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Items where Author is "Blangero, J"

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Blackburn, AN, Blondell, L, Kos, MZ, Blackburn, NB ORCID: 0000-0002-9774-1539, Peralta, JM, Stevens, PT, Lehman, DM, Blangero, J and Goring, HHH 2020 , 'Genotype phasing in pedigrees using whole-genome sequence data' , European Journal of Human Genetics, vol. 28, no. 6 , pp. 790-803 , doi: 10.1038/s41431-020-0574-3.

Blackburn, NB ORCID: 0000-0002-9774-1539, Leandro, AC, Nahvi, N, Devlin, MA, Leandro, M, Martinez Escobedo, I, Peralta Fernandez, JM, George, J, Stacy, BA, deMaar, TW, Blangero, J, Keniry, M and Curran, JE 2021 , 'Transcriptomic profiling of fibropapillomatosis in green sea turtles (Chelonia mydas) from south Texas' , Frontiers in Immunology, vol. 12 , pp. 1-16 , doi: 10.3389/fimmu.2021.630988.

Blackburn, NB, Marthick, JR, Banks, A, Charlesworth, JC ORCID: 0000-0001-6201-3518, Marsden, KA, Lowenthal, RM, Blangero, J and Dickinson, JL ORCID: 0000-0003-4621-1703 2017 , 'Evaluating a CLL susceptibility variant in ITGB2 in families with multiple sub-types of hematological malignancies' , Blood, vol. 130, no. 1 , pp. 86-88 , doi: 10.1182/blood-2017-03-774232.

Blackburn, NB ORCID: 0000-0002-9774-1539, Meikle, PJ, Peralta, JM, Kumar, S, Leandro, AC, Bellinger, MA, Giles, C, Huynh, K, Mahaney, MC, Goring, HHH, VandeBerg, JL, Williams-Blangero, S, Glahn, DC, Duggirala, R, Blangero, J, Michael, LF and Curran, JE 2021 , 'Identifying the lipidomic effects of a rare loss-of-function deletion in ANGPTL3' , Circulation. Genomic and Precision Medicine , doi: 10.1161/CIRCGEN.120.003232.

Blackburn, NB, Michael, LF, Meikle, PJ, Peralta, JM, Mosior, M, McAhren, S, Bui, HH, Bellinger, MA, Giles, C, Kumar, S, Leandro, AC, Almeida, M, Weir, JM, Mahaney, MC, Dyer, TD, Almasy, L, VandeBerg, JL, Williams-Blangero, S, Glahn, DC, Duggirala, R, Kowala, M, Blangero, J and Curran, JE 2019 , 'Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway' , Journal of Lipid Research, vol. 60, no. 9 , pp. 1630-1639 , doi: 10.1194/jlr.P094433.

Blackburn, NB ORCID: 0000-0002-9774-1539, Porto, A, Peralta, JM and Blangero, J 2018 , 'Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships' , BMC Proceedings, vol. 12, no. Suppl , pp. 129-258 , doi: 10.1186/s12919-018-0133-x.

Cadby, G, Melton, PE ORCID: 0000-0003-4026-2964, McCarthy, NS, Almeida, M, Williams-Blangero, S, Curran, JE, VandeBerg, JL, Hui, J, Beilby, J, Musk, AW, James, AL, Hung, J, Blangero, J and Moses, EK 2018 , 'Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study' , Human Genetics, vol. 137, no. 1 , pp. 45-53 , doi: 10.1007/s00439-017-1856-x.

Cadby, G, Melton, PE ORCID: 0000-0003-4026-2964, McCarthy, NS, Giles, C, Mellett, NA, Huynh, K, Hung, J, Beilby, J, Dube, M-P, Watts, GF, Blangero, J, Meikle, PJ and Moses, EK 2020 , 'Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study' , Journal of Lipid Research, vol. 61, no. 4 , pp. 537-545 , doi: 10.1194/jlr.RA119000594.

