Zobrazeno 1 - 10
of 404
pro vyhledávání: '"HIVERT MF"'
Autor:
Aris IM, Perng W, Dabelea D, Ganiban JM, Liu C, Marceau K, Robertson OC, Hockett CW, Mihalopoulos NL, Kong X, Herting MM, O'Shea TM, Jensen ET, Hivert MF, Oken E
Publikováno v:
Yearbook of Paediatric Endocrinology.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Kazmi, N, Sharp, GC, Reese, SE, Vehmeijer, FO, Lahti, J, Page, CM, Zhang, WM, Rifas-Shiman, SL, Rezwan, FI, Simpkin, AJ, Burrows, K, Richardson, TG, Ferreira, D L S, Fraser, A, Harmon, QE, Zhao, SS, Jaddoe, Vincent, Czamara, D, Binder, EB, Magnus, MC, Haberg, SE, Nystad, W, Nohr, EA, Starling, AP, Kechris, KJ, Yang, IV, DeMeo, DL, Litonjua, AA, Baccarelli, A, Oken, E, Holloway, JW, Karmaus, W, Arshad, SH, Dabelea, D, Sorensen, TIA, Laivuori, H, Raikkonen, K, Felix, Janine, London, SJ, Hivert, MF, Gaunt, TR, Lawlor, DA, Relton, CL
Publikováno v:
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings from the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Ferreira, D L S, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Haberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sorensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Hypertension, 74(2), 375-383. Lippincott Williams & Wilkins
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Santos Ferreira, D L, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Håberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sørensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns : Findings from the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Kazmi, N, Sharp, G C, Reese, S E, Vehmeijer, F O, Lahti, J, Page, C M, Zhang, W, Rifas-Shiman, S L, Rezwan, F I, Simpkin, A J, Burrows, K, Richardson, T G, Ferreira, D L S, Fraser, A, Harmon, Q E, Zhao, S, Jaddoe, V W V, Czamara, D, Binder, E B, Magnus, M C, Haberg, S E, Nystad, W, Nohr, E A, Starling, A P, Kechris, K J, Yang, I V, DeMeo, D L, Litonjua, A A, Baccarelli, A, Oken, E, Holloway, J W, Karmaus, W, Arshad, S H, Dabelea, D, Sorensen, T I A, Laivuori, H, Raikkonen, K, Felix, J F, London, S J, Hivert, M-F, Gaunt, T R, Lawlor, D A & Relton, C L 2019, ' Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium ', Hypertension, vol. 74, no. 2, pp. 375-383 . https://doi.org/10.1161/HYPERTENSIONAHA.119.12634
Hypertension, 74(2), 375-383. Lippincott Williams & Wilkins
Hypertensive disorders of pregnancy (HDP) are associated with low birth weight, shorter gestational age, and increased risk of maternal and offspring cardiovascular diseases later in life. The mechanisms involved are poorly understood, but epigenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d0f69e0963999a0ada775a2eb5de460f
http://www.scopus.com/inward/record.url?scp=85069621483&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85069621483&partnerID=8YFLogxK
Autor:
Hivert, MF, Christophi, CA, Franks, PW, Jablonski, KA, Ehrmann, DA, Kahn, SE, Horton, ES, Pollin, TI, Mather, KJ, Perreault, L, Barrett-Connor, E, Knowler, WC, Florez, JC
Publikováno v:
Hivert, MF; Christophi, CA; Franks, PW; Jablonski, KA; Ehrmann, DA; Kahn, SE; et al.(2016). Lifestyle and metformin ameliorate insulin sensitivity independently of the genetic burden of established insulin resistance variants in diabetes prevention program participants. Diabetes, 65(2), 520-526. doi: 10.2337/db15-0950. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1422z0tf
© 2016 by the American Diabetes Association.Large genome-wide association studies of glycemic traits have identified genetics variants that are associated with insulin resistance (IR) in the general population. It is unknown whether people with gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::f0d3630576f38e8a9ef70ad6649aae2b
http://www.escholarship.org/uc/item/1422z0tf
http://www.escholarship.org/uc/item/1422z0tf
Autor:
Wessel, J, Chu, AY, Willems, SM, Wang, S, Yaghootkar, H, Brody, JA, Dauriz, M, Hivert, MF, Raghavan, S, Lipovich, L, Hidalgo, B, Fox, K, Huffman, JE, An, P, Lu, Y, Rasmussen-Torvik, LJ, Grarup, N, Ehm, MG, Li, L, Baldridge, AS, Stančáková, A, Abrol, R, Besse, C, Boland, A, Bork-Jensen, J, Fornage, M, Freitag, DF, Garcia, ME, Guo, X, Hara, K, Isaacs, A, Jakobsdottir, J, Lange, LA, Layton, JC, Li, M, Hua Zhao, J, Meidtner, K, Morrison, AC, Nalls, MA, Peters, MJ, Sabater-Lleal, M, Schurmann, C, Silveira, A, Smith, AV, Southam, L, Stoiber, MH, Strawbridge, RJ, Taylor, KD, Varga, TV, Allin, KH, Amin, N, Aponte, JL, Aung, T, Barbieri, C, Bihlmeyer, NA, Boehnke, M, Bombieri, C, Bowden, DW, Burns, SM, Chen, Y, Chen, YD, Cheng, CY, Correa, A, Czajkowski, J, Dehghan, A, Ehret, GB, Eiriksdottir, G, Escher, SA, Farmaki, AE, Frånberg, M, Gambaro, G, Giulianini, F, Goddard, WA
