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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 1
1949 1
1950 3
1954 2
1966 2
1971 1
1973 1
1998 1
1999 2
2000 5
2001 5
2002 3
2003 3
2004 3
2005 5
2006 3
2007 2
2008 3
2009 11
2010 11
2011 13
2012 6
2013 7
2014 9
2015 8
2016 3
2017 2
2018 7
2019 4
2020 9
2021 5
2022 7
2023 6
2024 1

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135 results

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Page 1
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study.
BIRTH-GENE (BIG) Study Working Group; Huang T, Wang T, Zheng Y, Ellervik C, Li X, Gao M, Fang Z, Chai JF, Ahluwalia TVS, Wang Y, Voortman T, Noordam R, Frazier-Wood A, Scholz M, Sonestedt E, Akiyama M, Dorajoo R, Zhou A, Kilpeläinen TO, Kleber ME, Crozier SR, Godfrey KM, Lemaitre R, Felix JF, Shi Y, Gupta P, Khor CC, Lehtimäki T, Wang CA, Tiesler CMT, Thiering E, Standl M, Rzehak P, Marouli E, He M, Lecoeur C, Corella D, Lai CQ, Moreno LA, Pitkänen N, Boreham CA, Zhang T, Saw SM, Ridker PM, Graff M, van Rooij FJA, Uitterlinden AG, Hofman A, van Heemst D, Rosendaal FR, de Mutsert R, Burkhardt R, Schulz CA, Ericson U, Kamatani Y, Yuan JM, Power C, Hansen T, Sørensen TIA, Tjønneland A, Overvad K, Delgado G, Cooper C, Djousse L, Rivadeneira F, Jameson K, Zhao W, Liu J, Lee NR, Raitakari O, Kähönen M, Viikari J, Grote V, Langhendries JP, Koletzko B, Escribano J, Verduci E, Dedoussis G, Yu C, Tham YC, Lim B, Lim SH, Froguel P, Balkau B, Fink NR, Vinding RK, Sevelsted A, Bisgaard H, Coltell O, Dallongeville J, Gottrand F, Pahkala K, Niinikoski H, Hyppönen E, Pedersen O, März W, Inskip H, Jaddoe VWV, Dennison E, Wong TY, Sabanayagam C, Tai ES, Mohlke KL, Mackey DA, Gruszfeld D, Deloukas P… See abstract for full author list ➔ BIRTH-GENE (BIG) Study Working Group, et al. Among authors: meirhaeghe a. JAMA Netw Open. 2019 Sep 4;2(9):e1910915. doi: 10.1001/jamanetworkopen.2019.10915. JAMA Netw Open. 2019. PMID: 31539074 Free PMC article.
A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia.
Vanhoye X, Bardel C, Rimbert A, Moulin P, Rollat-Farnier PA, Muntaner M, Marmontel O, Dumont S, Charrière S, Cornélis F, Ducluzeau PH, Fonteille A, Nobecourt E, Peretti N, Schillo F, Wargny M, Cariou B, Meirhaeghe A, Di Filippo M. Vanhoye X, et al. Among authors: meirhaeghe a. Transl Res. 2023 May;255:119-127. doi: 10.1016/j.trsl.2022.12.002. Epub 2022 Dec 15. Transl Res. 2023. PMID: 36528340
Impact of genetic variation of PPARgamma in humans.
Meirhaeghe A, Amouyel P. Meirhaeghe A, et al. Mol Genet Metab. 2004 Sep-Oct;83(1-2):93-102. doi: 10.1016/j.ymgme.2004.08.014. Mol Genet Metab. 2004. PMID: 15464424 Review.
Development of a genetic risk score to predict the risk of hypertension in European adolescents from the HELENA study.