Glahn, DC, Nimgaonkar, VL, Raventos, H, Contreras, J, McIntosh, AM, Thomson, PA, Jablensky, A, McCarthy, NS, Charlesworth, JC ORCID: 0000-0001-6201-3518, Blackburn, NB, Peralta, JM, Knowles, EEM, Mathias, SR, Ament, SA, McMahon, FJ, Gur, RC, Bucan, M, Curran, JE, Almasy, L, Gur, RE and Blangero, J 2018 , 'Rediscovering the value of families for psychiatric genetics research' , Molecular Psychiatry , pp. 1-13 , doi: 10.1038/s41380-018-0073-x.

Johnson, MP, Keyho, R, Blackburn, NB, Laston, S, Kumar, S, Peralta, J, Thapa, SS, Towne, B, Subedi, J, Blangero, J and Williams-Blangero, S 2019 , 'Glycated serum protein genetics and pleiotropy with cardiometabolic risk factors' , Journal of Diabetes Research , pp. 1-9 , doi: 10.1155/2019/2310235.

McCarthy, NS, Badcock, JC, Clark, ML, Knowles, EEM, Cadby, G, Melton, PE ORCID: 0000-0003-4026-2964, Morgan, VA, Blangero, J, Moses, EK, Glahn, DC and Jablensky, A 2018 , 'Assessment of cognition and personality as potential endophenotypes in the Western Australian Family Study of Schizophrenia' , Schizophrenia Bulletin, vol. 44, no. 4 , pp. 908-921 , doi: 10.1093/schbul/sbx141.

McCarthy, NS, Melton, PE ORCID: 0000-0003-4026-2964, Ward, SV, Allan, SM, Dragovic, M, Clark, ML, Morar, B, Rubio, JP, Blangero, J, Badcock, JC, Morgan, VA, Moses, EK and Jablensky, A 2017 , 'Exome array analysis suggests an increased variant burden in families with schizophrenia' , Schizophrenia Research, vol. 185 , pp. 9-16 , doi: 10.1016/j.schres.2016.12.007.

Melton, PE ORCID: 0000-0003-4026-2964, Johnson, MP, Gokhale-Agashe, D, Rea, AJ, Ariff, A, Cadby, G, Peralta, JM, McNab, TJ, Allcock, RJn, Abraham, LJ, Blangero, J, Brennecke, SP and Moses, EK 2019 , 'Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes' , Journal of Hypertension, vol. 37, no. 5 , pp. 997-1011 , doi: 10.1097/HJH.0000000000002023.

Merino, J, Dashti, HS, Li, SX, Sarnowski, C, Justice, AE, Graff, M, Papoutsakis, C, Smith, CE, Dedoussis, GV, Lemaitre, RN, Wojczynski, MK, Mannisto, S, Ngwa, JS, Kho, M, Ahluwalia, TS, Pervjakova, N, Houston, DK, Bouchard, C, Huang, T, Orho-Melander, M, Frazier-Wood, AC, Mook-Kanamori, DO, Perusse, L, Pennell, CE, de Vries, PS, Voortman, T, Li, O, Kanoni, S, Rose, LM, Lehtimaki, T, Zhao, JH, Feitosa, MF, Luan, J, McKeown, NM, Smith, JA, Hansen, T, Eklund, N, Nalls, MA, Rankinen, T, Huang, J, Hernandez, DG, Schulz, CA, Manichaikul, A, Li-Gao, R, Vohl, MC, Wang, CA, van Rooij, FJA, Shin, J, Kalafati, IP, Day, F, Ridker, PM, Kahonen, M, Siscovick, DS, Langenberg, C, Zhao, W, Astrup, A, Knekt, P, Garcia, M, Rao, DC, Qi, Q, Ferrucci, L, Ericson, U, Blangero, J, Hofman, A, Pausova, Z, Mikkila, V, Wareham, NJ, Kardia, SLR, Pedersen, O, Jula, A, Curran, JE, Zillikens, MC, Viikari, JS, Forouhi, NG, Ordovas, JM, Lieske, JC, Rissanen, H, Uitterlinden, AG, Raitakari, OT, Kiefte-de Jong, JC, Dupuis, J, Rotter, JI, North, KE, Scott, RA, Province, MA, Perola, M, Cupples, LA, Turner, ST, Sorensen, TIA, Salomaa, V, Liu, Y, Sung, YJ, Qi, L, Bandinelli, S, Rich, SS, de Mutsert, R, Tremblay, A, Oddy, WH ORCID: 0000-0002-6119-7017, Franco, OH, Paus, T, Florez, JC, Deloukas, P, Lyytikainen, LP, Chasman, DI, Chu, AY and Tanaka, T 2018 , 'Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium' , Molecular Psychiatry, no. July , pp. 1-13 , doi: 10.1038/s41380-018-0079-4.