Publikováno v:
Wessel, J; Chu, AY; Willems, SM; Wang, S; Yaghootkar, H; Brody, JA; et al.(2015). Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications, 6. doi: 10.1038/ncomms6897. UCLA: Retrieved from: http://www.escholarship.org/uc/item/8rr9g67v
© 2015 Macmillan Publishers Limited. All rights reserved. Fasting glucose and insulin are intermediate traits for type 2 diabetes. Here we explore the role of coding variation on these traits by analysis of variants on the HumanExome BeadChip in 60,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e1e08b2b78e9f8ea0f2ec1d6cbe5b83e
http://www.escholarship.org/uc/item/8rr9g67v
http://www.escholarship.org/uc/item/8rr9g67v
Autor:
Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, Boomsma DI, de Geus E, Penninx B, Willemsen G, Wright AF, Yaghootkar H, Zelenika D, Zemunik T, Zgaga L, DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Multiple Tissue Human Expression Resource (MUTHER) Consortium, Wareham NJ, McCarthy MI, Barroso I, Watanabe RM, Florez JC, Dupuis J, Meigs JB, Langenberg C, Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, Boomsma DI, de Geus E, Penninx B, Willemsen G, Wright AF, Yaghootkar H, Zelenika D, Zemunik T, Zgaga L, Multiple Tissue Human Expression Resource (MUTHER) Consortium, Wareham NJ, McCarthy MI, Barroso I, Watanabe RM, Florez JC, Dupuis J, Meigs JB, Langenberg C
Publikováno v:
Nature Genetics.
Autor:
NETTLETON JA, MCKEOWN NM, KANONI S, LEMAITRE RN, HIVERT MF, NGWA J, VAN ROOIJ, SONESTEDT E, WOJCZYNSKI MK, YE Z, TANAKA T, GARCIA M, ANDERSON JS, FOLLIS JL, DJOUSSE L, MUKAMAL K, PAPOUTSAKIS C, MOZAFFARIAN D, ZILLIKENS MC, BANDINELLI S, BENNETT AJ, BORECKI IB, FEITOSA MF, FERRUCCI L, FOROUHI NG, GROVES CJ, HALLMANS, G, HARRIS T, HOFMAN A, HOUSTON DK, HU FB, JOHANSSON I, KRITCHEVSKY SB, LANGENBERG, C, LAUNER L, LIU Y, LOOS RJ, NALLS M, ORHO MELANDER M, RENSTROM F, RICE K, RISERUS U, ROLANDSSON O, ROTTER JI, SAYLOR G, SIJBRANDS EJ, SJOGREN P, SMITH A, STEINGRÍMSDÓTTIR L, UITTERLINDEN AG, WAREHAM NJ, PROKOPENKO I, PANKOW JS, VAN, DUIJN CM, FLOREZ JC, WITTEMAN JC, MAGIC INVESTIGATORS, DUPUIS J, DEDOUSSIS GV, ORDOVAS JM, INGELSSON E, CUPPLES LA, SISCOVICK DS, FRANKS PW, MEIGS JB, PAOLISSO, Giuseppe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::851cb1ecd5cbc12863367a30ed027582
http://hdl.handle.net/11591/191046
http://hdl.handle.net/11591/191046
Autor:
Nettleton, JA, McKeown, NM, Kanoni, S, Lemaitre, RN, Hivert, MF, Ngwa, J, van Rooij, FJA, Sonestedt, E, Wojczynski, MK, Ye, Z, Tanaka, T
Publikováno v:
Diabetes Care, 33(12), 2684-2691. American Diabetes Association Inc.
OBJECTIVE - Whole-grain foods are touted for multiple health benefits including enhancing insulin sensitivity and reducing type 2 diabetes risk Recent genome-wide association studies (GWAS) have identified several single nucleotide polymorphisms (SNP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::1e3b365610acf089227431ee3a1ed52f
https://pure.eur.nl/en/publications/d536d5ea-45c8-42df-8882-64a0ec5fb1cc
https://pure.eur.nl/en/publications/d536d5ea-45c8-42df-8882-64a0ec5fb1cc
Autor:
Hivert, MF, Sullivan, LM, Shrader, P, Fox, CS, Nathan, DM, D’Agostino, RB, Wilson, PWF, Benjamin, EJ, Meigs, JB
Tumor necrosis factor alpha (TNFalpha) is a proinflammatory adipokine hypothesized to link obesity with insulin resistance. Functional studies suggest that TNFalpha acts through pathways involving adipokines and fatty acids to induce insulin resistan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8b48672809ed860a5c3e1bbeaaa4574
https://europepmc.org/articles/PMC2843788/
https://europepmc.org/articles/PMC2843788/
Autor:
Allard, C, Desgagné, V, Patenaude, J, Lacroix, M, Guillemette, L, Battista, MC, Doyon, M, Ménard, J, Ardilouze, JL, Perron, P, Bouchard, L, Hivert, MF
Publikováno v:
Epigenetics; 2015, Vol. 10 Issue 4, p342-351, 10p