Pérez-Gimeno G, Seral-Cortes M, Sabroso-Lasa S, Esteban LM, Lurbe E, Béghin L, Gottrand F, Meirhaeghe A, Muntaner M, Kafatos A, Molnár D, Leclercq C, Widhalm K, Kersting M, Nova E, Salazar-Tortosa DF, Gonzalez-Gross M, Breidenassel C, Sinningen K, De Ruyter T, Labayen I, Rupérez AI, Bueno-Lozano G, Moreno LA. Pérez-Gimeno G, et al. Among authors: meirhaeghe a. Front Cardiovasc Med. 2023 Jun 1;10:1118919. doi: 10.3389/fcvm.2023.1118919. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37324619 Free PMC article.
Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood.
Zheng Y, Huang T, Wang T, Mei Z, Sun Z, Zhang T, Ellervik C, Chai JF, Sim X, van Dam RM, Tai ES, Koh WP, Dorajoo R, Saw SM, Sabanayagam C, Wong TY, Gupta P, Rossing P, Ahluwalia TS, Vinding RK, Bisgaard H, Bønnelykke K, Wang Y, Graff M, Voortman T, van Rooij FJA, Hofman A, van Heemst D, Noordam R, Estampador AC, Varga TV, Enzenbach C, Scholz M, Thiery J, Burkhardt R, Orho-Melander M, Schulz CA, Ericson U, Sonestedt E, Kubo M, Akiyama M, Zhou A, Kilpeläinen TO, Hansen T, Kleber ME, Delgado G, McCarthy M, Lemaitre RN, Felix JF, Jaddoe VWV, Wu Y, Mohlke KL, Lehtimäki T, Wang CA, Pennell CE, Schunkert H, Kessler T, Zeng L, Willenborg C, Peters A, Lieb W, Grote V, Rzehak P, Koletzko B, Erdmann J, Munz M, Wu T, He M, Yu C, Lecoeur C, Froguel P, Corella D, Moreno LA, Lai CQ, Pitkänen N, Boreham CA, Ridker PM, Rosendaal FR, de Mutsert R, Power C, Paternoster L, Sørensen TIA, Tjønneland A, Overvad K, Djousse L, Rivadeneira F, Lee NR, Raitakari OT, Kähönen M, Viikari J, Langhendries JP, Escribano J, Verduci E, Dedoussis G, König I, Balkau B, Coltell O, Dallongeville J, Meirhaeghe A, Amouyel P, Gottrand F, Pahkala K, Niinikoski H, Hyppönen E, März W, Mackey DA, Gruszfeld D, Tucker KL,… See abstract for full author list ➔ Zheng Y, et al. Among authors: meirhaeghe a. Eur J Epidemiol. 2020 Jul;35(7):685-697. doi: 10.1007/s10654-020-00638-z. Epub 2020 May 7. Eur J Epidemiol. 2020. PMID: 32383070 Free PMC article.
Development of a Genetic Risk Score to predict the risk of overweight and obesity in European adolescents from the HELENA study.
Seral-Cortes M, Sabroso-Lasa S, De Miguel-Etayo P, Gonzalez-Gross M, Gesteiro E, Molina-Hidalgo C, De Henauw S, Gottrand F, Mavrogianni C, Manios Y, Plada M, Widhalm K, Kafatos A, Erhardt É, Meirhaeghe A, Salazar-Tortosa D, Ruiz J, Moreno LA, Esteban LM, Labayen I. Seral-Cortes M, et al. Among authors: meirhaeghe a. Sci Rep. 2021 Feb 4;11(1):3067. doi: 10.1038/s41598-021-82712-4. Sci Rep. 2021. PMID: 33542408 Free PMC article.
PCSK9 post-transcriptional regulation: Role of a 3'UTR microRNA-binding site variant in linkage disequilibrium with c.1420G.
Decourt C, Janin A, Moindrot M, Chatron N, Nony S, Muntaner M, Dumont S, Divry E, Dauchet L, Meirhaeghe A, Marmontel O, Bardel C, Charrière S, Cariou B, Moulin P, Di Filippo M. Decourt C, et al. Among authors: meirhaeghe a. Atherosclerosis. 2020 Dec;314:63-70. doi: 10.1016/j.atherosclerosis.2020.10.010. Epub 2020 Oct 10. Atherosclerosis. 2020. PMID: 33186855
135 results