul; 7(7):e1002162. PMID: 21750684; PMCID: PMC3131293.
      Citations: 69     Fields:    Translation:HumansCells
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