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Items where Author is "Peralta, JM"

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Number of items: 10.

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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, 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.

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.

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.

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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