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Nature genetics. Apr 2024
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Nature. Feb 2024
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Nature genetics. May 2022
(DOI : 10.1038/s41588-022-01058-3)
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
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American journal of human genetics. Dec 2021
(DOI : 10.1016/j.ajhg.2022.06.012)
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(DOI : 10.1002/ehf2.13517)
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Nature. Sep 2020
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Nature genetics. Jul 2020
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Nature communications. Jan 2020
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Nature genetics. Jun 2019
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Nature communications. Feb 2019
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American journal of human genetics. Feb 2019
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American journal of human genetics. May 2018
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Disentangling the genetics of lean mass.
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The American Journal of Clinical Nutrition. Mar 2018
(DOI : 10.1093/ajcn/nqy272)
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Nature genetics. Mar 2018
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Nature genetics. Mar 2018
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Nature genetics. Jan 2018
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Nature genetics. Dec 2017
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Nature genetics. Nov 2017
(DOI : 10.1038/s41588-018-0334-2)
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American journal of human genetics. Oct 2017
(DOI : 10.1016/j.ajhg.2018.01.015)
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I, Ng FL, Evangelou M, Witkowska K, Tzanis E, Hellwege JN, Giri A, Velez Edwards DR, Sun YV, Cho K, Gaziano JM, Wilson PWF, Tsao PS, Kovesdy CP, Esko T, Mägi R, Milani L, Almgren P, Boutin T, Debette S, Ding J, Giulianini F, Holliday EG, Jackson AU, Li-Gao R, Lin WY, Luan J, Mangino M, Oldmeadow C, Prins BP, Qian Y, Sargurupremraj M, Shah N, Surendran P, Thériault S, Verweij N, Willems SM, Zhao JH, Amouyel P, Connell J, de Mutsert R, Doney ASF, Farrall M, Menni C, Morris AD, Noordam R, Pare G, Poulter NR, Shields DC, Stanton A, Thom S, Abecasis G, Amin N, Arking DE, Ayers KL, Barbieri CM, Batini C, Bis JC, Blake T, Bochud M, Boehnke M, Boerwinkle E, Boomsma DI, Bottinger EP, Braund PS, Brumat M, Campbell A, Campbell H, Chakravarti A, Chambers JC, Chauhan G, Ciullo M, Cocca M, Collins F, Cordell HJ, Davies G, de Borst MH, de Geus EJ, Deary IJ, Deelen J, Del Greco M F, Demirkale CY, Dörr M, Ehret GB, Elosua R, Enroth S, Erzurumluoglu AM, Ferreira T, Frånberg M, Franco OH, Gandin I, Gasparini P, Giedraitis V, Gieger C, Girotto G, Goel A, Gow AJ, Gudnason V, Guo X, Gyllensten U, Hamsten A, Harris TB, Harris SE, Hartman CA, Havulinna AS, Hicks AA, Hofer E, Hofman A, Hottenga JJ, Huffman JE, Hwang SJ, Ingelsson E, James A, Jansen R, Järvelin MR, Joehanes R, Johansson Å, Johnson AD, Joshi PK, Jousilahti P, Jukema JW, Jula A, Kähönen M, Kathiresan S, Keavney BD, Khaw KT, Knekt P, Knight J, Kolcic I, Kooner JS, Koskinen S, Kristiansson K, Kutalik Z, Laan M, Larson M, Launer LJ, Lehne B, Lehtimäki T, Liewald DCM, Lin L, Lind L, Lindgren CM, Liu Y, Loos RJF, Lopez LM, Lu Y, Lyytikäinen LP, Mahajan A, Mamasoula C, Marrugat J, Marten J, Milaneschi Y, Morgan A, Morris AP, Morrison AC, Munson PJ, Nalls MA, Nandakumar P, Nelson CP, Niiranen T, Nolte IM, Nutile T, Oldehinkel AJ, Oostra BA, O'Reilly PF, Org E, Padmanabhan S, Palmas W, Palotie A, Pattie A, Penninx BWJH, Perola M, Peters A, Polasek O, Pramstaller PP, Nguyen QT, Raitakari OT, Ren M, Rettig R, Rice K, Ridker PM, Ried JS, Riese H, Ripatti S, Robino A, Rose LM, Rotter JI, Rudan I, Ruggiero D, Saba Y, Sala CF, Salomaa V, Samani NJ, Sarin AP, Schmidt R, Schmidt H, Shrine N, Siscovick D, Smith AV, Snieder H, Sõber S, Sorice R, Starr JM, Stott DJ, Strachan DP, Strawbridge RJ, Sundström J, Swertz MA, Taylor KD, Teumer A, Tobin MD, Tomaszewski M, Toniolo D, Traglia M, Trompet S, Tuomilehto J, Tzourio