Peralta, JM, Blackburn, NB, Porto, A, Blangero, J and Charlesworth, J ORCID: 0000-0001-6201-3518 2018 , 'Genome-wide linkage scan for loci influencing plasma triglyceride levels' , BMC Proceedings, vol. 12, no. Suppl , pp. 1-6 , doi: 10.1186/s12919-018-0137-6.

Porto, A, Peralta, JM, Blackburn, NB ORCID: 0000-0002-9774-1539 and Blangero, J 2018 , 'Reliability of genomic predictions of complex human phenotypes' , BMC Proceedings, vol. 12, no. Suppl , pp. 157-258 , doi: 10.1186/s12919-018-0138-5.

Sonderby, IE, Gustafsson, O, Doan, NT, Hibar, DP, Martin-Brevet, S, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB ORCID: 0000-0002-9774-1539, Blangero, J, Boomsma, DI, Bralten, J, Brattbak, H-R, Brodaty, H, Brouwe, RM, Bulow, R, Calhoun, V, Caspers, S, Cavalleri, G, Chen, C-H, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dale, AM, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Donohoe, G, Draganski, B, Ehrlich, S, Espeseth, T, Fisher, SE, Franke, B, Frouin, V, Fukunaga, M, Hashimoto, R, Hehir-Kwa, JY, Heinz, A, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff, HE, Ikeda, M, Jahanshad, N, Jernigan, T, Jockwitz, C, Johansson, S, Jonsdottir, GA, Jonsson, EG, Kahn, R, Kaufmann, T, Kelly, S, Kikuchi, M, Knowles, EEM, Kolskar, KK, Kwok, JB, Le Hellard, S, Leu, C, Liu, J, Lundervold, AJ, Lundervold, A, Martin, NG, Mather, K, Mathias, SR, McCormack, M, McMahon, KL, McRae, A, Milaneschi, Y, Moreau, C, Morris, D, Mothersill, D, Muhleisen, TW, Murray, R, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, R, Paus, T, Pausova, Z, Penninx, B, Peralta, JM, Pike, B, Prieto, C, Pudas, S, Quinlan, E, Quintana, DS, Reinbold, CS, Reis Marques, T, Reymond, A, Richard, G, Rodriguez-Herreros, B, Roiz-Santianez, R, Rokicki, J, Rucker, J, Sachdev, P, Sanders, A-M, Sando, SB, Schmaal, L, Schofield, PR, Schork, AJ, Schumann, G, Shin, J, Shumskaya, E, Sisodiya, S, Steen, VM, Stein, DJ, Steinberg, S, Strike, L, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Turner, J, Ueland, T, Uhlmann, A, Ulfarsson, MO, van 't En, D, van der Meer, D, van Haren, NEM, Vaskinn, A, Vassos, E, Walters, GB, Wang, Y, Wen, W, Whelan, CD, Wittfeld, K, Wright, M, Yamamori, H, Zayats, T, Agartz, I, Westlye, LT, Jacquemont, S, Djurovic, S, Stefansson, H, Stefansson, K, Thompson, P and Andreassen, OA 2020 , 'Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia' , Molecular Psychiatry, vol. 25, no. 3 , pp. 584-602 , doi: 10.1038/s41380-018-0118-1.

van der Meer, D, Sonderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB ORCID: 0000-0002-9774-1539, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bulow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gustafsson, O, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jonsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Muhleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Burke Quinlan, E, Reinbold, CS, Marques, TR, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Uhlmann, A, Ulfarsson, MO, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefansson, H, Stefansson, K, Thompson, PM and Andreassen, OA 2020 , 'Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition' , JAMA Psychiatry, vol. 77, no. 4 , pp. 420-430 , doi: 10.1001/jamapsychiatry.2019.3779.

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