C, Uitterlinden AG, Vaez A, van der Most PJ, van Duijn CM, Vergnaud AC, Verwoert GC, Vitart V, Völker U, Vollenweider P, Vuckovic D, Watkins H, Wild SH, Willemsen G, Wilson JF, Wright AF, Yao J, Zemunik T, Zhang W, Attia JR, Butterworth AS, Chasman DI, Conen D, Cucca F, Danesh J, Hayward C, Howson JMM, Laakso M, Lakatta EG, Langenberg C, Melander O, Mook-Kanamori DO, Palmer CNA, Risch L, Scott RA, Scott RJ, Sever P, Spector TD, van der Harst P, Wareham NJ, Zeggini E, Levy D, Munroe PB, Newton-Cheh C, Brown MJ, Metspalu A, Hung AM, O'Donnell CJ, Edwards TL, Psaty BM, Tzoulaki I, Barnes MR, Wain LV, Elliott P, Caulfield MJ, Million Veteran Program Million Veteran Program
Nature genetics. Oct 2017
(DOI : 10.1038/s41588-018-0205-x)
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Nature genetics. Aug 2017
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Strawbridge RJ, Silveira A, Hoed MD, Gustafsson S, Luan J, Rybin D, Dupuis J, Li-Gao R, Kavousi M, Dehghan A, Haljas K, Lahti J, Gådin JR, Bäcklund A, de Faire U, Gertow K, Giral P, Goel A, Humphries SE, Kurl S, Langenberg C, Lannfelt LL, Lind L, Lindgren CCM, Mannarino E, Mook-Kanamori DO, Morris AP, de Mutsert R, Rauramaa R, Saliba-Gustafsson P, Sennblad B, Smit AJ, Syvänen AC, Tremoli E, Veglia F, Zethelius B, Björck HM, Eriksson JG, Hofman A, Franco OH, Watkins H, Jukema JW, Florez JC, Wareham NJ, Meigs JB, Ingelsson E, Baldassarre D, Hamsten A, IMPROVE study group
Atherosclerosis. Jul 2017
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Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
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Scientific data. May 2017
(DOI : 10.1038/sdata.2017.179)
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Nature genetics. May 2017
(DOI : 10.1038/s41588-018-0084-1)
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals.
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Circulation. Cardiovascular genetics. Apr 2017
(DOI : 10.1161/CIRCGENETICS.117.001778)
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Hypertension (Dallas, Tex. : 1979). Mar 2017
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PLoS Medicine. Feb 2017
(DOI : 10.1371/journal.pmed.1002383)
Exome-wide association study of plasma lipids in >300,000 individuals.
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Nature genetics. Jan 2017
(DOI : 10.1038/ng.3977)
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
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American journal of human genetics. Nov 2016
(DOI : 10.1016/j.ajhg.2017.04.014)
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Diabetes. Nov 2016
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
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Diabetes. Oct 2016
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Nature genetics. Jul 2016
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Rare and low-frequency coding variants alter human adult height.
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Science translational medicine. Sep 2015
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Nature genetics. Jul 2015
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PLoS Medicine. Jun 2015
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Nature communications. Jun 2015
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Nature communications. Jun 2015
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Nature genetics. Dec 2013
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Nature genetics. Dec 2013
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Nature. Nov 2013
(DOI : 10.1038/nature14132)
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Nature. Nov 2013
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Gene-lifestyle interaction and type 2 diabetes: the EPIC interact case-cohort study.
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Nature genetics. Sep 2013
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Nature genetics. Jan 2012
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Low-frequency variants in HMGA1 are not associated with type 2 diabetes risk.
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Nature genetics. Apr 2011
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Nature. Apr 2010
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